geneid | 682 |
---|---|
ensemblid | ENSG00000172270.22 |
hgncid | 1116 |
symbol | BSG |
name | basigin (Ok blood group) |
refseq_nuc | NM_001728.4 |
refseq_prot | NP_001719.2 |
ensembl_nuc | ENST00000333511.9 |
ensembl_prot | ENSP00000333769.3 |
mane_status | MANE Select |
chr | chr19 |
start | 572596 |
end | 583493 |
strand | + |
ver | v1.2 |
region | chr19:572596-583493 |
region5000 | chr19:567596-588493 |
regionname0 | BSG_chr19_572596_583493 |
regionname5000 | BSG_chr19_567596_588493 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 385 | 294 | 71 | 70 | 99 | 16 | 36 | 66 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0002 | 0/0 | 385 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0003 | 0/0 | 385 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0004 | 0/0 | 385 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0005 | 0/0 | 385 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0006 | 0/0 | 385 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0007 | 0/0 | 385 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0008 | 0/0 | 385 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0009 | 0/0 | 385 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1158 | 139 | 37 | 42 | 37 | 10 | 11 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0002 | 0/0 | 1158 | 88 | 16 | 16 | 41 | 1 | 14 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0003 | 0/0 | 1158 | 54 | 12 | 10 | 20 | 3 | 9 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0004 | 0/0 | 1158 | 3 | 3 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0005 | 0/0 | 1158 | 2 | 0 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0006 | 0/0 | 1158 | 2 | 0 | 1 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0007 | 0/0 | 1158 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0008 | 0/0 | 1158 | 2 | 0 | 1 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0009 | 0/0 | 1158 | 2 | 0 | 0 | 1 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0010 | 0/0 | 1158 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0011 | 0/0 | 1158 | 2 | 1 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0012 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0013 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0014 | 0/0 | 1158 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0015 | 0/0 | 1158 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0016 | 0/0 | 1158 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0017 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0018 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
c0019 | 0/0 | 1158 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 789 | 99 | 20 | 19 | 44 | 2 | 14 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0002 | 1/1 | 789 | 76 | 4 | 25 | 26 | 11 | 8 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0003 | 0/0 | 789 | 40 | 25 | 5 | 9 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0004 | 0/0 | 789 | 36 | 6 | 6 | 13 | 2 | 9 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0005 | 0/0 | 789 | 17 | 1 | 12 | 2 | 0 | 2 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0006 | 0/0 | 789 | 8 | 6 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0007 | 0/0 | 789 | 8 | 2 | 3 | 0 | 0 | 3 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0008 | 0/0 | 789 | 3 | 0 | 1 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0009 | 0/0 | 789 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0010 | 0/0 | 789 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0011 | 0/0 | 789 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0012 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0013 | 0/0 | 788 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0014 | 0/0 | 789 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0015 | 0/0 | 789 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0016 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0017 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0018 | 0/0 | 789 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0019 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0020 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0021 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0022 | 0/0 | 789 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0023 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
t0024 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 26 | 3 | 4 | 15 | 0 | 4 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0002 | 1/1 | 23 | 1 | 5 | 12 | 1 | 2 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0003 | 0/0 | 18 | 4 | 6 | 4 | 1 | 3 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0004 | 0/0 | 11 | 2 | 2 | 1 | 3 | 3 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0005 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0006 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0009 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0011 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0022 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1158 | 139 | 37 | 42 | 37 | 10 | 11 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0002 | 0/0 | 1158 | 88 | 16 | 16 | 41 | 1 | 14 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0003 | 0/0 | 1158 | 54 | 12 | 10 | 20 | 3 | 9 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0004 | 0/0 | 1158 | 3 | 3 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0006 | 0/0 | 1158 | 2 | 0 | 1 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0008 | 0/0 | 1158 | 2 | 0 | 1 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0010 | 0/0 | 1158 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0013 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0015 | 0/0 | 1158 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0016 | 0/0 | 1158 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0018 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0002c0005 | 0/0 | 1158 | 2 | 0 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0003c0011 | 0/0 | 1158 | 2 | 1 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0004c0009 | 0/0 | 1158 | 2 | 0 | 0 | 1 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0005c0007 | 0/0 | 1158 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0006c0019 | 0/0 | 1158 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0007c0014 | 0/0 | 1158 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0008c0017 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0009c0012 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1946 | 3 | 3 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0001t0002 | 1/1 | 1946 | 69 | 3 | 23 | 25 | 9 | 7 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0001t0003 | 0/0 | 1946 | 36 | 22 | 5 | 9 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0001t0005 | 0/0 | 1946 | 15 | 1 | 11 | 2 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0001t0007 | 0/0 | 1946 | 8 | 2 | 3 | 0 | 0 | 3 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0001t0011 | 0/0 | 1946 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0001t0015 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0001t0017 | 0/0 | 1945 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0001t0020 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0001t0021 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0001t0023 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0001t0024 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0002t0001 | 0/0 | 1946 | 83 | 14 | 15 | 40 | 1 | 13 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0002t0002 | 0/0 | 1946 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0002t0012 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0002t0016 | 0/0 | 1945 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0002t0018 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0002t0019 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0003t0001 | 0/0 | 1946 | 3 | 0 | 1 | 0 | 1 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0003t0004 | 0/0 | 1946 | 35 | 6 | 6 | 13 | 2 | 8 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0003t0006 | 0/0 | 1946 | 8 | 6 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0003t0008 | 0/0 | 1946 | 3 | 0 | 1 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0003t0009 | 0/0 | 1946 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0003t0010 | 0/0 | 1946 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0003t0014 | 0/0 | 1946 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0004t0003 | 0/0 | 1946 | 3 | 3 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0006t0002 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0006t0013 | 0/0 | 1945 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0008t0002 | 0/0 | 1946 | 2 | 0 | 1 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0010t0001 | 0/0 | 1946 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0013t0001 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0015t0004 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0016t0005 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0001c0018t0001 | 0/0 | 1946 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0002c0005t0001 | 0/0 | 1946 | 2 | 0 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0003c0011t0002 | 0/0 | 1946 | 2 | 1 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0004c0009t0003 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0004c0009t0022 | 0/0 | 1946 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0005c0007t0001 | 0/0 | 1946 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0006c0019t0005 | 0/0 | 1946 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0007c0014t0001 | 0/0 | 1946 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0008c0017t0002 | 0/0 | 1946 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
a0009c0012t0001 | 0/0 | 1946 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | copy fasta | chr19 | 567596 | 588493 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0002 | 1/1 | 23 | 1 | 5 | 12 | 1 | 2 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0004 | 0/0 | 8 | 1 | 2 | 1 | 2 | 2 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0005g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0007g0009 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0007g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0007g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0015g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0017g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0020g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0021g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0023g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0001t0024g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0001 | 0/0 | 22 | 1 | 3 | 15 | 0 | 3 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0006 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0016g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0018g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0002t0019g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0003 | 0/0 | 9 | 0 | 4 | 1 | 1 | 3 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0006g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0008g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0009g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0010g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0010g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0003t0014g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0004t0003g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0004t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0006t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0006t0013g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0008t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0008t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0010t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0010t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0013t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0015t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0016t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0001c0018t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0002c0005t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0002c0005t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0003c0011t0002g0004 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0004c0009t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0004c0009t0022g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0005c0007t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0006c0019t0005g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0007c0014t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0008c0017t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
a0009c0012t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | GBR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0058 | EUR | GBR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00140 | hp1 | a0001 | c0001 | t0015 | g0004 | EUR | GBR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0126 | EUR | GBR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0130 | EUR | FIN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | FIN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | FIN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0157 | EUR | FIN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00408 | hp1 | a0001 | c0003 | t0004 | g0160 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00423 | hp1 | a0001 | c0018 | t0001 | g0133 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00544 | hp2 | a0001 | c0003 | t0008 | g0003 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00621 | hp2 | a0001 | c0003 | t0014 | g0055 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00639 | hp1 | a0006 | c0019 | t0005 | g0005 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00642 | hp2 | a0001 | c0003 | t0004 | g0003 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00673 | hp2 | a0001 | c0003 | t0009 | g0003 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0108 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01074 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01099 | hp1 | a0001 | c0003 | t0004 | g0003 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0082 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01106 | hp2 | a0001 | c0003 | t0004 | g0063 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01109 | hp2 | a0001 | c0003 | t0006 | g0038 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01167 | hp1 | a0001 | c0001 | t0007 | g0009 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01167 | hp2 | a0001 | c0008 | t0002 | g0007 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01168 | hp2 | a0001 | c0006 | t0013 | g0149 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01169 | hp2 | a0001 | c0001 | t0007 | g0105 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01243 | hp2 | a0001 | c0003 | t0006 | g0003 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01256 | hp1 | a0001 | c0003 | t0004 | g0003 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01346 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01361 | hp2 | a0001 | c0003 | t0004 | g0003 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0049 | EUR | IBS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01516 | hp2 | a0001 | c0003 | t0004 | g0003 | EUR | IBS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0153 | EUR | IBS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01517 | hp2 | a0001 | c0003 | t0004 | g0020 | EUR | IBS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01884 | hp2 | a0001 | c0001 | t0020 | g0023 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01891 | hp1 | a0001 | c0004 | t0003 | g0034 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0077 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01943 | hp1 | a0001 | c0001 | t0007 | g0112 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01943 | hp2 | a0002 | c0005 | t0001 | g0116 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01952 | hp1 | a0002 | c0005 | t0001 | g0001 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01975 | hp2 | a0001 | c0003 | t0004 | g0019 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0172 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01981 | hp2 | a0007 | c0014 | t0001 | g0119 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0040 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02015 | hp2 | a0001 | c0003 | t0004 | g0020 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02027 | hp2 | a0001 | c0003 | t0009 | g0037 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02040 | hp1 | a0005 | c0007 | t0001 | g0010 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0168 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02056 | hp1 | a0001 | c0001 | t0017 | g0022 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02074 | hp1 | a0001 | c0003 | t0004 | g0033 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02129 | hp1 | a0001 | c0003 | t0004 | g0033 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02129 | hp2 | a0001 | c0003 | t0004 | g0003 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02145 | hp2 | a0001 | c0003 | t0004 | g0008 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0110 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CDX | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02155 | hp2 | a0001 | c0001 | t0005 | g0080 | EAS | CDX | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0079 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02300 | hp2 | a0001 | c0003 | t0008 | g0003 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02451 | hp1 | a0001 | c0003 | t0006 | g0060 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02451 | hp2 | a0001 | c0010 | t0001 | g0070 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02572 | hp2 | a0001 | c0003 | t0006 | g0062 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02602 | hp2 | a0001 | c0003 | t0004 | g0003 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02630 | hp2 | a0001 | c0003 | t0006 | g0003 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02647 | hp2 | a0001 | c0003 | t0006 | g0003 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02698 | hp2 | a0001 | c0003 | t0004 | g0071 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02717 | hp2 | a0001 | c0001 | t0011 | g0111 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0009 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0173 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02896 | hp1 | a0001 | c0002 | t0019 | g0090 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02896 | hp2 | a0001 | c0003 | t0004 | g0067 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02922 | hp1 | a0001 | c0003 | t0004 | g0008 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02965 | hp2 | a0001 | c0003 | t0004 | g0008 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02970 | hp1 | a0001 | c0001 | t0024 | g0072 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03017 | hp1 | a0001 | c0016 | t0005 | g0075 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03041 | hp1 | a0001 | c0001 | t0011 | g0151 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03098 | hp2 | a0001 | c0003 | t0004 | g0054 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03209 | hp2 | a0001 | c0003 | t0006 | g0003 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03239 | hp1 | a0004 | c0009 | t0003 | g0092 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0076 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03516 | hp2 | a0001 | c0004 | t0003 | g0034 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03540 | hp2 | a0001 | c0010 | t0001 | g0084 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03579 | hp1 | a0001 | c0003 | t0004 | g0008 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03579 | hp2 | a0001 | c0003 | t0006 | g0003 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03654 | hp1 | a0001 | c0002 | t0018 | g0001 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03704 | hp2 | a0003 | c0011 | t0002 | g0004 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0137 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03831 | hp1 | a0001 | c0001 | t0007 | g0031 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03831 | hp2 | a0001 | c0003 | t0004 | g0039 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03834 | hp1 | a0001 | c0015 | t0004 | g0065 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03942 | hp2 | a0001 | c0003 | t0004 | g0059 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG04184 | hp1 | a0001 | c0003 | t0004 | g0003 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG04184 | hp2 | a0001 | c0003 | t0004 | g0019 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG04199 | hp1 | a0001 | c0001 | t0007 | g0031 | SAS | STU | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG04199 | hp2 | a0001 | c0003 | t0004 | g0056 | SAS | STU | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0101 | SAS | STU | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | STU | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG04228 | hp2 | a0001 | c0003 | t0004 | g0003 | SAS | STU | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18522 | hp1 | a0001 | c0004 | t0003 | g0166 | AFR | YRI | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | YRI | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18939 | hp1 | a0001 | c0003 | t0008 | g0064 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18952 | hp2 | a0001 | c0003 | t0004 | g0017 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18964 | hp1 | a0001 | c0003 | t0004 | g0159 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18970 | hp2 | a0001 | c0003 | t0004 | g0057 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18972 | hp2 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18979 | hp1 | a0001 | c0003 | t0004 | g0167 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18982 | hp1 | a0001 | c0002 | t0016 | g0122 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18995 | hp2 | a0001 | c0003 | t0004 | g0017 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA18998 | hp2 | a0001 | c0003 | t0004 | g0061 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19007 | hp1 | a0001 | c0003 | t0010 | g0003 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | LWK | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19043 | hp2 | a0001 | c0002 | t0012 | g0001 | AFR | LWK | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19060 | hp2 | a0008 | c0017 | t0002 | g0007 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19066 | hp2 | a0001 | c0003 | t0004 | g0052 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19074 | hp1 | a0001 | c0003 | t0010 | g0053 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19082 | hp2 | a0004 | c0009 | t0022 | g0091 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19085 | hp2 | a0009 | c0012 | t0001 | g0148 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19088 | hp2 | a0005 | c0007 | t0001 | g0010 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19091 | hp1 | a0001 | c0003 | t0004 | g0017 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ASW | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA20752 | hp1 | a0001 | c0006 | t0002 | g0103 | EUR | TSI | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA20805 | hp2 | a0001 | c0008 | t0002 | g0011 | EUR | TSI | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0106 | SAS | GIH | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA20905 | hp2 | a0001 | c0003 | t0001 | g0066 | SAS | GIH | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02109 | hp1 | a0001 | c0013 | t0001 | g0001 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02486 | hp1 | a0001 | c0001 | t0021 | g0074 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG06807 | hp1 | a0003 | c0011 | t0002 | g0004 | AFR | USA | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
HG06807 | hp2 | a0001 | c0001 | t0023 | g0068 | AFR | USA | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | LWK | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | LWK | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0002 | REF | REF | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0002 | REF | REF | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:572663
|
G | A | 1 | a0002 | 2 | HG01943.hp2 HG01952.hp1 |
missense_variant | MODERATE | c.29G>A | p.Gly10Glu | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/9 | 68/1946 | 29/1158 | 10/385 | chr19 | 572663 | ||
chr19:572680
|
A | G | 1 | a0003 | 2 | HG03704.hp2 HG06807.hp1 |
missense_variant | MODERATE | c.46A>G | p.Thr16Ala | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/9 | 85/1946 | 46/1158 | 16/385 | chr19 | 572680 | ||
chr19:577776
|
G | A | 1 | a0009 | 1 | NA19085.hp2 | missense_variant&splice_region_variant | MODERATE | c.70G>A | p.Gly24Ser | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/9 | 109/1946 | 70/1158 | 24/385 | chr19 | 577776 | ||
chr19:577782
|
G | T | 1 | a0006 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.76G>T | p.Val26Phe | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/9 | 115/1946 | 76/1158 | 26/385 | chr19 | 577782 | ||
chr19:577963
|
A | G | 1 | a0008 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.257A>G | p.His86Arg | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/9 | 296/1946 | 257/1158 | 86/385 | chr19 | 577963 | ||
chr19:580389
|
G | A | 1 | a0007 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.583G>A | p.Asp195Asn | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/9 | 622/1946 | 583/1158 | 195/385 | chr19 | 580389 | ||
chr19:580389
|
G | C | 1 | a0005 | 2 | HG02040.hp1 NA19088.hp2 |
missense_variant | MODERATE | c.583G>C | p.Asp195His | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/9 | 622/1946 | 583/1158 | 195/385 | chr19 | 580389 | ||
chr19:582310
|
C | G | 1 | a0004 | 2 | HG03239.hp1 NA19082.hp2 |
missense_variant | MODERATE | c.1074C>G | p.Asp358Glu | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 7/9 | 1113/1946 | 1074/1158 | 358/385 | chr19 | 582310 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:577793
|
G | A | 1 | a0001c0006 | 2 | HG01168.hp2 NA20752.hp1 |
synonymous_variant | LOW | c.87G>A | p.Pro29Pro | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/9 | 126/1946 | 87/1158 | 29/385 | chr19 | 577793 | ||
chr19:577952
|
C | T | 1 | a0001c0018 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.246C>T | p.His82His | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/9 | 285/1946 | 246/1158 | 82/385 | chr19 | 577952 | ||
chr19:578105
|
C | T | 1 | a0001c0010 | 2 | HG02451.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.399C>T | p.Val133Val | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/9 | 438/1946 | 399/1158 | 133/385 | chr19 | 578105 | ||
chr19:579519
|
C | T | 1 | a0001c0016 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.435C>T | p.Thr145Thr | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/9 | 474/1946 | 435/1158 | 145/385 | chr19 | 579519 | ||
chr19:579627
|
C | T | 2 | a0001c0003a0001c0015 | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
synonymous_variant | LOW | c.543C>T | p.Asp181Asp | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/9 | 582/1946 | 543/1158 | 181/385 | chr19 | 579627 | ||
chr19:579630
|
G | A | 1 | a0001c0013 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.546G>A | p.Ala182Ala | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/9 | 585/1946 | 546/1158 | 182/385 | chr19 | 579630 | ||
chr19:580388
|
C | G | 2 | a0001c0003a0001c0015 | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
synonymous_variant | LOW | c.582C>G | p.Ser194Ser | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/9 | 621/1946 | 582/1158 | 194/385 | chr19 | 580388 | ||
chr19:580665
|
T | C | 8 | a0001c0002a0001c0010a0001c0013others(5): Show | 98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
synonymous_variant | LOW | c.675T>C | p.Ala225Ala | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/9 | 714/1946 | 675/1158 | 225/385 | chr19 | 580665 | ||
chr19:580710
|
G | A | 1 | a0001c0008 | 2 | HG01167.hp2 NA20805.hp2 |
synonymous_variant | LOW | c.720G>A | p.Leu240Leu | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/9 | 759/1946 | 720/1158 | 240/385 | chr19 | 580710 | ||
chr19:581332
|
C | G | 1 | a0001c0015 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.810C>G | p.Ser270Ser | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/9 | 849/1946 | 810/1158 | 270/385 | chr19 | 581332 | ||
chr19:581371
|
A | G | 1 | a0001c0004 | 3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.849A>G | p.Ser283Ser | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/9 | 888/1946 | 849/1158 | 283/385 | chr19 | 581371 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:572596
|
A | G | 1 | a0001c0001t0024 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/9 | 39 | chr19 | 572596 | |||||
chr19:572602
|
T | A | 1 | a0001c0002t0012 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-33T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/9 | 33 | chr19 | 572602 | |||||
chr19:572610
|
G | T | 1 | a0001c0001t0023 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-25G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/9 | 25 | chr19 | 572610 | |||||
chr19:572628
|
A | G | 1 | a0001c0003t0008 | 3 | HG00544.hp2 HG02300.hp2 NA18939.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/9 | chr19 | 572628 | ||||||
chr19:582775
|
A | G | 34 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(31): Show | 227 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*31A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 198 | chr19 | 582775 | |||||
chr19:582878
|
CT | C | 3 | a0001c0001t0017a0001c0002t0016a0001c0006t0013 | 3 | HG01168.hp2 HG02056.hp1 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*140delT | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 307 | INFO_REALIGN_3_PRIME | chr19 | 582878 | ||||
chr19:582927
|
T | A | 21 | a0001c0001t0001a0001c0002t0001a0001c0002t0012others(18): Show | 155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*183T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 350 | chr19 | 582927 | |||||
chr19:582982
|
C | T | 1 | a0001c0003t0006 | 8 | HG01109.hp2 HG01243.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*238C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 405 | chr19 | 582982 | |||||
chr19:583224
|
T | G | 1 | a0001c0001t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*480T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 647 | chr19 | 583224 | |||||
chr19:583255
|
C | T | 1 | a0004c0009t0022 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 678 | chr19 | 583255 | |||||
chr19:583256
|
G | A | 1 | a0001c0002t0018 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 679 | chr19 | 583256 | |||||
chr19:583268
|
G | A | 3 | a0001c0001t0005a0001c0016t0005a0006c0019t0005 | 17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*524G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 691 | chr19 | 583268 | |||||
chr19:583314
|
C | T | 1 | a0001c0001t0021 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*570C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 737 | chr19 | 583314 | |||||
chr19:583361
|
G | A | 1 | a0001c0002t0019 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 784 | chr19 | 583361 | |||||
chr19:583418
|
T | C | 7 | a0001c0003t0004a0001c0003t0006a0001c0003t0008others(4): Show | 52 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*674T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 841 | chr19 | 583418 | |||||
chr19:583435
|
C | T | 1 | a0001c0003t0010 | 2 | NA19007.hp1 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*691C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 858 | chr19 | 583435 | |||||
chr19:583443
|
C | G | 1 | a0001c0001t0011 | 2 | HG02717.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*699C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 866 | chr19 | 583443 | |||||
chr19:583450
|
C | T | 1 | a0001c0001t0007 | 8 | HG01167.hp1 HG01169.hp2 HG01943.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*706C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 873 | chr19 | 583450 | |||||
chr19:583460
|
G | A | 6 | a0001c0003t0004a0001c0003t0006a0001c0003t0008others(3): Show | 50 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*716G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 883 | chr19 | 583460 | |||||
chr19:583490
|
C | T | 1 | a0001c0001t0015 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*746C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 913 | chr19 | 583490 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:572721
|
C | CG | 14 | a0001c0001t0002g0018a0001c0001t0002g0045a0001c0001t0002g0046others(11): Show | 15 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+25dupG | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 572721 | |||||
chr19:572721
|
C | G | 2 | a0001c0001t0005g0172a0001c0002t0001g0173 | 2 | HG01978.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.67+20C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572721 | ||||||
chr19:572764
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.67+63C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572764 | ||||||
chr19:572811
|
G | T | 2 | a0001c0001t0002g0036a0001c0001t0002g0049 | 3 | HG00099.hp1 HG00323.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.67+110G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572811 | ||||||
chr19:572860
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.67+159G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572860 | ||||||
chr19:572878
|
T | C | 32 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0023g0068others(29): Show | 50 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+177T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572878 | ||||||
chr19:572884
|
G | C | 1 | a0001c0001t0003g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.67+183G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572884 | ||||||
chr19:572934
|
TCCGGCCT others(5): Show |
T | 32 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0023g0068others(29): Show | 50 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+242_67+253delGA others(10): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 572934 | |||||
chr19:572988
|
G | A | 4 | a0001c0001t0003g0021a0001c0001t0003g0073a0001c0001t0021g0074others(1): Show | 5 | HG02257.hp2 HG02486.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+287G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572988 | ||||||
chr19:572998
|
G | C | 11 | a0001c0001t0005g0005a0001c0001t0005g0040a0001c0001t0005g0076others(8): Show | 17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.67+297G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572998 | ||||||
chr19:573068
|
T | TTTCCCGG others(11): Show |
32 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0023g0068others(29): Show | 50 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+367_67+368insTT others(16): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573068 | ||||||
chr19:573070
|
A | ATCTCG | 32 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0023g0068others(29): Show | 50 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+369_67+370insTC others(3): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573070 | ||||||
chr19:573132
|
T | C | 1 | a0001c0016t0005g0075 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.67+431T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573132 | ||||||
chr19:573145
|
G | T | 2 | a0001c0001t0002g0035a0001c0001t0002g0170 | 3 | HG02155.hp1 NA18983.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.67+444G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573145 | ||||||
chr19:573188
|
C | G | 1 | a0001c0001t0005g0081 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.67+487C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573188 | ||||||
chr19:573205
|
T | C | 32 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0023g0068others(29): Show | 50 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+504T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573205 | ||||||
chr19:573522
|
C | T | 2 | a0001c0002t0001g0168a0001c0002t0001g0169 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.67+821C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573522 | ||||||
chr19:573623
|
A | C | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.67+922A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573623 | ||||||
chr19:573698
|
C | G | 7 | a0001c0001t0003g0021a0001c0001t0003g0073a0001c0001t0003g0165others(4): Show | 9 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+997C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573698 | ||||||
chr19:573712
|
AG | A | 31 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0023g0068others(28): Show | 49 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.67+1016delG | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 573712 | |||||
chr19:573777
|
C | G | 3 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0023g0068 | 3 | HG02723.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67+1076C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573777 | ||||||
chr19:573869
|
G | A | 1 | a0001c0001t0005g0076 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.67+1168G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573869 | ||||||
chr19:573967
|
T | C | 1 | a0001c0003t0004g0052 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.67+1266T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573967 | ||||||
chr19:574025
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.67+1324C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574025 | ||||||
chr19:574199
|
G | A | 8 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(5): Show | 8 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+1498G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574199 | ||||||
chr19:574253
|
T | TA | 19 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(16): Show | 24 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.67+1568dupA | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 574253 | |||||
chr19:574253
|
T | TAA | 7 | a0001c0001t0003g0021a0001c0001t0003g0073a0001c0001t0003g0165others(4): Show | 9 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+1567_67+1568dup others(2): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 574253 | |||||
chr19:574253
|
TA | T | 53 | a0001c0001t0002g0007a0001c0001t0002g0154a0001c0001t0002g0155others(50): Show | 79 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.67+1568delA | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 574253 | |||||
chr19:574254
|
A | T | 1 | a0001c0001t0003g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.67+1553A>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574254 | ||||||
chr19:574255
|
A | T | 2 | a0001c0001t0003g0162a0001c0001t0003g0163 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.67+1554A>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574255 | ||||||
chr19:574301
|
C | T | 31 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(28): Show | 42 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.67+1600C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574301 | ||||||
chr19:574429
|
T | A | 11 | a0001c0001t0005g0005a0001c0001t0005g0040a0001c0001t0005g0076others(8): Show | 17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.67+1728T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574429 | ||||||
chr19:574448
|
G | A | 1 | a0001c0003t0004g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.67+1747G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574448 | ||||||
chr19:574449
|
A | G | 1 | a0001c0003t0004g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.67+1748A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574449 | ||||||
chr19:574477
|
A | C | 1 | a0001c0002t0001g0143 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.67+1776A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574477 | ||||||
chr19:574484
|
C | T | 1 | a0001c0003t0004g0052 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.67+1783C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574484 | ||||||
chr19:574489
|
C | G | 1 | a0001c0002t0001g0094 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.67+1788C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574489 | ||||||
chr19:574532
|
G | A | 3 | a0001c0001t0003g0021a0001c0001t0003g0073a0001c0001t0024g0072 | 4 | HG02257.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+1831G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574532 | ||||||
chr19:574545
|
C | T | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+1844C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574545 | ||||||
chr19:574547
|
C | T | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+1846C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574547 | ||||||
chr19:574552
|
C | CA | 35 | a0001c0001t0003g0165a0001c0002t0001g0101a0001c0003t0001g0058others(32): Show | 56 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+1860dupA | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 574552 | |||||
chr19:574562
|
C | A | 1 | a0001c0003t0004g0056 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.67+1861C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574562 | ||||||
chr19:574568
|
AAAAATTT others(20): Show |
A | 1 | a0001c0001t0005g0078 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.67+1870_67+1896del others(27): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 574568 | |||||
chr19:574573
|
T | A | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+1872T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574573 | ||||||
chr19:574636
|
C | G | 1 | a0001c0003t0004g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.67+1935C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574636 | ||||||
chr19:574641
|
G | A | 3 | a0001c0001t0003g0048a0001c0001t0003g0162a0001c0001t0003g0163 | 3 | HG02922.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.67+1940G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574641 | ||||||
chr19:574824
|
G | A | 1 | a0009c0012t0001g0148 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.67+2123G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574824 | ||||||
chr19:574852
|
CAGAT | C | 1 | a0001c0003t0004g0008 | 4 | HG02145.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+2154_67+2157del others(4): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 574852 | |||||
chr19:574861
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.67+2160G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574861 | ||||||
chr19:574882
|
G | A | 2 | a0004c0009t0003g0092a0004c0009t0022g0091 | 2 | HG03239.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.67+2181G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574882 | ||||||
chr19:574893
|
C | T | 1 | a0001c0002t0001g0142 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.67+2192C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574893 | ||||||
chr19:574927
|
C | T | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+2226C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574927 | ||||||
chr19:574951
|
G | A | 1 | a0001c0001t0005g0078 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.67+2250G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574951 | ||||||
chr19:574973
|
T | G | 1 | a0001c0002t0001g0102 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.67+2272T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574973 | ||||||
chr19:575083
|
G | C | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+2382G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575083 | ||||||
chr19:575159
|
G | A | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+2458G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575159 | ||||||
chr19:575255
|
G | A | 17 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(14): Show | 22 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.68-2519G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575255 | ||||||
chr19:575353
|
G | T | 3 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0023g0068 | 3 | HG02723.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.68-2421G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575353 | ||||||
chr19:575406
|
C | T | 1 | a0001c0002t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.68-2368C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575406 | ||||||
chr19:575445
|
C | T | 11 | a0001c0001t0005g0005a0001c0001t0005g0040a0001c0001t0005g0076others(8): Show | 17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-2329C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575445 | ||||||
chr19:575605
|
TGGGTGGG others(9): Show |
T | 1 | a0001c0001t0002g0141 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.68-2160_68-2145del others(16): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 575605 | |||||
chr19:575647
|
G | C | 2 | a0001c0006t0002g0103a0001c0006t0013g0149 | 2 | HG01168.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.68-2127G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575647 | ||||||
chr19:575675
|
C | A | 1 | a0001c0002t0001g0104 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.68-2099C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575675 | ||||||
chr19:575697
|
TG | T | 35 | a0001c0001t0007g0105a0001c0003t0001g0058a0001c0003t0001g0066others(32): Show | 56 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.68-2074delG | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 575697 | |||||
chr19:575754
|
T | C | 10 | a0001c0002t0001g0016a0001c0002t0001g0042a0001c0002t0001g0106others(7): Show | 12 | HG00735.hp1 HG00738.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.68-2020T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575754 | ||||||
chr19:575780
|
T | A | 1 | a0001c0001t0003g0095 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.68-1994T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575780 | ||||||
chr19:575782
|
C | T | 1 | a0001c0001t0005g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.68-1992C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575782 | ||||||
chr19:575805
|
G | T | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-1969G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575805 | ||||||
chr19:575818
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0158 | 4 | HG00423.hp2 HG01070.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-1956C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575818 | ||||||
chr19:575886
|
G | A | 1 | a0001c0001t0024g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.68-1888G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575886 | ||||||
chr19:575910
|
G | A | 1 | a0001c0003t0004g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.68-1864G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575910 | ||||||
chr19:575921
|
A | G | 3 | a0001c0001t0003g0013a0001c0001t0003g0100a0001c0001t0003g0145 | 5 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-1853A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575921 | ||||||
chr19:575942
|
C | T | 20 | a0001c0002t0001g0012a0001c0002t0001g0016a0001c0002t0001g0042others(17): Show | 25 | HG00735.hp1 HG00738.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-1832C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575942 | ||||||
chr19:575943
|
G | GC | 18 | a0001c0001t0002g0011a0001c0001t0002g0050a0001c0001t0002g0138others(15): Show | 25 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-1824dupC | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 575943 | |||||
chr19:575964
|
C | T | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-1810C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575964 | ||||||
chr19:575997
|
C | T | 3 | a0001c0001t0003g0048a0001c0001t0003g0162a0001c0001t0003g0163 | 3 | HG02922.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.68-1777C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575997 | ||||||
chr19:576010
|
G | A | 1 | a0001c0002t0001g0150 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.68-1764G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576010 | ||||||
chr19:576157
|
C | G | 1 | a0001c0018t0001g0133 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.68-1617C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576157 | ||||||
chr19:576377
|
G | T | 11 | a0001c0001t0005g0005a0001c0001t0005g0040a0001c0001t0005g0076others(8): Show | 17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-1397G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576377 | ||||||
chr19:576466
|
A | C | 11 | a0001c0001t0005g0005a0001c0001t0005g0040a0001c0001t0005g0076others(8): Show | 17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-1308A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576466 | ||||||
chr19:576487
|
C | G | 2 | a0001c0010t0001g0070a0001c0010t0001g0084 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.68-1287C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576487 | ||||||
chr19:576499
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.68-1275C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576499 | ||||||
chr19:576500
|
G | A | 3 | a0001c0001t0003g0146a0001c0001t0003g0147a0001c0001t0003g0161 | 3 | HG03195.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-1274G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576500 | ||||||
chr19:576552
|
G | C | 3 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0023g0068 | 3 | HG02723.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.68-1222G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576552 | ||||||
chr19:576589
|
G | A | 1 | a0001c0002t0001g0027 | 2 | HG00609.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.68-1185G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576589 | ||||||
chr19:576628
|
G | A | 1 | a0001c0003t0004g0052 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.68-1146G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576628 | ||||||
chr19:576675
|
T | C | 149 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(146): Show | 223 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.68-1099T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576675 | ||||||
chr19:576686
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.68-1088G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576686 | ||||||
chr19:576716
|
A | G | 142 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(139): Show | 212 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.68-1058A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576716 | ||||||
chr19:576748
|
CA | C | 64 | a0001c0001t0002g0036a0001c0001t0002g0049a0001c0001t0002g0132others(61): Show | 101 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.68-1012delA | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 576748 | |||||
chr19:576760
|
A | AAAG | 36 | a0001c0001t0003g0013a0001c0001t0003g0022a0001c0001t0003g0023others(33): Show | 46 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.68-1006_68-1004dup others(3): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 576760 | |||||
chr19:576768
|
AGAG | A | 30 | a0001c0003t0001g0066a0001c0003t0001g0082a0001c0003t0004g0003others(27): Show | 50 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-1002_68-1000del others(3): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 576768 | |||||
chr19:576771
|
G | A | 4 | a0001c0003t0001g0058a0001c0003t0004g0019a0001c0003t0004g0071others(1): Show | 5 | HG00099.hp2 HG01975.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-1003G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576771 | ||||||
chr19:576777
|
A | G | 2 | a0001c0001t0003g0051a0001c0001t0003g0069 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.68-997A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576777 | ||||||
chr19:576919
|
A | G | 1 | a0001c0001t0003g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.68-855A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576919 | ||||||
chr19:576932
|
T | C | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-842T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576932 | ||||||
chr19:576936
|
TTG | T | 3 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0023g0068 | 3 | HG02723.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.68-830_68-829delGT | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 576936 | |||||
chr19:576961
|
C | CGTGTGTG others(1): Show |
28 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(25): Show | 47 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.68-813_68-812insGT others(6): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576961 | ||||||
chr19:576961
|
C | CGTGTGTG others(3): Show |
4 | a0001c0003t0004g0020a0001c0003t0004g0059a0001c0003t0004g0071others(1): Show | 5 | HG01517.hp2 HG02015.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-813_68-812insGT others(8): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576961 | ||||||
chr19:576961
|
C | CGTGTGTG others(5): Show |
1 | a0001c0003t0004g0033 | 2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.68-813_68-812insGT others(10): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576961 | ||||||
chr19:576962
|
T | G | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-812T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576962 | ||||||
chr19:576962
|
TTG | T | 79 | a0001c0001t0003g0021a0001c0001t0003g0048a0001c0001t0003g0051others(76): Show | 117 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.68-796_68-795delGT | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 576962 | |||||
chr19:577157
|
G | C | 12 | a0001c0001t0003g0021a0001c0001t0003g0051a0001c0001t0003g0069others(9): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-617G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577157 | ||||||
chr19:577157
|
G | T | 11 | a0001c0001t0005g0005a0001c0001t0005g0040a0001c0001t0005g0076others(8): Show | 17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-617G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577157 | ||||||
chr19:577246
|
G | A | 31 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(28): Show | 42 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.68-528G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577246 | ||||||
chr19:577247
|
CCT | C | 62 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(59): Show | 98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.68-520_68-519delCT | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 577247 | |||||
chr19:577261
|
G | A | 1 | a0001c0003t0006g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-513G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577261 | ||||||
chr19:577321
|
C | T | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-453C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577321 | ||||||
chr19:577347
|
C | T | 62 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(59): Show | 98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.68-427C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577347 | ||||||
chr19:577426
|
T | G | 151 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(148): Show | 225 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.68-348T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577426 | ||||||
chr19:577435
|
G | A | 1 | a0001c0002t0001g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68-339G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577435 | ||||||
chr19:577436
|
G | C | 151 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(148): Show | 225 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.68-338G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577436 | ||||||
chr19:577489
|
C | T | 1 | a0001c0002t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.68-285C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577489 | ||||||
chr19:577596
|
C | G | 2 | a0001c0002t0001g0168a0001c0002t0001g0169 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.68-178C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577596 | ||||||
chr19:577622
|
T | G | 1 | a0001c0001t0011g0151 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.68-152T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577622 | ||||||
chr19:577664
|
G | C | 3 | a0001c0001t0003g0048a0001c0001t0003g0162a0001c0001t0003g0163 | 3 | HG02922.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.68-110G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577664 | ||||||
chr19:577665
|
G | A | 3 | a0001c0001t0003g0048a0001c0001t0003g0162a0001c0001t0003g0163 | 3 | HG02922.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.68-109G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577665 | ||||||
chr19:577707
|
T | C | 1 | a0001c0001t0005g0078 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.68-67T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577707 | ||||||
chr19:577760
|
T | C | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-14T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577760 | ||||||
chr19:578157
|
G | C | 1 | a0001c0001t0005g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.415+36G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578157 | ||||||
chr19:578208
|
C | T | 34 | a0001c0002t0001g0029a0001c0003t0001g0058a0001c0003t0001g0066others(31): Show | 56 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.415+87C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578208 | ||||||
chr19:578236
|
C | G | 1 | a0001c0001t0007g0105 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.415+115C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578236 | ||||||
chr19:578239
|
C | T | 110 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(107): Show | 161 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.415+118C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578239 | ||||||
chr19:578268
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.415+147C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578268 | ||||||
chr19:578316
|
G | T | 6 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0003g0146others(3): Show | 6 | HG02723.hp2 HG03195.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.415+195G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578316 | ||||||
chr19:578345
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.415+224C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578345 | ||||||
chr19:578394
|
C | G | 1 | a0001c0003t0001g0066 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.415+273C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578394 | ||||||
chr19:578417
|
G | A | 3 | a0001c0001t0003g0146a0001c0001t0003g0147a0001c0001t0003g0161 | 3 | HG03195.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.415+296G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578417 | ||||||
chr19:578549
|
A | G | 1 | a0001c0002t0001g0142 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.415+428A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578549 | ||||||
chr19:578556
|
G | C | 1 | a0001c0001t0002g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.415+435G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578556 | ||||||
chr19:578661
|
C | T | 1 | a0009c0012t0001g0148 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.415+540C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578661 | ||||||
chr19:578668
|
G | T | 1 | a0001c0003t0004g0008 | 4 | HG02145.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+547G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578668 | ||||||
chr19:578718
|
C | CA | 142 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(139): Show | 212 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.415+597_415+598ins others(1): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578718 | ||||||
chr19:578734
|
AT | A | 49 | a0001c0001t0002g0127a0001c0001t0003g0013a0001c0001t0003g0022others(46): Show | 73 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.415+627delT | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 578734 | |||||
chr19:578759
|
G | T | 1 | a0001c0002t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.415+638G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578759 | ||||||
chr19:578763
|
C | G | 1 | a0001c0003t0001g0058 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.415+642C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578763 | ||||||
chr19:578785
|
T | C | 109 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(106): Show | 158 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.415+664T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578785 | ||||||
chr19:578794
|
A | G | 151 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(148): Show | 225 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.415+673A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578794 | ||||||
chr19:578812
|
C | A | 1 | a0001c0001t0007g0105 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.416-688C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578812 | ||||||
chr19:578813
|
T | C | 1 | a0001c0001t0007g0105 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.416-687T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578813 | ||||||
chr19:578815
|
C | T | 1 | a0001c0001t0007g0105 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.416-685C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578815 | ||||||
chr19:578907
|
T | C | 2 | a0001c0002t0001g0115a0001c0002t0001g0135 | 2 | HG02056.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.416-593T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578907 | ||||||
chr19:578924
|
G | T | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-576G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578924 | ||||||
chr19:578976
|
C | T | 1 | a0001c0001t0005g0076 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.416-524C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578976 | ||||||
chr19:579010
|
G | A | 142 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(139): Show | 212 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.416-490G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579010 | ||||||
chr19:579022
|
G | A | 1 | a0001c0002t0001g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.416-478G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579022 | ||||||
chr19:579035
|
C | T | 61 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(58): Show | 97 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.416-465C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579035 | ||||||
chr19:579084
|
G | C | 1 | a0001c0002t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.416-416G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579084 | ||||||
chr19:579100
|
C | T | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.416-400C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579100 | ||||||
chr19:579157
|
T | C | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.416-343T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579157 | ||||||
chr19:579175
|
T | C | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-325T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579175 | ||||||
chr19:579186
|
G | C | 3 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0023g0068 | 3 | HG02723.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-314G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579186 | ||||||
chr19:579192
|
C | T | 2 | a0001c0001t0003g0147a0001c0001t0003g0161 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.416-308C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579192 | ||||||
chr19:579222
|
C | T | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-278C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579222 | ||||||
chr19:579224
|
T | A | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-276T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579224 | ||||||
chr19:579250
|
G | A | 1 | a0001c0003t0004g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.416-250G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579250 | ||||||
chr19:579252
|
AGGGTGCC others(10): Show |
A | 34 | a0001c0001t0002g0127a0001c0003t0001g0058a0001c0003t0001g0066others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.416-228_416-212del others(17): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 579252 | |||||
chr19:579254
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.416-246G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579254 | ||||||
chr19:579267
|
AGGGGGTG others(11): Show |
A | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-229_416-212del others(18): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 579267 | |||||
chr19:579282
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.416-218G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579282 | ||||||
chr19:579354
|
C | G | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-146C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579354 | ||||||
chr19:579356
|
G | T | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-144G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579356 | ||||||
chr19:579357
|
T | C | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-143T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579357 | ||||||
chr19:579383
|
A | T | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-117A>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579383 | ||||||
chr19:579384
|
T | A | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-116T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579384 | ||||||
chr19:579432
|
G | C | 15 | a0001c0001t0003g0013a0001c0001t0003g0022a0001c0001t0003g0023others(12): Show | 19 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.416-68G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579432 | ||||||
chr19:579448
|
G | T | 1 | a0001c0002t0001g0110 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.416-52G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579448 | ||||||
chr19:579450
|
G | A | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.416-50G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579450 | ||||||
chr19:579687
|
T | A | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.572+31T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579687 | ||||||
chr19:579699
|
C | T | 35 | a0001c0001t0003g0024a0001c0003t0001g0058a0001c0003t0001g0066others(32): Show | 57 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.572+43C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579699 | ||||||
chr19:579700
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.572+44G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579700 | ||||||
chr19:579701
|
G | C | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.572+45G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579701 | ||||||
chr19:579707
|
T | C | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.572+51T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579707 | ||||||
chr19:579713
|
C | T | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.572+57C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579713 | ||||||
chr19:579768
|
G | A | 2 | a0001c0002t0001g0115a0001c0002t0001g0135 | 2 | HG02056.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.572+112G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579768 | ||||||
chr19:579773
|
T | G | 1 | a0001c0003t0004g0061 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.572+117T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579773 | ||||||
chr19:579809
|
C | A | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.572+153C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579809 | ||||||
chr19:579825
|
G | C | 1 | a0002c0005t0001g0116 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.572+169G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579825 | ||||||
chr19:579907
|
G | A | 2 | a0001c0002t0001g0136a0001c0002t0001g0153 | 2 | HG01517.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.572+251G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579907 | ||||||
chr19:579913
|
G | A | 1 | a0001c0001t0003g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.572+257G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579913 | ||||||
chr19:579915
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.572+259G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579915 | ||||||
chr19:579944
|
C | T | 1 | a0001c0001t0003g0125 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.572+288C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579944 | ||||||
chr19:580012
|
C | A | 33 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(30): Show | 54 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.572+356C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580012 | ||||||
chr19:580012
|
C | G | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.572+356C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580012 | ||||||
chr19:580014
|
G | C | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.572+358G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580014 | ||||||
chr19:580100
|
A | G | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.573-279A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580100 | ||||||
chr19:580101
|
G | A | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.573-278G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580101 | ||||||
chr19:580115
|
GTGGGGT | G | 4 | a0001c0002t0001g0010a0001c0002t0001g0029a0001c0002t0001g0152others(1): Show | 7 | HG00558.hp2 HG02040.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.573-263_573-258del others(6): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580115 | ||||||
chr19:580124
|
A | AC | 4 | a0001c0002t0001g0010a0001c0002t0001g0029a0001c0002t0001g0152others(1): Show | 7 | HG00558.hp2 HG02040.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.573-255_573-254ins others(1): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580124 | ||||||
chr19:580154
|
A | G | 142 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(139): Show | 212 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.573-225A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580154 | ||||||
chr19:580163
|
GA | G | 146 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(143): Show | 220 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.573-214delA | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr19 | 580163 | |||||
chr19:580206
|
C | A | 1 | a0001c0001t0007g0105 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.573-173C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580206 | ||||||
chr19:580230
|
G | A | 1 | a0001c0002t0001g0113 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.573-149G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580230 | ||||||
chr19:580268
|
G | C | 62 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(59): Show | 98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.573-111G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580268 | ||||||
chr19:580299
|
T | C | 1 | a0001c0001t0002g0030 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.573-80T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580299 | ||||||
chr19:580333
|
G | A | 62 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(59): Show | 98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.573-46G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580333 | ||||||
chr19:580335
|
C | G | 1 | a0001c0001t0002g0130 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.573-44C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580335 | ||||||
chr19:580349
|
A | G | 3 | a0001c0001t0003g0048a0001c0001t0003g0162a0001c0001t0003g0163 | 3 | HG02922.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.573-30A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580349 | ||||||
chr19:580353
|
G | A | 2 | a0001c0001t0003g0147a0001c0001t0003g0161 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.573-26G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580353 | ||||||
chr19:580486
|
G | C | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.655+25G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/8 | chr19 | 580486 | ||||||
chr19:580575
|
C | T | 35 | a0001c0001t0002g0156a0001c0003t0001g0058a0001c0003t0001g0066others(32): Show | 56 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-71C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/8 | chr19 | 580575 | ||||||
chr19:580602
|
G | C | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.656-44G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/8 | chr19 | 580602 | ||||||
chr19:580603
|
C | T | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.656-43C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/8 | chr19 | 580603 | ||||||
chr19:580613
|
G | T | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.656-33G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/8 | chr19 | 580613 | ||||||
chr19:580793
|
A | C | 108 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(105): Show | 157 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.792+11A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580793 | ||||||
chr19:580799
|
GCTGGGGG others(39): Show |
G | 1 | a0001c0001t0005g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.792+28_792+73delTG others(44): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580799 | |||||
chr19:580810
|
T | C | 148 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(145): Show | 222 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.792+28T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580810 | ||||||
chr19:580811
|
G | A | 62 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(59): Show | 98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.792+29G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580811 | ||||||
chr19:580822
|
T | G | 20 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(17): Show | 25 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.792+40T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580822 | ||||||
chr19:580837
|
A | AGGCCTAG others(177): Show |
3 | a0001c0002t0001g0085a0001c0002t0001g0087a0001c0002t0001g0089 | 3 | HG01192.hp2 HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.792+104_792+105ins others(184): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580837 | |||||
chr19:580837
|
A | G | 44 | a0001c0001t0005g0005a0001c0001t0005g0040a0001c0001t0005g0076others(41): Show | 71 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.792+55A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580837 | ||||||
chr19:580841
|
C | T | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.792+59C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580841 | ||||||
chr19:580856
|
C | G | 33 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(30): Show | 54 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.792+74C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580856 | ||||||
chr19:580870
|
A | AGGACTGG others(39): Show |
1 | a0001c0002t0001g0086 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.792+104_792+105ins others(46): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580870 | |||||
chr19:580870
|
A | AGGACTGG others(223): Show |
2 | a0001c0002t0001g0083a0001c0002t0001g0088 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.792+104_792+105ins others(230): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580870 | |||||
chr19:580870
|
A | AGGACTGG others(223): Show |
1 | a0001c0002t0001g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.792+104_792+105ins others(230): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580870 | |||||
chr19:580870
|
A | AGGACTGG others(269): Show |
1 | a0001c0002t0019g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.792+104_792+105ins others(276): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580870 | |||||
chr19:580870
|
A | C | 33 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(30): Show | 54 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.792+88A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580870 | ||||||
chr19:580870
|
A | T | 1 | a0001c0003t0008g0064 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.792+88A>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580870 | ||||||
chr19:580883
|
G | A | 35 | a0001c0001t0005g0080a0001c0003t0001g0058a0001c0003t0001g0066others(32): Show | 56 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.792+101G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580883 | ||||||
chr19:580884
|
G | A | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.792+102G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580884 | ||||||
chr19:580887
|
C | CAAG | 33 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(30): Show | 54 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.792+105_792+106ins others(3): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580887 | ||||||
chr19:580887
|
C | G | 57 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(54): Show | 93 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.792+105C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580887 | ||||||
chr19:580888
|
T | A | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+106T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580888 | ||||||
chr19:580888
|
T | G | 33 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(30): Show | 54 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.792+106T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580888 | ||||||
chr19:580891
|
A | G | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.792+109A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580891 | ||||||
chr19:580892
|
C | A | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+110C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580892 | ||||||
chr19:580893
|
T | G | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+111T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580893 | ||||||
chr19:580916
|
A | AGGACTGG others(39): Show |
1 | a0001c0001t0002g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.792+226_793-262dup others(46): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580916 | |||||
chr19:580916
|
A | C | 96 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(93): Show | 153 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.792+134A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580916 | ||||||
chr19:580927
|
A | C | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+145A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580927 | ||||||
chr19:580928
|
G | A | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+146G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580928 | ||||||
chr19:580929
|
G | A | 32 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(29): Show | 53 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.792+147G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580929 | ||||||
chr19:580930
|
G | A | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+148G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580930 | ||||||
chr19:580945
|
T | G | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+163T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580945 | ||||||
chr19:580946
|
C | T | 1 | a0001c0003t0004g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+164C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580946 | ||||||
chr19:580962
|
C | A | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.792+180C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580962 | ||||||
chr19:580975
|
G | A | 3 | a0001c0001t0003g0051a0001c0001t0003g0069a0001c0001t0023g0068 | 3 | HG02723.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.792+193G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580975 | ||||||
chr19:580979
|
C | G | 1 | a0001c0003t0004g0059 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.792+197C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580979 | ||||||
chr19:580999
|
C | CCAGCCCT others(269): Show |
1 | a0001c0001t0003g0163 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.793-262_793-261ins others(276): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580999 | |||||
chr19:580999
|
C | CCAGCCCT others(223): Show |
2 | a0001c0001t0003g0048a0001c0001t0003g0162 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.793-262_793-261ins others(230): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580999 | |||||
chr19:581008
|
C | A | 2 | a0001c0002t0001g0086a0001c0003t0006g0062 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.792+226C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581008 | ||||||
chr19:581008
|
CGGACTGG others(39): Show |
C | 12 | a0001c0001t0003g0021a0001c0001t0003g0051a0001c0001t0003g0069others(9): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.792+233_793-255del others(46): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581008 | |||||
chr19:581008
|
CGGACTGG others(100): Show |
C | 1 | a0001c0002t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.793-261_793-155del | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581008 | |||||
chr19:581009
|
GGACTGGG others(54): Show |
G | 1 | a0001c0015t0004g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.793-261_793-201del others(61): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581009 | |||||
chr19:581015
|
G | T | 1 | a0001c0002t0016g0122 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.792+233G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581015 | ||||||
chr19:581025
|
C | G | 2 | a0001c0002t0001g0086a0001c0002t0001g0087 | 2 | HG01192.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.792+243C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581025 | ||||||
chr19:581045
|
CCAGCCCT others(8): Show |
C | 35 | a0001c0002t0001g0139a0001c0002t0019g0090a0001c0003t0001g0058others(32): Show | 56 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.793-261_793-247del others(15): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581045 | |||||
chr19:581054
|
T | A | 52 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(49): Show | 88 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.793-261T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581054 | ||||||
chr19:581054
|
T | C | 41 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(38): Show | 52 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.793-261T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581054 | ||||||
chr19:581055
|
GGACTGCA others(8): Show |
G | 3 | a0001c0002t0001g0012a0001c0002t0001g0104a0001c0002t0001g0140 | 6 | HG01978.hp1 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-254_793-240del others(15): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581055 | |||||
chr19:581060
|
G | GGGTGAGG others(24): Show |
1 | a0001c0002t0001g0117 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.793-255_793-254ins others(31): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581060 | ||||||
chr19:581060
|
G | GGGTGAGG others(24): Show |
5 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0088others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-255_793-254ins others(31): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581060 | ||||||
chr19:581060
|
G | GGGTGAGG others(70): Show |
2 | a0001c0002t0001g0086a0001c0002t0001g0087 | 2 | HG01192.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.793-255_793-254ins others(77): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581060 | ||||||
chr19:581060
|
G | GGGTGAGG others(25): Show |
1 | a0001c0002t0001g0115 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.793-255_793-254ins others(32): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581060 | ||||||
chr19:581060
|
G | GGGTGAGG others(24): Show |
46 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(43): Show | 79 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.793-255_793-254ins others(31): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581060 | ||||||
chr19:581060
|
G | GGGTGAGG others(25): Show |
1 | a0001c0002t0001g0137 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.793-255_793-254ins others(32): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581060 | ||||||
chr19:581069
|
C | A | 1 | a0001c0002t0001g0121 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.793-246C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581069 | ||||||
chr19:581069
|
CA | C | 3 | a0001c0001t0003g0146a0001c0001t0003g0147a0001c0001t0003g0161 | 3 | HG03195.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.793-245delA | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581069 | ||||||
chr19:581070
|
A | G | 134 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(131): Show | 201 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.793-245A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581070 | ||||||
chr19:581072
|
A | G | 3 | a0001c0001t0003g0146a0001c0001t0003g0147a0001c0001t0003g0161 | 3 | HG03195.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.793-243A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581072 | ||||||
chr19:581086
|
C | G | 4 | a0001c0002t0001g0012a0001c0002t0001g0104a0001c0002t0001g0121others(1): Show | 7 | HG01978.hp1 HG02071.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.793-229C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581086 | ||||||
chr19:581115
|
A | C | 95 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(92): Show | 152 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.793-200A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581115 | ||||||
chr19:581152
|
CCAGCCCT others(39): Show |
C | 1 | a0001c0001t0002g0170 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.793-108_793-63delC others(45): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581152 | |||||
chr19:581167
|
G | A | 14 | a0001c0001t0003g0146a0001c0001t0003g0147a0001c0001t0003g0161others(11): Show | 20 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.793-148G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581167 | ||||||
chr19:581190
|
TCCCGGAC others(7): Show |
T | 50 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(47): Show | 83 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.793-124_793-111del others(14): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581190 | ||||||
chr19:581198
|
T | C | 46 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0085others(43): Show | 70 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.793-117T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581198 | ||||||
chr19:581204
|
C | CTCCGGAC others(25): Show |
9 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(6): Show | 9 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.793-110_793-79dupT others(31): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581204 | |||||
chr19:581236
|
TCCCGGAC others(7): Show |
T | 3 | a0001c0002t0001g0012a0001c0002t0001g0104a0001c0002t0001g0140 | 6 | HG01978.hp1 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-78_793-65delCC others(12): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581236 | ||||||
chr19:581239
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.793-76C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581239 | ||||||
chr19:581253
|
A | C | 37 | a0001c0002t0001g0012a0001c0002t0001g0104a0001c0002t0001g0140others(34): Show | 61 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.793-62A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581253 | ||||||
chr19:581624
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0096 | 3 | HG02559.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1069+33G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581624 | ||||||
chr19:581633
|
G | A | 44 | a0001c0001t0003g0021a0001c0001t0003g0073a0001c0001t0003g0165others(41): Show | 67 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1069+42G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581633 | ||||||
chr19:581714
|
A | C | 1 | a0001c0001t0011g0111 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1069+123A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581714 | ||||||
chr19:581729
|
G | A | 1 | a0001c0002t0001g0118 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1069+138G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581729 | ||||||
chr19:581783
|
A | C | 1 | a0001c0001t0003g0024 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1069+192A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581783 | ||||||
chr19:581786
|
G | A | 1 | a0001c0002t0001g0028 | 2 | HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1069+195G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581786 | ||||||
chr19:581806
|
C | T | 1 | a0001c0001t0005g0077 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1069+215C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581806 | ||||||
chr19:581815
|
C | T | 78 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0002g0154others(75): Show | 110 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1069+224C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581815 | ||||||
chr19:581846
|
C | T | 1 | a0001c0002t0001g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1069+255C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581846 | ||||||
chr19:581915
|
G | A | 1 | a0001c0001t0003g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1069+324G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581915 | ||||||
chr19:581920
|
C | G | 1 | a0001c0002t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1069+329C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581920 | ||||||
chr19:581944
|
C | T | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1069+353C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581944 | ||||||
chr19:581956
|
C | T | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1070-350C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581956 | ||||||
chr19:581974
|
C | T | 34 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0082others(31): Show | 55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1070-332C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581974 | ||||||
chr19:582006
|
G | A | 2 | a0001c0001t0003g0023a0001c0001t0020g0023 | 2 | HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1070-300G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582006 | ||||||
chr19:582077
|
A | G | 7 | a0001c0001t0003g0021a0001c0001t0003g0073a0001c0001t0003g0165others(4): Show | 9 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1070-229A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582077 | ||||||
chr19:582092
|
C | G | 1 | a0001c0001t0002g0129 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1070-214C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582092 | ||||||
chr19:582137
|
G | A | 1 | a0001c0001t0011g0111 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1070-169G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582137 | ||||||
chr19:582140
|
C | T | 1 | a0001c0002t0001g0143 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1070-166C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582140 | ||||||
chr19:582253
|
T | C | 164 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0002g0004others(161): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1070-53T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582253 | ||||||
chr19:582292
|
C | T | 1 | a0001c0002t0001g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1070-14C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582292 | ||||||
chr19:582352
|
C | T | 1 | a0001c0001t0005g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1094+22C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 7/8 | chr19 | 582352 | ||||||
chr19:582429
|
G | T | 1 | a0001c0003t0004g0063 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1095-85G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 7/8 | chr19 | 582429 | ||||||
chr19:582468
|
A | G | 141 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0003g0013others(138): Show | 211 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.1095-46A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 7/8 | chr19 | 582468 | ||||||
chr19:582481
|
G | T | 1 | a0004c0009t0003g0092 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1095-33G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 7/8 | chr19 | 582481 | ||||||
chr19:582505
|
G | A | 59 | a0001c0001t0003g0021a0001c0002t0001g0001a0001c0002t0001g0006others(56): Show | 96 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.1095-9G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 7/8 | chr19 | 582505 | ||||||
chr19:582586
|
C | T | 2 | a0004c0009t0003g0092a0004c0009t0022g0091 | 2 | HG03239.hp1 NA19082.hp2 |
splice_region_variant&intron_variant | LOW | c.*5+4C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 8/8 | chr19 | 582586 | ||||||
chr19:582693
|
C | T | 60 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0010others(57): Show | 96 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.*6-57C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 8/8 | chr19 | 582693 |