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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr16 | 50310957 | 50373988 |
a0002 | 0/0 | 651 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0003 | 0/0 | 651 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0004 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0005 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0006 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0007 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0008 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0009 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0010 | 0/0 | 651 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0011 | 0/0 | 651 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0012 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1956 | 288 | 64 | 71 | 106 | 13 | 33 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
c0002 | 0/1 | 1956 | 95 | 13 | 8 | 66 | 3 | 4 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
c0003 | 0/0 | 1956 | 6 | 6 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
c0004 | 0/0 | 1956 | 4 | 4 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
c0005 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
c0006 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
c0007 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
c0008 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
c0009 | 0/0 | 1956 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
c0010 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
c0011 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
c0012 | 0/0 | 1956 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
c0013 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3473 | 90 | 21 | 8 | 53 | 1 | 7 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0002 | 0/1 | 3468 | 84 | 13 | 6 | 59 | 3 | 2 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0003 | 0/0 | 3469 | 70 | 2 | 21 | 31 | 5 | 11 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0004 | 0/0 | 3473 | 32 | 12 | 9 | 3 | 2 | 6 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0005 | 0/0 | 3473 | 28 | 1 | 12 | 9 | 1 | 5 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0006 | 0/0 | 3469 | 19 | 1 | 12 | 0 | 2 | 4 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0007 | 0/0 | 3477 | 9 | 6 | 1 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0008 | 0/0 | 3477 | 5 | 5 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0009 | 0/0 | 3473 | 4 | 4 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0010 | 0/0 | 3465 | 4 | 4 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0011 | 0/0 | 3477 | 4 | 0 | 0 | 4 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0012 | 0/0 | 3469 | 4 | 0 | 4 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0013 | 0/0 | 3473 | 4 | 4 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0014 | 1/0 | 3469 | 4 | 0 | 0 | 3 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0015 | 0/0 | 3470 | 3 | 3 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0016 | 0/0 | 3470 | 3 | 3 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0017 | 0/0 | 3468 | 3 | 0 | 2 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0018 | 0/0 | 3464 | 3 | 1 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0019 | 0/0 | 3468 | 3 | 0 | 0 | 2 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0020 | 0/0 | 3469 | 2 | 0 | 1 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0021 | 0/0 | 3473 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0022 | 0/0 | 3473 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0023 | 0/0 | 3473 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0024 | 0/0 | 3455 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0025 | 0/0 | 3469 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0026 | 0/0 | 3473 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0027 | 0/0 | 3473 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0028 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0029 | 0/0 | 3473 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0030 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0031 | 0/0 | 3469 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0032 | 0/0 | 3470 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0033 | 0/0 | 3473 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0034 | 0/0 | 3464 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0035 | 0/0 | 3468 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0036 | 0/0 | 3468 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0037 | 0/0 | 3468 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0038 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0039 | 0/0 | 3468 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0040 | 0/0 | 3468 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
t0041 | 0/0 | 3469 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0002 | 0/0 | 5 | 0 | 2 | 0 | 3 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0007 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0253 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0312 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1956 | 288 | 64 | 71 | 106 | 13 | 33 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0002 | 0/1 | 1956 | 95 | 13 | 8 | 66 | 3 | 4 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0002c0003 | 0/0 | 1956 | 6 | 6 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0003c0004 | 0/0 | 1956 | 4 | 4 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0004c0013 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0005c0006 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0006c0011 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0007c0008 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0008c0007 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0009c0010 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0010c0009 | 0/0 | 1956 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0011c0012 | 0/0 | 1956 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0012c0005 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | 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 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0003 | 0/0 | 5424 | 70 | 2 | 21 | 31 | 5 | 11 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0004 | 0/0 | 5428 | 31 | 12 | 9 | 3 | 2 | 5 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0005 | 0/0 | 5428 | 27 | 1 | 11 | 9 | 1 | 5 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0006 | 0/0 | 5424 | 18 | 0 | 12 | 0 | 2 | 4 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0007 | 0/0 | 5432 | 9 | 6 | 1 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0009 | 0/0 | 5428 | 4 | 4 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0011 | 0/0 | 5432 | 4 | 0 | 0 | 4 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0012 | 0/0 | 5424 | 4 | 0 | 4 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0013 | 0/0 | 5428 | 4 | 4 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0014 | 1/0 | 5424 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0015 | 0/0 | 5425 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0016 | 0/0 | 5425 | 3 | 3 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0017 | 0/0 | 5423 | 3 | 0 | 2 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0020 | 0/0 | 5424 | 2 | 0 | 1 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0021 | 0/0 | 5428 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0022 | 0/0 | 5428 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0023 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0024 | 0/0 | 5410 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0025 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0027 | 0/0 | 5428 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0028 | 0/0 | 5412 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0029 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0031 | 0/0 | 5424 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0032 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0033 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0034 | 0/0 | 5419 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0035 | 0/0 | 5423 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0001t0041 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0002t0002 | 0/1 | 5423 | 82 | 12 | 6 | 58 | 3 | 2 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0002t0014 | 0/0 | 5424 | 3 | 0 | 0 | 3 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0002t0018 | 0/0 | 5419 | 3 | 1 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0002t0019 | 0/0 | 5423 | 3 | 0 | 0 | 2 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0002t0036 | 0/0 | 5423 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0002t0037 | 0/0 | 5423 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0002t0039 | 0/0 | 5423 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0001c0002t0040 | 0/0 | 5423 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0002c0003t0008 | 0/0 | 5432 | 5 | 5 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0002c0003t0023 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0003c0004t0010 | 0/0 | 5420 | 3 | 3 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0003c0004t0030 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0004c0013t0006 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0005c0006t0002 | 0/0 | 5423 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0006c0011t0038 | 0/0 | 5427 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0007c0008t0026 | 0/0 | 5428 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0008c0007t0015 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0009c0010t0002 | 0/0 | 5423 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0010c0009t0004 | 0/0 | 5428 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0011c0012t0005 | 0/0 | 5428 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
a0012c0005t0010 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | copy fasta | chr16 | 50310957 | 50373988 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 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 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0048 | 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 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0058 | 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 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0085 | 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 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0120 | 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 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0002 | 0/0 | 5 | 0 | 2 | 0 | 3 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
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 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0017 | 0/0 | 2 | 2 | 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 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0039 | 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 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0006g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0009g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0011g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0011g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0012g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0012g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0012g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0012g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0013g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0013g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0013g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0013g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0014g0253 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0015g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0015g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0016g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0016g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0016g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0017g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0017g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0020g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0020g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0021g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0021g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0022g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0022g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0023g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0024g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0025g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0027g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0028g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0029g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0031g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0032g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0033g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0034g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0035g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0001t0041g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0002t0002g0294 | 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 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0002t0002g0299 | 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 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0312 | 0/1 | 1 | 0 | 0 | 0 | 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 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0323 | 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 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 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 |
a0001c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0014g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0014g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0014g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0018g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0018g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0018g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0019g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0019g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0019g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0036g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0037g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0039g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0001c0002t0040g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0002c0003t0008g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0002c0003t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0002c0003t0008g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0002c0003t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0002c0003t0023g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0003c0004t0010g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0003c0004t0010g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0003c0004t0010g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0003c0004t0030g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0004c0013t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0005c0006t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0006c0011t0038g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0007c0008t0026g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0008c0007t0015g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0009c0010t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0010c0009t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0011c0012t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
a0012c0005t0010g0267 | 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 | g0362 | EUR | GBR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0210 | EUR | GBR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0283 | EUR | FIN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | FIN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00323 | hp1 | a0001 | c0001 | t0017 | g0327 | EUR | FIN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0170 | EUR | FIN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00408 | hp1 | a0001 | c0002 | t0019 | g0291 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0320 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0143 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0323 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0357 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00621 | hp1 | a0001 | c0001 | t0011 | g0112 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0305 | EAS | CHS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0247 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00639 | hp2 | a0001 | c0001 | t0024 | g0028 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0239 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0219 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0231 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0093 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0220 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0243 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG00741 | hp2 | a0001 | c0002 | t0040 | g0315 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0232 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01081 | hp1 | a0001 | c0001 | t0012 | g0233 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01099 | hp2 | a0001 | c0001 | t0012 | g0245 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01106 | hp1 | a0001 | c0001 | t0020 | g0043 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0360 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0338 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01167 | hp1 | a0001 | c0001 | t0007 | g0064 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01167 | hp2 | a0001 | c0001 | t0017 | g0023 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01168 | hp2 | a0001 | c0001 | t0012 | g0244 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01169 | hp1 | a0001 | c0001 | t0017 | g0023 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0226 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0122 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01255 | hp2 | a0001 | c0001 | t0012 | g0241 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0227 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0328 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0307 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0238 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0121 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0229 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01361 | hp1 | a0001 | c0002 | t0036 | g0310 | 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 | g0246 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0150 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0230 | EUR | IBS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0204 | EUR | IBS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0007 | EUR | IBS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0007 | EUR | IBS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01891 | hp1 | a0002 | c0003 | t0008 | g0021 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01891 | hp2 | a0005 | c0006 | t0002 | g0335 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01928 | hp2 | a0001 | c0001 | t0005 | g0117 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0345 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0130 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0124 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0330 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0083 | 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 | g0016 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01978 | hp2 | a0001 | c0001 | t0031 | g0224 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0303 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0356 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0339 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0326 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0105 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02056 | hp1 | a0001 | c0002 | t0018 | g0313 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0331 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0309 | 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 | g0333 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02083 | hp1 | a0001 | c0002 | t0019 | g0349 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02083 | hp2 | a0001 | c0001 | t0011 | g0113 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02129 | hp1 | a0007 | c0008 | t0026 | g0091 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0286 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02145 | hp2 | a0002 | c0003 | t0008 | g0274 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0184 | 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 | g0040 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02257 | hp2 | a0003 | c0004 | t0010 | g0269 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02258 | hp2 | a0001 | c0001 | t0013 | g0251 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02280 | hp1 | a0001 | c0001 | t0013 | g0254 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0108 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0242 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02300 | hp2 | a0011 | c0012 | t0005 | g0088 | AMR | PEL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02451 | hp2 | a0001 | c0001 | t0016 | g0265 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02622 | hp1 | a0003 | c0004 | t0010 | g0268 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02622 | hp2 | a0001 | c0001 | t0023 | g0273 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02630 | hp1 | a0001 | c0001 | t0013 | g0250 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02647 | hp1 | a0001 | c0001 | t0032 | g0260 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0138 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0033 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02717 | hp2 | a0001 | c0001 | t0015 | g0262 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0341 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02735 | hp1 | a0001 | c0002 | t0019 | g0279 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02809 | hp2 | a0002 | c0003 | t0023 | g0272 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02818 | hp1 | a0002 | c0003 | t0008 | g0275 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02818 | hp2 | a0003 | c0004 | t0030 | g0271 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02895 | hp1 | a0001 | c0001 | t0033 | g0266 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0252 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0065 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0139 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03098 | hp1 | a0001 | c0001 | t0021 | g0255 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0104 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0280 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0314 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03195 | hp1 | a0001 | c0001 | t0035 | g0278 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03195 | hp2 | a0001 | c0001 | t0016 | g0263 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0287 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03453 | hp2 | a0012 | c0005 | t0010 | g0267 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03486 | hp2 | a0001 | c0001 | t0021 | g0249 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0348 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0148 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0106 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03516 | hp2 | a0008 | c0007 | t0015 | g0259 | AFR | ESN | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03540 | hp2 | a0002 | c0003 | t0008 | g0276 | AFR | GWD | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03579 | hp2 | a0001 | c0001 | t0028 | g0248 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03654 | hp1 | a0001 | c0001 | t0006 | g0235 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0127 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03669 | hp2 | a0001 | c0001 | t0020 | g0035 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0234 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0215 | SAS | PJL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0157 | SAS | BEB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0218 | SAS | BEB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03942 | hp1 | a0010 | c0009 | t0004 | g0217 | SAS | BEB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0346 | SAS | BEB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0216 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0158 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0141 | SAS | BEB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04184 | hp2 | a0001 | c0001 | t0006 | g0228 | SAS | BEB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0212 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0140 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04204 | hp2 | a0001 | c0001 | t0006 | g0240 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04228 | hp1 | a0001 | c0002 | t0037 | g0290 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | STU | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18522 | hp1 | a0001 | c0001 | t0016 | g0264 | AFR | YRI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18522 | hp2 | a0003 | c0004 | t0010 | g0270 | AFR | YRI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0343 | EAS | CHB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18747 | hp1 | a0001 | c0001 | t0011 | g0076 | EAS | CHB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0302 | EAS | CHB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | YRI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | YRI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18947 | hp1 | a0001 | c0002 | t0014 | g0258 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18953 | hp1 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0319 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0125 | 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 | g0311 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18957 | hp1 | a0009 | c0010 | t0002 | g0324 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0340 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18969 | hp1 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18971 | hp2 | a0001 | c0001 | t0022 | g0073 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18973 | hp1 | a0001 | c0001 | t0025 | g0075 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0318 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0013 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18978 | hp1 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0353 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0352 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0354 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18982 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18985 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18986 | hp1 | a0001 | c0002 | t0014 | g0257 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0359 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18988 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18990 | hp1 | a0001 | c0002 | t0018 | g0293 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0347 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18991 | hp2 | a0001 | c0001 | t0007 | g0013 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0355 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0342 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0361 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0351 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0336 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0027 | 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 | g0010 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0325 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19004 | hp2 | a0001 | c0002 | t0039 | g0289 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19006 | hp2 | a0001 | c0002 | t0002 | g0350 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | LWK | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0308 | AFR | LWK | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19057 | hp2 | a0001 | c0001 | t0011 | g0074 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19059 | hp1 | a0001 | c0002 | t0002 | g0322 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19059 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0344 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19065 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0358 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19068 | hp1 | a0001 | c0001 | t0022 | g0072 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0337 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19077 | hp2 | a0001 | c0001 | t0027 | g0051 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19078 | hp1 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0321 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19082 | hp1 | a0001 | c0002 | t0014 | g0256 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0332 | 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 | g0003 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0317 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0062 | AFR | YRI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA19240 | hp2 | a0004 | c0013 | t0006 | g0236 | AFR | YRI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | ASW | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0096 | AFR | ASW | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | TSI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0147 | EUR | TSI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0094 | EUR | TSI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0225 | EUR | TSI | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | GIH | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | GIH | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01123 | hp1 | a0001 | c0001 | t0006 | g0237 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | CLM | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02109 | hp2 | a0001 | c0001 | t0034 | g0277 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02486 | hp1 | a0001 | c0001 | t0015 | g0261 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0221 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02559 | hp1 | a0006 | c0011 | t0038 | g0288 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG02559 | hp2 | a0001 | c0001 | t0029 | g0222 | AFR | ACB | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG03471 | hp2 | a0002 | c0003 | t0008 | g0021 | AFR | MSL | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | USA | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0334 | AFR | USA | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20300 | hp1 | a0001 | c0002 | t0018 | g0306 | AFR | USA | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | USA | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | LWK | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0312 | REF | REF | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0014 | g0253 | REF | REF | BRD7_chr16_50310957_50373988 | BRD7 | chr16 | 50310957 | 50373988 |
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 | a0007 | 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 | a0008 | 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 | a0006 | 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 | a0009 | 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 | a0003a0012 | 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 | a0005 | 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 | a0011 | 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 | a0004 | 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 | a0012 | 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 |
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 | a0001c0002a0005c0006a0006c0011others(1): Show | 98 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(95): 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 |
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 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(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 | a0001c0001t0003a0001c0001t0004a0001c0001t0024others(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 | a0001c0001t0015a0001c0001t0016a0001c0001t0032others(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 | a0001c0001t0016a0001c0001t0032 | 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 | a0001c0001t0006a0001c0001t0012a0001c0001t0028others(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 | a0001c0001t0005a0007c0008t0026a0011c0012t0005 | 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 | a0001c0001t0023a0002c0003t0008a0002c0003t0023 | 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 | a0001c0001t0004a0001c0001t0007a0001c0001t0029others(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 | a0001c0001t0006a0001c0001t0012a0001c0001t0025others(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 | a0001c0001t0034a0001c0001t0035 | 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 | a0001c0001t0017a0001c0001t0020 | 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 | a0001c0001t0034a0001c0001t0035 | 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 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(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 | a0003c0004t0010a0003c0004t0030a0012c0005t0010 | 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 | a0003c0004t0010a0012c0005t0010 | 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 | a0001c0001t0023a0002c0003t0008a0002c0003t0023 | 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 | a0001c0001t0017a0001c0001t0034a0001c0001t0035others(10): Show | 100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): 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 |
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 | a0001c0001t0001g0109 | 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 | a0001c0001t0004g0215a0001c0001t0004g0218a0001c0001t0004g0219others(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 | 128 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(125): 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 | a0001c0001t0003g0168a0001c0001t0006g0225a0001c0001t0006g0226others(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 | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(130): 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 | a0001c0002t0002g0357a0001c0002t0002g0358a0001c0002t0002g0359 | 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 | 79 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(76): 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 | a0001c0002t0002g0281a0001c0002t0002g0282a0001c0002t0002g0283 | 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 | a0001c0002t0002g0292 | 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0001t0001g0045 | 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 | a0001c0002t0002g0334 | 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 | a0001c0001t0003g0190a0001c0001t0004g0155a0001c0001t0004g0156 | 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 | a0001c0001t0034g0277 | 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 | a0001c0001t0003g0194a0001c0001t0013g0250a0001c0001t0015g0261others(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 | a0001c0001t0003g0158a0001c0001t0003g0175a0001c0001t0003g0179others(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 | 75 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(72): 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 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0066others(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 | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(110): 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0003c0004t0030g0271 | 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 | a0001c0001t0009g0011a0001c0001t0009g0105a0001c0001t0009g0108 | 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 | a0001c0001t0003g0146a0001c0001t0003g0149a0001c0001t0004g0005others(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 | a0001c0001t0033g0266 | 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 | a0001c0001t0005g0127 | 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 | a0001c0001t0007g0064 | 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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(129): 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0001t0006g0234 | 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 | a0001c0002t0002g0356 | 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0001t0003g0146a0001c0001t0004g0005a0001c0001t0004g0144others(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 | a0001c0001t0001g0120 | 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 | a0001c0002t0002g0344 | 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0003g0168a0001c0001t0006g0225a0001c0001t0006g0226others(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 | a0003c0004t0030g0271 | 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0002t0002g0303 | 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 | a0001c0001t0001g0069 | 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 | a0001c0002t0002g0287 | 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 | a0001c0001t0004g0211a0001c0001t0004g0213 | 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 | a0001c0001t0033g0266 | 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 | a0001c0001t0033g0266 | 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 | a0001c0002t0019g0291a0001c0002t0019g0349 | 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 | a0001c0002t0002g0284 | 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 | a0001c0001t0006g0235 | 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 | 6 | a0001c0001t0013g0250a0001c0001t0013g0251a0001c0001t0013g0252others(3): 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 | a0001c0001t0001g0120 | 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 | a0001c0002t0018g0313 | 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 | a0001c0001t0028g0248 | 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 | 3 | a0001c0001t0001g0012a0001c0001t0001g0067a0001c0001t0001g0110 | 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 | a0001c0002t0036g0310 | 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 | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(138): 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 | a0011c0012t0005g0088 | 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 | a0001c0002t0002g0314 | 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 | a0001c0001t0011g0113 | 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 | a0001c0002t0002g0357 | 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 | 5 | a0001c0001t0005g0083a0001c0001t0005g0086a0001c0001t0005g0087others(2): 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 | 128 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(125): 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0006g0231 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(176): 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 | 3 | a0001c0001t0013g0250a0001c0001t0013g0252a0001c0001t0013g0254 | 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 | a0001c0001t0015g0262 | 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 | a0001c0002t0002g0361 | 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 | a0001c0002t0002g0307a0001c0002t0002g0328 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0001t0005g0140 | 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 | a0001c0001t0028g0248 | 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 | a0003c0004t0030g0271 | 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 | 4 | a0001c0001t0013g0250a0001c0001t0013g0251a0001c0001t0013g0252others(1): Show | 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 | 59 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(56): 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 | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(351): Show | 394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.1088-885C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 9/16 | chr16 | 50327276 | ||||||
chr16:50327466
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(125): 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 | a0001c0001t0005g0125 | 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 | a0001c0001t0005g0125 | 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0004g0155a0001c0001t0004g0156 | 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 | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(351): Show | 394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): 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 | a0003c0004t0010g0269a0003c0004t0010g0270a0012c0005t0010g0267 | 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 | a0001c0001t0034g0277 | 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0001t0033g0266 | 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | 128 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(125): 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 | a0001c0002t0002g0303 | 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 | a0001c0001t0006g0231 | 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 | a0001c0002t0002g0308 | 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 | 20 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(17): 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 | 90 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(87): 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0235others(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 | a0001c0001t0003g0186a0001c0001t0003g0188 | 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0001t0032g0260 | 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 | a0001c0002t0002g0331 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | 14 | a0001c0001t0003g0003a0001c0001t0003g0164a0001c0001t0003g0174others(11): 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 | a0001c0001t0003g0018a0001c0002t0002g0341 | 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 | 140 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(137): Show | 158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): 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 | a0001c0001t0003g0146a0001c0001t0003g0149a0001c0001t0003g0172others(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 | a0001c0001t0001g0041a0001c0001t0001g0059a0001c0001t0001g0060others(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 | 43 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0069others(40): 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0001t0034g0277 | 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | 360 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(357): Show | 400 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(397): Show |
intron_variant | MODIFIER | c.1012-1855G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50330599 | ||||||
chr16:50330700
|
A | G | 59 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(56): 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 | a0001c0001t0009g0105a0001c0001t0015g0261a0001c0001t0015g0262others(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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0001t0001g0067 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0001t0004g0221 | 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 | a0001c0001t0033g0266 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(132): 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 | a0001c0001t0005g0125 | 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 | a0001c0002t0002g0281 | 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(124): 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 | a0001c0002t0002g0305 | 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0003c0004t0010g0269a0003c0004t0010g0270a0012c0005t0010g0267 | 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 | a0001c0001t0003g0164a0001c0001t0003g0175a0001c0001t0003g0192others(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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | 90 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(87): 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | 92 | a0001c0001t0003g0158a0001c0002t0002g0007a0001c0002t0002g0022others(89): Show | 99 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(96): 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0003g0157a0001c0001t0035g0278 | 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 | 4 | a0001c0001t0013g0250a0001c0001t0013g0251a0001c0001t0013g0252others(1): Show | 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 | a0001c0001t0034g0277 | 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 | a0001c0002t0002g0296 | 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 | 182 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(179): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1011+627G>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 8/16 | chr16 | 50332947 | ||||||
chr16:50333116
|
G | A | 2 | a0001c0001t0007g0062a0001c0001t0007g0106 | 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 | 7 | a0001c0001t0001g0037a0001c0001t0001g0066a0001c0001t0001g0077others(4): 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 | 360 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(357): Show | 400 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(397): 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0002t0018g0313 | 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 | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(350): Show | 393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.888-26dupT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 7/16 | chr16 | 50333722 | ||||||
chr16:50333779
|
T | C | 8 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0099 | 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 | a0001c0002t0002g0314 | 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 | a0001c0001t0003g0165a0001c0001t0003g0166 | 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0003g0178 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0001g0133 | 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 | a0001c0001t0033g0266 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0003c0004t0010g0269a0003c0004t0010g0270a0012c0005t0010g0267 | 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0001t0004g0214 | 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 | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(138): 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 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0042others(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 | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(136): 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 | 359 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(356): Show | 399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): 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 | a0001c0001t0033g0266 | 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 | a0001c0002t0002g0325 | 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0001t0031g0224 | 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 | 91 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(88): 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 | a0001c0001t0001g0142 | 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 | 58 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(55): 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 | a0001c0002t0002g0303 | 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 | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(136): 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(128): 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 | a0003c0004t0030g0271 | 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 | a0001c0001t0005g0126 | 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 | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(351): Show | 394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): 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 | a0001c0002t0002g0336 | 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 | a0001c0002t0002g0025a0001c0002t0002g0334a0001c0002t0002g0360others(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 | a0001c0001t0009g0105 | 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 | 5 | a0001c0001t0001g0036a0001c0001t0007g0062a0001c0001t0007g0064others(2): 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 | 58 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(55): 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 | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(240): Show | 267 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.703-2362delA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 6/16 | chr16 | 50337256 | ||||||
chr16:50337260
|
T | C | 1 | a0001c0001t0005g0139 | 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0001g0098 | 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 | a0001c0001t0035g0278 | 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 | a0001c0001t0033g0266 | 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 | a0001c0001t0006g0247 | 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 | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(138): 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 | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(130): 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 | 91 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(88): 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 | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(136): 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 | 91 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(88): 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 | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(123): 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 | a0001c0001t0003g0149 | 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 | a0004c0013t0006g0236 | 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 | a0001c0002t0002g0309 | 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 | a0001c0002t0002g0338 | 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 | a0001c0001t0005g0130 | 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 | a0001c0001t0005g0130 | 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 | a0001c0001t0021g0255 | 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 | a0001c0002t0002g0309 | 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0001t0020g0035 | 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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(128): 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0001t0012g0233a0001c0001t0012g0244a0001c0001t0012g0245 | 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 | a0001c0001t0004g0156 | 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 | a0001c0001t0004g0216 | 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 | a0002c0003t0023g0272 | 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 | a0003c0004t0010g0270 | 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 | a0003c0004t0010g0270 | 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(136): 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 | a0002c0003t0023g0272 | 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 | a0001c0001t0003g0209 | 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 | 331 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(328): Show | 371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): 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 | a0001c0001t0033g0266 | 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0001g0034a0001c0001t0001g0053 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | 91 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(88): 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 | a0001c0002t0002g0318a0001c0002t0002g0319a0001c0002t0002g0332 | 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0002t0002g0341 | 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 | a0002c0003t0008g0021a0002c0003t0008g0274a0002c0003t0008g0275others(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 | a0001c0001t0017g0023a0001c0001t0017g0327 | 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 | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044others(2): 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0001t0011g0113 | 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 | a0001c0001t0006g0247 | 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | 59 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(56): 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 | a0001c0002t0002g0292 | 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 | 96 | a0001c0001t0003g0146a0001c0001t0003g0149a0001c0001t0003g0166others(93): 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 | a0001c0001t0003g0158a0001c0001t0004g0147a0001c0001t0004g0159others(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 | a0001c0001t0004g0215a0001c0001t0033g0266a0001c0002t0002g0299others(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 | a0003c0004t0010g0268 | 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 | a0001c0001t0004g0218 | 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 | a0001c0001t0003g0191a0001c0001t0021g0255a0001c0001t0035g0278others(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 | 9 | a0001c0001t0001g0133a0001c0001t0003g0018a0001c0001t0003g0164others(6): 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 | a0001c0002t0002g0286a0001c0002t0002g0287a0006c0011t0038g0288 | 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 | 125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(122): 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 | a0002c0003t0008g0021a0002c0003t0008g0274a0002c0003t0008g0275others(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 | a0001c0001t0033g0266 | 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 | a0001c0001t0021g0249 | 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 | 17 | a0001c0001t0003g0003a0001c0001t0003g0163a0001c0001t0003g0164others(14): 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 | a0001c0002t0002g0331 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(130): 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0001t0006g0227 | 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 | a0001c0002t0002g0348 | 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 | a0001c0001t0028g0248 | 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 | a0001c0001t0034g0277a0001c0001t0035g0278a0003c0004t0010g0268others(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 | 57 | a0001c0001t0001g0111a0001c0001t0001g0128a0001c0001t0003g0002others(54): 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 | 125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(122): 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 | 92 | a0001c0001t0017g0023a0001c0001t0017g0327a0001c0001t0023g0273others(89): Show | 101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.592-1557delT | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 5/16 | chr16 | 50341642 | ||||||
chr16:50341927
|
T | TTC | 7 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0055others(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 | 22 | a0001c0001t0003g0168a0001c0001t0003g0170a0001c0001t0003g0171others(19): 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 | 30 | a0001c0001t0001g0037a0001c0001t0003g0019a0001c0001t0003g0184others(27): 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 | 43 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0114others(40): 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 |
32 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0005g0090others(29): Show | 35 | HG00323.hp1 HG00597.hp2 HG00741.hp2 others(32): 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 |
27 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(24): 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 | a0001c0001t0005g0086a0001c0001t0005g0124a0001c0001t0005g0127others(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 | a0001c0001t0005g0094a0001c0002t0002g0318a0001c0002t0002g0319others(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 | 34 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0029others(31): 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 | 23 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(20): 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 | a0001c0001t0001g0010a0001c0001t0001g0052a0001c0001t0001g0059others(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 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0053others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0003g0157a0001c0001t0003g0165a0001c0001t0003g0166others(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 | 31 | a0001c0001t0003g0003a0001c0001t0003g0163a0001c0001t0003g0164others(28): 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 | a0001c0001t0006g0226a0001c0001t0006g0246a0001c0001t0033g0266 | 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 | a0001c0001t0016g0263a0001c0001t0016g0264a0001c0001t0016g0265others(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 | a0001c0001t0028g0248 | 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 | a0001c0001t0007g0033a0001c0001t0007g0065a0001c0001t0007g0096 | 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 | a0001c0001t0001g0049a0001c0001t0001g0069a0001c0001t0001g0118others(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 | a0001c0001t0007g0033a0001c0001t0007g0065a0001c0001t0007g0096 | 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 | a0001c0001t0005g0138a0001c0001t0005g0139a0001c0001t0005g0140others(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 | a0001c0001t0006g0242 | 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 | 91 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(88): 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 | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(176): 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 | 144 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0054others(141): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): 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 | 32 | a0001c0001t0003g0157a0001c0001t0003g0163a0001c0001t0003g0176others(29): 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0003c0004t0030g0271 | 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0028g0248 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0001t0006g0227a0001c0001t0006g0228a0001c0001t0006g0230others(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 | a0001c0001t0003g0165 | 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 | a0001c0001t0007g0065a0001c0001t0007g0096 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | 91 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(88): 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 | a0001c0001t0028g0248 | 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 | a0001c0002t0002g0359 | 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | 93 | a0001c0001t0017g0023a0001c0001t0017g0327a0001c0002t0002g0007others(90): Show | 101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): 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 | a0001c0001t0017g0023 | 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 | a0001c0001t0003g0003a0001c0001t0003g0190a0001c0001t0003g0191 | 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0237others(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 | a0003c0004t0030g0271 | 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(123): 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 | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(351): Show | 394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): 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 | a0001c0002t0002g0026 | 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 | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(351): Show | 394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): 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 | a0003c0004t0030g0271 | 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 | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(351): Show | 394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): 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 | a0001c0001t0001g0068 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(123): 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 | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(123): 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | 3 | a0001c0001t0001g0012a0001c0001t0001g0067a0001c0001t0001g0110 | 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 | a0001c0002t0002g0353 | 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 | a0001c0002t0002g0292 | 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 | a0001c0001t0005g0086 | 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 | a0001c0001t0004g0211 | 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 | a0001c0001t0001g0066 | 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 | 91 | a0001c0002t0002g0007a0001c0002t0002g0022a0001c0002t0002g0024others(88): Show | 98 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(95): 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(138): 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 | a0001c0002t0002g0323 | 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0001t0001g0097 | 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 | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(132): 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 | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(132): 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 | a0001c0001t0033g0266 | 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 | a0001c0001t0005g0139 | 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 | a0001c0001t0003g0170 | 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0004g0221 | 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 | a0001c0001t0003g0146a0001c0001t0003g0149a0001c0001t0003g0170others(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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0021g0255a0001c0001t0023g0273a0002c0003t0008g0021others(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 | a0001c0001t0003g0203 | 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 | a0001c0001t0021g0255a0001c0001t0023g0273a0002c0003t0008g0021others(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 | a0001c0001t0004g0221 | 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 | a0001c0001t0009g0105 | 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 | a0001c0001t0003g0189 | 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 | a0001c0002t0002g0024a0001c0002t0002g0321a0001c0002t0002g0322others(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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | 90 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(87): 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 | 15 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0069others(12): 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 | a0001c0001t0004g0210 | 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0003g0206 | 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 | a0001c0002t0002g0356 | 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 | a0003c0004t0030g0271 | 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 | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(123): 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | 360 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(357): Show | 400 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(397): 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 | a0001c0001t0001g0078a0001c0001t0015g0261a0001c0001t0015g0262others(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 | a0001c0001t0001g0034a0001c0001t0001g0053 | 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 | a0001c0001t0033g0266 | 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 | a0001c0002t0002g0334 | 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 | a0001c0001t0033g0266 | 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 | a0001c0001t0004g0220 | 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 | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(136): 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 | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044others(2): 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 | a0001c0001t0003g0207 | 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 | 360 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(357): Show | 400 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(397): 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 | a0001c0001t0001g0103 | 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 | a0001c0002t0018g0293 | 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 | 91 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(88): 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0033g0266 | 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 | a0001c0002t0002g0026 | 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | 17 | a0001c0001t0003g0003a0001c0001t0003g0163a0001c0001t0003g0164others(14): 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 | a0001c0002t0002g0024a0009c0010t0002g0324 | 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 | a0001c0001t0033g0266 | 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 | a0001c0001t0005g0093a0001c0001t0005g0094a0001c0001t0005g0127 | 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 | a0001c0002t0002g0025a0001c0002t0002g0334a0001c0002t0002g0360others(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 | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(351): Show | 394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): 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 | a0001c0001t0004g0211 | 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 | a0001c0001t0003g0166 | 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0004g0221 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0007g0104 | 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 | a0001c0001t0028g0248 | 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 | a0001c0001t0003g0168 | 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 | a0001c0001t0007g0033a0001c0001t0007g0065a0001c0001t0007g0096 | 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 | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(123): 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0002c0003t0023g0272 | 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 | a0001c0002t0002g0025a0001c0002t0002g0334a0001c0002t0002g0360others(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 | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(130): 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 | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(130): 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 | a0001c0001t0006g0237a0001c0001t0015g0261a0001c0001t0015g0262others(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 | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(130): 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 | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(130): 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 | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(130): 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 | a0001c0001t0009g0108 | 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 | a0001c0001t0033g0266 | 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 | a0001c0002t0002g0026a0001c0002t0002g0338a0001c0002t0002g0341 | 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 | a0001c0001t0035g0278 | 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 | a0001c0001t0001g0133 | 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 | 184 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(181): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): 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 | a0001c0001t0021g0255a0001c0001t0023g0273a0002c0003t0008g0021others(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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0275others(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 | a0001c0001t0003g0167a0001c0001t0006g0225a0001c0001t0006g0226others(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 | a0001c0001t0004g0148a0001c0002t0002g0284 | 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 | 128 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(125): 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 | a0008c0007t0015g0259 | 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 | a0001c0001t0023g0273 | 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 | 7 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0067others(4): 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 | 35 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044others(32): 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 | 187 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0066others(184): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.446+1353delA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353071 | ||||||
chr16:50353258
|
T | C | 2 | a0001c0001t0016g0263a0001c0001t0016g0264 | 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0002t0002g0326 | 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 | 331 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(328): Show | 371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.446+665delA | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 4/16 | chr16 | 50353759 | ||||||
chr16:50353759
|
ATT | A | 12 | a0001c0001t0003g0199a0001c0001t0004g0148a0001c0001t0005g0125others(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 | 4 | a0001c0001t0013g0250a0001c0001t0013g0251a0001c0001t0013g0252others(1): Show | 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 | a0001c0001t0003g0146a0001c0001t0003g0149a0001c0001t0004g0005others(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 | 27 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0039others(24): 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 | a0001c0002t0002g0292 | 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 | 6 | a0001c0001t0003g0165a0001c0001t0003g0166a0001c0001t0003g0170others(3): 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 | a0001c0001t0001g0142 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0001t0033g0266 | 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 | a0001c0002t0002g0286a0001c0002t0002g0287a0006c0011t0038g0288 | 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 | a0001c0002t0002g0025a0001c0002t0002g0360 | 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 | a0001c0001t0001g0137 | 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 | a0001c0001t0034g0277a0001c0001t0035g0278a0003c0004t0010g0268others(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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0001t0034g0277 | 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | 360 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(357): Show | 400 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(397): 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0001t0004g0144 | 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 | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(48): 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 | 183 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(180): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | 14 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0053others(11): 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 | 4 | a0001c0001t0013g0250a0001c0001t0013g0251a0001c0001t0013g0252others(1): Show | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0002t0002g0331 | 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 | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(351): Show | 394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.259-1582T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356504 | ||||||
chr16:50356512
|
T | C | 93 | a0001c0001t0017g0023a0001c0001t0017g0327a0001c0002t0002g0007others(90): Show | 101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.259-1590A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50356512 | ||||||
chr16:50356576
|
T | TA | 4 | a0001c0001t0001g0037a0001c0001t0001g0077a0001c0001t0001g0078others(1): Show | 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0004g0017a0001c0001t0004g0151a0001c0001t0004g0152others(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 | 21 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(18): 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | 107 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0029others(104): 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 | 24 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(21): 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 | a0001c0001t0003g0200 | 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 | a0001c0001t0003g0146a0001c0001t0004g0005a0001c0001t0004g0144others(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 | a0001c0001t0007g0033 | 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 | 121 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(118): 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 | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(132): 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 | a0001c0001t0004g0210a0001c0002t0002g0329a0001c0002t0002g0330others(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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0003g0202 | 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 | 331 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(328): Show | 371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): 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 | a0001c0002t0002g0026 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0005g0121 | 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 | a0001c0002t0002g0331 | 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0003g0002a0001c0001t0003g0203a0001c0001t0003g0204others(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 | a0001c0002t0002g0285 | 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 | 331 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(328): Show | 371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.259-2477C>T | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50357399 | ||||||
chr16:50357475
|
C | G | 93 | a0001c0001t0017g0023a0001c0001t0017g0327a0001c0002t0002g0007others(90): Show | 101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): 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 | a0001c0001t0033g0266 | 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 | a0001c0001t0003g0146a0001c0001t0003g0149a0001c0001t0004g0005others(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 | a0001c0001t0004g0210 | 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 | a0001c0001t0001g0014a0001c0001t0001g0079a0001c0001t0001g0115others(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 | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(123): 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 | a0001c0001t0017g0023 | 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 | a0001c0001t0001g0120 | 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 | a0001c0001t0003g0146a0001c0001t0003g0149a0001c0001t0004g0005others(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 | 93 | a0001c0001t0017g0023a0001c0001t0017g0327a0001c0002t0002g0007others(90): Show | 101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): 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 | a0001c0001t0033g0266 | 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 |
228 | a0001c0001t0001g0133a0001c0001t0003g0002a0001c0001t0003g0003others(225): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): 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 |
125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(122): 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 | a0001c0001t0006g0228a0001c0001t0006g0242 | 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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(123): 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 | 117 | a0001c0001t0001g0132a0001c0001t0003g0002a0001c0001t0003g0003others(114): 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0020g0043 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0002t0037g0290 | 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 | a0001c0001t0003g0020 | 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 | 59 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(56): 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 | a0001c0001t0003g0165a0001c0001t0003g0166a0001c0001t0034g0277others(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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0001t0006g0240 | 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 | a0001c0001t0006g0246 | 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 | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(123): 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0001t0016g0265 | 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 | a0001c0002t0002g0332 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0034g0277 | 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 | a0001c0001t0003g0207 | 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 | a0001c0001t0028g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.259-5605A>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50360527 | ||||||
chr16:50360534
|
A | G | 361 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(358): Show | 401 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(398): Show |
intron_variant | MODIFIER | c.259-5612T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50360534 | ||||||
chr16:50360627
|
T | C | 2 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0002t0039g0289 | 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 | a0001c0001t0021g0255a0001c0001t0023g0273a0002c0003t0008g0021others(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 | a0001c0002t0002g0338 | 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 | a0001c0001t0029g0222 | 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 | a0001c0001t0035g0278 | 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 | 121 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(118): 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 | a0001c0001t0003g0208a0001c0001t0003g0209 | 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 | a0001c0001t0034g0277 | 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0002t0002g0286a0001c0002t0002g0287a0006c0011t0038g0288 | 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 | a0001c0001t0005g0093a0001c0001t0005g0094a0001c0001t0005g0127 | 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 | a0001c0001t0034g0277 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0002t0002g0357a0001c0002t0002g0358a0001c0002t0002g0359others(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 | a0001c0002t0002g0333 | 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0002t0002g0336a0001c0002t0002g0337a0001c0002t0014g0258 | 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 | a0001c0001t0021g0255a0001c0001t0023g0273a0002c0003t0008g0021others(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 | a0001c0001t0021g0255a0001c0001t0023g0273a0002c0003t0008g0021others(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 | a0001c0001t0004g0221 | 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 | 89 | a0001c0001t0017g0023a0001c0001t0017g0327a0001c0002t0002g0007others(86): Show | 96 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.258+5571T>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50362519 | ||||||
chr16:50362535
|
AGGT | A | 93 | a0001c0001t0017g0023a0001c0001t0017g0327a0001c0002t0002g0007others(90): Show | 101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): 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 | a0002c0003t0008g0021a0002c0003t0008g0274a0002c0003t0008g0275others(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 | 93 | a0001c0001t0017g0023a0001c0001t0017g0327a0001c0002t0002g0007others(90): Show | 101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): 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 | a0001c0001t0021g0255a0001c0001t0023g0273a0002c0003t0008g0021others(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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0003g0164 | 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 | a0001c0001t0006g0227 | 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 | a0001c0001t0003g0163 | 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 | a0001c0001t0001g0080 | 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 | 59 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(56): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0006g0226 | 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 | a0001c0001t0001g0095a0001c0001t0007g0096a0001c0001t0034g0277others(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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0002t0002g0022a0001c0002t0002g0281a0001c0002t0002g0284others(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 | a0001c0001t0006g0226a0001c0001t0006g0227a0001c0001t0006g0228others(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 | a0001c0001t0006g0239 | 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 | 68 | a0001c0001t0017g0023a0001c0001t0017g0327a0001c0002t0002g0007others(65): Show | 74 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(71): 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 | a0001c0001t0005g0117 | 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 | 15 | a0001c0002t0002g0026a0001c0002t0002g0280a0001c0002t0002g0336others(12): 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | 90 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(87): 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 | a0001c0001t0005g0039a0001c0002t0019g0349 | 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 | a0001c0001t0001g0095a0001c0001t0013g0254a0001c0001t0028g0248 | 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 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(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 | a0001c0001t0001g0097a0001c0001t0001g0132a0001c0001t0001g0135others(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 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0001g0004a0001c0001t0001g0098a0001c0001t0001g0099others(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 | a0001c0001t0001g0128a0001c0001t0001g0129 | 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 | a0001c0001t0033g0266 | 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 | a0001c0001t0001g0029a0001c0001t0001g0082a0001c0001t0001g0084others(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 | a0001c0001t0001g0032a0001c0001t0001g0118a0001c0001t0001g0119others(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 | a0001c0001t0005g0086a0001c0001t0005g0087a0001c0001t0005g0089others(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 | a0001c0001t0005g0015a0001c0001t0005g0117a0001c0001t0005g0121others(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 | a0001c0001t0005g0016 | 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 | a0001c0001t0005g0130 | 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 | a0001c0001t0005g0140a0001c0001t0006g0246 | 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 | a0001c0001t0005g0141 | 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 | a0001c0001t0001g0133a0001c0002t0002g0280a0001c0002t0002g0342others(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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | 88 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(85): Show | 96 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(93): 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 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0020g0035 | 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 | a0001c0001t0007g0033 | 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 | a0001c0001t0023g0273a0002c0003t0008g0021a0002c0003t0008g0274others(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 | a0001c0001t0021g0255a0001c0001t0023g0273a0002c0003t0008g0021others(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 | a0001c0001t0021g0255a0001c0001t0023g0273a0002c0003t0008g0021others(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 | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(219): 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 | 355 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(352): Show | 395 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(392): 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 | a0001c0002t0002g0350a0001c0002t0002g0351 | 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 | a0001c0001t0029g0222 | 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 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0015g0261others(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 | a0001c0001t0001g0133 | 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 | 355 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(352): Show | 395 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.258+3866G>C | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 2/16 | chr16 | 50364224 | ||||||
chr16:50364572
|
C | T | 89 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(86): 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 | a0003c0004t0030g0271 | 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 | a0001c0002t0002g0281a0001c0002t0002g0282a0001c0002t0002g0283 | 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 | a0001c0002t0002g0027a0001c0002t0002g0354a0001c0002t0002g0355others(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 | a0001c0001t0033g0266 | 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 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032 | 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 | a0001c0001t0001g0030 | 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 | a0002c0003t0008g0021a0002c0003t0008g0274a0002c0003t0008g0275others(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 | a0001c0001t0004g0017a0001c0001t0004g0151a0001c0001t0004g0152others(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 | a0001c0001t0003g0223 | 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 | a0001c0001t0035g0278 | 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 | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(138): 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 | a0001c0001t0001g0134 | 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 | 356 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(353): Show | 396 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(393): 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0001g0135a0001c0001t0001g0136 | 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 | 128 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(125): 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 | a0001c0002t0002g0280 | 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 | a0001c0001t0006g0247 | 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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(123): 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 | a0001c0001t0004g0159a0001c0001t0004g0160a0001c0001t0004g0161others(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 | 129 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(126): 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 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 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 | a0001c0002t0019g0279 | 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 | a0001c0001t0005g0138a0001c0001t0005g0139a0001c0001t0005g0140others(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 | a0001c0001t0005g0138a0001c0001t0005g0139a0001c0001t0005g0140others(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 | 89 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(86): 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 | a0001c0001t0015g0261a0001c0001t0015g0262a0001c0001t0016g0263others(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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | a0001c0001t0028g0248 | 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 | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(124): 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 | 129 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(126): 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 | a0001c0001t0033g0266 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0006g0227others(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 | a0001c0002t0002g0357a0001c0002t0002g0358a0001c0002t0002g0359 | 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 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0155others(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 | a0001c0001t0004g0155a0001c0001t0004g0156 | 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 | a0001c0001t0023g0273a0001c0002t0002g0360a0002c0003t0008g0021others(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 | 91 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0006others(88): 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 | a0001c0001t0003g0157 | 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 | a0001c0001t0005g0143 | 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 | a0001c0001t0003g0146a0001c0001t0003g0149a0001c0001t0004g0005others(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 | a0001c0001t0003g0146a0001c0001t0003g0149a0001c0001t0004g0005others(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 | a0003c0004t0010g0268a0003c0004t0010g0269a0003c0004t0010g0270others(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 | a0001c0001t0034g0277a0001c0001t0035g0278 | 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 | 128 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(125): 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 | a0001c0002t0002g0361 | 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 | a0001c0002t0002g0361 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.49+39C>G | BRD7 | ENSG00000166164.17 | transcript | ENST00000394688.8 | protein_coding | 1/16 | chr16 | 50368687 |