Item | Value |
---|---|
geneid | 29117 |
ensemblid | ENSG00000166164.17 |
hgncid | 14310 |
symbol | BRD7 |
name | bromodomain containing 7 |
refseq_nuc | NM_013263.5 |
refseq_prot | NP_037395.2 |
ensembl_nuc | ENST00000394688.8 |
ensembl_prot | ENSP00000378180.3 |
mane_status | MANE Select |
chr | chr16 |
start | 50315957 |
end | 50368988 |
strand | - |
ver | v1.2 |
region | chr16:50315957-50368988 |
region5000 | chr16:50310957-50373988 |
regionname0 | BRD7_chr16_50315957_50368988 |
regionname5000 | BRD7_chr16_50310957_50373988 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 651 | 383 | 77 | 79 | 172 | 16 | 37 | 143 | BRD7_chr16_50310957_50373988 | BRD7 | MGKKH others(646): Show |
chr16 | 50310957 | 50373988 |
a0002 | 0/0 | 651 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | MGKKH others(646): Show |
chr16 | 50310957 | 50373988 |
a0003 | 0/0 | 651 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | MGKKH others(646): Show |
chr16 | 50310957 | 50373988 |
a0004 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | MGKKH others(646): Show |
chr16 | 50310957 | 50373988 |
a0005 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | MGKKH others(646): Show |
chr16 | 50310957 | 50373988 |
a0006 | 0/0 | 651 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | MGKKH others(646): Show |
chr16 | 50310957 | 50373988 |
a0007 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | MGKKH others(646): Show |
chr16 | 50310957 | 50373988 |
a0008 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | MGKKH others(646): Show |
chr16 | 50310957 | 50373988 |
a0009 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | MGKKH others(646): Show |
chr16 | 50310957 | 50373988 |
a0010 | 0/0 | 651 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | MGKKH others(646): Show |
chr16 | 50310957 | 50373988 |
a0011 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | MGKKH others(646): Show |
chr16 | 50310957 | 50373988 |
a0012 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | MGKKH others(646): Show |
chr16 | 50310957 | 50373988 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1953 | 288 | 64 | 71 | 106 | 13 | 33 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 | ||
a0001c0002 | 0/1 | 1953 | 95 | 13 | 8 | 66 | 3 | 4 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 | ||
a0002c0003 | 0/0 | 1953 | 6 | 6 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 | ||
a0003c0004 | 0/0 | 1953 | 4 | 4 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 | ||
a0004c0006 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 | ||
a0005c0008 | 0/0 | 1953 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 | ||
a0006c0012 | 0/0 | 1953 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 | ||
a0007c0011 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 | ||
a0008c0005 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 | ||
a0009c0007 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 | ||
a0010c0009 | 0/0 | 1953 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 | ||
a0011c0010 | 0/0 | 1953 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 | ||
a0012c0013 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | ATGGG others(1948): Show |
chr16 | 50310957 | 50373988 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5428 | 90 | 21 | 8 | 53 | 1 | 7 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0003 | 0/0 | 5424 | 70 | 2 | 21 | 31 | 5 | 11 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5419): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0004 | 0/0 | 5428 | 31 | 12 | 9 | 3 | 2 | 5 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0005 | 0/0 | 5428 | 27 | 1 | 11 | 9 | 1 | 5 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0006 | 0/0 | 5424 | 18 | 0 | 12 | 0 | 2 | 4 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5419): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0007 | 0/0 | 5432 | 9 | 6 | 1 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5427): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0009 | 0/0 | 5428 | 4 | 4 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0011 | 0/0 | 5432 | 4 | 0 | 0 | 4 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5427): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0012 | 0/0 | 5424 | 4 | 0 | 4 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5419): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0013 | 0/0 | 5428 | 4 | 4 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0014 | 1/0 | 5424 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5419): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0015 | 0/0 | 5425 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5420): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0016 | 0/0 | 5425 | 3 | 3 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5420): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0017 | 0/0 | 5423 | 3 | 0 | 2 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5418): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0020 | 0/0 | 5424 | 2 | 0 | 1 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5419): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0021 | 0/0 | 5428 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0022 | 0/0 | 5428 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0023 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0024 | 0/0 | 5410 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5405): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0025 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5419): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0027 | 0/0 | 5428 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0028 | 0/0 | 5412 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5407): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0029 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0031 | 0/0 | 5424 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5419): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0032 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5420): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0033 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0034 | 0/0 | 5419 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5414): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0035 | 0/0 | 5423 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5418): Show |
chr16 | 50310957 | 50373988 |
a0001c0001t0041 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5419): Show |
chr16 | 50310957 | 50373988 |
a0001c0002t0002 | 0/1 | 5423 | 82 | 12 | 6 | 58 | 3 | 2 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5418): Show |
chr16 | 50310957 | 50373988 |
a0001c0002t0014 | 0/0 | 5424 | 3 | 0 | 0 | 3 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5419): Show |
chr16 | 50310957 | 50373988 |
a0001c0002t0018 | 0/0 | 5419 | 3 | 1 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5414): Show |
chr16 | 50310957 | 50373988 |
a0001c0002t0019 | 0/0 | 5423 | 3 | 0 | 0 | 2 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5418): Show |
chr16 | 50310957 | 50373988 |
a0001c0002t0036 | 0/0 | 5423 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5418): Show |
chr16 | 50310957 | 50373988 |
a0001c0002t0037 | 0/0 | 5423 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5418): Show |
chr16 | 50310957 | 50373988 |
a0001c0002t0039 | 0/0 | 5423 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5418): Show |
chr16 | 50310957 | 50373988 |
a0001c0002t0040 | 0/0 | 5423 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5418): Show |
chr16 | 50310957 | 50373988 |
a0002c0003t0008 | 0/0 | 5432 | 5 | 5 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5427): Show |
chr16 | 50310957 | 50373988 |
a0002c0003t0023 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0003c0004t0010 | 0/0 | 5420 | 3 | 3 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5415): Show |
chr16 | 50310957 | 50373988 |
a0003c0004t0030 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5415): Show |
chr16 | 50310957 | 50373988 |
a0004c0006t0002 | 0/0 | 5423 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5418): Show |
chr16 | 50310957 | 50373988 |
a0005c0008t0026 | 0/0 | 5428 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0006c0012t0005 | 0/0 | 5428 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0007c0011t0038 | 0/0 | 5427 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5422): Show |
chr16 | 50310957 | 50373988 |
a0008c0005t0010 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5415): Show |
chr16 | 50310957 | 50373988 |
a0009c0007t0015 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5420): Show |
chr16 | 50310957 | 50373988 |
a0010c0009t0004 | 0/0 | 5428 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5423): Show |
chr16 | 50310957 | 50373988 |
a0011c0010t0002 | 0/0 | 5423 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5418): Show |
chr16 | 50310957 | 50373988 |
a0012c0013t0006 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | GCCCC others(5419): Show |
chr16 | 50310957 | 50373988 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0003 | 0/0 | 5 | 0 | 2 | 0 | 3 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0002 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0009g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0011g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0011g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0011g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0011g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0012g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0012g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0012g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0012g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0013g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0013g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0013g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0014g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0015g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0015g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0016g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0016g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0016g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0017g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0017g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0020g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0020g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0021g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0021g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0022g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0022g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0023g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0024g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0025g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0027g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0028g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0029g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0031g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0032g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0033g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0034g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0035g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0041g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0267 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0014g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0014g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0014g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0018g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0018g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0018g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0019g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0019g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0019g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0036g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0037g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0039g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0040g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0002c0003t0008g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0002c0003t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0002c0003t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0002c0003t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0002c0003t0023g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0003c0004t0010g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0003c0004t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0003c0004t0010g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0003c0004t0030g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0004c0006t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0005c0008t0026g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0006c0012t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0007c0011t0038g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0008c0005t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0009c0007t0015g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0010c0009t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0011c0010t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0012c0013t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0041 | g0343 | EUR | GBR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0195 | EUR | GBR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0266 | EUR | FIN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00323 | hp1 | a0001 | c0001 | t0017 | g0316 | EUR | FIN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0161 | EUR | FIN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00408 | hp1 | a0001 | c0002 | t0019 | g0294 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0134 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0312 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0338 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00621 | hp1 | a0001 | c0001 | t0011 | g0098 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0232 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00639 | hp2 | a0001 | c0001 | t0024 | g0038 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0231 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0204 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0223 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0205 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0213 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00741 | hp2 | a0001 | c0002 | t0040 | g0303 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0224 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01081 | hp1 | a0001 | c0001 | t0012 | g0225 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01099 | hp2 | a0001 | c0001 | t0012 | g0216 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01106 | hp1 | a0001 | c0001 | t0020 | g0114 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0341 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0326 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01167 | hp1 | a0001 | c0001 | t0007 | g0073 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01167 | hp2 | a0001 | c0001 | t0017 | g0032 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01168 | hp2 | a0001 | c0001 | t0012 | g0215 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01169 | hp1 | a0001 | c0001 | t0017 | g0032 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0218 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01255 | hp2 | a0001 | c0001 | t0012 | g0214 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0219 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0315 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0160 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0296 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0230 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0221 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01361 | hp1 | a0001 | c0002 | t0036 | g0299 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01433 | hp1 | a0001 | c0001 | t0006 | g0210 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0141 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0222 | EUR | IBS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0189 | EUR | IBS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0009 | EUR | IBS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0009 | EUR | IBS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01891 | hp1 | a0002 | c0003 | t0008 | g0030 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01891 | hp2 | a0004 | c0006 | t0002 | g0323 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01928 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0270 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0083 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0084 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0318 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01978 | hp2 | a0001 | c0001 | t0031 | g0209 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0290 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0337 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0314 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0071 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02056 | hp1 | a0001 | c0002 | t0018 | g0301 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0319 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0298 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0321 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02083 | hp1 | a0001 | c0002 | t0019 | g0268 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02083 | hp2 | a0001 | c0001 | t0011 | g0104 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02129 | hp1 | a0005 | c0008 | t0026 | g0081 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0274 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02145 | hp2 | a0002 | c0003 | t0008 | g0257 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02257 | hp2 | a0003 | c0004 | t0010 | g0252 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02258 | hp2 | a0001 | c0001 | t0013 | g0235 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02280 | hp1 | a0001 | c0001 | t0013 | g0029 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0076 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0212 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02300 | hp2 | a0006 | c0012 | t0005 | g0079 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02451 | hp2 | a0001 | c0001 | t0016 | g0248 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02622 | hp1 | a0003 | c0004 | t0010 | g0251 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02622 | hp2 | a0001 | c0001 | t0023 | g0256 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02630 | hp1 | a0001 | c0001 | t0013 | g0234 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02647 | hp1 | a0001 | c0001 | t0032 | g0243 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0192 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0131 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0107 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02717 | hp2 | a0001 | c0001 | t0015 | g0245 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0330 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02735 | hp1 | a0001 | c0002 | t0019 | g0262 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02809 | hp2 | a0002 | c0003 | t0023 | g0255 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02818 | hp1 | a0002 | c0003 | t0008 | g0258 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02818 | hp2 | a0003 | c0004 | t0030 | g0254 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02895 | hp1 | a0001 | c0001 | t0033 | g0249 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0029 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0075 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0132 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03098 | hp1 | a0001 | c0001 | t0021 | g0238 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0070 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0263 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0302 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03195 | hp1 | a0001 | c0001 | t0035 | g0261 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03195 | hp2 | a0001 | c0001 | t0016 | g0246 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0275 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03453 | hp2 | a0008 | c0005 | t0010 | g0250 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03486 | hp2 | a0001 | c0001 | t0021 | g0237 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0304 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0139 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03516 | hp2 | a0009 | c0007 | t0015 | g0242 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0036 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03540 | hp2 | a0002 | c0003 | t0008 | g0259 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03579 | hp2 | a0001 | c0001 | t0028 | g0233 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03654 | hp1 | a0001 | c0001 | t0006 | g0227 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0116 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03669 | hp2 | a0001 | c0001 | t0020 | g0058 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0226 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0200 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | BEB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0203 | SAS | BEB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03942 | hp1 | a0010 | c0009 | t0004 | g0202 | SAS | BEB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0271 | SAS | BEB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0201 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0149 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0129 | SAS | BEB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04184 | hp2 | a0001 | c0001 | t0006 | g0220 | SAS | BEB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0197 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0130 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04204 | hp2 | a0001 | c0001 | t0006 | g0211 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04228 | hp1 | a0001 | c0002 | t0037 | g0278 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0168 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18522 | hp1 | a0001 | c0001 | t0016 | g0247 | AFR | YRI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18522 | hp2 | a0003 | c0004 | t0010 | g0253 | AFR | YRI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0327 | EAS | CHB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18747 | hp1 | a0001 | c0001 | t0011 | g0103 | EAS | CHB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | CHB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | YRI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0015 | AFR | YRI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18947 | hp1 | a0001 | c0002 | t0014 | g0241 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18953 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0308 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0085 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18957 | hp1 | a0011 | c0010 | t0002 | g0313 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18969 | hp1 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18971 | hp2 | a0001 | c0001 | t0022 | g0096 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18973 | hp1 | a0001 | c0001 | t0025 | g0100 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18978 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0334 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0333 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0335 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18982 | hp2 | a0001 | c0001 | t0005 | g0082 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18985 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18986 | hp1 | a0001 | c0002 | t0014 | g0240 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0340 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18988 | hp2 | a0001 | c0002 | t0002 | g0283 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18990 | hp1 | a0001 | c0002 | t0018 | g0280 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18991 | hp2 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0336 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0342 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19004 | hp2 | a0001 | c0002 | t0039 | g0277 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19006 | hp2 | a0001 | c0002 | t0002 | g0331 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | LWK | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0297 | AFR | LWK | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19057 | hp2 | a0001 | c0001 | t0011 | g0099 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19059 | hp1 | a0001 | c0002 | t0002 | g0311 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19059 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0328 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19065 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0339 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19068 | hp1 | a0001 | c0001 | t0022 | g0093 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0325 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0317 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19077 | hp2 | a0001 | c0001 | t0027 | g0055 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19078 | hp1 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0310 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19082 | hp1 | a0001 | c0002 | t0014 | g0239 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0320 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | YRI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19240 | hp2 | a0012 | c0013 | t0006 | g0229 | AFR | YRI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ASW | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0120 | AFR | ASW | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0138 | EUR | TSI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0117 | EUR | TSI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0217 | EUR | TSI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | GIH | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | GIH | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01123 | hp1 | a0001 | c0001 | t0006 | g0228 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0153 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02109 | hp2 | a0001 | c0001 | t0034 | g0260 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02486 | hp1 | a0001 | c0001 | t0015 | g0244 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02559 | hp1 | a0007 | c0011 | t0038 | g0276 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02559 | hp2 | a0001 | c0001 | t0029 | g0207 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03471 | hp2 | a0002 | c0003 | t0008 | g0030 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | USA | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0322 | AFR | USA | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20300 | hp1 | a0001 | c0002 | t0018 | g0293 | AFR | USA | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0015 | AFR | USA | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | LWK | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0267 | REF | REF | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
homoSapiens | grch38p0 | a0001 | c0001 | t0014 | g0236 | REF | REF | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:50319994 | T | C | 1 | a0005 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.1793A>G | p.Gln598Arg | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 16/17 | 2007/5424 | 1793/1956 | 598/651 | chr16 | 50319994 | |||
chr16:50320389 | C | T | 1 | a0009 | 1 | HG03516.hp2 | missense_variant&splice_region_variant | MODERATE | c.1615G>A | p.Ala539Thr | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 15/17 | 1829/5424 | 1615/1956 | 539/651 | chr16 | 50320389 | |||
chr16:50323658 | C | T | 1 | a0002 | 6 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(3): Show |
missense_variant | MODERATE | c.1372G>A | p.Val458Ile | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 12/17 | 1586/5424 | 1372/1956 | 458/651 | chr16 | 50323658 | |||
chr16:50325785 | T | C | 1 | a0007 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.1294A>G | p.Thr432Ala | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/17 | 1508/5424 | 1294/1956 | 432/651 | chr16 | 50325785 | |||
chr16:50325796 | A | G | 1 | a0011 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.1283T>C | p.Leu428Ser | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/17 | 1497/5424 | 1283/1956 | 428/651 | chr16 | 50325796 | |||
chr16:50334736 | T | G | 1 | a0010 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.862A>C | p.Lys288Gln | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/17 | 1076/5424 | 862/1956 | 288/651 | chr16 | 50334736 | |||
chr16:50334759 | C | A | 2 | a0003 a0008 |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
missense_variant | MODERATE | c.839G>T | p.Gly280Val | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/17 | 1053/5424 | 839/1956 | 280/651 | chr16 | 50334759 | |||
chr16:50334837 | C | T | 1 | a0004 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.761G>A | p.Arg254Gln | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/17 | 975/5424 | 761/1956 | 254/651 | chr16 | 50334837 | |||
chr16:50340076 | T | C | 1 | a0006 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.602A>G | p.Lys201Arg | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/17 | 816/5424 | 602/1956 | 201/651 | chr16 | 50340076 | |||
chr16:50350157 | T | C | 1 | a0012 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.457A>G | p.Ser153Gly | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/17 | 671/5424 | 457/1956 | 153/651 | chr16 | 50350157 | |||
chr16:50368221 | C | T | 1 | a0008 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.127G>A | p.Gly43Arg | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/17 | 341/5424 | 127/1956 | 43/651 | chr16 | 50368221 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:50334752 | G | A | 4 | a0001c0002 a0004c0006 a0007c0011 others(1): Show |
97 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
synonymous_variant | LOW | c.846C>T | p.Ala282Ala | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/17 | 1060/5424 | 846/1956 | 282/651 | chr16 | 50334752 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:50316100 | T | G | 1 | a0001c0001t0027 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3111A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 3111 | chr16 | 50316100 | ||||||
chr16:50316101 | G | T | 1 | a0001c0001t0027 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3110C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 3110 | chr16 | 50316101 | ||||||
chr16:50316117 | T | C | 1 | a0002c0003t0008 | 5 | HG01891.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3094A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 3094 | chr16 | 50316117 | ||||||
chr16:50316299 | G | A | 22 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(19): Show |
164 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*2912C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 2912 | chr16 | 50316299 | ||||||
chr16:50316420 | G | A | 1 | a0001c0002t0036 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2791C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 2791 | chr16 | 50316420 | ||||||
chr16:50316768 | C | A | 1 | a0001c0001t0028 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2443G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 2443 | chr16 | 50316768 | ||||||
chr16:50316788 | T | C | 1 | a0001c0002t0037 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2423A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 2423 | chr16 | 50316788 | ||||||
chr16:50316972 | T | G | 7 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0024 others(4): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2239A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 2239 | chr16 | 50316972 | ||||||
chr16:50317031 | A | AAATT | 1 | a0002c0003t0008 | 5 | HG01891.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2176_*2179dupAATT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 2179 | chr16 | 50317031 | ||||||
chr16:50317040 | G | GT | 4 | a0001c0001t0015 a0001c0001t0016 a0001c0001t0032 others(1): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2170dupA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 2170 | chr16 | 50317040 | ||||||
chr16:50317063 | G | A | 2 | a0001c0001t0016 a0001c0001t0032 |
4 | HG02451.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2148C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 2148 | chr16 | 50317063 | ||||||
chr16:50317089 | T | C | 1 | a0001c0001t0013 | 4 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2122A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 2122 | chr16 | 50317089 | ||||||
chr16:50317317 | G | A | 1 | a0001c0001t0033 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1894C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 1894 | chr16 | 50317317 | ||||||
chr16:50317431 | A | G | 1 | a0001c0001t0012 | 4 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1780T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 1780 | chr16 | 50317431 | ||||||
chr16:50317533 | T | C | 6 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0028 others(3): Show |
26 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1678A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 1678 | chr16 | 50317533 | ||||||
chr16:50317635 | A | G | 3 | a0001c0001t0005 a0005c0008t0026 a0006c0012t0005 |
29 | HG00597.hp1 HG00735.hp2 HG01192.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1576T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 1576 | chr16 | 50317635 | ||||||
chr16:50317777 | TAACA | T | 1 | a0001c0002t0018 | 3 | HG02056.hp1 NA18990.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1430_*1433delTGTT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 1430 | chr16 | 50317777 | ||||||
chr16:50317845 | T | G | 3 | a0001c0001t0023 a0002c0003t0008 a0002c0003t0023 |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1366A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 1366 | chr16 | 50317845 | ||||||
chr16:50317894 | T | TAACA | 5 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0029 others(2): Show |
43 | HG00140.hp2 HG00733.hp1 HG00738.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1313_*1316dupTGTT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 1316 | chr16 | 50317894 | ||||||
chr16:50317894 | TAACA | T | 5 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0025 others(2): Show |
25 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1313_*1316delTGTT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 1313 | chr16 | 50317894 | ||||||
chr16:50317894 | TAACAAAC others(5): Show |
T | 1 | a0001c0001t0028 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1305_*1316delTGTT others(8): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 1305 | chr16 | 50317894 | ||||||
chr16:50318271 | T | C | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG02109.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*940A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 940 | chr16 | 50318271 | ||||||
chr16:50318286 | TACTA | T | 2 | a0001c0001t0017 a0001c0001t0020 |
5 | HG00323.hp1 HG01106.hp1 HG01167.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*921_*924delTAGT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 921 | chr16 | 50318286 | ||||||
chr16:50318352 | A | G | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG02109.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*859T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 859 | chr16 | 50318352 | ||||||
chr16:50318359 | T | C | 1 | a0001c0001t0022 | 2 | NA18971.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*852A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 852 | chr16 | 50318359 | ||||||
chr16:50318400 | G | GCTAT | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(17): Show |
178 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*807_*810dupATAG | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 810 | chr16 | 50318400 | ||||||
chr16:50318400 | G | GCTATCTA others(1): Show |
1 | a0001c0001t0011 | 4 | HG00621.hp1 HG02083.hp2 NA18747.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*803_*810dupATAGAT others(2): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 810 | chr16 | 50318400 | ||||||
chr16:50318400 | GCTAT | G | 3 | a0003c0004t0010 a0003c0004t0030 a0008c0005t0010 |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*807_*810delATAG | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 807 | chr16 | 50318400 | ||||||
chr16:50318630 | T | C | 1 | a0001c0001t0031 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*581A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 581 | chr16 | 50318630 | ||||||
chr16:50318716 | C | A | 1 | a0001c0002t0039 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*495G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 495 | chr16 | 50318716 | ||||||
chr16:50318860 | A | T | 2 | a0003c0004t0010 a0008c0005t0010 |
4 | HG02257.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*351T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 351 | chr16 | 50318860 | ||||||
chr16:50318965 | T | C | 1 | a0001c0001t0032 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 246 | chr16 | 50318965 | ||||||
chr16:50319033 | C | T | 1 | a0001c0001t0009 | 4 | HG02055.hp2 HG02280.hp2 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*178G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 178 | chr16 | 50319033 | ||||||
chr16:50319150 | G | C | 1 | a0001c0002t0040 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*61C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 61 | chr16 | 50319150 | ||||||
chr16:50319204 | G | C | 1 | a0001c0001t0033 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 17/17 | 7 | chr16 | 50319204 | ||||||
chr16:50368848 | G | A | 1 | a0002c0003t0008 | 5 | HG01891.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-74C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/17 | 74 | chr16 | 50368848 | ||||||
chr16:50368897 | G | C | 3 | a0001c0001t0023 a0002c0003t0008 a0002c0003t0023 |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-123C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/17 | 123 | chr16 | 50368897 | ||||||
chr16:50368899 | GGGGCGGC others(7): Show |
G | 1 | a0001c0001t0024 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-139_-126delGGCGCG others(8): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/17 | 126 | chr16 | 50368899 | ||||||
chr16:50368979 | CG | C | 13 | a0001c0001t0017 a0001c0001t0034 a0001c0001t0035 others(10): Show |
99 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(96): Show |
5_prime_UTR_variant | MODIFIER | c.-206delC | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/17 | 206 | chr16 | 50368979 | ||||||
chr16:50368981 | G | C | 1 | a0001c0001t0041 | 1 | HG00140.hp1 | 5_prime_UTR_variant | MODIFIER | c.-207C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/17 | 207 | chr16 | 50368981 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:50319349 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1901-83T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 16/16 | chr16 | 50319349 | |||||||
chr16:50319401 | C | G | 4 | a0001c0001t0004g0200 a0001c0001t0004g0203 a0001c0001t0004g0204 others(1): Show |
4 | HG00733.hp1 HG03710.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1901-135G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 16/16 | chr16 | 50319401 | |||||||
chr16:50319618 | C | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
145 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1900+269G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 16/16 | chr16 | 50319618 | |||||||
chr16:50319797 | C | T | 24 | a0001c0001t0003g0158 a0001c0001t0006g0210 a0001c0001t0006g0211 others(21): Show |
24 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1900+90G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 16/16 | chr16 | 50319797 | |||||||
chr16:50319799 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
150 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.1900+88T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 16/16 | chr16 | 50319799 | |||||||
chr16:50319838 | C | G | 3 | a0001c0002t0002g0338 a0001c0002t0002g0339 a0001c0002t0002g0340 |
3 | HG00609.hp2 NA18986.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1900+49G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 16/16 | chr16 | 50319838 | |||||||
chr16:50320128 | CAAAA | C | 76 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(73): Show |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1757-102_1757-99de others(5): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 15/16 | chr16 | 50320128 | |||||||
chr16:50320959 | T | C | 3 | a0001c0002t0002g0264 a0001c0002t0002g0265 a0001c0002t0002g0266 |
3 | HG00280.hp1 NA18961.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1501-185A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50320959 | |||||||
chr16:50320967 | A | T | 1 | a0001c0002t0002g0279 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1501-193T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50320967 | |||||||
chr16:50321096 | G | C | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1501-322C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321096 | |||||||
chr16:50321459 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1500+523G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321459 | |||||||
chr16:50321516 | G | A | 1 | a0001c0002t0002g0322 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1500+466C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321516 | |||||||
chr16:50321554 | G | A | 3 | a0001c0001t0003g0178 a0001c0001t0004g0146 a0001c0001t0004g0147 |
3 | HG02647.hp2 HG02809.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1500+428C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321554 | |||||||
chr16:50321561 | C | T | 1 | a0001c0001t0034g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1500+421G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321561 | |||||||
chr16:50321566 | C | CA | 18 | a0001c0001t0003g0182 a0001c0001t0013g0234 a0001c0001t0015g0244 others(15): Show |
18 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.1500+415dupT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321566 | |||||||
chr16:50321566 | CA | C | 103 | a0001c0001t0003g0149 a0001c0001t0003g0164 a0001c0001t0003g0168 others(100): Show |
112 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1500+415delT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321566 | |||||||
chr16:50321566 | CAA | C | 72 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(69): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.1500+414_1500+415d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321566 | |||||||
chr16:50321566 | CAAAAAAA | C | 9 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(6): Show |
9 | HG00621.hp1 HG01109.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1500+409_1500+415d others(9): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321566 | |||||||
chr16:50321566 | CAAAAAAA others(1): Show |
C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
130 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1500+408_1500+415d others(10): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321566 | |||||||
chr16:50321577 | A | G | 4 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(1): Show |
4 | HG02257.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1500+405T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321577 | |||||||
chr16:50321578 | A | G | 1 | a0003c0004t0030g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1500+404T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321578 | |||||||
chr16:50321668 | G | C | 3 | a0001c0001t0009g0015 a0001c0001t0009g0071 a0001c0001t0009g0076 |
4 | HG02055.hp2 HG02280.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1500+314C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321668 | |||||||
chr16:50321830 | G | A | 27 | a0001c0001t0003g0137 a0001c0001t0003g0140 a0001c0001t0004g0007 others(24): Show |
29 | HG00140.hp2 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1500+152C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321830 | |||||||
chr16:50321864 | C | T | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1500+118G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321864 | |||||||
chr16:50321867 | C | T | 1 | a0001c0001t0005g0116 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1500+115G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321867 | |||||||
chr16:50321904 | C | A | 1 | a0001c0001t0007g0073 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1500+78G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 13/16 | chr16 | 50321904 | |||||||
chr16:50322085 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
149 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.1444-47C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 12/16 | chr16 | 50322085 | |||||||
chr16:50322174 | C | A | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1444-136G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 12/16 | chr16 | 50322174 | |||||||
chr16:50322241 | T | G | 1 | a0001c0001t0006g0226 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1444-203A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 12/16 | chr16 | 50322241 | |||||||
chr16:50322403 | A | G | 1 | a0001c0002t0002g0337 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1444-365T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 12/16 | chr16 | 50322403 | |||||||
chr16:50322458 | G | C | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1444-420C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 12/16 | chr16 | 50322458 | |||||||
chr16:50322509 | C | T | 8 | a0001c0001t0003g0137 a0001c0001t0004g0007 a0001c0001t0004g0135 others(5): Show |
10 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1444-471G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 12/16 | chr16 | 50322509 | |||||||
chr16:50322510 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1444-472T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 12/16 | chr16 | 50322510 | |||||||
chr16:50322550 | T | C | 1 | a0001c0002t0002g0328 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1444-512A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 12/16 | chr16 | 50322550 | |||||||
chr16:50322790 | T | C | 14 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(11): Show |
15 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1444-752A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 12/16 | chr16 | 50322790 | |||||||
chr16:50323133 | A | G | 24 | a0001c0001t0003g0158 a0001c0001t0006g0210 a0001c0001t0006g0211 others(21): Show |
24 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1443+454T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 12/16 | chr16 | 50323133 | |||||||
chr16:50323222 | T | C | 1 | a0003c0004t0030g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1443+365A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 12/16 | chr16 | 50323222 | |||||||
chr16:50323899 | G | A | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1332-201C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50323899 | |||||||
chr16:50323927 | C | T | 1 | a0001c0002t0002g0290 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1332-229G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50323927 | |||||||
chr16:50323928 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1332-230C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50323928 | |||||||
chr16:50323930 | G | A | 1 | a0001c0002t0002g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1332-232C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50323930 | |||||||
chr16:50323961 | C | G | 2 | a0001c0001t0004g0196 a0001c0001t0004g0198 |
2 | NA18955.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1332-263G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50323961 | |||||||
chr16:50323983 | C | T | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1332-285G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50323983 | |||||||
chr16:50323992 | C | T | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1332-294G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50323992 | |||||||
chr16:50324169 | G | A | 2 | a0001c0002t0019g0268 a0001c0002t0019g0294 |
2 | HG00408.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1332-471C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50324169 | |||||||
chr16:50324244 | C | T | 1 | a0001c0002t0002g0269 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1332-546G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50324244 | |||||||
chr16:50324279 | G | C | 1 | a0001c0001t0006g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1332-581C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50324279 | |||||||
chr16:50324282 | T | C | 5 | a0001c0001t0013g0029 a0001c0001t0013g0234 a0001c0001t0013g0235 others(2): Show |
6 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332-584A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50324282 | |||||||
chr16:50324292 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1332-594G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50324292 | |||||||
chr16:50324748 | C | A | 1 | a0001c0002t0018g0301 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1331+1000G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50324748 | |||||||
chr16:50324840 | G | C | 1 | a0001c0001t0028g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1331+908C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50324840 | |||||||
chr16:50324878 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0088 |
4 | NA18962.hp1 NA18983.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331+870C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50324878 | |||||||
chr16:50324927 | C | T | 1 | a0001c0002t0036g0299 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1331+821G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50324927 | |||||||
chr16:50325014 | G | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
159 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.1331+734C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50325014 | |||||||
chr16:50325027 | G | A | 1 | a0006c0012t0005g0079 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1331+721C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50325027 | |||||||
chr16:50325101 | T | C | 1 | a0001c0002t0002g0302 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1331+647A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50325101 | |||||||
chr16:50325106 | A | G | 1 | a0001c0001t0011g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1331+642T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50325106 | |||||||
chr16:50325254 | A | G | 1 | a0001c0002t0002g0338 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1331+494T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50325254 | |||||||
chr16:50325527 | T | A | 4 | a0001c0001t0005g0016 a0001c0001t0005g0078 a0001c0001t0005g0082 others(1): Show |
5 | HG01975.hp1 HG02300.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1331+221A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50325527 | |||||||
chr16:50325528 | T | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
145 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1331+220A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50325528 | |||||||
chr16:50325617 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1331+131A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50325617 | |||||||
chr16:50325627 | A | G | 1 | a0001c0001t0006g0223 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1331+121T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 11/16 | chr16 | 50325627 | |||||||
chr16:50325987 | T | C | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196-104A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 10/16 | chr16 | 50325987 | |||||||
chr16:50325990 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
197 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.1196-107C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 10/16 | chr16 | 50325990 | |||||||
chr16:50326094 | C | A | 2 | a0001c0001t0013g0029 a0001c0001t0013g0234 |
3 | HG02280.hp1 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1195+190G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 10/16 | chr16 | 50326094 | |||||||
chr16:50326178 | A | T | 1 | a0001c0001t0015g0245 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1195+106T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 10/16 | chr16 | 50326178 | |||||||
chr16:50326611 | C | G | 1 | a0001c0002t0002g0342 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1088-220G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50326611 | |||||||
chr16:50326821 | G | C | 2 | a0001c0002t0002g0296 a0001c0002t0002g0315 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1088-430C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50326821 | |||||||
chr16:50326840 | G | A | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1088-449C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50326840 | |||||||
chr16:50326909 | C | T | 1 | a0001c0001t0005g0130 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1088-518G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50326909 | |||||||
chr16:50326983 | G | A | 1 | a0001c0001t0028g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1088-592C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50326983 | |||||||
chr16:50327000 | A | T | 1 | a0003c0004t0030g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1088-609T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50327000 | |||||||
chr16:50327117 | C | T | 3 | a0001c0001t0013g0029 a0001c0001t0013g0234 a0001c0001t0013g0235 |
4 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088-726G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50327117 | |||||||
chr16:50327259 | T | C | 56 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(53): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1088-868A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50327259 | |||||||
chr16:50327276 | G | C | 335 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(332): Show |
393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.1088-885C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50327276 | |||||||
chr16:50327466 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
145 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1088-1075A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50327466 | |||||||
chr16:50327773 | T | C | 1 | a0001c0001t0005g0085 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1087+896A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50327773 | |||||||
chr16:50327804 | G | A | 1 | a0001c0001t0005g0085 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1087+865C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50327804 | |||||||
chr16:50327828 | T | C | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1087+841A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50327828 | |||||||
chr16:50327859 | G | C | 2 | a0001c0001t0004g0146 a0001c0001t0004g0147 |
2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1087+810C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50327859 | |||||||
chr16:50328012 | A | AAT | 335 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(332): Show |
393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.1087+655_1087+656d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50328012 | |||||||
chr16:50328049 | T | C | 3 | a0003c0004t0010g0252 a0003c0004t0010g0253 a0008c0005t0010g0250 |
3 | HG02257.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1087+620A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50328049 | |||||||
chr16:50328145 | C | T | 1 | a0001c0001t0034g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1087+524G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50328145 | |||||||
chr16:50328226 | C | T | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087+443G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50328226 | |||||||
chr16:50328475 | T | C | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1087+194A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50328475 | |||||||
chr16:50328926 | T | C | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1012-182A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50328926 | |||||||
chr16:50328997 | T | C | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1012-253A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50328997 | |||||||
chr16:50329046 | T | A | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1012-302A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329046 | |||||||
chr16:50329153 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
145 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1012-409T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329153 | |||||||
chr16:50329244 | A | T | 1 | a0001c0002t0002g0290 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1012-500T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329244 | |||||||
chr16:50329256 | C | T | 1 | a0001c0001t0006g0223 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1012-512G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329256 | |||||||
chr16:50329613 | C | A | 1 | a0001c0002t0002g0297 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1012-869G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329613 | |||||||
chr16:50329613 | C | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(14): Show |
30 | HG01361.hp2 HG01975.hp2 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.1012-869G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329613 | |||||||
chr16:50329648 | C | T | 87 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(84): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1012-904G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329648 | |||||||
chr16:50329753 | T | C | 5 | a0001c0001t0006g0217 a0001c0001t0006g0218 a0001c0001t0006g0227 others(2): Show |
5 | HG00642.hp1 HG01123.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1012-1009A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329753 | |||||||
chr16:50329784 | G | T | 2 | a0001c0001t0003g0174 a0001c0001t0003g0176 |
2 | NA18980.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1012-1040C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329784 | |||||||
chr16:50329870 | A | G | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1012-1126T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329870 | |||||||
chr16:50329900 | C | T | 1 | a0001c0001t0032g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1012-1156G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329900 | |||||||
chr16:50329927 | C | A | 1 | a0001c0002t0002g0319 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1012-1183G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329927 | |||||||
chr16:50329975 | C | T | 4 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(1): Show |
4 | HG02257.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-1231G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50329975 | |||||||
chr16:50330014 | C | T | 13 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0155 others(10): Show |
17 | HG00639.hp2 NA18939.hp1 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.1012-1270G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330014 | |||||||
chr16:50330336 | ACT | A | 2 | a0001c0001t0003g0024 a0001c0002t0002g0330 |
3 | HG02723.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1012-1594_1012-159 others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330336 | |||||||
chr16:50330336 | ACTT | A | 136 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(133): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1012-1595_1012-159 others(7): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330336 | |||||||
chr16:50330336 | ACTTT | A | 39 | a0001c0001t0003g0023 a0001c0001t0003g0137 a0001c0001t0003g0140 others(36): Show |
42 | HG00140.hp2 HG00733.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1012-1596_1012-159 others(8): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330336 | |||||||
chr16:50330337 | C | CT | 8 | a0001c0001t0001g0011 a0001c0001t0001g0066 a0001c0001t0001g0067 others(5): Show |
8 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1012-1594dupA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330337 | |||||||
chr16:50330337 | CT | C | 42 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0090 others(39): Show |
43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1012-1594delA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330337 | |||||||
chr16:50330415 | A | G | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1012-1671T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330415 | |||||||
chr16:50330484 | G | C | 1 | a0001c0001t0034g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1012-1740C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330484 | |||||||
chr16:50330487 | A | C | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1012-1743T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330487 | |||||||
chr16:50330599 | C | G | 340 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(337): Show |
399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.1012-1855G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330599 | |||||||
chr16:50330700 | A | G | 56 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(53): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1012-1956T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330700 | |||||||
chr16:50330731 | T | TA | 8 | a0001c0001t0009g0071 a0001c0001t0015g0244 a0001c0001t0015g0245 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012-1988dupT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330731 | |||||||
chr16:50330731 | T | TAA | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1012-1989_1012-198 others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330731 | |||||||
chr16:50330789 | G | T | 1 | a0001c0001t0001g0088 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1012-2045C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330789 | |||||||
chr16:50330809 | A | G | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1012-2065T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330809 | |||||||
chr16:50330844 | G | A | 1 | a0001c0001t0004g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1012-2100C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330844 | |||||||
chr16:50330850 | T | C | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1012-2106A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330850 | |||||||
chr16:50330864 | G | A | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1012-2120C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330864 | |||||||
chr16:50330906 | A | AAT | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
152 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.1012-2164_1012-216 others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330906 | |||||||
chr16:50330940 | C | T | 1 | a0001c0001t0005g0085 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1012-2196G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330940 | |||||||
chr16:50330965 | G | T | 1 | a0001c0002t0002g0264 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1012-2221C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330965 | |||||||
chr16:50331079 | C | T | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1012-2335G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50331079 | |||||||
chr16:50331225 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
144 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1011+2349G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50331225 | |||||||
chr16:50331243 | C | T | 1 | a0001c0002t0002g0292 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1011+2331G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50331243 | |||||||
chr16:50331350 | G | C | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1011+2224C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50331350 | |||||||
chr16:50331460 | G | A | 3 | a0003c0004t0010g0252 a0003c0004t0010g0253 a0008c0005t0010g0250 |
3 | HG02257.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1011+2114C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50331460 | |||||||
chr16:50331511 | G | C | 7 | a0001c0001t0003g0155 a0001c0001t0003g0164 a0001c0001t0003g0180 others(4): Show |
7 | HG00639.hp2 NA18943.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.1011+2063C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50331511 | |||||||
chr16:50331699 | G | A | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1011+1875C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50331699 | |||||||
chr16:50331730 | T | G | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1011+1844A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50331730 | |||||||
chr16:50331914 | G | A | 87 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(84): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1011+1660C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50331914 | |||||||
chr16:50332003 | C | G | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1011+1571G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50332003 | |||||||
chr16:50332085 | A | C | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1011+1489T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50332085 | |||||||
chr16:50332092 | T | C | 4 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(1): Show |
4 | HG02257.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1011+1482A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50332092 | |||||||
chr16:50332227 | GAACTACG others(16): Show |
G | 90 | a0001c0001t0003g0149 a0001c0002t0002g0009 a0001c0002t0002g0031 others(87): Show |
98 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1011+1324_1011+134 others(27): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50332227 | |||||||
chr16:50332257 | G | A | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1011+1317C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50332257 | |||||||
chr16:50332360 | C | T | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1011+1214G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50332360 | |||||||
chr16:50332425 | T | C | 2 | a0001c0001t0003g0148 a0001c0001t0035g0261 |
2 | HG03195.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1011+1149A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50332425 | |||||||
chr16:50332637 | G | A | 3 | a0001c0001t0013g0029 a0001c0001t0013g0234 a0001c0001t0013g0235 |
4 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011+937C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50332637 | |||||||
chr16:50332833 | G | A | 1 | a0001c0001t0034g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1011+741C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50332833 | |||||||
chr16:50332847 | C | T | 1 | a0001c0002t0002g0283 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1011+727G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50332847 | |||||||
chr16:50332947 | C | A | 177 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(174): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1011+627G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50332947 | |||||||
chr16:50333116 | G | A | 1 | a0001c0001t0007g0014 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1011+458C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50333116 | |||||||
chr16:50333121 | C | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0074 a0001c0001t0001g0077 others(3): Show |
7 | HG02451.hp1 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1011+453G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50333121 | |||||||
chr16:50333150 | A | G | 340 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(337): Show |
399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.1011+424T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50333150 | |||||||
chr16:50333182 | T | A | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1011+392A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50333182 | |||||||
chr16:50333564 | G | A | 1 | a0001c0002t0018g0301 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1011+10C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50333564 | |||||||
chr16:50333722 | T | TA | 334 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(331): Show |
392 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.888-26dupT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/16 | chr16 | 50333722 | |||||||
chr16:50333779 | T | C | 8 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.888-82A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/16 | chr16 | 50333779 | |||||||
chr16:50333806 | A | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | NA18945.hp1 NA18957.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.888-109T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/16 | chr16 | 50333806 | |||||||
chr16:50333913 | T | A | 1 | a0001c0002t0002g0302 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.888-216A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/16 | chr16 | 50333913 | |||||||
chr16:50334354 | A | C | 2 | a0001c0001t0003g0156 a0001c0001t0003g0157 |
2 | HG01433.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.887+357T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/16 | chr16 | 50334354 | |||||||
chr16:50334491 | C | T | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.887+220G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/16 | chr16 | 50334491 | |||||||
chr16:50334610 | A | G | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.887+101T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/16 | chr16 | 50334610 | |||||||
chr16:50334671 | A | T | 1 | a0001c0001t0003g0167 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.887+40T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/16 | chr16 | 50334671 | |||||||
chr16:50334695 | C | T | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+16G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/16 | chr16 | 50334695 | |||||||
chr16:50334952 | GCATTTTT others(7): Show |
G | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.703-71_703-58delTG others(12): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50334952 | |||||||
chr16:50334968 | A | G | 8 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.703-73T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50334968 | |||||||
chr16:50335002 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.703-107T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50335002 | |||||||
chr16:50335143 | C | G | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.703-248G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50335143 | |||||||
chr16:50335289 | C | T | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-394G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50335289 | |||||||
chr16:50335410 | C | T | 3 | a0003c0004t0010g0252 a0003c0004t0010g0253 a0008c0005t0010g0250 |
3 | HG02257.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.703-515G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50335410 | |||||||
chr16:50335540 | G | GTTTCTCC others(7): Show |
2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.703-659_703-646dup others(14): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50335540 | |||||||
chr16:50335727 | C | T | 1 | a0001c0001t0004g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.703-832G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50335727 | |||||||
chr16:50335852 | C | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
159 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.703-957G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50335852 | |||||||
chr16:50335933 | G | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0053 others(3): Show |
7 | NA18945.hp1 NA18957.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.703-1038C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50335933 | |||||||
chr16:50335977 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
156 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.703-1082G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50335977 | |||||||
chr16:50335984 | C | A | 339 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(336): Show |
398 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(395): Show |
intron_variant | MODIFIER | c.703-1089G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50335984 | |||||||
chr16:50335997 | G | A | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.703-1102C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50335997 | |||||||
chr16:50336071 | A | C | 1 | a0001c0002t0002g0295 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.703-1176T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50336071 | |||||||
chr16:50336132 | T | C | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.703-1237A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50336132 | |||||||
chr16:50336169 | C | T | 1 | a0001c0001t0031g0209 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.703-1274G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50336169 | |||||||
chr16:50336294 | T | G | 88 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(85): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.703-1399A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50336294 | |||||||
chr16:50336377 | G | T | 1 | a0001c0001t0001g0133 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.703-1482C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50336377 | |||||||
chr16:50336487 | G | A | 55 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(52): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.703-1592C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50336487 | |||||||
chr16:50336544 | A | T | 1 | a0001c0002t0002g0290 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.703-1649T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50336544 | |||||||
chr16:50336632 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
156 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.703-1737G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50336632 | |||||||
chr16:50336713 | G | C | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.703-1818C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50336713 | |||||||
chr16:50336792 | G | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
147 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.703-1897C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50336792 | |||||||
chr16:50336840 | A | C | 1 | a0003c0004t0030g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.703-1945T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50336840 | |||||||
chr16:50336934 | T | C | 1 | a0001c0001t0005g0113 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.703-2039A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50336934 | |||||||
chr16:50337027 | C | T | 335 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(332): Show |
393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.703-2132G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337027 | |||||||
chr16:50337094 | T | C | 1 | a0001c0002t0002g0324 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.703-2199A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337094 | |||||||
chr16:50337104 | T | A | 4 | a0001c0002t0002g0034 a0001c0002t0002g0322 a0001c0002t0002g0341 others(1): Show |
5 | HG01106.hp2 HG01891.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.703-2209A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337104 | |||||||
chr16:50337134 | G | C | 1 | a0001c0001t0009g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.703-2239C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337134 | |||||||
chr16:50337236 | C | T | 4 | a0001c0001t0001g0108 a0001c0001t0007g0014 a0001c0001t0007g0070 others(1): Show |
5 | HG01167.hp1 HG03098.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-2341G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337236 | |||||||
chr16:50337256 | C | CT | 55 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(52): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.703-2362dupA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337256 | |||||||
chr16:50337256 | CT | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
266 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.703-2362delA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337256 | |||||||
chr16:50337260 | T | C | 1 | a0001c0001t0005g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.703-2365A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337260 | |||||||
chr16:50337298 | T | G | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.703-2403A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337298 | |||||||
chr16:50337307 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.703-2412G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337307 | |||||||
chr16:50337364 | G | A | 1 | a0001c0001t0035g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.703-2469C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337364 | |||||||
chr16:50337394 | G | A | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.703-2499C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337394 | |||||||
chr16:50337410 | A | G | 1 | a0001c0001t0006g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.703-2515T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337410 | |||||||
chr16:50337451 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
159 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.702+2525T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337451 | |||||||
chr16:50337552 | T | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
149 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.702+2424A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337552 | |||||||
chr16:50337699 | C | T | 88 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(85): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.702+2277G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337699 | |||||||
chr16:50337827 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
156 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.702+2149A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337827 | |||||||
chr16:50337889 | AGAC | A | 88 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(85): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.702+2084_702+2086d others(5): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337889 | |||||||
chr16:50337912 | G | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
142 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.702+2064C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337912 | |||||||
chr16:50338291 | G | C | 1 | a0001c0001t0003g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.702+1685C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338291 | |||||||
chr16:50338391 | A | G | 1 | a0012c0013t0006g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.702+1585T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338391 | |||||||
chr16:50338417 | G | C | 1 | a0001c0002t0002g0298 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.702+1559C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338417 | |||||||
chr16:50338428 | C | A | 1 | a0001c0002t0002g0326 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.702+1548G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338428 | |||||||
chr16:50338483 | A | C | 1 | a0001c0001t0005g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.702+1493T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338483 | |||||||
chr16:50338487 | A | T | 1 | a0001c0001t0005g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.702+1489T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338487 | |||||||
chr16:50338568 | A | C | 1 | a0001c0001t0021g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.702+1408T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338568 | |||||||
chr16:50338574 | G | A | 1 | a0001c0002t0002g0298 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.702+1402C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338574 | |||||||
chr16:50338646 | A | G | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+1330T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338646 | |||||||
chr16:50338686 | T | G | 1 | a0001c0001t0020g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.702+1290A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338686 | |||||||
chr16:50338767 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
147 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.702+1209C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338767 | |||||||
chr16:50338828 | G | A | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.702+1148C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338828 | |||||||
chr16:50338855 | GGTAT | G | 3 | a0001c0001t0012g0215 a0001c0001t0012g0216 a0001c0001t0012g0225 |
3 | HG01081.hp1 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.702+1117_702+1120d others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338855 | |||||||
chr16:50338906 | T | C | 1 | a0001c0001t0004g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.702+1070A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338906 | |||||||
chr16:50338917 | T | G | 1 | a0001c0001t0004g0201 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.702+1059A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338917 | |||||||
chr16:50338949 | A | C | 1 | a0002c0003t0023g0255 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.702+1027T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50338949 | |||||||
chr16:50339062 | G | A | 1 | a0003c0004t0010g0253 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.702+914C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339062 | |||||||
chr16:50339063 | C | A | 1 | a0003c0004t0010g0253 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.702+913G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339063 | |||||||
chr16:50339075 | A | G | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.702+901T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339075 | |||||||
chr16:50339361 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
156 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.702+615G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339361 | |||||||
chr16:50339424 | C | T | 1 | a0002c0003t0023g0255 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.702+552G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339424 | |||||||
chr16:50339508 | T | G | 1 | a0001c0001t0003g0194 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.702+468A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339508 | |||||||
chr16:50339620 | G | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(309): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.702+356C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339620 | |||||||
chr16:50339664 | C | T | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.702+312G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339664 | |||||||
chr16:50339667 | A | C | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.702+309T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339667 | |||||||
chr16:50339751 | G | C | 22 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(19): Show |
22 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.702+225C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339751 | |||||||
chr16:50339757 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.702+219C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339757 | |||||||
chr16:50339824 | AT | A | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+151delA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339824 | |||||||
chr16:50339873 | TAATA | T | 88 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(85): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.702+99_702+102delT others(3): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339873 | |||||||
chr16:50339929 | G | A | 3 | a0001c0002t0002g0307 a0001c0002t0002g0308 a0001c0002t0002g0320 |
3 | NA18954.hp1 NA18974.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.702+47C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50339929 | |||||||
chr16:50340268 | A | G | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-182T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50340268 | |||||||
chr16:50340288 | T | C | 1 | a0001c0002t0002g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.592-202A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50340288 | |||||||
chr16:50340306 | T | A | 5 | a0002c0003t0008g0030 a0002c0003t0008g0257 a0002c0003t0008g0258 others(2): Show |
6 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-220A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50340306 | |||||||
chr16:50340322 | C | A | 2 | a0001c0001t0017g0032 a0001c0001t0017g0316 |
3 | HG00323.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.592-236G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50340322 | |||||||
chr16:50340434 | A | AT | 4 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-349dupA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50340434 | |||||||
chr16:50340459 | T | G | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.592-373A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50340459 | |||||||
chr16:50340515 | T | A | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-429A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50340515 | |||||||
chr16:50340647 | T | C | 1 | a0001c0001t0011g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.592-561A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50340647 | |||||||
chr16:50340766 | T | G | 1 | a0001c0001t0006g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.592-680A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50340766 | |||||||
chr16:50340964 | T | A | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.592-878A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50340964 | |||||||
chr16:50341092 | G | C | 56 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(53): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.592-1006C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341092 | |||||||
chr16:50341120 | T | C | 1 | a0001c0002t0002g0279 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.592-1034A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341120 | |||||||
chr16:50341177 | T | TAC | 95 | a0001c0001t0003g0137 a0001c0001t0003g0140 a0001c0001t0003g0157 others(92): Show |
103 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.592-1093_592-1092d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341177 | |||||||
chr16:50341177 | T | TACAC | 25 | a0001c0001t0003g0149 a0001c0001t0004g0138 a0001c0001t0004g0150 others(22): Show |
27 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.592-1095_592-1092d others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341177 | |||||||
chr16:50341177 | T | TACACAC | 6 | a0001c0001t0004g0200 a0001c0001t0033g0249 a0001c0002t0002g0286 others(3): Show |
6 | HG01361.hp1 HG02895.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-1097_592-1092d others(8): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341177 | |||||||
chr16:50341177 | T | TACACACA others(3): Show |
1 | a0003c0004t0010g0251 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.592-1101_592-1092d others(12): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341177 | |||||||
chr16:50341177 | T | TACACACA others(9): Show |
1 | a0001c0001t0004g0203 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.592-1107_592-1092d others(18): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341177 | |||||||
chr16:50341177 | TAC | T | 4 | a0001c0001t0003g0179 a0001c0001t0021g0238 a0001c0001t0035g0261 others(1): Show |
4 | HG03098.hp1 HG03195.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-1093_592-1092d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341177 | |||||||
chr16:50341177 | TACAC | T | 8 | a0001c0001t0001g0124 a0001c0001t0003g0023 a0001c0001t0003g0024 others(5): Show |
10 | HG01168.hp1 HG01169.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.592-1095_592-1092d others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341177 | |||||||
chr16:50341177 | TACACACA others(5): Show |
T | 3 | a0001c0002t0002g0274 a0001c0002t0002g0275 a0007c0011t0038g0276 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.592-1103_592-1092d others(14): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341177 | |||||||
chr16:50341177 | TACACACA others(17): Show |
T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(108): Show |
141 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.592-1115_592-1092d others(26): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341177 | |||||||
chr16:50341177 | TACACACA others(19): Show |
T | 5 | a0002c0003t0008g0030 a0002c0003t0008g0257 a0002c0003t0008g0258 others(2): Show |
6 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-1117_592-1092d others(28): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341177 | |||||||
chr16:50341299 | T | A | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.592-1213A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341299 | |||||||
chr16:50341364 | G | A | 1 | a0001c0001t0021g0237 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.592-1278C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341364 | |||||||
chr16:50341374 | C | A | 16 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0154 others(13): Show |
20 | HG00423.hp1 HG00639.hp2 NA18939.hp1 others(17): Show |
intron_variant | MODIFIER | c.592-1288G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341374 | |||||||
chr16:50341406 | C | T | 1 | a0001c0002t0002g0319 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.592-1320G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341406 | |||||||
chr16:50341407 | G | A | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-1321C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341407 | |||||||
chr16:50341435 | G | GT | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
149 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.592-1350dupA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341435 | |||||||
chr16:50341555 | A | G | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.592-1469T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341555 | |||||||
chr16:50341572 | C | T | 1 | a0001c0001t0006g0219 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.592-1486G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341572 | |||||||
chr16:50341573 | G | A | 1 | a0001c0002t0002g0304 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.592-1487C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341573 | |||||||
chr16:50341580 | T | G | 1 | a0001c0001t0028g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.592-1494A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341580 | |||||||
chr16:50341642 | C | CA | 7 | a0001c0001t0034g0260 a0001c0001t0035g0261 a0003c0004t0010g0251 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.592-1557dupT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341642 | |||||||
chr16:50341642 | C | CAA | 55 | a0001c0001t0001g0097 a0001c0001t0001g0101 a0001c0001t0003g0003 others(52): Show |
66 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.592-1558_592-1557d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341642 | |||||||
chr16:50341642 | C | CAAA | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
144 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.592-1559_592-1557d others(5): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341642 | |||||||
chr16:50341642 | CA | C | 90 | a0001c0001t0017g0032 a0001c0001t0017g0316 a0001c0001t0023g0256 others(87): Show |
100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.592-1557delT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341642 | |||||||
chr16:50341927 | T | TTC | 7 | a0001c0001t0001g0047 a0001c0001t0001g0051 a0001c0001t0001g0062 others(4): Show |
7 | HG00408.hp2 HG00621.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.592-1843_592-1842d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341927 | |||||||
chr16:50341928 | T | TCA | 21 | a0001c0001t0003g0023 a0001c0001t0003g0158 a0001c0001t0003g0161 others(18): Show |
23 | HG00140.hp2 HG00323.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.592-1844_592-1843d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | T | TCACA | 28 | a0001c0001t0001g0105 a0001c0001t0003g0026 a0001c0001t0003g0172 others(25): Show |
32 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.592-1846_592-1843d others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | T | TCACACA | 41 | a0001c0001t0001g0020 a0001c0001t0001g0106 a0001c0001t0003g0149 others(38): Show |
48 | HG00408.hp1 HG01167.hp2 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.592-1848_592-1843d others(8): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | T | TCACACAC others(1): Show |
30 | a0001c0001t0001g0045 a0001c0001t0001g0068 a0001c0001t0005g0017 others(27): Show |
34 | HG00323.hp1 HG00597.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.592-1850_592-1843d others(10): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | T | TCACACAC others(3): Show |
23 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0046 others(20): Show |
29 | HG00597.hp1 HG00609.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.592-1852_592-1843d others(12): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | T | TCACACAC others(5): Show |
7 | a0001c0001t0005g0078 a0001c0001t0005g0083 a0001c0001t0005g0084 others(4): Show |
7 | HG01934.hp2 HG01952.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-1854_592-1843d others(14): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | T | TCACACAC others(7): Show |
4 | a0001c0001t0005g0117 a0001c0002t0002g0307 a0001c0002t0002g0308 others(1): Show |
4 | HG02723.hp1 NA18954.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-1856_592-1843d others(16): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | T | TCTCA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0018 others(26): Show |
43 | HG01361.hp2 HG01975.hp2 HG02055.hp2 others(40): Show |
intron_variant | MODIFIER | c.592-1843_592-1842i others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | T | TCTCACA | 21 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(18): Show |
26 | HG00544.hp1 HG01167.hp1 HG01981.hp1 others(23): Show |
intron_variant | MODIFIER | c.592-1843_592-1842i others(8): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | T | TCTCACAC others(1): Show |
10 | a0001c0001t0001g0012 a0001c0001t0001g0056 a0001c0001t0001g0057 others(7): Show |
11 | HG00642.hp2 HG01069.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.592-1843_592-1842i others(10): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | T | TCTCACAC others(3): Show |
6 | a0001c0001t0001g0021 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
7 | HG01109.hp1 HG02886.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.592-1843_592-1842i others(12): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | T | TCTCACAC others(5): Show |
1 | a0001c0001t0001g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.592-1843_592-1842i others(14): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | TCA | T | 17 | a0001c0001t0003g0148 a0001c0001t0003g0156 a0001c0001t0003g0157 others(14): Show |
17 | HG00639.hp1 HG00642.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.592-1844_592-1843d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | TCACA | T | 30 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0154 others(27): Show |
34 | HG00423.hp1 HG00639.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.592-1846_592-1843d others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | TCACACA | T | 3 | a0001c0001t0006g0210 a0001c0001t0006g0218 a0001c0001t0033g0249 |
3 | HG01175.hp1 HG01433.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.592-1848_592-1843d others(8): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | TCACACAC others(1): Show |
T | 4 | a0001c0001t0016g0246 a0001c0001t0016g0247 a0001c0001t0016g0248 others(1): Show |
4 | HG02451.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-1850_592-1843d others(10): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | TCACACAC others(7): Show |
T | 1 | a0001c0001t0028g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.592-1856_592-1843d others(16): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341928 | TCACACAC others(11): Show |
T | 3 | a0001c0001t0007g0075 a0001c0001t0007g0107 a0001c0001t0007g0120 |
3 | HG02717.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.592-1860_592-1843d others(20): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341928 | |||||||
chr16:50341930 | A | T | 5 | a0001c0001t0001g0050 a0001c0001t0001g0086 a0001c0001t0001g0090 others(2): Show |
5 | HG02280.hp2 HG02602.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-1844T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341930 | |||||||
chr16:50341948 | A | T | 3 | a0001c0001t0007g0075 a0001c0001t0007g0107 a0001c0001t0007g0120 |
3 | HG02717.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.592-1862T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341948 | |||||||
chr16:50341969 | T | C | 4 | a0001c0001t0005g0129 a0001c0001t0005g0130 a0001c0001t0005g0131 others(1): Show |
4 | HG02683.hp2 HG03017.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-1883A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341969 | |||||||
chr16:50342016 | T | C | 1 | a0001c0001t0006g0212 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.592-1930A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342016 | |||||||
chr16:50342044 | C | T | 88 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(85): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.592-1958G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342044 | |||||||
chr16:50342455 | C | CT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
198 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(195): Show |
intron_variant | MODIFIER | c.592-2370dupA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342455 | |||||||
chr16:50342455 | C | CTT | 140 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0061 others(137): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.592-2371_592-2370d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342455 | |||||||
chr16:50342455 | C | CTTT | 31 | a0001c0001t0003g0148 a0001c0001t0003g0154 a0001c0001t0003g0165 others(28): Show |
32 | HG01074.hp1 HG01891.hp2 HG02027.hp2 others(29): Show |
intron_variant | MODIFIER | c.592-2372_592-2370d others(5): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342455 | |||||||
chr16:50342497 | C | T | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-2411G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342497 | |||||||
chr16:50342519 | C | T | 1 | a0003c0004t0030g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.592-2433G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342519 | |||||||
chr16:50342521 | C | T | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.592-2435G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342521 | |||||||
chr16:50342531 | C | T | 1 | a0001c0001t0028g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.592-2445G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342531 | |||||||
chr16:50342574 | C | G | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-2488G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342574 | |||||||
chr16:50342586 | A | G | 7 | a0001c0001t0006g0210 a0001c0001t0006g0212 a0001c0001t0006g0219 others(4): Show |
7 | HG00639.hp1 HG00735.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.592-2500T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342586 | |||||||
chr16:50342604 | G | A | 1 | a0001c0001t0003g0156 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.592-2518C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342604 | |||||||
chr16:50342673 | G | C | 2 | a0001c0001t0007g0075 a0001c0001t0007g0120 |
2 | HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.592-2587C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342673 | |||||||
chr16:50342680 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.592-2594C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342680 | |||||||
chr16:50342873 | C | T | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-2787G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342873 | |||||||
chr16:50342885 | T | C | 88 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(85): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.592-2799A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50342885 | |||||||
chr16:50343052 | T | C | 1 | a0001c0001t0028g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.592-2966A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343052 | |||||||
chr16:50343119 | T | G | 1 | a0001c0002t0002g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.592-3033A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343119 | |||||||
chr16:50343219 | C | T | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-3133G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343219 | |||||||
chr16:50343436 | G | C | 91 | a0001c0001t0017g0032 a0001c0001t0017g0316 a0001c0002t0002g0009 others(88): Show |
100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.592-3350C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343436 | |||||||
chr16:50343510 | A | C | 1 | a0001c0001t0017g0032 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.592-3424T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343510 | |||||||
chr16:50343579 | A | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0178 a0001c0001t0003g0179 |
6 | NA18939.hp1 NA18955.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-3493T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343579 | |||||||
chr16:50343640 | G | A | 4 | a0001c0001t0006g0217 a0001c0001t0006g0218 a0001c0001t0006g0228 others(1): Show |
4 | HG00642.hp1 HG01123.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-3554C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343640 | |||||||
chr16:50343759 | C | T | 1 | a0003c0004t0030g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.592-3673G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343759 | |||||||
chr16:50343821 | A | T | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-3735T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343821 | |||||||
chr16:50343918 | T | C | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-3832A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343918 | |||||||
chr16:50343920 | C | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
142 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.592-3834G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343920 | |||||||
chr16:50343972 | A | G | 335 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(332): Show |
393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.592-3886T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343972 | |||||||
chr16:50343985 | C | T | 1 | a0001c0002t0002g0036 | 2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.592-3899G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50343985 | |||||||
chr16:50344140 | C | CCAGA | 335 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(332): Show |
393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.592-4055_592-4054i others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50344140 | |||||||
chr16:50344202 | C | T | 1 | a0003c0004t0030g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.592-4116G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50344202 | |||||||
chr16:50344286 | C | G | 335 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(332): Show |
393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.592-4200G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50344286 | |||||||
chr16:50344302 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.592-4216G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50344302 | |||||||
chr16:50344455 | T | C | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-4369A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50344455 | |||||||
chr16:50344596 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
142 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.592-4510A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50344596 | |||||||
chr16:50344671 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
142 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.592-4585A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50344671 | |||||||
chr16:50344745 | C | T | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.592-4659G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50344745 | |||||||
chr16:50344783 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0088 |
4 | NA18962.hp1 NA18983.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-4697T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50344783 | |||||||
chr16:50344924 | A | T | 1 | a0001c0002t0002g0334 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.592-4838T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50344924 | |||||||
chr16:50344980 | T | G | 1 | a0001c0002t0002g0279 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.592-4894A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50344980 | |||||||
chr16:50345084 | A | G | 1 | a0001c0001t0005g0078 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.591+4939T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50345084 | |||||||
chr16:50345144 | C | G | 1 | a0001c0001t0004g0196 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.591+4879G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50345144 | |||||||
chr16:50345164 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.591+4859T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50345164 | |||||||
chr16:50345236 | C | T | 89 | a0001c0002t0002g0009 a0001c0002t0002g0031 a0001c0002t0002g0033 others(86): Show |
97 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.591+4787G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50345236 | |||||||
chr16:50345386 | T | A | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.591+4637A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50345386 | |||||||
chr16:50345471 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
159 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.591+4552T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50345471 | |||||||
chr16:50345530 | T | C | 1 | a0001c0002t0002g0312 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.591+4493A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50345530 | |||||||
chr16:50345807 | C | T | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.591+4216G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50345807 | |||||||
chr16:50345808 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.591+4215C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50345808 | |||||||
chr16:50345857 | CG | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
152 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.591+4165delC | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50345857 | |||||||
chr16:50345860 | C | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
152 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.591+4163G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50345860 | |||||||
chr16:50346245 | G | A | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.591+3778C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50346245 | |||||||
chr16:50346267 | G | C | 1 | a0001c0001t0005g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.591+3756C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50346267 | |||||||
chr16:50346475 | T | C | 1 | a0001c0001t0003g0161 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.591+3548A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50346475 | |||||||
chr16:50346518 | C | T | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.591+3505G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50346518 | |||||||
chr16:50346724 | C | T | 1 | a0001c0001t0004g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.591+3299G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50346724 | |||||||
chr16:50346828 | G | T | 33 | a0001c0001t0003g0137 a0001c0001t0003g0140 a0001c0001t0003g0161 others(30): Show |
36 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.591+3195C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50346828 | |||||||
chr16:50347011 | A | G | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.591+3012T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50347011 | |||||||
chr16:50347063 | C | T | 7 | a0001c0001t0021g0238 a0001c0001t0023g0256 a0002c0003t0008g0030 others(4): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+2960G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50347063 | |||||||
chr16:50347144 | A | G | 1 | a0001c0001t0003g0188 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.591+2879T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50347144 | |||||||
chr16:50347187 | A | G | 7 | a0001c0001t0021g0238 a0001c0001t0023g0256 a0002c0003t0008g0030 others(4): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+2836T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50347187 | |||||||
chr16:50347238 | C | T | 1 | a0001c0001t0004g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.591+2785G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50347238 | |||||||
chr16:50347362 | A | C | 1 | a0001c0001t0009g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.591+2661T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50347362 | |||||||
chr16:50347469 | T | G | 1 | a0001c0001t0003g0177 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.591+2554A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50347469 | |||||||
chr16:50347485 | T | C | 5 | a0001c0002t0002g0033 a0001c0002t0002g0310 a0001c0002t0002g0311 others(2): Show |
6 | HG00609.hp1 NA18957.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+2538A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50347485 | |||||||
chr16:50347515 | C | T | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+2508G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50347515 | |||||||
chr16:50347516 | G | A | 87 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(84): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.591+2507C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50347516 | |||||||
chr16:50347916 | A | T | 14 | a0001c0001t0001g0018 a0001c0001t0001g0089 a0001c0001t0001g0090 others(11): Show |
16 | NA18939.hp2 NA18951.hp2 NA18971.hp2 others(13): Show |
intron_variant | MODIFIER | c.591+2107T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50347916 | |||||||
chr16:50347995 | A | C | 1 | a0001c0001t0004g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.591+2028T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50347995 | |||||||
chr16:50348027 | T | C | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.591+1996A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50348027 | |||||||
chr16:50348102 | T | C | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.591+1921A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50348102 | |||||||
chr16:50348415 | T | C | 1 | a0001c0001t0003g0191 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.591+1608A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50348415 | |||||||
chr16:50348496 | T | A | 1 | a0001c0002t0002g0337 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.591+1527A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50348496 | |||||||
chr16:50348619 | C | A | 1 | a0003c0004t0030g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.591+1404G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50348619 | |||||||
chr16:50348648 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
142 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.591+1375G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50348648 | |||||||
chr16:50348664 | C | A | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+1359G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50348664 | |||||||
chr16:50348674 | A | C | 340 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(337): Show |
399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.591+1349T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50348674 | |||||||
chr16:50348675 | G | A | 8 | a0001c0001t0001g0106 a0001c0001t0015g0244 a0001c0001t0015g0245 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.591+1348C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50348675 | |||||||
chr16:50348730 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.591+1293G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50348730 | |||||||
chr16:50348954 | C | T | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.591+1069G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50348954 | |||||||
chr16:50348985 | A | G | 1 | a0001c0002t0002g0322 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.591+1038T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50348985 | |||||||
chr16:50349018 | G | A | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.591+1005C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349018 | |||||||
chr16:50349094 | T | C | 1 | a0001c0001t0004g0205 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.591+929A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349094 | |||||||
chr16:50349166 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
156 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.591+857G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349166 | |||||||
chr16:50349199 | G | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+824C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349199 | |||||||
chr16:50349234 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.591+789G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349234 | |||||||
chr16:50349257 | C | T | 340 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(337): Show |
399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.591+766G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349257 | |||||||
chr16:50349323 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.591+700G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349323 | |||||||
chr16:50349342 | A | G | 1 | a0001c0002t0018g0280 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.591+681T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349342 | |||||||
chr16:50349347 | T | C | 88 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(85): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.591+676A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349347 | |||||||
chr16:50349491 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.591+532G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349491 | |||||||
chr16:50349632 | C | T | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.591+391G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349632 | |||||||
chr16:50349800 | G | A | 1 | a0001c0002t0002g0036 | 2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.591+223C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349800 | |||||||
chr16:50349830 | A | G | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.591+193T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349830 | |||||||
chr16:50349968 | T | C | 16 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0154 others(13): Show |
20 | HG00423.hp1 HG00639.hp2 NA18939.hp1 others(17): Show |
intron_variant | MODIFIER | c.591+55A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50349968 | |||||||
chr16:50350361 | T | G | 2 | a0001c0002t0002g0033 a0011c0010t0002g0313 |
3 | NA18957.hp1 NA18982.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.447-194A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50350361 | |||||||
chr16:50350495 | T | A | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.447-328A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50350495 | |||||||
chr16:50350532 | G | A | 3 | a0001c0001t0005g0115 a0001c0001t0005g0116 a0001c0001t0005g0117 |
3 | HG00735.hp2 HG03654.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.447-365C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50350532 | |||||||
chr16:50350622 | C | T | 4 | a0001c0002t0002g0034 a0001c0002t0002g0322 a0001c0002t0002g0341 others(1): Show |
5 | HG01106.hp2 HG01891.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.447-455G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50350622 | |||||||
chr16:50350647 | C | T | 335 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(332): Show |
393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.447-480G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50350647 | |||||||
chr16:50350796 | A | G | 1 | a0001c0001t0004g0196 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.447-629T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50350796 | |||||||
chr16:50350856 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.447-689C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50350856 | |||||||
chr16:50350909 | G | A | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.447-742C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50350909 | |||||||
chr16:50351033 | A | G | 1 | a0001c0001t0004g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.447-866T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351033 | |||||||
chr16:50351134 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.447-967A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351134 | |||||||
chr16:50351229 | G | T | 1 | a0001c0001t0007g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.447-1062C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351229 | |||||||
chr16:50351302 | G | C | 1 | a0001c0001t0028g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.447-1135C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351302 | |||||||
chr16:50351387 | C | T | 1 | a0001c0001t0003g0158 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.447-1220G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351387 | |||||||
chr16:50351436 | G | C | 3 | a0001c0001t0007g0075 a0001c0001t0007g0107 a0001c0001t0007g0120 |
3 | HG02717.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.447-1269C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351436 | |||||||
chr16:50351557 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
142 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.447-1390A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351557 | |||||||
chr16:50351625 | T | C | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.447-1458A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351625 | |||||||
chr16:50351713 | T | C | 1 | a0002c0003t0023g0255 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.447-1546A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351713 | |||||||
chr16:50351793 | T | A | 4 | a0001c0002t0002g0034 a0001c0002t0002g0322 a0001c0002t0002g0341 others(1): Show |
5 | HG01106.hp2 HG01891.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.447-1626A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351793 | |||||||
chr16:50351823 | GGT | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
149 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.447-1658_447-1657d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351823 | |||||||
chr16:50351830 | CCTTGTAT others(20): Show |
C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
149 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.447-1690_447-1664d others(29): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351830 | |||||||
chr16:50351832 | T | TTGTA | 8 | a0001c0001t0006g0228 a0001c0001t0015g0244 a0001c0001t0015g0245 others(5): Show |
8 | HG01123.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.447-1669_447-1666d others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351832 | |||||||
chr16:50351859 | A | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
149 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.447-1692T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351859 | |||||||
chr16:50351860 | G | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
149 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.447-1693C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351860 | |||||||
chr16:50351878 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
149 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.447-1711T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351878 | |||||||
chr16:50351912 | T | C | 1 | a0001c0001t0009g0076 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.447-1745A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351912 | |||||||
chr16:50351960 | T | G | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.447-1793A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50351960 | |||||||
chr16:50352025 | T | C | 3 | a0001c0002t0002g0036 a0001c0002t0002g0326 a0001c0002t0002g0330 |
4 | HG01109.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.447-1858A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352025 | |||||||
chr16:50352116 | G | A | 1 | a0001c0001t0035g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.447-1949C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352116 | |||||||
chr16:50352157 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.447-1990A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352157 | |||||||
chr16:50352491 | C | T | 179 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(176): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.446+1934G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352491 | |||||||
chr16:50352500 | T | G | 7 | a0001c0001t0021g0238 a0001c0001t0023g0256 a0002c0003t0008g0030 others(4): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.446+1925A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352500 | |||||||
chr16:50352504 | A | G | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.446+1921T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352504 | |||||||
chr16:50352559 | C | T | 4 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | HG02572.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.446+1866G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352559 | |||||||
chr16:50352697 | CTTTG | C | 5 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0258 others(2): Show |
6 | HG01891.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.446+1724_446+1727d others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352697 | |||||||
chr16:50352701 | G | GT | 25 | a0001c0001t0003g0159 a0001c0001t0006g0210 a0001c0001t0006g0211 others(22): Show |
25 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.446+1723dupA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352701 | |||||||
chr16:50352701 | G | T | 2 | a0001c0001t0004g0139 a0001c0002t0002g0269 |
2 | HG03491.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.446+1724C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352701 | |||||||
chr16:50352701 | GT | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
144 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.446+1723delA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352701 | |||||||
chr16:50352887 | C | T | 1 | a0009c0007t0015g0242 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.446+1538G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352887 | |||||||
chr16:50352944 | G | A | 1 | a0001c0001t0023g0256 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.446+1481C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50352944 | |||||||
chr16:50353071 | C | CT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0088 others(3): Show |
8 | HG02818.hp2 HG02970.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.446+1353dupA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353071 | |||||||
chr16:50353071 | C | CTT | 34 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0045 others(31): Show |
36 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.446+1352_446+1353d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353071 | |||||||
chr16:50353071 | CT | C | 181 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0077 others(178): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.446+1353delA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353071 | |||||||
chr16:50353258 | T | C | 2 | a0001c0001t0016g0246 a0001c0001t0016g0247 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.446+1167A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353258 | |||||||
chr16:50353361 | G | C | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.446+1064C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353361 | |||||||
chr16:50353393 | C | A | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.446+1032G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353393 | |||||||
chr16:50353722 | T | C | 1 | a0001c0002t0002g0314 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.446+703A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353722 | |||||||
chr16:50353759 | AT | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(309): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.446+665delA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353759 | |||||||
chr16:50353759 | ATT | A | 12 | a0001c0001t0003g0185 a0001c0001t0004g0139 a0001c0001t0005g0085 others(9): Show |
12 | HG00323.hp1 HG01256.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.446+664_446+665del others(2): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353759 | |||||||
chr16:50353763 | T | C | 3 | a0001c0001t0013g0029 a0001c0001t0013g0234 a0001c0001t0013g0235 |
4 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.446+662A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353763 | |||||||
chr16:50353800 | A | G | 10 | a0001c0001t0003g0137 a0001c0001t0003g0140 a0001c0001t0004g0007 others(7): Show |
12 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.446+625T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353800 | |||||||
chr16:50353807 | C | A | 22 | a0001c0001t0005g0002 a0001c0001t0005g0016 a0001c0001t0005g0017 others(19): Show |
29 | HG00597.hp1 HG00735.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.446+618G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353807 | |||||||
chr16:50353833 | C | T | 1 | a0001c0002t0002g0279 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.446+592G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353833 | |||||||
chr16:50353868 | G | T | 5 | a0001c0001t0003g0023 a0001c0001t0003g0156 a0001c0001t0003g0157 others(2): Show |
6 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.446+557C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353868 | |||||||
chr16:50353927 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.446+498A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353927 | |||||||
chr16:50354020 | C | T | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.446+405G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50354020 | |||||||
chr16:50354045 | C | A | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.446+380G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50354045 | |||||||
chr16:50354128 | T | G | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.446+297A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50354128 | |||||||
chr16:50354197 | T | C | 3 | a0001c0002t0002g0274 a0001c0002t0002g0275 a0007c0011t0038g0276 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.446+228A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50354197 | |||||||
chr16:50354216 | G | T | 2 | a0001c0002t0002g0034 a0001c0002t0002g0341 |
3 | HG01106.hp2 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.446+209C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50354216 | |||||||
chr16:50354320 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.446+105G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50354320 | |||||||
chr16:50354333 | C | A | 7 | a0001c0001t0034g0260 a0001c0001t0035g0261 a0003c0004t0010g0251 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.446+92G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50354333 | |||||||
chr16:50354583 | C | T | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.389-101G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 3/16 | chr16 | 50354583 | |||||||
chr16:50354661 | T | C | 1 | a0001c0001t0034g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.388+132A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 3/16 | chr16 | 50354661 | |||||||
chr16:50354681 | T | G | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.388+112A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 3/16 | chr16 | 50354681 | |||||||
chr16:50354704 | C | T | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.388+89G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 3/16 | chr16 | 50354704 | |||||||
chr16:50354746 | G | A | 340 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(337): Show |
399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.388+47C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 3/16 | chr16 | 50354746 | |||||||
chr16:50355096 | G | A | 8 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.259-174C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50355096 | |||||||
chr16:50355419 | A | G | 6 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-497T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50355419 | |||||||
chr16:50355450 | G | T | 1 | a0001c0001t0004g0135 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.259-528C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50355450 | |||||||
chr16:50355559 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(43): Show |
63 | HG00544.hp1 HG00621.hp1 HG01361.hp2 others(60): Show |
intron_variant | MODIFIER | c.259-637A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50355559 | |||||||
chr16:50355574 | A | G | 178 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(175): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.259-652T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50355574 | |||||||
chr16:50355611 | G | A | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.259-689C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50355611 | |||||||
chr16:50355927 | A | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0059 others(10): Show |
14 | HG00408.hp2 HG01106.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.259-1005T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50355927 | |||||||
chr16:50356001 | A | G | 3 | a0001c0001t0013g0029 a0001c0001t0013g0234 a0001c0001t0013g0235 |
4 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-1079T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356001 | |||||||
chr16:50356222 | C | A | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-1300G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356222 | |||||||
chr16:50356301 | G | A | 1 | a0001c0002t0002g0319 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.259-1379C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356301 | |||||||
chr16:50356504 | A | G | 335 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(332): Show |
393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.259-1582T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356504 | |||||||
chr16:50356512 | T | C | 91 | a0001c0001t0017g0032 a0001c0001t0017g0316 a0001c0002t0002g0009 others(88): Show |
100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.259-1590A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356512 | |||||||
chr16:50356576 | T | TA | 3 | a0001c0001t0001g0020 a0001c0001t0001g0105 a0001c0001t0001g0106 |
4 | HG02886.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-1655dupT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356576 | |||||||
chr16:50356714 | GA | G | 29 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(26): Show |
30 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.259-1793delT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356714 | |||||||
chr16:50356715 | A | G | 5 | a0001c0001t0004g0022 a0001c0001t0004g0142 a0001c0001t0004g0143 others(2): Show |
6 | HG02922.hp1 HG02965.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-1793T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356715 | |||||||
chr16:50356721 | A | AT | 18 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(15): Show |
31 | HG01361.hp2 HG01975.hp2 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.259-1800_259-1799i others(3): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356721 | |||||||
chr16:50356721 | AAAAT | A | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-1803_259-1800d others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356721 | |||||||
chr16:50356723 | A | AT | 96 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): Show |
113 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.259-1802_259-1801i others(3): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356723 | |||||||
chr16:50356723 | A | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(18): Show |
34 | HG01361.hp2 HG01975.hp2 HG01981.hp1 others(31): Show |
intron_variant | MODIFIER | c.259-1801T>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356723 | |||||||
chr16:50356725 | T | A | 1 | a0001c0001t0003g0025 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.259-1803A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356725 | |||||||
chr16:50356730 | A | G | 8 | a0001c0001t0003g0137 a0001c0001t0004g0007 a0001c0001t0004g0135 others(5): Show |
10 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-1808T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356730 | |||||||
chr16:50356735 | T | C | 1 | a0001c0001t0007g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.259-1813A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356735 | |||||||
chr16:50356737 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(105): Show |
137 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.259-1815A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356737 | |||||||
chr16:50356739 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
151 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.259-1817A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356739 | |||||||
chr16:50356739 | T | TAC | 4 | a0001c0001t0004g0195 a0001c0002t0002g0317 a0001c0002t0002g0318 others(1): Show |
4 | HG00140.hp2 HG01106.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-1819_259-1818d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356739 | |||||||
chr16:50356741 | C | T | 29 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(26): Show |
29 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.259-1819G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356741 | |||||||
chr16:50356763 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.259-1841A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356763 | |||||||
chr16:50356858 | C | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(309): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.259-1936G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356858 | |||||||
chr16:50357004 | G | C | 1 | a0001c0002t0002g0036 | 2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.259-2082C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357004 | |||||||
chr16:50357036 | GATTTTGC others(16): Show |
G | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.259-2137_259-2115d others(25): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357036 | |||||||
chr16:50357090 | C | T | 1 | a0001c0001t0005g0048 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.259-2168G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357090 | |||||||
chr16:50357241 | T | C | 1 | a0001c0002t0002g0319 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.259-2319A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357241 | |||||||
chr16:50357261 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.259-2339C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357261 | |||||||
chr16:50357318 | AGAAT | A | 6 | a0001c0001t0003g0003 a0001c0001t0003g0188 a0001c0001t0003g0189 others(3): Show |
10 | HG00140.hp1 HG00280.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-2400_259-2397d others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357318 | |||||||
chr16:50357373 | T | C | 1 | a0001c0002t0002g0272 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.259-2451A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357373 | |||||||
chr16:50357399 | G | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(309): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.259-2477C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357399 | |||||||
chr16:50357475 | C | G | 91 | a0001c0001t0017g0032 a0001c0001t0017g0316 a0001c0002t0002g0009 others(88): Show |
100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.259-2553G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357475 | |||||||
chr16:50357531 | G | A | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.259-2609C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357531 | |||||||
chr16:50357685 | C | T | 32 | a0001c0001t0003g0137 a0001c0001t0003g0140 a0001c0001t0004g0007 others(29): Show |
35 | HG00140.hp2 HG00733.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.259-2763G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357685 | |||||||
chr16:50357688 | C | T | 1 | a0001c0001t0004g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.259-2766G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357688 | |||||||
chr16:50357689 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
5 | HG00642.hp2 HG01069.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-2767C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357689 | |||||||
chr16:50357853 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
142 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.259-2931G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357853 | |||||||
chr16:50357905 | C | T | 1 | a0001c0001t0017g0032 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.259-2983G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357905 | |||||||
chr16:50357935 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.259-3013C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357935 | |||||||
chr16:50358110 | T | C | 32 | a0001c0001t0003g0137 a0001c0001t0003g0140 a0001c0001t0004g0007 others(29): Show |
35 | HG00140.hp2 HG00733.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.259-3188A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50358110 | |||||||
chr16:50358220 | C | T | 91 | a0001c0001t0017g0032 a0001c0001t0017g0316 a0001c0002t0002g0009 others(88): Show |
100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.259-3298G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50358220 | |||||||
chr16:50358345 | C | T | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.259-3423G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50358345 | |||||||
chr16:50358350 | T | TCCCGTCT others(22): Show |
223 | a0001c0001t0001g0124 a0001c0001t0003g0003 a0001c0001t0003g0004 others(220): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.259-3429_259-3428i others(31): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50358350 | |||||||
chr16:50358350 | T | TCCCGTCT others(22): Show |
111 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(108): Show |
141 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.259-3429_259-3428i others(31): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50358350 | |||||||
chr16:50358350 | T | TCCTGTCT others(22): Show |
2 | a0001c0001t0006g0212 a0001c0001t0006g0220 |
2 | HG02300.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.259-3429_259-3428i others(31): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50358350 | |||||||
chr16:50358374 | G | T | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.259-3452C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50358374 | |||||||
chr16:50358483 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
142 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.259-3561G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50358483 | |||||||
chr16:50358495 | C | CA | 114 | a0001c0001t0001g0123 a0001c0001t0003g0003 a0001c0001t0003g0004 others(111): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.259-3574dupT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50358495 | |||||||
chr16:50358535 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.259-3613T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50358535 | |||||||
chr16:50358738 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.259-3816C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50358738 | |||||||
chr16:50358924 | T | A | 1 | a0001c0001t0020g0114 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.259-4002A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50358924 | |||||||
chr16:50359015 | C | A | 4 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(1): Show |
4 | HG02257.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-4093G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359015 | |||||||
chr16:50359168 | A | G | 1 | a0001c0002t0037g0278 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.259-4246T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359168 | |||||||
chr16:50359188 | T | C | 1 | a0001c0001t0003g0028 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.259-4266A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359188 | |||||||
chr16:50359520 | C | T | 56 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(53): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.259-4598G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359520 | |||||||
chr16:50359626 | TA | T | 4 | a0001c0001t0003g0156 a0001c0001t0003g0157 a0001c0001t0034g0260 others(1): Show |
4 | HG01433.hp2 HG02109.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-4705delT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359626 | |||||||
chr16:50359664 | C | T | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.259-4742G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359664 | |||||||
chr16:50359715 | A | G | 1 | a0001c0001t0006g0211 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.259-4793T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359715 | |||||||
chr16:50359786 | C | T | 1 | a0001c0001t0006g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.259-4864G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359786 | |||||||
chr16:50359840 | GA | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
142 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.259-4919delT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359840 | |||||||
chr16:50359844 | G | C | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-4922C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359844 | |||||||
chr16:50359861 | G | C | 1 | a0001c0001t0016g0248 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.259-4939C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359861 | |||||||
chr16:50359912 | T | C | 1 | a0001c0002t0002g0320 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.259-4990A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359912 | |||||||
chr16:50359995 | T | C | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-5073A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50359995 | |||||||
chr16:50360115 | C | T | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.259-5193G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50360115 | |||||||
chr16:50360355 | T | C | 1 | a0001c0001t0034g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.259-5433A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50360355 | |||||||
chr16:50360488 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.259-5566C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50360488 | |||||||
chr16:50360527 | T | C | 1 | a0001c0001t0028g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.259-5605A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50360527 | |||||||
chr16:50360627 | T | C | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.259-5705A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50360627 | |||||||
chr16:50360790 | A | G | 1 | a0001c0002t0039g0277 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.259-5868T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50360790 | |||||||
chr16:50361027 | A | AC | 7 | a0001c0001t0021g0238 a0001c0001t0023g0256 a0002c0003t0008g0030 others(4): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-6106dupG | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361027 | |||||||
chr16:50361079 | A | G | 1 | a0001c0002t0002g0326 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.259-6157T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361079 | |||||||
chr16:50361091 | T | C | 1 | a0001c0001t0029g0207 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.259-6169A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361091 | |||||||
chr16:50361100 | C | T | 1 | a0001c0001t0035g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.259-6178G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361100 | |||||||
chr16:50361257 | T | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(105): Show |
137 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.259-6335A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361257 | |||||||
chr16:50361286 | G | A | 2 | a0001c0001t0003g0193 a0001c0001t0003g0194 |
2 | NA18943.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.259-6364C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361286 | |||||||
chr16:50361361 | A | G | 1 | a0001c0001t0034g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.259-6439T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361361 | |||||||
chr16:50361581 | C | T | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.258+6509G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361581 | |||||||
chr16:50361623 | C | T | 3 | a0001c0002t0002g0274 a0001c0002t0002g0275 a0007c0011t0038g0276 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.258+6467G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361623 | |||||||
chr16:50361764 | T | C | 3 | a0001c0001t0005g0115 a0001c0001t0005g0116 a0001c0001t0005g0117 |
3 | HG00735.hp2 HG03654.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.258+6326A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361764 | |||||||
chr16:50361781 | A | G | 1 | a0001c0001t0034g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.258+6309T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361781 | |||||||
chr16:50361857 | TAATCCTC others(11): Show |
T | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+6215_258+6232d others(20): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361857 | |||||||
chr16:50361951 | T | TA | 4 | a0001c0002t0002g0338 a0001c0002t0002g0339 a0001c0002t0002g0340 others(1): Show |
4 | HG00609.hp2 NA18986.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+6138dupT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361951 | |||||||
chr16:50361957 | T | C | 1 | a0001c0002t0002g0321 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.258+6133A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50361957 | |||||||
chr16:50362214 | G | T | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+5876C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50362214 | |||||||
chr16:50362256 | C | T | 3 | a0001c0002t0002g0324 a0001c0002t0002g0325 a0001c0002t0014g0241 |
3 | NA18947.hp1 NA19001.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.258+5834G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50362256 | |||||||
chr16:50362429 | C | T | 7 | a0001c0001t0021g0238 a0001c0001t0023g0256 a0002c0003t0008g0030 others(4): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+5661G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50362429 | |||||||
chr16:50362452 | T | C | 7 | a0001c0001t0021g0238 a0001c0001t0023g0256 a0002c0003t0008g0030 others(4): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+5638A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50362452 | |||||||
chr16:50362491 | T | C | 1 | a0001c0001t0004g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.258+5599A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50362491 | |||||||
chr16:50362519 | A | G | 87 | a0001c0001t0017g0032 a0001c0001t0017g0316 a0001c0002t0002g0009 others(84): Show |
95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.258+5571T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50362519 | |||||||
chr16:50362535 | AGGT | A | 91 | a0001c0001t0017g0032 a0001c0001t0017g0316 a0001c0002t0002g0009 others(88): Show |
100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.258+5552_258+5554d others(5): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50362535 | |||||||
chr16:50362800 | T | TG | 4 | a0002c0003t0008g0030 a0002c0003t0008g0257 a0002c0003t0008g0258 others(1): Show |
5 | HG01891.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+5289dupC | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50362800 | |||||||
chr16:50362826 | A | G | 91 | a0001c0001t0017g0032 a0001c0001t0017g0316 a0001c0002t0002g0009 others(88): Show |
100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.258+5264T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50362826 | |||||||
chr16:50362987 | T | C | 7 | a0001c0001t0021g0238 a0001c0001t0023g0256 a0002c0003t0008g0030 others(4): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+5103A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50362987 | |||||||
chr16:50363031 | G | GTACT | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.258+5055_258+5058d others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363031 | |||||||
chr16:50363051 | A | G | 1 | a0001c0001t0003g0155 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.258+5039T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363051 | |||||||
chr16:50363076 | C | T | 1 | a0001c0001t0006g0219 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.258+5014G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363076 | |||||||
chr16:50363137 | A | G | 1 | a0001c0001t0003g0154 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.258+4953T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363137 | |||||||
chr16:50363161 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.258+4929A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363161 | |||||||
chr16:50363243 | G | T | 56 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(53): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.258+4847C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363243 | |||||||
chr16:50363465 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.258+4625C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363465 | |||||||
chr16:50363626 | C | T | 1 | a0001c0001t0006g0218 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.258+4464G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363626 | |||||||
chr16:50363641 | T | G | 4 | a0001c0001t0001g0121 a0001c0001t0007g0120 a0001c0001t0034g0260 others(1): Show |
4 | HG02109.hp2 HG03195.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+4449A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363641 | |||||||
chr16:50363641 | T | TTG | 4 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(1): Show |
4 | HG02257.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+4447_258+4448d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363641 | |||||||
chr16:50363641 | T | TTGTA | 9 | a0001c0002t0002g0031 a0001c0002t0002g0264 a0001c0002t0002g0269 others(6): Show |
10 | HG01934.hp1 HG03942.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.258+4448_258+4449i others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363641 | |||||||
chr16:50363641 | T | TTGTGTGT others(1): Show |
13 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0220 others(10): Show |
13 | HG00735.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.258+4441_258+4448d others(10): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363641 | |||||||
chr16:50363641 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0006g0231 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.258+4439_258+4448d others(12): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363641 | |||||||
chr16:50363643 | G | GTA | 67 | a0001c0001t0017g0032 a0001c0001t0017g0316 a0001c0002t0002g0009 others(64): Show |
73 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.258+4446_258+4447i others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363643 | |||||||
chr16:50363643 | G | T | 1 | a0001c0001t0005g0043 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.258+4447C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363643 | |||||||
chr16:50363645 | G | A | 14 | a0001c0002t0002g0035 a0001c0002t0002g0036 a0001c0002t0002g0263 others(11): Show |
16 | HG00609.hp2 HG01109.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.258+4445C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363645 | |||||||
chr16:50363655 | G | GTGTC | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+4434_258+4435i others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363655 | |||||||
chr16:50363656 | TGTGTGCG others(9): Show |
T | 87 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(84): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.258+4418_258+4433d others(18): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363656 | |||||||
chr16:50363660 | T | C | 2 | a0001c0001t0005g0002 a0001c0002t0019g0268 |
2 | HG02083.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.258+4430A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGC | 3 | a0001c0001t0001g0121 a0001c0001t0013g0029 a0001c0001t0028g0233 |
3 | HG02280.hp1 HG03579.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.258+4428_258+4429d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGC | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0054 others(2): Show |
5 | HG01106.hp1 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+4429_258+4430i others(6): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGCGC | 5 | a0001c0001t0001g0065 a0001c0001t0001g0123 a0001c0001t0001g0126 others(2): Show |
5 | HG00544.hp1 HG02738.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+4429_258+4430i others(8): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGTGC | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
62 | HG00408.hp2 HG01109.hp1 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.258+4429_258+4430i others(8): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGTGCG others(1): Show |
21 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(18): Show |
23 | HG00621.hp1 HG00642.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.258+4429_258+4430i others(10): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGTGCG others(3): Show |
2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18943.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.258+4429_258+4430i others(12): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGTGCG others(5): Show |
1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258+4429_258+4430i others(14): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGTGTG others(1): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0092 others(5): Show |
8 | HG01255.hp2 HG01975.hp1 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+4429_258+4430i others(10): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGTGTG others(3): Show |
4 | a0001c0001t0001g0018 a0001c0001t0001g0041 a0001c0001t0001g0086 others(1): Show |
4 | HG02602.hp1 NA19004.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+4429_258+4430i others(12): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGTGTG others(3): Show |
16 | a0001c0001t0005g0002 a0001c0001t0005g0016 a0001c0001t0005g0017 others(13): Show |
16 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.258+4429_258+4430i others(12): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGTGTG others(5): Show |
9 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0043 others(6): Show |
10 | HG01192.hp2 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.258+4429_258+4430i others(14): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0005g0002 | 2 | HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.258+4429_258+4430i others(16): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0005g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.258+4429_258+4430i others(18): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGTGTG others(5): Show |
2 | a0001c0001t0005g0130 a0001c0001t0006g0210 |
2 | HG01433.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.258+4429_258+4430i others(14): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0005g0129 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.258+4429_258+4430i others(16): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | TGC | T | 5 | a0001c0001t0001g0124 a0001c0002t0002g0035 a0001c0002t0002g0263 others(2): Show |
5 | HG02970.hp2 HG03130.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+4428_258+4429d others(4): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363660 | TGCGCGC | T | 5 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(2): Show |
6 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+4424_258+4429d others(8): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363660 | |||||||
chr16:50363662 | C | T | 87 | a0001c0001t0001g0059 a0001c0001t0001g0105 a0001c0001t0001g0108 others(84): Show |
95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.258+4428G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363662 | |||||||
chr16:50363664 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0108 a0001c0001t0020g0058 |
3 | HG02886.hp1 HG03225.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.258+4426G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363664 | |||||||
chr16:50363665 | G | T | 1 | a0001c0001t0007g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.258+4425C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363665 | |||||||
chr16:50363668 | C | T | 5 | a0001c0001t0023g0256 a0002c0003t0008g0030 a0002c0003t0008g0257 others(2): Show |
6 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+4422G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363668 | |||||||
chr16:50363670 | C | T | 7 | a0001c0001t0021g0238 a0001c0001t0023g0256 a0002c0003t0008g0030 others(4): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+4420G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363670 | |||||||
chr16:50363672 | C | T | 7 | a0001c0001t0021g0238 a0001c0001t0023g0256 a0002c0003t0008g0030 others(4): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+4418G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363672 | |||||||
chr16:50363680 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(202): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.258+4410A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363680 | |||||||
chr16:50363780 | T | C | 336 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(333): Show |
394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.258+4310A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363780 | |||||||
chr16:50363897 | G | C | 2 | a0001c0002t0002g0331 a0001c0002t0002g0332 |
2 | NA19000.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.258+4193C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50363897 | |||||||
chr16:50364016 | T | C | 1 | a0001c0001t0029g0207 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.258+4074A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364016 | |||||||
chr16:50364069 | G | GA | 14 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0015g0244 others(11): Show |
14 | HG02257.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.258+4020dupT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364069 | |||||||
chr16:50364188 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.258+3902C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364188 | |||||||
chr16:50364224 | C | G | 336 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(333): Show |
394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.258+3866G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364224 | |||||||
chr16:50364572 | C | T | 86 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(83): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.258+3518G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364572 | |||||||
chr16:50364573 | C | A | 1 | a0003c0004t0030g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.258+3517G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364573 | |||||||
chr16:50364706 | CA | C | 3 | a0001c0002t0002g0264 a0001c0002t0002g0265 a0001c0002t0002g0266 |
3 | HG00280.hp1 NA18961.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.258+3383delT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364706 | |||||||
chr16:50364754 | G | A | 4 | a0001c0002t0002g0037 a0001c0002t0002g0335 a0001c0002t0002g0336 others(1): Show |
5 | HG02015.hp2 NA18980.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+3336C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364754 | |||||||
chr16:50364795 | A | G | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258+3295T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364795 | |||||||
chr16:50364935 | A | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0042 |
4 | NA18997.hp1 NA19004.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+3155T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364935 | |||||||
chr16:50364989 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.258+3101G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364989 | |||||||
chr16:50364998 | A | G | 5 | a0002c0003t0008g0030 a0002c0003t0008g0257 a0002c0003t0008g0258 others(2): Show |
6 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+3092T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364998 | |||||||
chr16:50365076 | C | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0142 a0001c0001t0004g0143 others(2): Show |
6 | HG02922.hp1 HG02965.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+3014G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50365076 | |||||||
chr16:50365158 | G | A | 1 | a0001c0001t0003g0208 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.258+2932C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50365158 | |||||||
chr16:50365163 | G | A | 1 | a0001c0001t0035g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258+2927C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50365163 | |||||||
chr16:50365171 | A | AG | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
158 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(155): Show |
intron_variant | MODIFIER | c.258+2918_258+2919i others(3): Show |
BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50365171 | |||||||
chr16:50365375 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.258+2715C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50365375 | |||||||
chr16:50365436 | C | A | 337 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(334): Show |
395 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.258+2654G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50365436 | |||||||
chr16:50365438 | C | T | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.258+2652G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50365438 | |||||||
chr16:50365704 | A | C | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+2386T>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50365704 | |||||||
chr16:50365832 | G | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA18974.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.258+2258C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50365832 | |||||||
chr16:50365977 | AG | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
144 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.258+2112delC | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50365977 | |||||||
chr16:50366014 | C | T | 1 | a0001c0002t0002g0263 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.258+2076G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366014 | |||||||
chr16:50366029 | G | A | 1 | a0001c0001t0006g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.258+2061C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366029 | |||||||
chr16:50366120 | A | G | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+1970T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366120 | |||||||
chr16:50366176 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
142 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.258+1914A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366176 | |||||||
chr16:50366215 | A | G | 4 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0004g0152 others(1): Show |
4 | HG01074.hp1 HG01081.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+1875T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366215 | |||||||
chr16:50366361 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
145 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.258+1729T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366361 | |||||||
chr16:50366545 | T | C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG00544.hp1 NA18974.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.258+1545A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366545 | |||||||
chr16:50366556 | A | G | 1 | a0001c0002t0019g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.258+1534T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366556 | |||||||
chr16:50366813 | T | A | 5 | a0001c0001t0005g0129 a0001c0001t0005g0130 a0001c0001t0005g0131 others(2): Show |
5 | HG00597.hp1 HG02683.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+1277A>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366813 | |||||||
chr16:50366828 | G | C | 5 | a0001c0001t0005g0129 a0001c0001t0005g0130 a0001c0001t0005g0131 others(2): Show |
5 | HG00597.hp1 HG02683.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+1262C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366828 | |||||||
chr16:50366869 | G | A | 86 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(83): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.258+1221C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366869 | |||||||
chr16:50366885 | T | G | 7 | a0001c0001t0015g0244 a0001c0001t0015g0245 a0001c0001t0016g0246 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+1205A>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366885 | |||||||
chr16:50366920 | A | G | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.258+1170T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50366920 | |||||||
chr16:50367246 | A | G | 1 | a0001c0001t0028g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.258+844T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50367246 | |||||||
chr16:50367277 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
143 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.258+813G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50367277 | |||||||
chr16:50367408 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
145 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.258+682C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50367408 | |||||||
chr16:50367423 | T | C | 1 | a0001c0001t0033g0249 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258+667A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50367423 | |||||||
chr16:50367580 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.258+510A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50367580 | |||||||
chr16:50367599 | A | G | 1 | a0001c0001t0001g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+491T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50367599 | |||||||
chr16:50367672 | A | G | 23 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(20): Show |
23 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.258+418T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50367672 | |||||||
chr16:50367713 | G | A | 3 | a0001c0002t0002g0338 a0001c0002t0002g0339 a0001c0002t0002g0340 |
3 | HG00609.hp2 NA18986.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.258+377C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50367713 | |||||||
chr16:50367768 | C | G | 4 | a0001c0001t0004g0135 a0001c0001t0004g0136 a0001c0001t0004g0146 others(1): Show |
4 | HG02647.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+322G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50367768 | |||||||
chr16:50367894 | T | C | 2 | a0001c0001t0004g0146 a0001c0001t0004g0147 |
2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.258+196A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50367894 | |||||||
chr16:50368304 | AAAAAG | A | 7 | a0001c0001t0023g0256 a0001c0002t0002g0341 a0002c0003t0008g0030 others(4): Show |
8 | HG01106.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.50-11_50-7delCTTTT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/16 | chr16 | 50368304 | |||||||
chr16:50368329 | C | G | 88 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(85): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.50-31G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/16 | chr16 | 50368329 | |||||||
chr16:50368408 | G | T | 1 | a0001c0001t0003g0148 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.50-110C>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/16 | chr16 | 50368408 | |||||||
chr16:50368427 | T | C | 1 | a0001c0001t0005g0134 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.50-129A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/16 | chr16 | 50368427 | |||||||
chr16:50368567 | CG | C | 15 | a0001c0001t0003g0137 a0001c0001t0003g0140 a0001c0001t0004g0007 others(12): Show |
18 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.49+158delC | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/16 | chr16 | 50368567 | |||||||
chr16:50368574 | C | T | 15 | a0001c0001t0003g0137 a0001c0001t0003g0140 a0001c0001t0004g0007 others(12): Show |
18 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.49+152G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/16 | chr16 | 50368574 | |||||||
chr16:50368634 | G | A | 5 | a0003c0004t0010g0251 a0003c0004t0010g0252 a0003c0004t0010g0253 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+92C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/16 | chr16 | 50368634 | |||||||
chr16:50368650 | C | A | 2 | a0001c0001t0034g0260 a0001c0001t0035g0261 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.49+76G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/16 | chr16 | 50368650 | |||||||
chr16:50368658 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
144 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.49+68G>A | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/16 | chr16 | 50368658 | |||||||
chr16:50368686 | C | G | 1 | a0001c0002t0002g0342 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.49+40G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/16 | chr16 | 50368686 | |||||||
chr16:50368687 | G | C | 1 | a0001c0002t0002g0342 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.49+39C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/16 | chr16 | 50368687 |