geneid | 22820 |
---|---|
ensemblid | ENSG00000181789.14 |
hgncid | 2236 |
symbol | COPG1 |
name | COPI coat complex subunit gamma 1 |
refseq_nuc | NM_016128.4 |
refseq_prot | NP_057212.1 |
ensembl_nuc | ENST00000314797.10 |
ensembl_prot | ENSP00000325002.6 |
mane_status | MANE Select |
chr | chr3 |
start | 129249606 |
end | 129277773 |
strand | + |
ver | v1.2 |
region | chr3:129249606-129277773 |
region5000 | chr3:129244606-129282773 |
regionname0 | COPG1_chr3_129249606_129277773 |
regionname5000 | COPG1_chr3_129244606_129282773 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 874 | 307 | 83 | 65 | 112 | 10 | 35 | 76 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0002 | 0/0 | 874 | 14 | 3 | 5 | 1 | 2 | 3 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0003 | 0/0 | 874 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0004 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0005 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0006 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2625 | 216 | 31 | 52 | 91 | 10 | 30 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0002 | 0/0 | 2625 | 27 | 6 | 0 | 16 | 0 | 5 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0003 | 0/0 | 2625 | 26 | 25 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0004 | 0/0 | 2625 | 16 | 10 | 6 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0005 | 0/0 | 2625 | 14 | 3 | 5 | 1 | 2 | 3 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0006 | 0/0 | 2625 | 10 | 7 | 3 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0007 | 0/0 | 2625 | 4 | 0 | 0 | 4 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0008 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0009 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0010 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0011 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0012 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0013 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0014 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0015 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0016 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0017 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
c0018 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 455 | 156 | 24 | 34 | 73 | 6 | 18 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
t0002 | 1/0 | 454 | 126 | 35 | 26 | 40 | 5 | 19 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
t0003 | 0/0 | 453 | 31 | 20 | 9 | 0 | 1 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
t0004 | 0/0 | 455 | 8 | 8 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
t0005 | 0/0 | 454 | 2 | 1 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
t0006 | 0/0 | 454 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
t0007 | 0/0 | 454 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 24 | 0 | 5 | 16 | 1 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0002 | 0/0 | 16 | 3 | 2 | 7 | 1 | 3 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0003 | 0/0 | 10 | 6 | 4 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0004 | 0/0 | 10 | 4 | 5 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0006 | 0/0 | 8 | 1 | 5 | 0 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0007 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0008 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0020 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0022 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0035 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2625 | 216 | 31 | 52 | 91 | 10 | 30 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0002 | 0/0 | 2625 | 27 | 6 | 0 | 16 | 0 | 5 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0003 | 0/0 | 2625 | 26 | 25 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0004 | 0/0 | 2625 | 16 | 10 | 6 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0006 | 0/0 | 2625 | 10 | 7 | 3 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0007 | 0/0 | 2625 | 4 | 0 | 0 | 4 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0009 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0010 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0011 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0012 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0013 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0015 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0017 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0002c0005 | 0/0 | 2625 | 14 | 3 | 5 | 1 | 2 | 3 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0003c0008 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0004c0014 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0005c0018 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0006c0016 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3079 | 143 | 18 | 32 | 69 | 6 | 17 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0001t0002 | 1/0 | 3078 | 60 | 5 | 20 | 19 | 3 | 12 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0001t0003 | 0/0 | 3077 | 2 | 0 | 0 | 0 | 1 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0001t0004 | 0/0 | 3079 | 8 | 8 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0001t0006 | 0/0 | 3078 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0001t0007 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0002t0001 | 0/0 | 3079 | 3 | 1 | 0 | 1 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0002t0002 | 0/0 | 3078 | 23 | 4 | 0 | 15 | 0 | 4 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0002t0005 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0003t0001 | 0/0 | 3079 | 3 | 3 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0003t0002 | 0/0 | 3078 | 11 | 11 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0003t0003 | 0/0 | 3077 | 12 | 11 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0004t0002 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0004t0003 | 0/0 | 3077 | 15 | 9 | 6 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0006t0002 | 0/0 | 3078 | 10 | 7 | 3 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0007t0002 | 0/0 | 3078 | 4 | 0 | 0 | 4 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0009t0002 | 0/0 | 3078 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0010t0005 | 0/0 | 3078 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0011t0002 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0012t0002 | 0/0 | 3078 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0013t0002 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0015t0001 | 0/0 | 3079 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0001c0017t0001 | 0/0 | 3079 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0002c0005t0001 | 0/0 | 3079 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0002c0005t0002 | 0/0 | 3078 | 11 | 3 | 2 | 1 | 2 | 3 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0002c0005t0003 | 0/0 | 3077 | 2 | 0 | 2 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0003c0008t0001 | 0/0 | 3079 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0004c0014t0001 | 0/0 | 3079 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0005c0018t0001 | 0/0 | 3079 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
a0006c0016t0002 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | copy fasta | chr3 | 129244606 | 129282773 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 18 | 0 | 3 | 13 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0002 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0004 | 0/0 | 10 | 4 | 5 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0006 | 0/0 | 7 | 1 | 4 | 0 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0035 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0002 | 0/0 | 10 | 1 | 1 | 4 | 1 | 3 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0007 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0004g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0006g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0002t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0003g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0003g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0003t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0004t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0004t0003g0003 | 0/0 | 10 | 6 | 4 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0004t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0004t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0004t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0004t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0004t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0006t0002g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0006t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0006t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0006t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0006t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0006t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0007t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0007t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0007t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0007t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0009t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0009t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0010t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0011t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0012t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0013t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0015t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0001c0017t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0002c0005t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0002c0005t0002g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0002c0005t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0002c0005t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0002c0005t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0002c0005t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0002c0005t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0002c0005t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0003c0008t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0003c0008t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0004c0014t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0005c0018t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
a0006c0016t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0115 | EUR | FIN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00280 | hp2 | a0002 | c0005 | t0002 | g0045 | EUR | FIN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00408 | hp2 | a0001 | c0017 | t0001 | g0122 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00639 | hp2 | a0001 | c0003 | t0003 | g0030 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00642 | hp2 | a0001 | c0010 | t0005 | g0079 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00735 | hp1 | a0001 | c0004 | t0003 | g0087 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00738 | hp1 | a0001 | c0004 | t0003 | g0003 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01069 | hp1 | a0002 | c0005 | t0002 | g0010 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01071 | hp2 | a0002 | c0005 | t0002 | g0010 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01167 | hp2 | a0001 | c0004 | t0003 | g0003 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01169 | hp1 | a0001 | c0004 | t0003 | g0003 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01175 | hp2 | a0001 | c0004 | t0003 | g0090 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01243 | hp1 | a0001 | c0006 | t0002 | g0012 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01255 | hp2 | a0001 | c0006 | t0002 | g0076 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01261 | hp1 | a0002 | c0005 | t0001 | g0049 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01346 | hp1 | a0001 | c0004 | t0003 | g0003 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01361 | hp2 | a0001 | c0015 | t0001 | g0001 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01496 | hp1 | a0001 | c0012 | t0002 | g0092 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01884 | hp1 | a0001 | c0003 | t0003 | g0082 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01884 | hp2 | a0002 | c0005 | t0002 | g0014 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0176 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01934 | hp2 | a0002 | c0005 | t0003 | g0024 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02027 | hp1 | a0001 | c0001 | t0007 | g0186 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02055 | hp1 | a0001 | c0003 | t0002 | g0011 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02055 | hp2 | a0001 | c0006 | t0002 | g0012 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02071 | hp1 | a0006 | c0016 | t0002 | g0023 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02083 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02145 | hp1 | a0001 | c0003 | t0003 | g0029 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CDX | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | CDX | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02257 | hp1 | a0001 | c0002 | t0005 | g0078 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02257 | hp2 | a0002 | c0005 | t0002 | g0014 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02258 | hp1 | a0001 | c0004 | t0003 | g0003 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02273 | hp1 | a0002 | c0005 | t0003 | g0024 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02280 | hp1 | a0001 | c0003 | t0002 | g0055 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02451 | hp2 | a0001 | c0004 | t0002 | g0084 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0101 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02615 | hp2 | a0001 | c0004 | t0003 | g0003 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02622 | hp1 | a0001 | c0003 | t0003 | g0009 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02622 | hp2 | a0001 | c0003 | t0002 | g0011 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02647 | hp1 | a0001 | c0003 | t0003 | g0009 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02647 | hp2 | a0001 | c0009 | t0002 | g0072 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02698 | hp2 | a0002 | c0005 | t0002 | g0010 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02717 | hp1 | a0001 | c0003 | t0002 | g0053 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02723 | hp1 | a0001 | c0003 | t0003 | g0085 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02735 | hp2 | a0002 | c0005 | t0002 | g0010 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0065 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02809 | hp2 | a0001 | c0011 | t0002 | g0088 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02818 | hp2 | a0001 | c0004 | t0003 | g0086 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02886 | hp1 | a0001 | c0009 | t0002 | g0073 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02896 | hp1 | a0001 | c0004 | t0003 | g0089 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02896 | hp2 | a0001 | c0006 | t0002 | g0028 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02970 | hp2 | a0003 | c0008 | t0001 | g0135 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02976 | hp2 | a0001 | c0006 | t0002 | g0093 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03098 | hp2 | a0001 | c0003 | t0002 | g0050 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03139 | hp1 | a0001 | c0003 | t0003 | g0009 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03139 | hp2 | a0001 | c0004 | t0003 | g0081 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03195 | hp1 | a0001 | c0004 | t0003 | g0003 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03195 | hp2 | a0001 | c0003 | t0003 | g0029 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0057 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03239 | hp1 | a0002 | c0005 | t0002 | g0046 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03453 | hp1 | a0001 | c0003 | t0003 | g0030 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03486 | hp1 | a0001 | c0004 | t0003 | g0003 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03486 | hp2 | a0001 | c0006 | t0002 | g0028 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03516 | hp1 | a0003 | c0008 | t0001 | g0136 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03579 | hp1 | a0001 | c0003 | t0002 | g0052 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03579 | hp2 | a0001 | c0003 | t0003 | g0009 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0056 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0063 | SAS | STU | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | STU | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18522 | hp1 | a0001 | c0003 | t0002 | g0011 | AFR | YRI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18522 | hp2 | a0001 | c0006 | t0002 | g0077 | AFR | YRI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18612 | hp2 | a0002 | c0005 | t0002 | g0047 | EAS | CHB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18747 | hp2 | a0001 | c0007 | t0002 | g0060 | EAS | CHB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18906 | hp1 | a0001 | c0006 | t0002 | g0012 | AFR | YRI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18906 | hp2 | a0001 | c0003 | t0003 | g0009 | AFR | YRI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18939 | hp1 | a0001 | c0007 | t0002 | g0069 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18954 | hp1 | a0005 | c0018 | t0001 | g0096 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18966 | hp1 | a0001 | c0007 | t0002 | g0064 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18972 | hp2 | a0001 | c0007 | t0002 | g0066 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18973 | hp1 | a0004 | c0014 | t0001 | g0041 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19030 | hp2 | a0001 | c0003 | t0002 | g0054 | AFR | LWK | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0137 | AFR | LWK | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0061 | AFR | LWK | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19240 | hp1 | a0001 | c0003 | t0002 | g0051 | AFR | YRI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA20129 | hp1 | a0001 | c0004 | t0003 | g0003 | AFR | ASW | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA20129 | hp2 | a0001 | c0003 | t0002 | g0011 | AFR | ASW | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA20805 | hp1 | a0002 | c0005 | t0002 | g0048 | EUR | TSI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | GIH | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG01123 | hp2 | a0001 | c0006 | t0002 | g0075 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02109 | hp2 | a0001 | c0003 | t0002 | g0025 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02486 | hp1 | a0001 | c0004 | t0003 | g0003 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02486 | hp2 | a0001 | c0006 | t0002 | g0012 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03471 | hp1 | a0001 | c0003 | t0003 | g0083 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | USA | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | USA | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA20300 | hp1 | a0002 | c0005 | t0002 | g0014 | AFR | USA | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA21309 | hp1 | a0001 | c0013 | t0002 | g0091 | AFR | LWK | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0035 | REF | REF | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0165 | REF | REF | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:129252354
|
T | C | 1 | a0003 | 2 | HG02970.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.164T>C | p.Ile55Thr | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 3/24 | 268/3078 | 164/2625 | 55/874 | chr3 | 129252354 | ||
chr3:129257608
|
C | G | 1 | a0002 | 14 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
missense_variant | MODERATE | c.718C>G | p.Leu240Val | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 9/24 | 822/3078 | 718/2625 | 240/874 | chr3 | 129257608 | ||
chr3:129257791
|
T | A | 1 | a0004 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.802T>A | p.Tyr268Asn | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/24 | 906/3078 | 802/2625 | 268/874 | chr3 | 129257791 | ||
chr3:129271868
|
C | T | 1 | a0005 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.1945C>T | p.Arg649Cys | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 19/24 | 2049/3078 | 1945/2625 | 649/874 | chr3 | 129271868 | ||
chr3:129274944
|
C | T | 1 | a0006 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.2363C>T | p.Thr788Met | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 22/24 | 2467/3078 | 2363/2625 | 788/874 | chr3 | 129274944 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:129252340
|
G | A | 1 | a0001c0010 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.150G>A | p.Lys50Lys | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 3/24 | 254/3078 | 150/2625 | 50/874 | chr3 | 129252340 | ||
chr3:129252649
|
G | A | 1 | a0001c0011 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.198G>A | p.Ala66Ala | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 4/24 | 302/3078 | 198/2625 | 66/874 | chr3 | 129252649 | ||
chr3:129254716
|
C | T | 1 | a0001c0007 | 4 | NA18747.hp2 NA18939.hp1 NA18966.hp1 others(1): Show |
synonymous_variant | LOW | c.372C>T | p.Ala124Ala | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/24 | 476/3078 | 372/2625 | 124/874 | chr3 | 129254716 | ||
chr3:129257553
|
T | C | 11 | a0001c0002a0001c0003a0001c0004others(8): Show | 103 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(100): Show |
synonymous_variant | LOW | c.663T>C | p.His221His | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 9/24 | 767/3078 | 663/2625 | 221/874 | chr3 | 129257553 | ||
chr3:129257820
|
G | A | 2 | a0001c0012a0001c0013 | 2 | HG01496.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.831G>A | p.Leu277Leu | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/24 | 935/3078 | 831/2625 | 277/874 | chr3 | 129257820 | ||
chr3:129257850
|
G | A | 1 | a0001c0006 | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
synonymous_variant | LOW | c.861G>A | p.Pro287Pro | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/24 | 965/3078 | 861/2625 | 287/874 | chr3 | 129257850 | ||
chr3:129260732
|
G | A | 1 | a0001c0015 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.1053G>A | p.Thr351Thr | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/24 | 1157/3078 | 1053/2625 | 351/874 | chr3 | 129260732 | ||
chr3:129260750
|
C | T | 1 | a0001c0013 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1071C>T | p.Ile357Ile | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/24 | 1175/3078 | 1071/2625 | 357/874 | chr3 | 129260750 | ||
chr3:129265566
|
G | A | 2 | a0001c0004a0001c0011 | 17 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(14): Show |
synonymous_variant | LOW | c.1242G>A | p.Lys414Lys | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/24 | 1346/3078 | 1242/2625 | 414/874 | chr3 | 129265566 | ||
chr3:129265740
|
C | T | 4 | a0001c0002a0001c0007a0001c0009others(1): Show | 34 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(31): Show |
synonymous_variant | LOW | c.1416C>T | p.Tyr472Tyr | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/24 | 1520/3078 | 1416/2625 | 472/874 | chr3 | 129265740 | ||
chr3:129267976
|
C | G | 1 | a0001c0010 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.1584C>G | p.Ala528Ala | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/24 | 1688/3078 | 1584/2625 | 528/874 | chr3 | 129267976 | ||
chr3:129272366
|
C | T | 1 | a0001c0017 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.2109C>T | p.Pro703Pro | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 20/24 | 2213/3078 | 2109/2625 | 703/874 | chr3 | 129272366 | ||
chr3:129275276
|
C | T | 1 | a0001c0009 | 2 | HG02647.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.2478C>T | p.His826His | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/24 | 2582/3078 | 2478/2625 | 826/874 | chr3 | 129275276 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:129249638
|
A | G | 1 | a0001c0001t0006 | 2 | HG02083.hp2 NA18951.hp2 |
5_prime_UTR_variant | MODIFIER | c.-72A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/24 | 72 | chr3 | 129249638 | |||||
chr3:129249670
|
C | G | 1 | a0001c0001t0007 | 1 | HG02027.hp1 | 5_prime_UTR_variant | MODIFIER | c.-40C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/24 | 40 | chr3 | 129249670 | |||||
chr3:129277601
|
C | CT | 9 | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(6): Show | 156 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*196dupT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 24/24 | 197 | INFO_REALIGN_3_PRIME | chr3 | 129277601 | ||||
chr3:129277601
|
CT | C | 4 | a0001c0001t0003a0001c0003t0003a0001c0004t0003others(1): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*196delT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 24/24 | 196 | INFO_REALIGN_3_PRIME | chr3 | 129277601 | ||||
chr3:129277620
|
T | TA | 1 | a0001c0001t0004 | 8 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*199dupA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 24/24 | 200 | INFO_REALIGN_3_PRIME | chr3 | 129277620 | ||||
chr3:129277765
|
T | A | 2 | a0001c0002t0005a0001c0010t0005 | 2 | HG00642.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*341T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 24/24 | 341 | chr3 | 129277765 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:129249799
|
T | C | 64 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(61): Show | 101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.37+53T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249799 | ||||||
chr3:129249812
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.37+66C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249812 | ||||||
chr3:129249911
|
C | T | 17 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(14): Show | 32 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.37+165C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249911 | ||||||
chr3:129249964
|
G | A | 8 | a0002c0005t0001g0049a0002c0005t0002g0010a0002c0005t0002g0014others(5): Show | 14 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.37+218G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249964 | ||||||
chr3:129249972
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.37+226C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249972 | ||||||
chr3:129249973
|
A | AC | 17 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0179others(14): Show | 23 | HG00323.hp2 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+238dupC | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr3 | 129249973 | |||||
chr3:129249973
|
ACC | A | 44 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0002g0005others(41): Show | 72 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.37+237_37+238delCC | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr3 | 129249973 | |||||
chr3:129249973
|
ACCC | A | 17 | a0001c0003t0001g0025a0001c0003t0002g0011a0001c0003t0002g0025others(14): Show | 26 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.37+236_37+238delCC others(1): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr3 | 129249973 | |||||
chr3:129249982
|
C | A | 16 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(13): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.37+236C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249982 | ||||||
chr3:129249987
|
G | A | 2 | a0001c0002t0005g0078a0001c0010t0005g0079 | 2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.37+241G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249987 | ||||||
chr3:129250069
|
G | T | 1 | a0001c0001t0001g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.37+323G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129250069 | ||||||
chr3:129250304
|
G | C | 14 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(11): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.38-378G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129250304 | ||||||
chr3:129250315
|
G | C | 2 | a0001c0003t0002g0050a0001c0003t0002g0051 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.38-367G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129250315 | ||||||
chr3:129250438
|
T | C | 1 | a0001c0002t0002g0056 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.38-244T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129250438 | ||||||
chr3:129250668
|
G | T | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.38-14G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129250668 | ||||||
chr3:129250810
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.90+76A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250810 | ||||||
chr3:129250863
|
T | C | 2 | a0001c0002t0002g0026a0001c0002t0002g0057 | 3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.90+129T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250863 | ||||||
chr3:129250896
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.90+162T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250896 | ||||||
chr3:129250912
|
CT | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(69): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.90+205delT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr3 | 129250912 | |||||
chr3:129250912
|
CTT | C | 9 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0006t0002g0012others(6): Show | 13 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.90+204_90+205delTT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr3 | 129250912 | |||||
chr3:129250912
|
CTTT | C | 10 | a0001c0002t0002g0074a0001c0003t0003g0029a0001c0003t0003g0030others(7): Show | 21 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.90+203_90+205delTT others(1): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr3 | 129250912 | |||||
chr3:129250912
|
CTTTT | C | 46 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(43): Show | 68 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.90+202_90+205delTT others(2): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr3 | 129250912 | |||||
chr3:129250947
|
A | G | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.90+213A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250947 | ||||||
chr3:129250952
|
C | A | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.90+218C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250952 | ||||||
chr3:129250969
|
G | T | 3 | a0001c0001t0001g0138a0001c0012t0002g0092a0001c0013t0002g0091 | 3 | HG01433.hp1 HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.90+235G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250969 | ||||||
chr3:129250992
|
C | T | 2 | a0001c0003t0001g0137a0001c0003t0001g0176 | 2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.90+258C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250992 | ||||||
chr3:129250993
|
G | A | 1 | a0002c0005t0002g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.90+259G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250993 | ||||||
chr3:129251016
|
C | G | 2 | a0001c0012t0002g0092a0001c0013t0002g0091 | 2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.90+282C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251016 | ||||||
chr3:129251054
|
G | A | 2 | a0001c0001t0002g0019a0001c0001t0002g0139 | 4 | NA18941.hp1 NA18970.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+320G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251054 | ||||||
chr3:129251178
|
C | T | 2 | a0001c0009t0002g0072a0001c0009t0002g0073 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.90+444C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251178 | ||||||
chr3:129251212
|
C | T | 18 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0002g0005others(15): Show | 26 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.90+478C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251212 | ||||||
chr3:129251269
|
A | G | 2 | a0001c0002t0002g0026a0001c0002t0002g0057 | 3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.90+535A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251269 | ||||||
chr3:129251326
|
G | A | 4 | a0001c0002t0005g0078a0001c0009t0002g0072a0001c0009t0002g0073others(1): Show | 4 | HG00642.hp2 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+592G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251326 | ||||||
chr3:129251327
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0094 | 4 | HG00609.hp2 NA18944.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+593G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251327 | ||||||
chr3:129251368
|
T | A | 64 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(61): Show | 101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.90+634T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251368 | ||||||
chr3:129251371
|
T | A | 6 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0140others(3): Show | 6 | NA18955.hp1 NA18959.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+637T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251371 | ||||||
chr3:129251371
|
TTA | T | 23 | a0001c0003t0001g0025a0001c0003t0002g0011a0001c0003t0002g0025others(20): Show | 36 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.90+653_90+654delAT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr3 | 129251371 | |||||
chr3:129251371
|
TTATA | T | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.90+651_90+654delAT others(2): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr3 | 129251371 | |||||
chr3:129251508
|
A | G | 58 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(55): Show | 91 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.91-773A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251508 | ||||||
chr3:129251582
|
G | C | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.91-699G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251582 | ||||||
chr3:129251607
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.91-674G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251607 | ||||||
chr3:129251675
|
C | T | 14 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(11): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.91-606C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251675 | ||||||
chr3:129251805
|
G | A | 2 | a0001c0003t0003g0029a0001c0003t0003g0085 | 3 | HG02145.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.91-476G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251805 | ||||||
chr3:129251812
|
C | G | 2 | a0003c0008t0001g0135a0003c0008t0001g0136 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.91-469C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251812 | ||||||
chr3:129251877
|
G | A | 1 | a0001c0006t0002g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.91-404G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251877 | ||||||
chr3:129251985
|
G | A | 4 | a0001c0002t0005g0078a0001c0009t0002g0072a0001c0009t0002g0073others(1): Show | 4 | HG00642.hp2 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-296G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251985 | ||||||
chr3:129252059
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.91-222A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129252059 | ||||||
chr3:129252150
|
A | G | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.91-131A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129252150 | ||||||
chr3:129252270
|
T | C | 64 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(61): Show | 101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.91-11T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129252270 | ||||||
chr3:129252403
|
G | T | 2 | a0001c0001t0001g0036a0001c0001t0002g0036 | 2 | NA18952.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.171+42G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 3/23 | chr3 | 129252403 | ||||||
chr3:129252416
|
G | C | 2 | a0001c0002t0005g0078a0001c0010t0005g0079 | 2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.171+55G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 3/23 | chr3 | 129252416 | ||||||
chr3:129253315
|
A | G | 66 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(63): Show | 103 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.323+360A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129253315 | ||||||
chr3:129253750
|
A | G | 2 | a0001c0003t0001g0137a0001c0003t0001g0176 | 2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.323+795A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129253750 | ||||||
chr3:129253807
|
C | G | 1 | a0001c0001t0002g0133 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.323+852C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129253807 | ||||||
chr3:129253994
|
G | C | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.324-674G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129253994 | ||||||
chr3:129254000
|
C | CA | 13 | a0001c0001t0001g0097a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01891.hp2 HG02572.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.324-651dupA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr3 | 129254000 | |||||
chr3:129254000
|
CA | C | 16 | a0001c0003t0001g0025a0001c0003t0002g0011a0001c0003t0002g0025others(13): Show | 25 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.324-651delA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr3 | 129254000 | |||||
chr3:129254000
|
CAA | C | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.324-652_324-651del others(2): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr3 | 129254000 | |||||
chr3:129254032
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.324-636C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254032 | ||||||
chr3:129254087
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.324-581G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254087 | ||||||
chr3:129254104
|
C | G | 1 | a0001c0001t0001g0035 | 2 | HG03710.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.324-564C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254104 | ||||||
chr3:129254154
|
G | A | 1 | a0001c0013t0002g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.324-514G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254154 | ||||||
chr3:129254217
|
T | C | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.324-451T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254217 | ||||||
chr3:129254248
|
C | T | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.324-420C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254248 | ||||||
chr3:129254295
|
C | CA | 42 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(39): Show | 66 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.324-362dupA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr3 | 129254295 | |||||
chr3:129254609
|
T | A | 1 | a0001c0004t0003g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.324-59T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254609 | ||||||
chr3:129254750
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | splice_region_variant&intron_variant | LOW | c.399+7C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/23 | chr3 | 129254750 | ||||||
chr3:129254755
|
C | G | 21 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(18): Show | 30 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.399+12C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/23 | chr3 | 129254755 | ||||||
chr3:129254783
|
A | C | 2 | a0001c0002t0005g0078a0001c0010t0005g0079 | 2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.399+40A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/23 | chr3 | 129254783 | ||||||
chr3:129254820
|
T | C | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.399+77T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/23 | chr3 | 129254820 | ||||||
chr3:129254838
|
C | T | 8 | a0001c0001t0004g0018a0001c0001t0004g0101a0001c0001t0004g0128others(5): Show | 10 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.399+95C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/23 | chr3 | 129254838 | ||||||
chr3:129254904
|
A | C | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.400-81A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/23 | chr3 | 129254904 | ||||||
chr3:129255135
|
A | C | 66 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(63): Show | 103 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.492+58A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255135 | ||||||
chr3:129255135
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.492+58A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255135 | ||||||
chr3:129255141
|
C | T | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.492+64C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255141 | ||||||
chr3:129255179
|
C | CT | 46 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(43): Show | 74 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.492+115dupT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr3 | 129255179 | |||||
chr3:129255201
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.492+124C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255201 | ||||||
chr3:129255297
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.492+220G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255297 | ||||||
chr3:129255321
|
G | T | 1 | a0001c0001t0002g0133 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.492+244G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255321 | ||||||
chr3:129255346
|
T | C | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.492+269T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255346 | ||||||
chr3:129255350
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.492+273T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255350 | ||||||
chr3:129255478
|
C | T | 14 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(11): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.492+401C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255478 | ||||||
chr3:129255487
|
C | CT | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0002g0005others(38): Show | 68 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.492+423dupT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr3 | 129255487 | |||||
chr3:129255773
|
C | T | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.493-295C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255773 | ||||||
chr3:129255968
|
C | T | 14 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(11): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.493-100C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255968 | ||||||
chr3:129256169
|
A | G | 2 | a0001c0002t0002g0026a0001c0002t0002g0057 | 3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.579+15A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256169 | ||||||
chr3:129256201
|
G | C | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.579+47G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256201 | ||||||
chr3:129256202
|
T | G | 20 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0002g0005others(17): Show | 29 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.579+48T>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256202 | ||||||
chr3:129256237
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.579+83C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256237 | ||||||
chr3:129256275
|
C | A | 21 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(18): Show | 30 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.579+121C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256275 | ||||||
chr3:129256491
|
C | T | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.579+337C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256491 | ||||||
chr3:129256657
|
C | G | 1 | a0001c0001t0001g0175 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.579+503C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256657 | ||||||
chr3:129256702
|
C | T | 16 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(13): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.579+548C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256702 | ||||||
chr3:129256714
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.579+560G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256714 | ||||||
chr3:129256814
|
A | G | 16 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(13): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.580-656A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256814 | ||||||
chr3:129257028
|
C | T | 2 | a0001c0002t0005g0078a0001c0010t0005g0079 | 2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.580-442C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129257028 | ||||||
chr3:129257702
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG03654.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.738-25C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 9/23 | chr3 | 129257702 | ||||||
chr3:129257886
|
C | G | 4 | a0002c0005t0002g0010a0002c0005t0002g0046a0002c0005t0002g0047others(1): Show | 8 | HG01069.hp1 HG01071.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.871+26C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129257886 | ||||||
chr3:129257897
|
A | G | 14 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(11): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.871+37A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129257897 | ||||||
chr3:129258315
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.871+455G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129258315 | ||||||
chr3:129258448
|
C | T | 64 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(61): Show | 101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.871+588C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129258448 | ||||||
chr3:129258800
|
G | C | 1 | a0001c0007t0002g0060 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.871+940G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129258800 | ||||||
chr3:129259439
|
C | T | 1 | a0001c0001t0001g0034 | 2 | HG02602.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.872-894C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129259439 | ||||||
chr3:129259460
|
C | CA | 7 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0140others(4): Show | 8 | HG01081.hp2 HG02145.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.872-853dupA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr3 | 129259460 | |||||
chr3:129259460
|
CA | C | 5 | a0001c0001t0001g0033a0001c0001t0001g0124a0001c0001t0001g0179others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.872-853delA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr3 | 129259460 | |||||
chr3:129259477
|
AAAAG | A | 9 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(6): Show | 15 | HG00639.hp2 HG01175.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.872-852_872-849del others(4): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr3 | 129259477 | |||||
chr3:129259478
|
AAAG | A | 28 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(25): Show | 46 | HG00408.hp1 HG00544.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.872-852_872-850del others(3): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr3 | 129259478 | |||||
chr3:129259487
|
G | A | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.872-846G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129259487 | ||||||
chr3:129259612
|
T | A | 20 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0002g0005others(17): Show | 29 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.872-721T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129259612 | ||||||
chr3:129259763
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.872-570G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129259763 | ||||||
chr3:129259845
|
A | C | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.872-488A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129259845 | ||||||
chr3:129259958
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.872-375C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129259958 | ||||||
chr3:129260153
|
A | G | 1 | a0001c0002t0002g0071 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.872-180A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129260153 | ||||||
chr3:129260165
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(50): Show | 86 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.872-168C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129260165 | ||||||
chr3:129260221
|
G | A | 16 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(13): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.872-112G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129260221 | ||||||
chr3:129260265
|
T | C | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.872-68T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129260265 | ||||||
chr3:129260272
|
C | T | 1 | a0001c0003t0002g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.872-61C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129260272 | ||||||
chr3:129260319
|
C | G | 1 | a0001c0001t0001g0172 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.872-14C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129260319 | ||||||
chr3:129260413
|
C | G | 64 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(61): Show | 101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.939+13C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 11/23 | chr3 | 129260413 | ||||||
chr3:129260954
|
G | C | 16 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(13): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1128+147G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129260954 | ||||||
chr3:129261189
|
G | A | 8 | a0002c0005t0001g0049a0002c0005t0002g0010a0002c0005t0002g0014others(5): Show | 14 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1128+382G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261189 | ||||||
chr3:129261268
|
A | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0166 | 5 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1128+461A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261268 | ||||||
chr3:129261395
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(197): Show | 325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1128+588T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261395 | ||||||
chr3:129261397
|
G | T | 2 | a0001c0002t0005g0078a0001c0010t0005g0079 | 2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1128+590G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261397 | ||||||
chr3:129261449
|
T | C | 17 | a0001c0003t0001g0025a0001c0003t0002g0011a0001c0003t0002g0025others(14): Show | 26 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1128+642T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261449 | ||||||
chr3:129261620
|
A | G | 21 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(18): Show | 30 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.1128+813A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261620 | ||||||
chr3:129261625
|
C | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0151a0001c0001t0001g0153others(1): Show | 5 | HG03490.hp1 HG03492.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1128+818C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261625 | ||||||
chr3:129261628
|
CT | C | 17 | a0001c0003t0001g0025a0001c0003t0002g0011a0001c0003t0002g0025others(14): Show | 26 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1128+822delT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261628 | ||||||
chr3:129261658
|
G | T | 17 | a0001c0003t0001g0025a0001c0003t0002g0011a0001c0003t0002g0025others(14): Show | 26 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1128+851G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261658 | ||||||
chr3:129261681
|
C | T | 1 | a0001c0017t0001g0122 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1128+874C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261681 | ||||||
chr3:129261836
|
T | C | 64 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(61): Show | 101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1128+1029T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261836 | ||||||
chr3:129261855
|
G | C | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1128+1048G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261855 | ||||||
chr3:129261983
|
A | G | 2 | a0001c0012t0002g0092a0001c0013t0002g0091 | 2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1128+1176A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261983 | ||||||
chr3:129262013
|
T | C | 4 | a0001c0002t0005g0078a0001c0009t0002g0072a0001c0009t0002g0073others(1): Show | 4 | HG00642.hp2 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+1206T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262013 | ||||||
chr3:129262065
|
T | C | 1 | a0001c0002t0002g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1128+1258T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262065 | ||||||
chr3:129262074
|
C | T | 16 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(13): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1128+1267C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262074 | ||||||
chr3:129262133
|
T | G | 64 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(61): Show | 101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1128+1326T>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262133 | ||||||
chr3:129262250
|
CA | C | 16 | a0001c0003t0001g0025a0001c0003t0002g0011a0001c0003t0002g0025others(13): Show | 25 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1128+1446delA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129262250 | |||||
chr3:129262253
|
A | T | 1 | a0001c0003t0002g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1128+1446A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262253 | ||||||
chr3:129262253
|
AT | A | 51 | a0001c0001t0001g0098a0001c0001t0001g0106a0001c0001t0001g0116others(48): Show | 79 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1128+1463delT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129262253 | |||||
chr3:129262256
|
T | A | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1128+1449T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262256 | ||||||
chr3:129262256
|
T | G | 1 | a0001c0001t0002g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1128+1449T>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262256 | ||||||
chr3:129262401
|
C | T | 5 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(2): Show | 9 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1129-1503C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262401 | ||||||
chr3:129262472
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1129-1432C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262472 | ||||||
chr3:129262542
|
C | T | 2 | a0001c0012t0002g0092a0001c0013t0002g0091 | 2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1129-1362C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262542 | ||||||
chr3:129262575
|
T | C | 1 | a0001c0001t0002g0185 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1129-1329T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262575 | ||||||
chr3:129262665
|
G | C | 1 | a0001c0001t0002g0107 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1129-1239G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262665 | ||||||
chr3:129262722
|
G | GAA | 35 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0002g0005others(32): Show | 57 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1129-1170_1129-116 others(6): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129262722 | |||||
chr3:129262722
|
G | GAAA | 5 | a0001c0002t0002g0027a0001c0002t0002g0058a0001c0002t0002g0062others(2): Show | 7 | HG00408.hp1 HG02080.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-1171_1129-116 others(7): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129262722 | |||||
chr3:129262722
|
GA | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 19 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1129-1169delA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129262722 | |||||
chr3:129262736
|
T | C | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1129-1168T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262736 | ||||||
chr3:129262788
|
G | T | 16 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(13): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1129-1116G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262788 | ||||||
chr3:129262977
|
C | A | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1129-927C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262977 | ||||||
chr3:129263014
|
C | CA | 25 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0102others(22): Show | 39 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1129-869dupA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263014 | |||||
chr3:129263033
|
AAAGAGTC others(6): Show |
A | 1 | a0001c0007t0002g0069 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1129-870_1129-858d others(15): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263033 | ||||||
chr3:129263034
|
AAGAGTCC others(5): Show |
A | 12 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0002g0005others(9): Show | 20 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1129-869_1129-858d others(14): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263034 | ||||||
chr3:129263034
|
AAGAGTCC others(6): Show |
A | 1 | a0001c0007t0002g0066 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1129-867_1129-855d others(15): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263034 | |||||
chr3:129263035
|
AGAGTCCT others(3): Show |
A | 5 | a0001c0002t0001g0080a0001c0002t0002g0026a0001c0002t0002g0057others(2): Show | 6 | HG00642.hp2 HG02257.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129-867_1129-858d others(12): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263035 | |||||
chr3:129263035
|
AGAGTCCT others(4): Show |
A | 6 | a0001c0002t0002g0056a0001c0002t0002g0063a0001c0002t0002g0065others(3): Show | 6 | HG02647.hp2 HG02738.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129-865_1129-855d others(13): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263035 | |||||
chr3:129263036
|
G | A | 16 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(13): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1129-868G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263036 | ||||||
chr3:129263037
|
A | T | 17 | a0001c0003t0001g0025a0001c0003t0002g0011a0001c0003t0002g0025others(14): Show | 26 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1129-867A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263037 | ||||||
chr3:129263037
|
AGTCCTTC others(1): Show |
A | 12 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(9): Show | 27 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1129-865_1129-858d others(10): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263037 | |||||
chr3:129263037
|
AGTCCTTC others(2): Show |
A | 3 | a0001c0004t0002g0084a0001c0012t0002g0092a0001c0013t0002g0091 | 3 | HG01496.hp1 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1129-865_1129-857d others(11): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263037 | |||||
chr3:129263045
|
T | A | 1 | a0001c0004t0003g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1129-859T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263045 | ||||||
chr3:129263046
|
G | A | 18 | a0001c0002t0001g0080a0001c0002t0002g0026a0001c0002t0002g0057others(15): Show | 34 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1129-858G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263046 | ||||||
chr3:129263099
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1129-805G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263099 | ||||||
chr3:129263105
|
A | T | 2 | a0001c0002t0002g0026a0001c0002t0002g0057 | 3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1129-799A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263105 | ||||||
chr3:129263121
|
C | G | 1 | a0001c0007t0002g0066 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1129-783C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263121 | ||||||
chr3:129263122
|
G | C | 1 | a0001c0007t0002g0066 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1129-782G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263122 | ||||||
chr3:129263244
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0123a0001c0001t0002g0036others(1): Show | 4 | HG02040.hp1 NA18952.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1129-660C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263244 | ||||||
chr3:129263262
|
G | A | 3 | a0001c0001t0004g0018a0001c0001t0004g0101a0001c0001t0004g0128 | 5 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1129-642G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263262 | ||||||
chr3:129263378
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1129-526G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263378 | ||||||
chr3:129263394
|
A | T | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1129-510A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263394 | ||||||
chr3:129263395
|
G | A | 3 | a0001c0003t0003g0009a0001c0003t0003g0082a0001c0003t0003g0083 | 7 | HG01884.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-509G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263395 | ||||||
chr3:129263459
|
A | C | 1 | a0001c0002t0005g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1129-445A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263459 | ||||||
chr3:129263507
|
G | A | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1129-397G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263507 | ||||||
chr3:129263725
|
G | T | 16 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(13): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1129-179G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263725 | ||||||
chr3:129263740
|
CCTTCAAG | C | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1129-155_1129-149d others(9): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263740 | |||||
chr3:129263898
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02523.hp2 | splice_region_variant&intron_variant | LOW | c.1129-6A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263898 | ||||||
chr3:129264008
|
CA | C | 2 | a0001c0002t0002g0026a0001c0002t0002g0057 | 3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1224+10delA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264008 | ||||||
chr3:129264018
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG00323.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1224+19C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264018 | ||||||
chr3:129264067
|
C | T | 1 | a0001c0001t0002g0043 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1224+68C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264067 | ||||||
chr3:129264135
|
C | T | 2 | a0001c0012t0002g0092a0001c0013t0002g0091 | 2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1224+136C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264135 | ||||||
chr3:129264357
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1224+358C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264357 | ||||||
chr3:129264381
|
C | T | 64 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(61): Show | 101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1224+382C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264381 | ||||||
chr3:129264421
|
C | T | 16 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(13): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1224+422C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264421 | ||||||
chr3:129264453
|
A | C | 1 | a0002c0005t0002g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1224+454A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264453 | ||||||
chr3:129264467
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1224+468A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264467 | ||||||
chr3:129264616
|
T | C | 64 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(61): Show | 101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1224+617T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264616 | ||||||
chr3:129264640
|
T | C | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1224+641T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264640 | ||||||
chr3:129264676
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1224+677G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264676 | ||||||
chr3:129264775
|
G | C | 1 | a0001c0007t0002g0066 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1225-774G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264775 | ||||||
chr3:129264776
|
C | G | 1 | a0001c0007t0002g0066 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1225-773C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264776 | ||||||
chr3:129264821
|
G | GT | 7 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0104others(4): Show | 7 | HG02145.hp2 HG02738.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225-715dupT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr3 | 129264821 | |||||
chr3:129264837
|
G | T | 58 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(55): Show | 91 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1225-712G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264837 | ||||||
chr3:129264850
|
C | T | 16 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(13): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1225-699C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264850 | ||||||
chr3:129264852
|
C | T | 2 | a0001c0003t0001g0137a0001c0003t0001g0176 | 2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1225-697C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264852 | ||||||
chr3:129265010
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1225-539A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129265010 | ||||||
chr3:129265100
|
C | T | 1 | a0001c0002t0002g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1225-449C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129265100 | ||||||
chr3:129265117
|
G | A | 17 | a0001c0003t0001g0025a0001c0003t0002g0011a0001c0003t0002g0025others(14): Show | 26 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1225-432G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129265117 | ||||||
chr3:129265315
|
T | C | 64 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(61): Show | 101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1225-234T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129265315 | ||||||
chr3:129265335
|
A | G | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1225-214A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129265335 | ||||||
chr3:129265497
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1225-52A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129265497 | ||||||
chr3:129265891
|
G | A | 2 | a0001c0012t0002g0092a0001c0013t0002g0091 | 2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1468+99G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129265891 | ||||||
chr3:129265974
|
GT | G | 8 | a0002c0005t0001g0049a0002c0005t0002g0010a0002c0005t0002g0014others(5): Show | 14 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1468+186delT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr3 | 129265974 | |||||
chr3:129266221
|
C | T | 21 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(18): Show | 30 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.1468+429C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266221 | ||||||
chr3:129266222
|
G | A | 1 | a0001c0013t0002g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1468+430G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266222 | ||||||
chr3:129266237
|
C | T | 2 | a0001c0002t0002g0026a0001c0002t0002g0057 | 3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1468+445C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266237 | ||||||
chr3:129266315
|
G | A | 2 | a0001c0002t0002g0026a0001c0002t0002g0057 | 3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1468+523G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266315 | ||||||
chr3:129266320
|
G | T | 2 | a0001c0002t0002g0026a0001c0002t0002g0057 | 3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1468+528G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266320 | ||||||
chr3:129266490
|
G | A | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1469-534G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266490 | ||||||
chr3:129266536
|
T | G | 1 | a0001c0003t0003g0029 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1469-488T>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266536 | ||||||
chr3:129266659
|
T | A | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1469-365T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266659 | ||||||
chr3:129266719
|
T | G | 2 | a0001c0012t0002g0092a0001c0013t0002g0091 | 2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1469-305T>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266719 | ||||||
chr3:129266738
|
C | T | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1469-286C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266738 | ||||||
chr3:129266804
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1469-220C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266804 | ||||||
chr3:129266806
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1469-218C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266806 | ||||||
chr3:129266838
|
G | A | 2 | a0001c0002t0005g0078a0001c0010t0005g0079 | 2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1469-186G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266838 | ||||||
chr3:129266849
|
T | C | 41 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(38): Show | 65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1469-175T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266849 | ||||||
chr3:129266875
|
C | T | 10 | a0001c0002t0001g0067a0001c0002t0002g0027a0001c0002t0002g0058others(7): Show | 11 | HG00408.hp1 HG02056.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1469-149C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266875 | ||||||
chr3:129266932
|
T | A | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1469-92T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266932 | ||||||
chr3:129266965
|
G | A | 2 | a0001c0002t0005g0078a0001c0010t0005g0079 | 2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1469-59G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266965 | ||||||
chr3:129267169
|
TA | T | 14 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(11): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1544+71delA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267169 | ||||||
chr3:129267236
|
G | A | 1 | a0001c0003t0003g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1544+137G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267236 | ||||||
chr3:129267317
|
T | A | 1 | a0001c0001t0002g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1544+218T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267317 | ||||||
chr3:129267388
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1544+289A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267388 | ||||||
chr3:129267423
|
C | T | 1 | a0001c0010t0005g0079 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1544+324C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267423 | ||||||
chr3:129267424
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1544+325G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267424 | ||||||
chr3:129267438
|
G | A | 1 | a0001c0003t0002g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1544+339G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267438 | ||||||
chr3:129267439
|
C | G | 1 | a0001c0003t0002g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1544+340C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267439 | ||||||
chr3:129267830
|
T | C | 1 | a0001c0001t0002g0109 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1545-107T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267830 | ||||||
chr3:129267872
|
A | C | 67 | a0001c0001t0002g0038a0001c0001t0002g0121a0001c0001t0002g0147others(64): Show | 105 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1545-65A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267872 | ||||||
chr3:129268183
|
G | C | 1 | a0001c0001t0001g0151 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1648+143G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/23 | chr3 | 129268183 | ||||||
chr3:129268231
|
T | TGAATTGA others(3): Show |
1 | a0001c0006t0002g0076 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1648+193_1648+202d others(12): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr3 | 129268231 | |||||
chr3:129268241
|
C | T | 1 | a0001c0004t0003g0089 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1648+201C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/23 | chr3 | 129268241 | ||||||
chr3:129268260
|
CTT | C | 3 | a0001c0003t0001g0025a0001c0003t0002g0025a0001c0003t0002g0053 | 3 | HG02109.hp2 HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1648+222_1648+223d others(4): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr3 | 129268260 | |||||
chr3:129268316
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0138a0001c0001t0002g0008 | 7 | HG00609.hp1 HG01081.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1649-179C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/23 | chr3 | 129268316 | ||||||
chr3:129268347
|
G | A | 25 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(22): Show | 34 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1649-148G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/23 | chr3 | 129268347 | ||||||
chr3:129268826
|
C | T | 14 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(11): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1775-106C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 17/23 | chr3 | 129268826 | ||||||
chr3:129268887
|
G | A | 66 | a0001c0001t0002g0038a0001c0001t0002g0147a0001c0001t0002g0159others(63): Show | 104 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1775-45G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 17/23 | chr3 | 129268887 | ||||||
chr3:129269056
|
T | A | 60 | a0001c0001t0002g0038a0001c0001t0002g0147a0001c0001t0002g0159others(57): Show | 94 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1843+56T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269056 | ||||||
chr3:129269202
|
A | G | 60 | a0001c0001t0002g0038a0001c0001t0002g0147a0001c0001t0002g0159others(57): Show | 94 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1843+202A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269202 | ||||||
chr3:129269209
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0103a0001c0001t0001g0162 | 4 | HG03654.hp1 HG03669.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1843+209G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269209 | ||||||
chr3:129269287
|
G | C | 14 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(11): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1843+287G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269287 | ||||||
chr3:129269332
|
A | G | 4 | a0002c0005t0002g0010a0002c0005t0002g0046a0002c0005t0002g0047others(1): Show | 8 | HG01069.hp1 HG01071.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1843+332A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269332 | ||||||
chr3:129269382
|
C | T | 21 | a0001c0001t0002g0038a0001c0001t0002g0147a0001c0001t0002g0159others(18): Show | 31 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1843+382C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269382 | ||||||
chr3:129269449
|
G | A | 14 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(11): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1843+449G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269449 | ||||||
chr3:129269606
|
C | T | 2 | a0001c0002t0005g0078a0001c0010t0005g0079 | 2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1843+606C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269606 | ||||||
chr3:129269660
|
T | C | 39 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(36): Show | 63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1843+660T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269660 | ||||||
chr3:129269699
|
C | T | 39 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(36): Show | 63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1843+699C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269699 | ||||||
chr3:129269708
|
A | G | 39 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(36): Show | 63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1843+708A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269708 | ||||||
chr3:129269797
|
T | C | 18 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0002g0005others(15): Show | 26 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.1843+797T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269797 | ||||||
chr3:129269853
|
C | T | 1 | a0001c0003t0002g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1843+853C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269853 | ||||||
chr3:129269968
|
C | T | 1 | a0001c0001t0001g0032 | 2 | HG00438.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1843+968C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269968 | ||||||
chr3:129269969
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1843+969G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269969 | ||||||
chr3:129269983
|
C | T | 1 | a0001c0002t0002g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1843+983C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269983 | ||||||
chr3:129270060
|
C | G | 1 | a0001c0009t0002g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1843+1060C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270060 | ||||||
chr3:129270110
|
C | A | 1 | a0001c0006t0002g0077 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1843+1110C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270110 | ||||||
chr3:129270116
|
T | C | 1 | a0003c0008t0001g0135 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1843+1116T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270116 | ||||||
chr3:129270122
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1843+1122A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270122 | ||||||
chr3:129270134
|
C | A | 1 | a0001c0001t0007g0186 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1843+1134C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270134 | ||||||
chr3:129270194
|
A | G | 2 | a0001c0009t0002g0072a0001c0009t0002g0073 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1843+1194A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270194 | ||||||
chr3:129270278
|
G | T | 18 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0002g0005others(15): Show | 26 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.1843+1278G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270278 | ||||||
chr3:129270388
|
C | T | 2 | a0001c0009t0002g0072a0001c0009t0002g0073 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1844-1379C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270388 | ||||||
chr3:129270428
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1844-1339T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270428 | ||||||
chr3:129270474
|
C | A | 4 | a0001c0001t0004g0018a0001c0001t0004g0101a0001c0001t0004g0128others(1): Show | 6 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1844-1293C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270474 | ||||||
chr3:129270618
|
A | G | 39 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(36): Show | 63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1844-1149A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270618 | ||||||
chr3:129270911
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1844-856A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270911 | ||||||
chr3:129270943
|
TGTA | T | 18 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0002g0005others(15): Show | 26 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.1844-819_1844-817d others(5): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr3 | 129270943 | |||||
chr3:129271239
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1844-528C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129271239 | ||||||
chr3:129271426
|
C | T | 1 | a0001c0002t0002g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1844-341C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129271426 | ||||||
chr3:129271574
|
A | G | 39 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(36): Show | 63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1844-193A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129271574 | ||||||
chr3:129271578
|
G | A | 2 | a0001c0012t0002g0092a0001c0013t0002g0091 | 2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1844-189G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129271578 | ||||||
chr3:129271629
|
T | C | 1 | a0001c0003t0002g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1844-138T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129271629 | ||||||
chr3:129272155
|
T | C | 66 | a0001c0001t0002g0038a0001c0001t0002g0147a0001c0001t0002g0159others(63): Show | 104 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1987-89T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 19/23 | chr3 | 129272155 | ||||||
chr3:129272163
|
A | C | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1987-81A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 19/23 | chr3 | 129272163 | ||||||
chr3:129272193
|
C | T | 2 | a0001c0009t0002g0072a0001c0009t0002g0073 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1987-51C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 19/23 | chr3 | 129272193 | ||||||
chr3:129272565
|
CTCT | C | 4 | a0001c0002t0005g0078a0001c0009t0002g0072a0001c0009t0002g0073others(1): Show | 4 | HG00642.hp2 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2158+155_2158+157d others(5): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr3 | 129272565 | |||||
chr3:129272577
|
A | T | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2158+162A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 20/23 | chr3 | 129272577 | ||||||
chr3:129272578
|
A | T | 39 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(36): Show | 63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2158+163A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 20/23 | chr3 | 129272578 | ||||||
chr3:129273085
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2256+181C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273085 | ||||||
chr3:129273104
|
C | T | 18 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0002g0005others(15): Show | 26 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.2256+200C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273104 | ||||||
chr3:129273163
|
C | T | 2 | a0001c0001t0001g0123a0005c0018t0001g0096 | 2 | HG02040.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.2256+259C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273163 | ||||||
chr3:129273204
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.2256+300G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273204 | ||||||
chr3:129273284
|
A | G | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2256+380A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273284 | ||||||
chr3:129273315
|
C | T | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2256+411C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273315 | ||||||
chr3:129273316
|
G | A | 3 | a0002c0005t0001g0049a0002c0005t0002g0045a0002c0005t0002g0048 | 3 | HG00280.hp2 HG01261.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2256+412G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273316 | ||||||
chr3:129273357
|
T | C | 21 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(18): Show | 30 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.2256+453T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273357 | ||||||
chr3:129273505
|
T | C | 2 | a0001c0002t0002g0026a0001c0002t0002g0057 | 3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2256+601T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273505 | ||||||
chr3:129273532
|
A | G | 66 | a0001c0001t0002g0038a0001c0001t0002g0147a0001c0001t0002g0159others(63): Show | 104 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.2256+628A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273532 | ||||||
chr3:129273655
|
A | C | 14 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(11): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2256+751A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273655 | ||||||
chr3:129273881
|
T | C | 4 | a0001c0002t0005g0078a0001c0009t0002g0072a0001c0009t0002g0073others(1): Show | 4 | HG00642.hp2 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2257-957T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273881 | ||||||
chr3:129273980
|
T | C | 25 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(22): Show | 34 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.2257-858T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273980 | ||||||
chr3:129274020
|
G | A | 1 | a0001c0001t0002g0038 | 2 | HG01358.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2257-818G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129274020 | ||||||
chr3:129274104
|
A | ATGACCCC others(214): Show |
1 | a0001c0001t0002g0115 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2257-731_2257-511d others(223): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr3 | 129274104 | |||||
chr3:129274161
|
C | G | 1 | a0001c0011t0002g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2257-677C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129274161 | ||||||
chr3:129274186
|
G | GA | 8 | a0001c0001t0002g0007a0001c0001t0002g0043a0001c0001t0002g0107others(5): Show | 16 | HG00639.hp2 HG01123.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.2257-640dupA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr3 | 129274186 | |||||
chr3:129274199
|
G | A | 38 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0002g0005others(35): Show | 62 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.2257-639G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129274199 | ||||||
chr3:129274628
|
C | T | 21 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(18): Show | 30 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.2257-210C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129274628 | ||||||
chr3:129274803
|
A | G | 39 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(36): Show | 63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2257-35A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129274803 | ||||||
chr3:129274816
|
A | T | 1 | a0001c0006t0002g0075 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2257-22A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129274816 | ||||||
chr3:129275035
|
T | C | 1 | a0001c0002t0005g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2395+59T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 22/23 | chr3 | 129275035 | ||||||
chr3:129275040
|
G | A | 2 | a0001c0009t0002g0072a0001c0009t0002g0073 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2395+64G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 22/23 | chr3 | 129275040 | ||||||
chr3:129275359
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2494+67C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275359 | ||||||
chr3:129275532
|
G | A | 14 | a0001c0003t0003g0009a0001c0003t0003g0029a0001c0003t0003g0030others(11): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2494+240G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275532 | ||||||
chr3:129275564
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2494+272C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275564 | ||||||
chr3:129275667
|
A | G | 2 | a0001c0009t0002g0072a0001c0009t0002g0073 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2494+375A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275667 | ||||||
chr3:129275790
|
C | G | 1 | a0001c0001t0002g0115 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2494+498C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275790 | ||||||
chr3:129275862
|
T | C | 39 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(36): Show | 63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2494+570T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275862 | ||||||
chr3:129275967
|
C | T | 2 | a0001c0002t0005g0078a0001c0010t0005g0079 | 2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.2494+675C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275967 | ||||||
chr3:129275968
|
G | A | 1 | a0001c0002t0002g0065 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2494+676G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275968 | ||||||
chr3:129275971
|
T | TAC | 7 | a0001c0001t0001g0031a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | HG01934.hp1 HG02145.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.2494+705_2494+706d others(4): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129275971 | |||||
chr3:129275971
|
TAC | T | 9 | a0001c0001t0001g0094a0001c0001t0001g0184a0001c0001t0002g0159others(6): Show | 9 | HG01891.hp2 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2494+705_2494+706d others(4): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129275971 | |||||
chr3:129275971
|
TACAC | T | 27 | a0001c0001t0001g0180a0001c0001t0002g0038a0001c0001t0002g0147others(24): Show | 41 | HG00280.hp2 HG00642.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+703_2494+706d others(6): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129275971 | |||||
chr3:129275971
|
TACACAC | T | 33 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(30): Show | 56 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2494+701_2494+706d others(8): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129275971 | |||||
chr3:129275971
|
TACACACA others(1): Show |
T | 2 | a0001c0002t0002g0026a0001c0002t0002g0057 | 3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2494+699_2494+706d others(10): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129275971 | |||||
chr3:129276099
|
C | T | 21 | a0001c0001t0002g0038a0001c0001t0002g0147a0001c0001t0002g0159others(18): Show | 31 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.2494+807C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276099 | ||||||
chr3:129276234
|
T | A | 1 | a0001c0001t0001g0168 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2494+942T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276234 | ||||||
chr3:129276505
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2495-789T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276505 | ||||||
chr3:129276530
|
T | A | 1 | a0002c0005t0002g0010 | 4 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-764T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276530 | ||||||
chr3:129276542
|
C | T | 1 | a0001c0002t0002g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2495-752C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276542 | ||||||
chr3:129276687
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2495-607A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276687 | ||||||
chr3:129276698
|
G | C | 6 | a0001c0006t0002g0012a0001c0006t0002g0028a0001c0006t0002g0075others(3): Show | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2495-596G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276698 | ||||||
chr3:129276760
|
T | C | 2 | a0001c0012t0002g0092a0001c0013t0002g0091 | 2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2495-534T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276760 | ||||||
chr3:129276779
|
A | G | 39 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(36): Show | 63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2495-515A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276779 | ||||||
chr3:129276793
|
G | A | 2 | a0001c0002t0002g0026a0001c0002t0002g0057 | 3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2495-501G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276793 | ||||||
chr3:129276823
|
C | CT | 77 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(74): Show | 120 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.2495-453dupT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129276823 | |||||
chr3:129276823
|
C | CTT | 22 | a0001c0001t0002g0159a0001c0001t0002g0188a0001c0002t0001g0067others(19): Show | 30 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.2495-454_2495-453d others(4): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129276823 | |||||
chr3:129276823
|
C | CTTTT | 12 | a0001c0002t0001g0080a0001c0003t0003g0009a0001c0003t0003g0029others(9): Show | 27 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.2495-456_2495-453d others(6): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129276823 | |||||
chr3:129276846
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2495-448C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276846 | ||||||
chr3:129276940
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2495-354C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276940 | ||||||
chr3:129276955
|
C | G | 21 | a0001c0001t0002g0038a0001c0001t0002g0147a0001c0001t0002g0159others(18): Show | 31 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.2495-339C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276955 | ||||||
chr3:129276970
|
T | C | 39 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(36): Show | 63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2495-324T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276970 | ||||||
chr3:129277039
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2495-255G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129277039 | ||||||
chr3:129277064
|
T | C | 39 | a0001c0002t0001g0067a0001c0002t0001g0070a0001c0002t0001g0080others(36): Show | 63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2495-230T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129277064 | ||||||
chr3:129277185
|
G | A | 2 | a0001c0002t0002g0026a0001c0002t0002g0057 | 3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2495-109G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129277185 | ||||||
chr3:129277262
|
G | A | 1 | a0001c0002t0005g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2495-32G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129277262 |