geneid | 65980 |
---|---|
ensemblid | ENSG00000028310.18 |
hgncid | 25818 |
symbol | BRD9 |
name | bromodomain containing 9 |
refseq_nuc | NM_023924.5 |
refseq_prot | NP_076413.3 |
ensembl_nuc | ENST00000467963.6 |
ensembl_prot | ENSP00000419765.1 |
mane_status | MANE Select |
chr | chr5 |
start | 863741 |
end | 892801 |
strand | - |
ver | v1.2 |
region | chr5:863741-892801 |
region5000 | chr5:858741-897801 |
regionname0 | BRD9_chr5_863741_892801 |
regionname5000 | BRD9_chr5_858741_897801 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 597 | 346 | 83 | 70 | 139 | 9 | 43 | 97 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0002 | 0/0 | 597 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0003 | 0/0 | 597 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0004 | 0/0 | 597 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0005 | 0/0 | 597 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0006 | 0/0 | 597 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0007 | 0/0 | 597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1794 | 314 | 62 | 63 | 138 | 9 | 40 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
c0002 | 0/0 | 1794 | 20 | 12 | 6 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
c0003 | 0/0 | 1794 | 9 | 8 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
c0004 | 0/0 | 1794 | 7 | 6 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
c0005 | 0/0 | 1794 | 3 | 3 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
c0006 | 0/0 | 1794 | 3 | 0 | 0 | 3 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
c0007 | 0/0 | 1794 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
c0008 | 0/0 | 1794 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
c0009 | 0/0 | 1794 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
c0010 | 0/0 | 1794 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
c0011 | 0/0 | 1794 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
c0012 | 0/0 | 1794 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
c0013 | 0/0 | 1794 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 872 | 250 | 34 | 62 | 103 | 10 | 39 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0002 | 0/0 | 872 | 66 | 24 | 3 | 37 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0003 | 0/0 | 872 | 7 | 6 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0004 | 0/0 | 872 | 5 | 0 | 3 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0005 | 0/0 | 872 | 5 | 4 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0006 | 0/0 | 872 | 5 | 5 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0007 | 0/0 | 872 | 5 | 5 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0008 | 0/0 | 871 | 5 | 5 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0009 | 0/0 | 880 | 4 | 4 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0010 | 0/0 | 871 | 3 | 3 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0011 | 0/0 | 872 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0012 | 0/0 | 871 | 2 | 1 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0013 | 0/0 | 872 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0014 | 0/0 | 872 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0015 | 0/0 | 872 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0016 | 0/0 | 872 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
t0017 | 0/0 | 872 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 48 | 3 | 9 | 30 | 1 | 4 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0002 | 0/0 | 22 | 0 | 7 | 12 | 0 | 3 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0003 | 0/0 | 15 | 0 | 0 | 14 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0004 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0006 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0009 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0010 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0011 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0014 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0017 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1794 | 314 | 62 | 63 | 138 | 9 | 40 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0002 | 0/0 | 1794 | 20 | 12 | 6 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0004 | 0/0 | 1794 | 7 | 6 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0005 | 0/0 | 1794 | 3 | 3 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0008 | 0/0 | 1794 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0013 | 0/0 | 1794 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0002c0003 | 0/0 | 1794 | 9 | 8 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0002c0012 | 0/0 | 1794 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0003c0006 | 0/0 | 1794 | 3 | 0 | 0 | 3 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0004c0007 | 0/0 | 1794 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0005c0010 | 0/0 | 1794 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0006c0011 | 0/0 | 1794 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0007c0009 | 0/0 | 1794 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2665 | 240 | 34 | 61 | 97 | 9 | 37 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0001t0002 | 0/0 | 2665 | 57 | 18 | 0 | 37 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0001t0005 | 0/0 | 2665 | 5 | 4 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0001t0007 | 0/0 | 2665 | 5 | 5 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0001t0011 | 0/0 | 2665 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0001t0013 | 0/0 | 2665 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0001t0014 | 0/0 | 2665 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0001t0015 | 0/0 | 2665 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0001t0016 | 0/0 | 2665 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0001t0017 | 0/0 | 2665 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0002t0002 | 0/0 | 2665 | 6 | 3 | 3 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0002t0004 | 0/0 | 2665 | 5 | 0 | 3 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0002t0006 | 0/0 | 2665 | 5 | 5 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0002t0009 | 0/0 | 2673 | 4 | 4 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0004t0003 | 0/0 | 2665 | 7 | 6 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0005t0002 | 0/0 | 2665 | 3 | 3 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0008t0001 | 0/0 | 2665 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0001c0013t0001 | 0/0 | 2665 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0002c0003t0008 | 0/0 | 2664 | 4 | 4 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0002c0003t0010 | 0/0 | 2664 | 3 | 3 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0002c0003t0012 | 0/0 | 2664 | 2 | 1 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0002c0012t0008 | 0/0 | 2664 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0003c0006t0001 | 0/0 | 2665 | 3 | 0 | 0 | 3 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0004c0007t0001 | 0/0 | 2665 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0005c0010t0001 | 0/0 | 2665 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0006c0011t0001 | 0/0 | 2665 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
a0007c0009t0001 | 0/0 | 2665 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | copy fasta | chr5 | 858741 | 897801 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 48 | 3 | 9 | 30 | 1 | 4 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0002 | 0/0 | 22 | 0 | 7 | 12 | 0 | 3 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0006 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0017 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0003 | 0/0 | 15 | 0 | 0 | 14 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0004 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0005g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0007g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0007g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0011g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0013g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0014g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0015g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0016g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0001t0017g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0002t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0002t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0002t0004g0011 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0002t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0002t0006g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0002t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0002t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0002t0009g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0002t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0004t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0004t0003g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0004t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0005t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0005t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0005t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0008t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0001c0013t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0002c0003t0008g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0002c0003t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0002c0003t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0002c0003t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0002c0003t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0002c0003t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0002c0003t0010g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0002c0003t0012g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0002c0003t0012g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0002c0012t0008g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0003c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0003c0006t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0003c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0004c0007t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0005c0010t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0006c0011t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
a0007c0009t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0054 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0152 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01175 | hp1 | a0001 | c0002 | t0004 | g0011 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01192 | hp2 | a0001 | c0001 | t0013 | g0056 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01243 | hp1 | a0001 | c0004 | t0003 | g0039 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01261 | hp2 | a0002 | c0003 | t0012 | g0066 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01433 | hp2 | a0001 | c0002 | t0004 | g0052 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | IBS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01884 | hp1 | a0002 | c0003 | t0008 | g0183 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01891 | hp2 | a0001 | c0002 | t0009 | g0020 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02040 | hp2 | a0001 | c0001 | t0011 | g0022 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02083 | hp2 | a0001 | c0001 | t0011 | g0022 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02129 | hp2 | a0001 | c0001 | t0016 | g0165 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02132 | hp2 | a0001 | c0001 | t0014 | g0109 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02148 | hp1 | a0001 | c0002 | t0004 | g0011 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02258 | hp2 | a0001 | c0001 | t0017 | g0110 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02280 | hp2 | a0002 | c0003 | t0010 | g0051 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02300 | hp1 | a0007 | c0009 | t0001 | g0072 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0048 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02723 | hp2 | a0002 | c0003 | t0008 | g0186 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02735 | hp2 | a0001 | c0002 | t0004 | g0011 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02738 | hp2 | a0001 | c0001 | t0015 | g0070 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02809 | hp2 | a0001 | c0005 | t0002 | g0080 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0048 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02818 | hp2 | a0001 | c0002 | t0009 | g0177 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02886 | hp1 | a0001 | c0005 | t0002 | g0086 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02965 | hp2 | a0001 | c0004 | t0003 | g0012 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03041 | hp1 | a0002 | c0003 | t0008 | g0185 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03098 | hp2 | a0001 | c0004 | t0003 | g0012 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03139 | hp1 | a0002 | c0003 | t0008 | g0184 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03139 | hp2 | a0002 | c0003 | t0012 | g0065 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03195 | hp1 | a0001 | c0004 | t0003 | g0012 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03195 | hp2 | a0001 | c0002 | t0006 | g0179 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03209 | hp1 | a0002 | c0012 | t0008 | g0182 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03453 | hp2 | a0001 | c0002 | t0006 | g0046 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0151 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03516 | hp1 | a0001 | c0002 | t0006 | g0178 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03516 | hp2 | a0001 | c0002 | t0009 | g0020 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03579 | hp2 | a0001 | c0004 | t0003 | g0039 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03654 | hp1 | a0001 | c0013 | t0001 | g0172 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03669 | hp2 | a0006 | c0011 | t0001 | g0108 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18522 | hp2 | a0001 | c0004 | t0003 | g0012 | AFR | YRI | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18950 | hp1 | a0003 | c0006 | t0001 | g0101 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18974 | hp2 | a0004 | c0007 | t0001 | g0024 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18997 | hp1 | a0003 | c0006 | t0001 | g0100 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19043 | hp2 | a0001 | c0005 | t0002 | g0088 | AFR | LWK | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19058 | hp1 | a0003 | c0006 | t0001 | g0077 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19058 | hp2 | a0001 | c0008 | t0001 | g0063 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19059 | hp1 | a0004 | c0007 | t0001 | g0024 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19059 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0181 | AFR | YRI | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA19240 | hp2 | a0001 | c0002 | t0009 | g0020 | AFR | YRI | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA20129 | hp1 | a0001 | c0002 | t0006 | g0046 | AFR | ASW | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ASW | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA20752 | hp2 | a0005 | c0010 | t0001 | g0096 | EUR | TSI | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | GIH | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA20905 | hp2 | a0001 | c0002 | t0004 | g0011 | SAS | GIH | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02486 | hp1 | a0001 | c0002 | t0006 | g0180 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02486 | hp2 | a0001 | c0004 | t0003 | g0150 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG02559 | hp2 | a0002 | c0003 | t0010 | g0049 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG03471 | hp2 | a0002 | c0003 | t0010 | g0050 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | USA | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0017 | REF | REF | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:865498
|
C | T | 1 | a0006 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1609G>A | p.Ala537Thr | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/16 | 1753/2665 | 1609/1794 | 537/597 | chr5 | 865498 | ||
chr5:870526
|
G | A | 1 | a0003 | 3 | NA18950.hp1 NA18997.hp1 NA19058.hp1 |
missense_variant | MODERATE | c.1472C>T | p.Ser491Leu | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/16 | 1616/2665 | 1472/1794 | 491/597 | chr5 | 870526 | ||
chr5:878428
|
C | T | 1 | a0004 | 2 | NA18974.hp2 NA19059.hp1 |
missense_variant | MODERATE | c.1198G>A | p.Asp400Asn | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/16 | 1342/2665 | 1198/1794 | 400/597 | chr5 | 878428 | ||
chr5:878436
|
A | G | 1 | a0005 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1190T>C | p.Val397Ala | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/16 | 1334/2665 | 1190/1794 | 397/597 | chr5 | 878436 | ||
chr5:886629
|
C | T | 1 | a0002 | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
missense_variant | MODERATE | c.796G>A | p.Ala266Thr | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/16 | 940/2665 | 796/1794 | 266/597 | chr5 | 886629 | ||
chr5:886668
|
C | T | 1 | a0007 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.757G>A | p.Glu253Lys | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/16 | 901/2665 | 757/1794 | 253/597 | chr5 | 886668 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:865448
|
C | T | 2 | a0002c0003a0002c0012 | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
synonymous_variant | LOW | c.1659G>A | p.Leu553Leu | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/16 | 1803/2665 | 1659/1794 | 553/597 | chr5 | 865448 | ||
chr5:865469
|
C | T | 1 | a0001c0005 | 3 | HG02809.hp2 HG02886.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.1638G>A | p.Pro546Pro | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/16 | 1782/2665 | 1638/1794 | 546/597 | chr5 | 865469 | ||
chr5:870504
|
A | G | 4 | a0001c0002a0001c0004a0002c0003others(1): Show | 37 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(34): Show |
synonymous_variant | LOW | c.1494T>C | p.Val498Val | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/16 | 1638/2665 | 1494/1794 | 498/597 | chr5 | 870504 | ||
chr5:881123
|
G | A | 2 | a0002c0003a0002c0012 | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
synonymous_variant | LOW | c.1026C>T | p.Ala342Ala | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/16 | 1170/2665 | 1026/1794 | 342/597 | chr5 | 881123 | ||
chr5:881138
|
G | A | 1 | a0002c0003 | 9 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(6): Show |
synonymous_variant | LOW | c.1011C>T | p.Ser337Ser | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/16 | 1155/2665 | 1011/1794 | 337/597 | chr5 | 881138 | ||
chr5:883944
|
G | A | 2 | a0002c0003a0002c0012 | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
synonymous_variant | LOW | c.960C>T | p.Gly320Gly | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/16 | 1104/2665 | 960/1794 | 320/597 | chr5 | 883944 | ||
chr5:886609
|
C | T | 1 | a0001c0004 | 7 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
synonymous_variant | LOW | c.816G>A | p.Pro272Pro | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/16 | 960/2665 | 816/1794 | 272/597 | chr5 | 886609 | ||
chr5:887418
|
G | A | 1 | a0001c0013 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.660C>T | p.Thr220Thr | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/16 | 804/2665 | 660/1794 | 220/597 | chr5 | 887418 | ||
chr5:887418
|
G | C | 2 | a0002c0003a0002c0012 | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
synonymous_variant | LOW | c.660C>G | p.Thr220Thr | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/16 | 804/2665 | 660/1794 | 220/597 | chr5 | 887418 | ||
chr5:891258
|
C | T | 1 | a0001c0008 | 1 | NA19058.hp2 | synonymous_variant | LOW | c.297G>A | p.Glu99Glu | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/16 | 441/2665 | 297/1794 | 99/597 | chr5 | 891258 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:863745
|
G | A | 1 | a0001c0001t0017 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*723C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 723 | chr5 | 863745 | |||||
chr5:863938
|
A | G | 7 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(4): Show | 84 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*530T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 530 | chr5 | 863938 | |||||
chr5:864017
|
G | A | 1 | a0001c0002t0009 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*451C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 451 | chr5 | 864017 | |||||
chr5:864065
|
C | T | 4 | a0002c0003t0008a0002c0003t0010a0002c0003t0012others(1): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*403G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 403 | chr5 | 864065 | |||||
chr5:864073
|
A | G | 4 | a0002c0003t0008a0002c0003t0010a0002c0003t0012others(1): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*395T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 395 | chr5 | 864073 | |||||
chr5:864075
|
C | T | 1 | a0001c0001t0016 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 393 | chr5 | 864075 | |||||
chr5:864091
|
A | G | 4 | a0002c0003t0008a0002c0003t0010a0002c0003t0012others(1): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*377T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 377 | chr5 | 864091 | |||||
chr5:864110
|
C | T | 1 | a0001c0001t0015 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*358G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 358 | chr5 | 864110 | |||||
chr5:864165
|
C | T | 1 | a0001c0004t0003 | 7 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*303G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 303 | chr5 | 864165 | |||||
chr5:864189
|
C | T | 1 | a0001c0001t0014 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*279G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 279 | chr5 | 864189 | |||||
chr5:864193
|
T | TATGACTC others(1): Show |
1 | a0001c0002t0009 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*267_*274dupGGAGTC others(2): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 274 | chr5 | 864193 | |||||
chr5:864216
|
AC | A | 4 | a0002c0003t0008a0002c0003t0010a0002c0003t0012others(1): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*251delG | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 251 | chr5 | 864216 | |||||
chr5:864351
|
G | A | 1 | a0001c0002t0004 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*117C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 117 | chr5 | 864351 | |||||
chr5:864464
|
A | G | 1 | a0001c0002t0006 | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 4 | chr5 | 864464 | |||||
chr5:892693
|
G | T | 1 | a0001c0001t0013 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-36C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/16 | 36 | chr5 | 892693 | |||||
chr5:892714
|
A | C | 1 | a0001c0001t0011 | 2 | HG02040.hp2 HG02083.hp2 |
5_prime_UTR_variant | MODIFIER | c.-57T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/16 | 57 | chr5 | 892714 | |||||
chr5:892722
|
C | T | 1 | a0001c0001t0005 | 5 | HG01099.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-65G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/16 | 65 | chr5 | 892722 | |||||
chr5:892731
|
C | T | 2 | a0001c0002t0004a0002c0003t0010 | 8 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-74G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/16 | 74 | chr5 | 892731 | |||||
chr5:892746
|
G | A | 1 | a0001c0002t0006 | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-89C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/16 | 89 | chr5 | 892746 | |||||
chr5:892754
|
G | A | 3 | a0001c0001t0007a0002c0003t0008a0002c0012t0008 | 10 | HG01884.hp1 HG02451.hp2 HG02630.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-97C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/16 | 97 | chr5 | 892754 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:864708
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1694-140A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 864708 | ||||||
chr5:864813
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1694-245A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 864813 | ||||||
chr5:864912
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1694-344A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 864912 | ||||||
chr5:864940
|
C | A | 3 | a0002c0003t0010g0049a0002c0003t0010g0050a0002c0003t0010g0051 | 3 | HG02280.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1694-372G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 864940 | ||||||
chr5:864941
|
A | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1694-373T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 864941 | ||||||
chr5:865175
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1693+239C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 865175 | ||||||
chr5:865296
|
C | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(96): Show | 185 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(182): Show |
intron_variant | MODIFIER | c.1693+118G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 865296 | ||||||
chr5:865327
|
A | G | 7 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+87T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 865327 | ||||||
chr5:865587
|
T | C | 1 | a0002c0012t0008g0182 | 1 | HG03209.hp1 | splice_region_variant&intron_variant | LOW | c.1526-6A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865587 | ||||||
chr5:865781
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1526-200C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865781 | ||||||
chr5:865855
|
G | A | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1526-274C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865855 | ||||||
chr5:865865
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1526-284G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865865 | ||||||
chr5:865880
|
C | T | 4 | a0001c0001t0002g0004a0001c0001t0002g0085a0001c0001t0002g0087others(1): Show | 15 | HG00609.hp2 HG02080.hp1 NA18962.hp2 others(12): Show |
intron_variant | MODIFIER | c.1526-299G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865880 | ||||||
chr5:865900
|
G | C | 1 | a0001c0001t0001g0104 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1526-319C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865900 | ||||||
chr5:865921
|
C | T | 1 | a0002c0003t0010g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1526-340G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865921 | ||||||
chr5:865948
|
G | A | 4 | a0001c0002t0006g0046a0001c0002t0006g0178a0001c0002t0006g0179others(1): Show | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1526-367C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865948 | ||||||
chr5:866183
|
C | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1526-602G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866183 | ||||||
chr5:866276
|
A | G | 1 | a0001c0008t0001g0063 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1526-695T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866276 | ||||||
chr5:866489
|
A | G | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1526-908T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866489 | ||||||
chr5:866521
|
A | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1526-940T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866521 | ||||||
chr5:866554
|
T | C | 3 | a0002c0003t0010g0049a0002c0003t0010g0050a0002c0003t0010g0051 | 3 | HG02280.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1526-973A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866554 | ||||||
chr5:866602
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1526-1021G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866602 | ||||||
chr5:866603
|
G | A | 49 | a0001c0001t0001g0045a0001c0001t0002g0003a0001c0001t0002g0004others(46): Show | 99 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1526-1022C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866603 | ||||||
chr5:866761
|
A | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1526-1180T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866761 | ||||||
chr5:866856
|
A | T | 69 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0133others(66): Show | 119 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(116): Show |
intron_variant | MODIFIER | c.1526-1275T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866856 | ||||||
chr5:867138
|
G | A | 1 | a0002c0003t0010g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1526-1557C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867138 | ||||||
chr5:867154
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1526-1573C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867154 | ||||||
chr5:867213
|
G | C | 41 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0007others(38): Show | 84 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(81): Show |
intron_variant | MODIFIER | c.1526-1632C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867213 | ||||||
chr5:867487
|
G | A | 1 | a0001c0001t0001g0016 | 3 | HG02132.hp1 NA18950.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1526-1906C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867487 | ||||||
chr5:867490
|
A | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0161a0001c0001t0001g0164others(2): Show | 8 | HG01192.hp1 HG01981.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1526-1909T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867490 | ||||||
chr5:867564
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1526-1983G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867564 | ||||||
chr5:867745
|
C | T | 1 | a0003c0006t0001g0100 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1526-2164G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867745 | ||||||
chr5:867879
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0073 | 2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1526-2298C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867879 | ||||||
chr5:868453
|
C | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1525+2020G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 868453 | ||||||
chr5:868570
|
T | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525+1903A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 868570 | ||||||
chr5:868626
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1525+1847A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 868626 | ||||||
chr5:868686
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1525+1787G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 868686 | ||||||
chr5:868731
|
G | A | 1 | a0001c0001t0001g0017 | 3 | HG00323.hp2 HG01109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1525+1742C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 868731 | ||||||
chr5:868924
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1525+1549G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 868924 | ||||||
chr5:869301
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1525+1172T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869301 | ||||||
chr5:869309
|
G | A | 7 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(4): Show | 13 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1525+1164C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869309 | ||||||
chr5:869431
|
C | T | 21 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(18): Show | 32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1525+1042G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869431 | ||||||
chr5:869450
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1525+1023A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869450 | ||||||
chr5:869467
|
A | C | 17 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(14): Show | 23 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1525+1006T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869467 | ||||||
chr5:869514
|
C | CAAGTCTC others(7): Show |
10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525+945_1525+958d others(16): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869514 | ||||||
chr5:869733
|
T | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525+740A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869733 | ||||||
chr5:869752
|
G | T | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525+721C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869752 | ||||||
chr5:869764
|
G | A | 1 | a0002c0003t0010g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1525+709C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869764 | ||||||
chr5:869806
|
C | T | 4 | a0001c0002t0006g0046a0001c0002t0006g0178a0001c0002t0006g0179others(1): Show | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525+667G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869806 | ||||||
chr5:869861
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1525+612T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869861 | ||||||
chr5:869873
|
G | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1525+600C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869873 | ||||||
chr5:870072
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1525+401G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 870072 | ||||||
chr5:870179
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0113a0001c0001t0001g0114 | 5 | HG00323.hp2 HG01070.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525+294C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 870179 | ||||||
chr5:870181
|
T | C | 1 | a0001c0001t0002g0090 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1525+292A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 870181 | ||||||
chr5:870339
|
G | T | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525+134C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 870339 | ||||||
chr5:870341
|
C | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525+132G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 870341 | ||||||
chr5:870440
|
A | G | 21 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(18): Show | 32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1525+33T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 870440 | ||||||
chr5:870625
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0059a0001c0001t0001g0098others(2): Show | 7 | HG00323.hp1 HG00738.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1423-50G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 870625 | ||||||
chr5:870725
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1423-150C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 870725 | ||||||
chr5:870811
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1423-236G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 870811 | ||||||
chr5:870828
|
G | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02056.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1423-253C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 870828 | ||||||
chr5:870990
|
C | CT | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1423-416dupA | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 870990 | ||||||
chr5:870999
|
ACT | A | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1423-426_1423-425d others(4): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 870999 | ||||||
chr5:871018
|
G | A | 1 | a0001c0001t0001g0041 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1423-443C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 871018 | ||||||
chr5:871018
|
G | C | 3 | a0003c0006t0001g0077a0003c0006t0001g0100a0003c0006t0001g0101 | 3 | NA18950.hp1 NA18997.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1423-443C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 871018 | ||||||
chr5:871066
|
T | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0148 | 3 | HG00099.hp1 HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1422+460A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 871066 | ||||||
chr5:871069
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1422+457G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 871069 | ||||||
chr5:871233
|
T | C | 21 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(18): Show | 32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1422+293A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 871233 | ||||||
chr5:871483
|
T | C | 21 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(18): Show | 32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1422+43A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 871483 | ||||||
chr5:871657
|
T | C | 7 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(4): Show | 13 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1384-93A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 871657 | ||||||
chr5:871790
|
G | A | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-226C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 871790 | ||||||
chr5:871842
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1384-278C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 871842 | ||||||
chr5:872001
|
G | T | 1 | a0001c0001t0005g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1384-437C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872001 | ||||||
chr5:872052
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0019others(5): Show | 16 | HG00140.hp2 HG00741.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.1384-488G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872052 | ||||||
chr5:872053
|
G | A | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-489C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872053 | ||||||
chr5:872087
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0097a0001c0001t0001g0105others(2): Show | 13 | HG00544.hp1 HG00558.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.1384-523C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872087 | ||||||
chr5:872105
|
T | TGGGCC | 3 | a0001c0005t0002g0080a0001c0005t0002g0086a0001c0005t0002g0088 | 3 | HG02809.hp2 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1384-546_1384-542d others(7): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872105 | ||||||
chr5:872111
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1384-547C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872111 | ||||||
chr5:872148
|
C | T | 6 | a0001c0002t0006g0046a0001c0002t0006g0178a0001c0002t0006g0179others(3): Show | 9 | HG01891.hp2 HG02486.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1384-584G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872148 | ||||||
chr5:872151
|
G | A | 1 | a0002c0012t0008g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1384-587C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872151 | ||||||
chr5:872160
|
G | A | 1 | a0002c0003t0010g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1384-596C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872160 | ||||||
chr5:872194
|
T | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02976.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1384-630A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872194 | ||||||
chr5:872195
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1384-631C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872195 | ||||||
chr5:872239
|
A | G | 3 | a0001c0001t0002g0031a0001c0001t0002g0125a0001c0001t0002g0126 | 4 | HG02257.hp2 HG02258.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-675T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872239 | ||||||
chr5:872251
|
C | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-687G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872251 | ||||||
chr5:872252
|
G | A | 1 | a0001c0002t0004g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1384-688C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872252 | ||||||
chr5:872314
|
A | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-750T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872314 | ||||||
chr5:872324
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1384-760C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872324 | ||||||
chr5:872471
|
A | G | 4 | a0001c0002t0006g0046a0001c0002t0006g0178a0001c0002t0006g0179others(1): Show | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1384-907T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872471 | ||||||
chr5:872506
|
G | A | 4 | a0001c0002t0006g0046a0001c0002t0006g0178a0001c0002t0006g0179others(1): Show | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1384-942C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872506 | ||||||
chr5:872515
|
G | C | 1 | a0001c0005t0002g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1384-951C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872515 | ||||||
chr5:872515
|
G | T | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-951C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872515 | ||||||
chr5:872641
|
G | C | 3 | a0002c0003t0010g0049a0002c0003t0010g0050a0002c0003t0010g0051 | 3 | HG02280.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1384-1077C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872641 | ||||||
chr5:872650
|
T | G | 21 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(18): Show | 32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1384-1086A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872650 | ||||||
chr5:872693
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02056.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1384-1129G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872693 | ||||||
chr5:872707
|
A | T | 1 | a0001c0001t0001g0005 | 9 | HG00544.hp1 HG00558.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1384-1143T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872707 | ||||||
chr5:872962
|
A | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-1398T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872962 | ||||||
chr5:873033
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-1469G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873033 | ||||||
chr5:873107
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-1543C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873107 | ||||||
chr5:873222
|
T | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-1658A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873222 | ||||||
chr5:873237
|
C | T | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-1673G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873237 | ||||||
chr5:873336
|
T | C | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-1772A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873336 | ||||||
chr5:873476
|
A | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0016g0165 | 10 | HG01070.hp2 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1384-1912T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873476 | ||||||
chr5:873484
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1384-1920A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873484 | ||||||
chr5:873591
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(39): Show | 78 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1384-2027G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873591 | ||||||
chr5:873669
|
C | G | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-2105G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873669 | ||||||
chr5:873683
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(82): Show | 166 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(163): Show |
intron_variant | MODIFIER | c.1384-2119T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873683 | ||||||
chr5:873745
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-2181G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873745 | ||||||
chr5:873788
|
A | T | 3 | a0001c0004t0003g0012a0001c0004t0003g0039a0001c0004t0003g0150 | 7 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1384-2224T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873788 | ||||||
chr5:873805
|
T | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-2241A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873805 | ||||||
chr5:873806
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-2242C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873806 | ||||||
chr5:873833
|
G | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2268C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873833 | ||||||
chr5:873886
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0019others(4): Show | 15 | HG00140.hp2 HG00741.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1383+2215C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873886 | ||||||
chr5:873904
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1383+2197C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873904 | ||||||
chr5:873907
|
G | A | 1 | a0001c0001t0007g0047 | 2 | HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1383+2194C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873907 | ||||||
chr5:873995
|
T | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2106A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873995 | ||||||
chr5:874047
|
A | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2054T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874047 | ||||||
chr5:874068
|
C | T | 1 | a0001c0001t0001g0019 | 3 | HG01123.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1383+2033G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874068 | ||||||
chr5:874148
|
C | CCTAGA | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1948_1383+195 others(9): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874148 | ||||||
chr5:874324
|
T | TA | 3 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0152 | 5 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1383+1776dupT | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874324 | ||||||
chr5:874362
|
G | A | 6 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0152others(3): Show | 12 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1383+1739C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874362 | ||||||
chr5:874391
|
T | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1710A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874391 | ||||||
chr5:874402
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1699G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874402 | ||||||
chr5:874479
|
G | A | 1 | a0001c0002t0002g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1383+1622C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874479 | ||||||
chr5:874610
|
C | A | 1 | a0002c0012t0008g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1383+1491G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874610 | ||||||
chr5:874645
|
A | G | 1 | a0001c0001t0001g0036 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1383+1456T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874645 | ||||||
chr5:874658
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1443C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874658 | ||||||
chr5:874750
|
C | T | 2 | a0002c0003t0010g0050a0002c0003t0010g0051 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1383+1351G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874750 | ||||||
chr5:874788
|
C | T | 7 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(4): Show | 13 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1383+1313G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874788 | ||||||
chr5:874873
|
C | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(27): Show | 66 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1383+1228G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874873 | ||||||
chr5:874930
|
G | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1171C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874930 | ||||||
chr5:874937
|
G | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1164C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874937 | ||||||
chr5:874977
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1383+1124A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874977 | ||||||
chr5:875144
|
G | A | 4 | a0001c0002t0006g0046a0001c0002t0006g0178a0001c0002t0006g0179others(1): Show | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1383+957C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875144 | ||||||
chr5:875338
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1383+763C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875338 | ||||||
chr5:875347
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+754G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875347 | ||||||
chr5:875349
|
C | CA | 5 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0004t0003g0012others(2): Show | 11 | HG01081.hp1 HG01168.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1383+751_1383+752i others(3): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875349 | ||||||
chr5:875349
|
C | CT | 8 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0143others(5): Show | 8 | HG02055.hp2 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1383+751dupA | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875349 | ||||||
chr5:875349
|
CT | C | 11 | a0001c0001t0001g0028a0002c0003t0008g0183a0002c0003t0008g0184others(8): Show | 12 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1383+751delA | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875349 | ||||||
chr5:875373
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+728C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875373 | ||||||
chr5:875379
|
G | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0104 | 6 | HG00408.hp1 HG00673.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1383+722C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875379 | ||||||
chr5:875474
|
A | T | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1383+627T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875474 | ||||||
chr5:875505
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1383+596C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875505 | ||||||
chr5:875889
|
G | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(22): Show | 58 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1383+212C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875889 | ||||||
chr5:875946
|
C | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1383+155G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875946 | ||||||
chr5:875961
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1383+140G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875961 | ||||||
chr5:875973
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1383+128G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875973 | ||||||
chr5:875981
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+120G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875981 | ||||||
chr5:875998
|
C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0041others(2): Show | 10 | HG02109.hp2 HG02145.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+103G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875998 | ||||||
chr5:876010
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+91C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876010 | ||||||
chr5:876046
|
G | A | 12 | a0001c0001t0001g0029a0001c0001t0001g0130a0002c0003t0008g0183others(9): Show | 13 | HG00738.hp1 HG01069.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1383+55C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876046 | ||||||
chr5:876064
|
G | C | 1 | a0005c0010t0001g0096 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1383+37C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876064 | ||||||
chr5:876072
|
C | T | 10 | a0001c0001t0001g0142a0001c0002t0002g0037a0001c0002t0002g0038others(7): Show | 18 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1383+29G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876072 | ||||||
chr5:876077
|
A | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+24T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876077 | ||||||
chr5:876082
|
C | T | 2 | a0003c0006t0001g0100a0003c0006t0001g0101 | 2 | NA18950.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1383+19G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876082 | ||||||
chr5:876087
|
C | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+14G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876087 | ||||||
chr5:876224
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0120others(2): Show | 6 | HG02280.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1272-12C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876224 | ||||||
chr5:876262
|
G | A | 1 | a0002c0003t0010g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1272-50C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876262 | ||||||
chr5:876317
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0079 | 3 | HG02109.hp2 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1272-105G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876317 | ||||||
chr5:876321
|
G | C | 8 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272-109C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876321 | ||||||
chr5:876347
|
T | G | 29 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0133others(26): Show | 38 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.1272-135A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876347 | ||||||
chr5:876421
|
G | A | 3 | a0001c0005t0002g0080a0001c0005t0002g0086a0001c0005t0002g0088 | 3 | HG02809.hp2 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1272-209C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876421 | ||||||
chr5:876518
|
G | A | 1 | a0003c0006t0001g0077 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1272-306C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876518 | ||||||
chr5:876588
|
T | A | 1 | a0001c0001t0002g0093 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1272-376A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876588 | ||||||
chr5:876594
|
C | T | 7 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(4): Show | 13 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1272-382G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876594 | ||||||
chr5:876721
|
A | C | 1 | a0001c0001t0001g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1272-509T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876721 | ||||||
chr5:876755
|
C | G | 9 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(6): Show | 9 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272-543G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876755 | ||||||
chr5:876791
|
A | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272-579T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876791 | ||||||
chr5:876851
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272-639C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876851 | ||||||
chr5:876865
|
C | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272-653G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876865 | ||||||
chr5:876888
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272-676C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876888 | ||||||
chr5:876911
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1272-699C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876911 | ||||||
chr5:876911
|
G | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272-699C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876911 | ||||||
chr5:876961
|
C | A | 1 | a0001c0001t0002g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1272-749G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876961 | ||||||
chr5:877048
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1272-836G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877048 | ||||||
chr5:877073
|
G | A | 8 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(5): Show | 8 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272-861C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877073 | ||||||
chr5:877152
|
A | G | 7 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0133others(4): Show | 8 | HG02280.hp1 HG02818.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272-940T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877152 | ||||||
chr5:877213
|
G | A | 4 | a0002c0003t0010g0049a0002c0003t0010g0050a0002c0003t0010g0051others(1): Show | 4 | HG02280.hp2 HG02559.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-1001C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877213 | ||||||
chr5:877238
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272-1026G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877238 | ||||||
chr5:877344
|
G | A | 9 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(6): Show | 9 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1271+1011C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877344 | ||||||
chr5:877377
|
G | A | 21 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(18): Show | 32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1271+978C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877377 | ||||||
chr5:877567
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0098 | 2 | HG00738.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1271+788T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877567 | ||||||
chr5:877584
|
C | A | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1271+771G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877584 | ||||||
chr5:877635
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+720G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877635 | ||||||
chr5:877667
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1271+688C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877667 | ||||||
chr5:877701
|
A | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+654T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877701 | ||||||
chr5:877724
|
T | G | 1 | a0001c0001t0002g0124 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1271+631A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877724 | ||||||
chr5:877734
|
G | A | 4 | a0001c0002t0006g0046a0001c0002t0006g0178a0001c0002t0006g0179others(1): Show | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271+621C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877734 | ||||||
chr5:877742
|
T | A | 1 | a0001c0001t0001g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1271+613A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877742 | ||||||
chr5:877779
|
T | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+576A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877779 | ||||||
chr5:877785
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1271+570G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877785 | ||||||
chr5:877924
|
A | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+431T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877924 | ||||||
chr5:877937
|
C | T | 11 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0133others(8): Show | 18 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1271+418G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877937 | ||||||
chr5:877942
|
C | G | 1 | a0002c0003t0010g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1271+413G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877942 | ||||||
chr5:877967
|
G | C | 1 | a0002c0003t0010g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1271+388C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877967 | ||||||
chr5:878018
|
A | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+337T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878018 | ||||||
chr5:878033
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1271+322C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878033 | ||||||
chr5:878068
|
T | C | 21 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(18): Show | 32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1271+287A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878068 | ||||||
chr5:878145
|
A | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+210T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878145 | ||||||
chr5:878238
|
A | C | 3 | a0002c0003t0010g0049a0002c0003t0010g0050a0002c0003t0010g0051 | 3 | HG02280.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1271+117T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878238 | ||||||
chr5:878271
|
G | A | 1 | a0001c0001t0001g0030 | 2 | NA18962.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1271+84C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878271 | ||||||
chr5:878281
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1271+74C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878281 | ||||||
chr5:878284
|
A | G | 1 | a0001c0001t0001g0036 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1271+71T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878284 | ||||||
chr5:878289
|
A | G | 1 | a0001c0001t0001g0036 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1271+66T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878289 | ||||||
chr5:878290
|
C | G | 1 | a0001c0001t0001g0036 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1271+65G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878290 | ||||||
chr5:878306
|
A | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+49T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878306 | ||||||
chr5:878333
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+22C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878333 | ||||||
chr5:878334
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1271+21G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878334 | ||||||
chr5:878492
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18959.hp1 | splice_region_variant&intron_variant | LOW | c.1139-5C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878492 | ||||||
chr5:878550
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1139-63G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878550 | ||||||
chr5:878632
|
A | G | 25 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(22): Show | 37 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.1139-145T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878632 | ||||||
chr5:878642
|
T | G | 15 | a0001c0001t0001g0169a0001c0002t0006g0046a0001c0002t0006g0178others(12): Show | 16 | HG01261.hp2 HG01884.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.1139-155A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878642 | ||||||
chr5:878645
|
C | A | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1139-158G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878645 | ||||||
chr5:878684
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01106.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1139-197A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878684 | ||||||
chr5:878685
|
T | G | 1 | a0002c0003t0008g0185 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1139-198A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878685 | ||||||
chr5:878758
|
T | C | 6 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0152others(3): Show | 12 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1139-271A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878758 | ||||||
chr5:878768
|
C | T | 1 | a0001c0001t0001g0043 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1139-281G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878768 | ||||||
chr5:878808
|
A | G | 1 | a0001c0004t0003g0039 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1139-321T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878808 | ||||||
chr5:878820
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1139-333G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878820 | ||||||
chr5:878827
|
A | G | 2 | a0001c0001t0011g0022a0001c0002t0002g0151 | 3 | HG02040.hp2 HG02083.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1139-340T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878827 | ||||||
chr5:878838
|
C | T | 1 | a0001c0005t0002g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1139-351G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878838 | ||||||
chr5:878985
|
A | G | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1139-498T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878985 | ||||||
chr5:878990
|
C | CA | 11 | a0001c0002t0002g0151a0002c0003t0008g0183a0002c0003t0008g0184others(8): Show | 11 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1139-504dupT | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878990 | ||||||
chr5:879017
|
G | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1139-530C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879017 | ||||||
chr5:879064
|
A | AC | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1139-578_1139-577i others(3): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879064 | ||||||
chr5:879068
|
A | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1139-581T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879068 | ||||||
chr5:879069
|
A | C | 1 | a0001c0002t0009g0177 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1139-582T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879069 | ||||||
chr5:879107
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1139-620C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879107 | ||||||
chr5:879308
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1138+486A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879308 | ||||||
chr5:879321
|
C | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0148a0002c0003t0010g0049others(3): Show | 7 | HG00099.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1138+473G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879321 | ||||||
chr5:879339
|
G | A | 30 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0007others(27): Show | 67 | HG00609.hp2 HG01099.hp1 HG01192.hp2 others(64): Show |
intron_variant | MODIFIER | c.1138+455C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879339 | ||||||
chr5:879357
|
T | C | 1 | a0001c0004t0003g0012 | 4 | HG02965.hp2 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1138+437A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879357 | ||||||
chr5:879391
|
T | C | 49 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0133others(46): Show | 91 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(88): Show |
intron_variant | MODIFIER | c.1138+403A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879391 | ||||||
chr5:879392
|
G | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0062a0001c0001t0002g0078others(2): Show | 11 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1138+402C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879392 | ||||||
chr5:879398
|
T | G | 55 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0133others(52): Show | 99 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1138+396A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879398 | ||||||
chr5:879414
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0091 | 2 | NA18980.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1138+380C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879414 | ||||||
chr5:879450
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1138+344C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879450 | ||||||
chr5:879462
|
A | G | 8 | a0001c0001t0002g0003a0001c0001t0002g0033a0001c0001t0002g0058others(5): Show | 23 | HG02027.hp2 HG03927.hp1 NA18943.hp1 others(20): Show |
intron_variant | MODIFIER | c.1138+332T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879462 | ||||||
chr5:879491
|
A | G | 4 | a0001c0002t0006g0046a0001c0002t0006g0178a0001c0002t0006g0179others(1): Show | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138+303T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879491 | ||||||
chr5:879527
|
G | A | 7 | a0001c0002t0004g0011a0001c0002t0004g0052a0001c0002t0009g0020others(4): Show | 12 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1138+267C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879527 | ||||||
chr5:879543
|
C | T | 26 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0007others(23): Show | 59 | HG00609.hp2 HG01099.hp1 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.1138+251G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879543 | ||||||
chr5:879582
|
T | C | 1 | a0001c0002t0009g0020 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1138+212A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879582 | ||||||
chr5:879597
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1138+197G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879597 | ||||||
chr5:879622
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1138+172C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879622 | ||||||
chr5:879655
|
T | G | 1 | a0001c0001t0002g0128 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1138+139A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879655 | ||||||
chr5:879722
|
T | C | 6 | a0001c0001t0001g0144a0001c0002t0004g0011a0001c0002t0004g0052others(3): Show | 11 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1138+72A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879722 | ||||||
chr5:879974
|
C | A | 7 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1043-85G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 879974 | ||||||
chr5:879984
|
G | C | 1 | a0001c0001t0002g0129 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1043-95C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 879984 | ||||||
chr5:879991
|
T | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1043-102A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 879991 | ||||||
chr5:879998
|
A | G | 31 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0076others(28): Show | 43 | HG00639.hp1 HG01081.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.1043-109T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 879998 | ||||||
chr5:880031
|
C | G | 2 | a0001c0002t0002g0038a0001c0002t0002g0152 | 3 | HG01081.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1043-142G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880031 | ||||||
chr5:880102
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1043-213C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880102 | ||||||
chr5:880207
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1043-318G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880207 | ||||||
chr5:880208
|
G | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043-319C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880208 | ||||||
chr5:880211
|
T | C | 11 | a0001c0001t0001g0130a0002c0003t0008g0183a0002c0003t0008g0184others(8): Show | 11 | HG00738.hp1 HG01261.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1043-322A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880211 | ||||||
chr5:880235
|
T | C | 4 | a0001c0002t0006g0046a0001c0002t0006g0178a0001c0002t0006g0179others(1): Show | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043-346A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880235 | ||||||
chr5:880335
|
C | G | 9 | a0002c0003t0008g0183a0002c0003t0008g0185a0002c0003t0008g0186others(6): Show | 9 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1043-446G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880335 | ||||||
chr5:880458
|
G | A | 1 | a0001c0001t0001g0032 | 2 | HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1043-569C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880458 | ||||||
chr5:880485
|
C | G | 1 | a0001c0001t0002g0085 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1043-596G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880485 | ||||||
chr5:880498
|
T | C | 8 | a0001c0001t0001g0084a0001c0002t0002g0037a0001c0002t0002g0038others(5): Show | 14 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1042+609A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880498 | ||||||
chr5:880500
|
A | C | 10 | a0001c0001t0001g0084a0001c0002t0002g0037a0001c0002t0002g0038others(7): Show | 18 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1042+607T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880500 | ||||||
chr5:880501
|
G | A | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042+606C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880501 | ||||||
chr5:880538
|
C | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0162others(1): Show | 6 | HG02559.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042+569G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880538 | ||||||
chr5:880561
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+546G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880561 | ||||||
chr5:880564
|
G | A | 1 | a0001c0001t0002g0033 | 2 | NA18974.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.1042+543C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880564 | ||||||
chr5:880569
|
C | T | 1 | a0002c0003t0012g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1042+538G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880569 | ||||||
chr5:880572
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1042+535C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880572 | ||||||
chr5:880578
|
G | A | 1 | a0001c0001t0001g0018 | 3 | HG00741.hp1 HG01256.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1042+529C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880578 | ||||||
chr5:880604
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+503G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880604 | ||||||
chr5:880616
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1042+491T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880616 | ||||||
chr5:880656
|
C | T | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042+451G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880656 | ||||||
chr5:880672
|
A | C | 7 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(4): Show | 13 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1042+435T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880672 | ||||||
chr5:880676
|
T | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+431A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880676 | ||||||
chr5:880725
|
A | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+382T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880725 | ||||||
chr5:880768
|
T | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+339A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880768 | ||||||
chr5:880860
|
A | G | 3 | a0001c0001t0002g0157a0001c0002t0004g0011a0001c0002t0004g0052 | 6 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042+247T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880860 | ||||||
chr5:880874
|
G | A | 1 | a0001c0001t0007g0048 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1042+233C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880874 | ||||||
chr5:880889
|
C | A | 2 | a0001c0002t0006g0179a0001c0002t0006g0180 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1042+218G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880889 | ||||||
chr5:880952
|
G | A | 1 | a0001c0001t0001g0034 | 2 | HG00597.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1042+155C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880952 | ||||||
chr5:880972
|
C | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(26): Show | 65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1042+135G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880972 | ||||||
chr5:880972
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+135G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880972 | ||||||
chr5:880978
|
AGGTCG | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0133others(1): Show | 5 | HG02280.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042+124_1042+128d others(7): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880978 | ||||||
chr5:881042
|
A | G | 1 | a0001c0001t0002g0035 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1042+65T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 881042 | ||||||
chr5:881090
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1042+17G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 881090 | ||||||
chr5:881516
|
C | T | 3 | a0001c0004t0003g0012a0001c0004t0003g0039a0001c0004t0003g0150 | 7 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-334G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881516 | ||||||
chr5:881532
|
C | T | 6 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(3): Show | 6 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-350G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881532 | ||||||
chr5:881596
|
C | T | 8 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0152others(5): Show | 16 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.967-414G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881596 | ||||||
chr5:881610
|
GATCC | G | 7 | a0001c0001t0005g0021a0001c0001t0005g0053a0001c0001t0005g0054others(4): Show | 10 | HG01099.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.967-432_967-429del others(4): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881610 | ||||||
chr5:881679
|
G | A | 3 | a0001c0001t0001g0131a0001c0002t0009g0020a0001c0002t0009g0177 | 5 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-497C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881679 | ||||||
chr5:881763
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.967-581G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881763 | ||||||
chr5:881795
|
G | C | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-613C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881795 | ||||||
chr5:881855
|
G | A | 14 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(11): Show | 21 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.967-673C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881855 | ||||||
chr5:881908
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.967-726C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881908 | ||||||
chr5:882133
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.967-951C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882133 | ||||||
chr5:882362
|
A | T | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-1180T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882362 | ||||||
chr5:882425
|
T | C | 4 | a0001c0002t0006g0046a0001c0002t0006g0178a0001c0002t0006g0179others(1): Show | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-1243A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882425 | ||||||
chr5:882434
|
C | T | 4 | a0001c0001t0001g0149a0002c0003t0010g0049a0002c0003t0010g0050others(1): Show | 4 | HG02280.hp2 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-1252G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882434 | ||||||
chr5:882441
|
C | G | 1 | a0001c0002t0002g0037 | 2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.967-1259G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882441 | ||||||
chr5:882471
|
C | T | 7 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-1289G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882471 | ||||||
chr5:882518
|
C | T | 1 | a0001c0005t0002g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.967-1336G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882518 | ||||||
chr5:882524
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.967-1342G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882524 | ||||||
chr5:882525
|
G | A | 1 | a0001c0001t0001g0041 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.967-1343C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882525 | ||||||
chr5:882635
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+1303G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882635 | ||||||
chr5:882742
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+1196C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882742 | ||||||
chr5:882750
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.966+1188G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882750 | ||||||
chr5:882811
|
G | C | 1 | a0001c0002t0009g0177 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.966+1127C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882811 | ||||||
chr5:882829
|
T | G | 10 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0133others(7): Show | 11 | HG02280.hp1 HG02572.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.966+1109A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882829 | ||||||
chr5:882854
|
T | A | 1 | a0001c0001t0001g0019 | 3 | HG01123.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.966+1084A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882854 | ||||||
chr5:882909
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+1029G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882909 | ||||||
chr5:882944
|
G | T | 3 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0152 | 5 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.966+994C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882944 | ||||||
chr5:882947
|
AACCACAA others(24): Show |
A | 7 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+960_966+990del others(31): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882947 | ||||||
chr5:882950
|
C | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(26): Show | 65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.966+988G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882950 | ||||||
chr5:882999
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.966+939C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882999 | ||||||
chr5:883052
|
T | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+886A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883052 | ||||||
chr5:883108
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0079 | 3 | HG02109.hp2 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.966+830G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883108 | ||||||
chr5:883129
|
CCACA | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0133others(1): Show | 5 | HG02280.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.966+805_966+808del others(4): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883129 | ||||||
chr5:883172
|
C | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+766G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883172 | ||||||
chr5:883185
|
T | G | 7 | a0001c0002t0004g0011a0001c0002t0004g0052a0001c0002t0009g0020others(4): Show | 16 | HG01175.hp1 HG01243.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.966+753A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883185 | ||||||
chr5:883190
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.966+748A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883190 | ||||||
chr5:883196
|
C | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+742G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883196 | ||||||
chr5:883204
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+734G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883204 | ||||||
chr5:883228
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.966+710C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883228 | ||||||
chr5:883266
|
T | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+672A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883266 | ||||||
chr5:883509
|
T | C | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+429A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883509 | ||||||
chr5:883522
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(26): Show | 65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.966+416C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883522 | ||||||
chr5:883540
|
C | T | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+398G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883540 | ||||||
chr5:883561
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.966+377T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883561 | ||||||
chr5:883821
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.966+117G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883821 | ||||||
chr5:883846
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+92C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883846 | ||||||
chr5:883903
|
C | T | 1 | a0003c0006t0001g0077 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.966+35G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883903 | ||||||
chr5:884136
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(26): Show | 65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.834-66C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884136 | ||||||
chr5:884244
|
G | A | 11 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(8): Show | 22 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.834-174C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884244 | ||||||
chr5:884324
|
A | C | 11 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(8): Show | 22 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.834-254T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884324 | ||||||
chr5:884334
|
A | G | 1 | a0001c0002t0002g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.834-264T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884334 | ||||||
chr5:884388
|
T | C | 6 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0152others(3): Show | 12 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.834-318A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884388 | ||||||
chr5:884523
|
T | G | 7 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(4): Show | 13 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.834-453A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884523 | ||||||
chr5:884569
|
T | C | 21 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(18): Show | 32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.834-499A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884569 | ||||||
chr5:884655
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0076 | 6 | HG00639.hp1 HG01255.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.834-585G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884655 | ||||||
chr5:884709
|
T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0133others(1): Show | 5 | HG02280.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.834-639A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884709 | ||||||
chr5:885045
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.834-975G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885045 | ||||||
chr5:885046
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.834-976G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885046 | ||||||
chr5:885092
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.834-1022C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885092 | ||||||
chr5:885203
|
A | C | 7 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.834-1133T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885203 | ||||||
chr5:885237
|
C | G | 3 | a0001c0004t0003g0012a0001c0004t0003g0039a0001c0004t0003g0150 | 7 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.834-1167G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885237 | ||||||
chr5:885319
|
C | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(26): Show | 65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.834-1249G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885319 | ||||||
chr5:885321
|
A | G | 1 | a0001c0001t0001g0042 | 2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.834-1251T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885321 | ||||||
chr5:885339
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+1253G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885339 | ||||||
chr5:885426
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+1166C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885426 | ||||||
chr5:885462
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.833+1130A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885462 | ||||||
chr5:885464
|
T | G | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.833+1128A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885464 | ||||||
chr5:885517
|
G | A | 21 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(18): Show | 32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.833+1075C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885517 | ||||||
chr5:885529
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.833+1063G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885529 | ||||||
chr5:885530
|
T | A | 1 | a0001c0001t0005g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.833+1062A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885530 | ||||||
chr5:885533
|
A | C | 1 | a0001c0001t0005g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.833+1059T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885533 | ||||||
chr5:885552
|
A | G | 1 | a0001c0002t0009g0020 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.833+1040T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885552 | ||||||
chr5:885563
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.833+1029G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885563 | ||||||
chr5:885593
|
C | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(26): Show | 65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.833+999G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885593 | ||||||
chr5:885607
|
T | C | 1 | a0002c0003t0010g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.833+985A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885607 | ||||||
chr5:885720
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01106.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.833+872C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885720 | ||||||
chr5:885792
|
T | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+800A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885792 | ||||||
chr5:885796
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+796C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885796 | ||||||
chr5:885799
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.833+793G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885799 | ||||||
chr5:885802
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.833+790A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885802 | ||||||
chr5:885850
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.833+742A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885850 | ||||||
chr5:885935
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.833+657G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885935 | ||||||
chr5:885950
|
C | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+642G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885950 | ||||||
chr5:886084
|
C | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.833+508G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886084 | ||||||
chr5:886111
|
G | A | 11 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(8): Show | 22 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.833+481C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886111 | ||||||
chr5:886276
|
G | A | 3 | a0001c0001t0001g0138a0001c0002t0004g0011a0001c0002t0004g0052 | 6 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.833+316C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886276 | ||||||
chr5:886475
|
T | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+117A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886475 | ||||||
chr5:886482
|
G | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+110C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886482 | ||||||
chr5:886574
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.833+18A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886574 | ||||||
chr5:886584
|
A | G | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.833+8T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886584 | ||||||
chr5:886891
|
G | A | 1 | a0001c0001t0007g0048 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.718-184C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/15 | chr5 | 886891 | ||||||
chr5:886928
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.718-221C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/15 | chr5 | 886928 | ||||||
chr5:887013
|
A | AGCCACTG others(6): Show |
2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-307_718-306ins others(13): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/15 | chr5 | 887013 | ||||||
chr5:887062
|
T | A | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+299A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/15 | chr5 | 887062 | ||||||
chr5:887172
|
T | C | 3 | a0002c0003t0010g0049a0002c0003t0010g0050a0002c0003t0010g0051 | 3 | HG02280.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.717+189A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/15 | chr5 | 887172 | ||||||
chr5:887211
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.717+150C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/15 | chr5 | 887211 | ||||||
chr5:887611
|
T | C | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-140A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887611 | ||||||
chr5:887687
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.607-216C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887687 | ||||||
chr5:887726
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.607-255C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887726 | ||||||
chr5:887744
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.607-273C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887744 | ||||||
chr5:887787
|
G | A | 1 | a0002c0012t0008g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.607-316C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887787 | ||||||
chr5:887829
|
G | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.607-358C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887829 | ||||||
chr5:887993
|
T | A | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.607-522A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887993 | ||||||
chr5:888051
|
C | T | 1 | a0001c0001t0002g0071 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.607-580G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888051 | ||||||
chr5:888076
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.607-605C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888076 | ||||||
chr5:888101
|
C | T | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.607-630G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888101 | ||||||
chr5:888173
|
G | A | 3 | a0001c0002t0006g0046a0001c0002t0006g0179a0001c0002t0006g0180 | 4 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-702C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888173 | ||||||
chr5:888209
|
G | A | 1 | a0001c0004t0003g0039 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.607-738C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888209 | ||||||
chr5:888285
|
G | T | 1 | a0002c0003t0010g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.606+736C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888285 | ||||||
chr5:888377
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.606+644C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888377 | ||||||
chr5:888618
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.606+403C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888618 | ||||||
chr5:888728
|
G | A | 1 | a0001c0001t0002g0035 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.606+293C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888728 | ||||||
chr5:888858
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.606+163C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888858 | ||||||
chr5:888900
|
G | A | 6 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(3): Show | 6 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+121C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888900 | ||||||
chr5:888953
|
G | C | 10 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.606+68C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888953 | ||||||
chr5:888976
|
C | T | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.606+45G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888976 | ||||||
chr5:888980
|
G | T | 1 | a0001c0001t0015g0070 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.606+41C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888980 | ||||||
chr5:889189
|
C | T | 7 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.462-24G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889189 | ||||||
chr5:889254
|
C | T | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.462-89G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889254 | ||||||
chr5:889279
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.462-114T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889279 | ||||||
chr5:889281
|
G | A | 11 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(8): Show | 22 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.462-116C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889281 | ||||||
chr5:889382
|
C | A | 4 | a0001c0002t0004g0011a0001c0002t0004g0052a0001c0002t0009g0020others(1): Show | 9 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.461+205G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889382 | ||||||
chr5:889421
|
T | C | 1 | a0001c0001t0001g0036 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.461+166A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889421 | ||||||
chr5:889450
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.461+137C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889450 | ||||||
chr5:889542
|
C | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0041a0001c0001t0001g0154 | 7 | HG02273.hp2 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.461+45G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889542 | ||||||
chr5:889571
|
A | G | 11 | a0001c0002t0006g0046a0001c0002t0006g0178a0001c0002t0006g0179others(8): Show | 12 | HG01261.hp2 HG01884.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.461+16T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889571 | ||||||
chr5:889579
|
C | A | 11 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0151others(8): Show | 22 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
splice_region_variant&intron_variant | LOW | c.461+8G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889579 | ||||||
chr5:889679
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.401-32T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889679 | ||||||
chr5:889808
|
C | T | 4 | a0001c0002t0004g0011a0001c0002t0004g0052a0001c0002t0009g0020others(1): Show | 9 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.401-161G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889808 | ||||||
chr5:889809
|
C | G | 4 | a0001c0002t0004g0011a0001c0002t0004g0052a0001c0002t0009g0020others(1): Show | 9 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.401-162G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889809 | ||||||
chr5:889817
|
G | T | 4 | a0001c0002t0004g0011a0001c0002t0004g0052a0001c0002t0009g0020others(1): Show | 9 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.401-170C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889817 | ||||||
chr5:889818
|
C | T | 4 | a0001c0002t0004g0011a0001c0002t0004g0052a0001c0002t0009g0020others(1): Show | 9 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.401-171G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889818 | ||||||
chr5:889820
|
G | A | 1 | a0001c0001t0001g0040 | 2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.401-173C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889820 | ||||||
chr5:889914
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.401-267A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889914 | ||||||
chr5:889915
|
G | C | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-268C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889915 | ||||||
chr5:890009
|
T | C | 4 | a0001c0002t0004g0011a0001c0002t0004g0052a0001c0002t0009g0020others(1): Show | 9 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.401-362A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890009 | ||||||
chr5:890062
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0041a0001c0001t0001g0154 | 7 | HG02273.hp2 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.401-415C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890062 | ||||||
chr5:890188
|
G | A | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-541C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890188 | ||||||
chr5:890189
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.401-542A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890189 | ||||||
chr5:890241
|
G | A | 11 | a0001c0002t0004g0011a0001c0002t0004g0052a0001c0002t0009g0020others(8): Show | 16 | HG01175.hp1 HG01261.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.401-594C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890241 | ||||||
chr5:890279
|
A | T | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.401-632T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890279 | ||||||
chr5:890314
|
C | A | 7 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.401-667G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890314 | ||||||
chr5:890315
|
C | A | 7 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.401-668G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890315 | ||||||
chr5:890393
|
C | T | 2 | a0001c0001t0001g0068a0004c0007t0001g0024 | 3 | HG02015.hp1 NA18974.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.401-746G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890393 | ||||||
chr5:890416
|
T | C | 1 | a0002c0003t0008g0185 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.400+739A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890416 | ||||||
chr5:890484
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.400+671G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890484 | ||||||
chr5:890519
|
T | G | 2 | a0001c0002t0004g0011a0001c0002t0004g0052 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+636A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890519 | ||||||
chr5:890596
|
T | G | 7 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.400+559A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890596 | ||||||
chr5:890639
|
A | G | 7 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.400+516T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890639 | ||||||
chr5:890773
|
T | C | 5 | a0001c0002t0004g0011a0001c0002t0004g0052a0002c0003t0010g0049others(2): Show | 8 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.400+382A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890773 | ||||||
chr5:890846
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400+309G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890846 | ||||||
chr5:891015
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.400+140C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 891015 | ||||||
chr5:891019
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.400+136G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 891019 | ||||||
chr5:891325
|
T | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(27): Show | 66 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.268-38A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 2/15 | chr5 | 891325 | ||||||
chr5:891370
|
G | C | 5 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-83C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 2/15 | chr5 | 891370 | ||||||
chr5:891875
|
T | G | 1 | a0001c0001t0005g0055 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-21A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 891875 | ||||||
chr5:891921
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.53-67C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 891921 | ||||||
chr5:891980
|
G | C | 4 | a0002c0003t0008g0183a0002c0003t0008g0184a0002c0003t0008g0185others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-126C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 891980 | ||||||
chr5:892089
|
G | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(26): Show | 65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.53-235C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892089 | ||||||
chr5:892124
|
A | C | 3 | a0002c0003t0010g0049a0002c0003t0010g0050a0002c0003t0010g0051 | 3 | HG02280.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.53-270T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892124 | ||||||
chr5:892276
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.52+330C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892276 | ||||||
chr5:892365
|
T | A | 2 | a0001c0002t0009g0020a0001c0002t0009g0177 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+241A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892365 | ||||||
chr5:892474
|
C | A | 1 | a0002c0003t0008g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.52+132G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892474 | ||||||
chr5:892501
|
GCCAGGAC others(12): Show |
G | 1 | a0001c0001t0011g0022 | 2 | HG02040.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.52+86_52+104delGCA others(16): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892501 | ||||||
chr5:892531
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.52+75G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892531 | ||||||
chr5:892563
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.52+43G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892563 | ||||||
chr5:892567
|
A | AC | 6 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0059others(3): Show | 7 | HG01109.hp2 HG01175.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+38dupG | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892567 |