geneid | 1633 |
---|---|
ensemblid | ENSG00000156136.10 |
hgncid | 2704 |
symbol | DCK |
name | deoxycytidine kinase |
refseq_nuc | NM_000788.3 |
refseq_prot | NP_000779.1 |
ensembl_nuc | ENST00000286648.10 |
ensembl_prot | ENSP00000286648.5 |
mane_status | MANE Select |
chr | chr4 |
start | 70993649 |
end | 71030914 |
strand | + |
ver | v1.2 |
region | chr4:70993649-71030914 |
region5000 | chr4:70988649-71035914 |
regionname0 | DCK_chr4_70993649_71030914 |
regionname5000 | DCK_chr4_70988649_71035914 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 260 | 260 | 84 | 55 | 77 | 10 | 32 | 49 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0002 | 0/0 | 260 | 16 | 2 | 1 | 11 | 0 | 2 | 9 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0003 | 0/0 | 260 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0004 | 0/0 | 260 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0005 | 0/0 | 260 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0006 | 0/0 | 260 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 783 | 254 | 83 | 53 | 77 | 8 | 32 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
c0002 | 0/0 | 783 | 16 | 2 | 1 | 11 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
c0003 | 0/1 | 783 | 6 | 1 | 2 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
c0004 | 0/0 | 783 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
c0005 | 0/0 | 783 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
c0006 | 0/0 | 783 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
c0007 | 0/0 | 783 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1724 | 189 | 30 | 45 | 76 | 9 | 29 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0002 | 1/0 | 1724 | 48 | 26 | 5 | 11 | 3 | 2 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0003 | 0/0 | 1724 | 12 | 10 | 0 | 0 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0004 | 0/0 | 1722 | 9 | 9 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0005 | 0/0 | 1724 | 4 | 4 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0006 | 0/0 | 1724 | 3 | 3 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0007 | 0/1 | 1724 | 3 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0008 | 0/0 | 1724 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0009 | 0/0 | 1724 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0010 | 0/0 | 1724 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0011 | 0/0 | 1724 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0012 | 0/0 | 1724 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0013 | 0/0 | 1724 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0014 | 0/0 | 1724 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0015 | 0/0 | 1724 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0016 | 0/0 | 1724 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0017 | 0/0 | 1724 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0018 | 0/0 | 1724 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
t0019 | 0/0 | 1724 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0002 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0003 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0008 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0009 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0012 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0013 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0017 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0019 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 783 | 254 | 83 | 53 | 77 | 8 | 32 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0003 | 0/1 | 783 | 6 | 1 | 2 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0002c0002 | 0/0 | 783 | 16 | 2 | 1 | 11 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0003c0004 | 0/0 | 783 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0004c0005 | 0/0 | 783 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0005c0006 | 0/0 | 783 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0006c0007 | 0/0 | 783 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2506 | 184 | 29 | 45 | 76 | 5 | 29 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0002 | 1/0 | 2506 | 31 | 23 | 4 | 0 | 3 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0003 | 0/0 | 2506 | 12 | 10 | 0 | 0 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0004 | 0/0 | 2504 | 9 | 9 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0005 | 0/0 | 2506 | 4 | 4 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0006 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0008 | 0/0 | 2506 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0009 | 0/0 | 2506 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0010 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0011 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0012 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0013 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0014 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0015 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0016 | 0/0 | 2506 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0017 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0001t0018 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0003t0001 | 0/0 | 2506 | 3 | 1 | 0 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0001c0003t0007 | 0/1 | 2506 | 3 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0002c0002t0002 | 0/0 | 2506 | 15 | 1 | 1 | 11 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0002c0002t0019 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0003c0004t0006 | 0/0 | 2506 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0004c0005t0002 | 0/0 | 2506 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0005c0006t0001 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
a0006c0007t0001 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | copy fasta | chr4 | 70988649 | 71035914 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0008 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0003g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0004g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0009g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0011g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0012g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0013g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0014g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0015g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0016g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0017g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0001t0018g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0001c0003t0007g0019 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0002c0002t0019g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0003c0004t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0003c0004t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0004c0005t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0005c0006t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
a0006c0007t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00140 | hp1 | a0005 | c0006 | t0001 | g0013 | EUR | GBR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0040 | EUR | FIN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00735 | hp1 | a0001 | c0001 | t0015 | g0129 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01106 | hp2 | a0001 | c0001 | t0011 | g0018 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01109 | hp2 | a0001 | c0001 | t0013 | g0173 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01255 | hp2 | a0001 | c0001 | t0018 | g0132 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01256 | hp2 | a0001 | c0003 | t0007 | g0019 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01258 | hp2 | a0001 | c0003 | t0007 | g0019 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01515 | hp1 | a0006 | c0007 | t0001 | g0089 | EUR | IBS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | IBS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0033 | EUR | IBS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01517 | hp1 | a0001 | c0003 | t0001 | g0033 | EUR | IBS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | IBS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0162 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0163 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01891 | hp2 | a0004 | c0005 | t0002 | g0039 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02083 | hp2 | a0001 | c0001 | t0016 | g0095 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0021 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0127 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02717 | hp2 | a0002 | c0002 | t0002 | g0174 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02723 | hp1 | a0002 | c0002 | t0019 | g0058 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02723 | hp2 | a0004 | c0005 | t0002 | g0039 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02886 | hp2 | a0003 | c0004 | t0006 | g0171 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0074 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0073 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03130 | hp1 | a0001 | c0001 | t0014 | g0051 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03453 | hp1 | a0001 | c0001 | t0017 | g0012 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | STU | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03710 | hp1 | a0001 | c0001 | t0012 | g0027 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0182 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0020 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | YRI | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | YRI | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | YRI | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18997 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | LWK | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | LWK | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | LWK | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19240 | hp1 | a0003 | c0004 | t0006 | g0172 | AFR | YRI | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | YRI | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ASW | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | GIH | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0181 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG06807 | hp1 | a0001 | c0001 | t0009 | g0097 | AFR | USA | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | USA | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | USA | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0007 | g0019 | REF | REF | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0066 | REF | REF | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:70993905
|
A | G | 1 | a0004 | 2 | HG01891.hp2 HG02723.hp2 |
missense_variant | MODERATE | c.70A>G | p.Ile24Val | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/7 | 257/2506 | 70/783 | 24/260 | chr4 | 70993905 | ||
chr4:71022428
|
A | G | 1 | a0006 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.269A>G | p.Glu90Gly | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/7 | 456/2506 | 269/783 | 90/260 | chr4 | 71022428 | ||
chr4:71022515
|
C | G | 1 | a0003 | 2 | HG02886.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.356C>G | p.Ala119Gly | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/7 | 543/2506 | 356/783 | 119/260 | chr4 | 71022515 | ||
chr4:71022523
|
C | T | 1 | a0002 | 16 | HG00673.hp1 HG01123.hp2 HG02129.hp2 others(13): Show |
missense_variant | MODERATE | c.364C>T | p.Pro122Ser | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/7 | 551/2506 | 364/783 | 122/260 | chr4 | 71022523 | ||
chr4:71023570
|
C | T | 1 | a0005 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.413C>T | p.Ala138Val | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/7 | 600/2506 | 413/783 | 138/260 | chr4 | 71023570 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:71022459
|
C | T | 2 | a0001c0003a0006c0007 | 7 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(4): Show |
synonymous_variant | LOW | c.300C>T | p.Ala100Ala | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/7 | 487/2506 | 300/783 | 100/260 | chr4 | 71022459 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:70993694
|
C | G | 1 | a0002c0002t0019 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-142C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/7 | 142 | chr4 | 70993694 | |||||
chr4:70993784
|
G | A | 3 | a0001c0001t0005a0001c0001t0008a0001c0001t0010 | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-52G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/7 | 52 | chr4 | 70993784 | |||||
chr4:70993807
|
C | A | 1 | a0001c0001t0011 | 1 | HG01106.hp2 | 5_prime_UTR_variant | MODIFIER | c.-29C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/7 | 29 | chr4 | 70993807 | |||||
chr4:70993824
|
C | G | 1 | a0001c0001t0018 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-12C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/7 | 12 | chr4 | 70993824 | |||||
chr4:71029523
|
T | A | 1 | a0001c0001t0012 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*145T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 145 | chr4 | 71029523 | |||||
chr4:71029543
|
C | T | 13 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(10): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*165C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 165 | chr4 | 71029543 | |||||
chr4:71029923
|
C | A | 1 | a0001c0001t0005 | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*545C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 545 | chr4 | 71029923 | |||||
chr4:71029925
|
T | G | 1 | a0001c0001t0015 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*547T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 547 | chr4 | 71029925 | |||||
chr4:71029948
|
C | T | 1 | a0001c0001t0005 | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*570C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 570 | chr4 | 71029948 | |||||
chr4:71029951
|
T | C | 1 | a0001c0001t0004 | 9 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*573T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 573 | chr4 | 71029951 | |||||
chr4:71030118
|
A | G | 1 | a0001c0001t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*740A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 740 | chr4 | 71030118 | |||||
chr4:71030303
|
T | C | 1 | a0001c0001t0013 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*925T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 925 | chr4 | 71030303 | |||||
chr4:71030333
|
G | A | 1 | a0001c0001t0014 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*955G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 955 | chr4 | 71030333 | |||||
chr4:71030503
|
C | T | 4 | a0001c0001t0005a0001c0001t0006a0001c0001t0013others(1): Show | 8 | HG01109.hp2 HG01884.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1125C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1125 | chr4 | 71030503 | |||||
chr4:71030572
|
C | A | 1 | a0001c0003t0007 | 3 | HG01256.hp2 HG01258.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1194C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1194 | chr4 | 71030572 | |||||
chr4:71030649
|
T | C | 1 | a0001c0001t0016 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1271 | chr4 | 71030649 | |||||
chr4:71030700
|
A | T | 1 | a0001c0001t0003 | 12 | HG02055.hp1 HG02602.hp1 HG02818.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1322A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1322 | chr4 | 71030700 | |||||
chr4:71030750
|
T | C | 1 | a0001c0001t0009 | 2 | HG01891.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1372T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1372 | chr4 | 71030750 | |||||
chr4:71030804
|
A | G | 1 | a0001c0001t0013 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1426A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1426 | chr4 | 71030804 | |||||
chr4:71030848
|
CTT | C | 1 | a0001c0001t0004 | 9 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1473_*1474delTT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1473 | INFO_REALIGN_3_PRIME | chr4 | 71030848 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:70993963
|
G | C | 3 | a0001c0001t0002g0022a0001c0001t0002g0040a0001c0001t0002g0041 | 4 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+37G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70993963 | ||||||
chr4:70994180
|
G | T | 1 | a0004c0005t0002g0039 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.91+254G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994180 | ||||||
chr4:70994202
|
G | A | 1 | a0001c0001t0001g0023 | 2 | NA19005.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.91+276G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994202 | ||||||
chr4:70994249
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.91+323A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994249 | ||||||
chr4:70994438
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.91+512A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994438 | ||||||
chr4:70994594
|
A | G | 24 | a0001c0001t0001g0185a0001c0001t0002g0021a0001c0001t0002g0187others(21): Show | 28 | HG00673.hp1 HG01109.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.91+668A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994594 | ||||||
chr4:70994642
|
G | C | 1 | a0001c0001t0002g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.91+716G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994642 | ||||||
chr4:70994688
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.91+762A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994688 | ||||||
chr4:70994791
|
T | C | 1 | a0001c0001t0005g0043 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.91+865T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994791 | ||||||
chr4:70994807
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.91+881A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994807 | ||||||
chr4:70994882
|
A | C | 1 | a0001c0001t0001g0169 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.91+956A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994882 | ||||||
chr4:70994925
|
T | A | 3 | a0001c0001t0013g0173a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.91+999T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994925 | ||||||
chr4:70994944
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.91+1018A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994944 | ||||||
chr4:70994950
|
A | T | 9 | a0001c0001t0002g0021a0001c0001t0002g0167a0001c0001t0002g0168others(6): Show | 11 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+1024A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994950 | ||||||
chr4:70994958
|
A | T | 4 | a0001c0001t0001g0169a0001c0001t0013g0173a0003c0004t0006g0171others(1): Show | 4 | HG01109.hp2 HG02165.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+1032A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994958 | ||||||
chr4:70995036
|
C | T | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG02109.hp1 HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.91+1110C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995036 | ||||||
chr4:70995037
|
T | G | 9 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0003g0005others(6): Show | 14 | HG01243.hp2 HG02055.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.91+1111T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995037 | ||||||
chr4:70995093
|
A | C | 1 | a0001c0001t0009g0163 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91+1167A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995093 | ||||||
chr4:70995168
|
A | G | 3 | a0001c0001t0013g0173a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.91+1242A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995168 | ||||||
chr4:70995387
|
G | C | 1 | a0001c0001t0002g0191 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.91+1461G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995387 | ||||||
chr4:70995469
|
A | G | 1 | a0001c0001t0001g0038 | 2 | HG00673.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.91+1543A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995469 | ||||||
chr4:70995553
|
T | C | 6 | a0001c0001t0002g0022a0001c0001t0002g0025a0001c0001t0002g0040others(3): Show | 8 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+1627T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995553 | ||||||
chr4:70995783
|
A | G | 4 | a0001c0001t0006g0162a0001c0001t0013g0173a0003c0004t0006g0171others(1): Show | 4 | HG01109.hp2 HG01884.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+1857A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995783 | ||||||
chr4:70995997
|
G | A | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-2070G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995997 | ||||||
chr4:70996204
|
CA | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.92-1848delA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 70996204 | |||||
chr4:70996377
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.92-1690T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70996377 | ||||||
chr4:70996886
|
T | A | 2 | a0003c0004t0006g0171a0003c0004t0006g0172 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.92-1181T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70996886 | ||||||
chr4:70996957
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.92-1110T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70996957 | ||||||
chr4:70997287
|
C | T | 1 | a0001c0001t0001g0037 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.92-780C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997287 | ||||||
chr4:70997351
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0012g0027 | 2 | HG03710.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.92-716T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997351 | ||||||
chr4:70997382
|
C | T | 3 | a0001c0001t0013g0173a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.92-685C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997382 | ||||||
chr4:70997393
|
T | C | 31 | a0001c0001t0002g0021a0001c0001t0002g0056a0001c0001t0002g0057others(28): Show | 40 | HG00673.hp1 HG01123.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.92-674T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997393 | ||||||
chr4:70997399
|
G | A | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.92-668G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997399 | ||||||
chr4:70997479
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 7 | HG00738.hp1 HG01069.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-588T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997479 | ||||||
chr4:70997580
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.92-487A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997580 | ||||||
chr4:70997806
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.92-261C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997806 | ||||||
chr4:70997893
|
G | A | 37 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0025others(34): Show | 48 | HG00323.hp2 HG00673.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.92-174G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997893 | ||||||
chr4:70997957
|
T | G | 1 | a0001c0001t0002g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.92-110T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997957 | ||||||
chr4:70998016
|
CT | C | 5 | a0001c0001t0002g0064a0001c0001t0002g0164a0001c0001t0002g0165others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-44delT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 70998016 | |||||
chr4:70998296
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.207+114A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998296 | ||||||
chr4:70998329
|
A | G | 1 | a0001c0001t0002g0166 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.207+147A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998329 | ||||||
chr4:70998362
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.207+180A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998362 | ||||||
chr4:70998367
|
G | A | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+185G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998367 | ||||||
chr4:70998368
|
A | T | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.207+186A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998368 | ||||||
chr4:70998455
|
G | A | 2 | a0003c0004t0006g0171a0003c0004t0006g0172 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+273G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998455 | ||||||
chr4:70998525
|
A | C | 1 | a0001c0003t0007g0019 | 3 | HG01256.hp2 HG01258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.207+343A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998525 | ||||||
chr4:70998527
|
A | G | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+345A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998527 | ||||||
chr4:70998548
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.207+366G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998548 | ||||||
chr4:70998588
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0008g0073a0001c0001t0008g0074 | 5 | HG02647.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+406G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998588 | ||||||
chr4:70998638
|
T | C | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.207+456T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998638 | ||||||
chr4:70998671
|
C | T | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+489C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998671 | ||||||
chr4:70998733
|
C | G | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+551C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998733 | ||||||
chr4:70998751
|
C | T | 1 | a0001c0001t0002g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.207+569C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998751 | ||||||
chr4:70998812
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.207+630G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998812 | ||||||
chr4:70998816
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA18975.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.207+634G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998816 | ||||||
chr4:70998824
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.207+642G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998824 | ||||||
chr4:70998859
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.207+677G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998859 | ||||||
chr4:70998879
|
C | A | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+697C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998879 | ||||||
chr4:70998925
|
C | CA | 13 | a0001c0001t0001g0055a0001c0001t0001g0158a0001c0001t0002g0021others(10): Show | 15 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+756dupA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 70998925 | |||||
chr4:70999023
|
T | G | 1 | a0001c0001t0001g0079 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.207+841T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999023 | ||||||
chr4:70999185
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.207+1003G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999185 | ||||||
chr4:70999418
|
T | C | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.207+1236T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999418 | ||||||
chr4:70999591
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.207+1409C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999591 | ||||||
chr4:70999591
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.207+1409C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999591 | ||||||
chr4:70999701
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | NA18968.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.207+1519A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999701 | ||||||
chr4:70999766
|
T | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0082 | 6 | HG00609.hp2 HG02027.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+1584T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999766 | ||||||
chr4:70999798
|
G | T | 1 | a0001c0001t0002g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.207+1616G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999798 | ||||||
chr4:71000096
|
T | C | 4 | a0001c0001t0006g0162a0001c0001t0013g0173a0003c0004t0006g0171others(1): Show | 4 | HG01109.hp2 HG01884.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+1914T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71000096 | ||||||
chr4:71000161
|
T | G | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+1979T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71000161 | ||||||
chr4:71000336
|
G | A | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+2154G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71000336 | ||||||
chr4:71000453
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.207+2271A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71000453 | ||||||
chr4:71001164
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.207+2982A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001164 | ||||||
chr4:71001256
|
G | C | 1 | a0002c0002t0002g0174 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.207+3074G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001256 | ||||||
chr4:71001421
|
T | TC | 4 | a0001c0001t0004g0004a0001c0001t0004g0061a0001c0001t0004g0062others(1): Show | 9 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.207+3240dupC | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71001421 | |||||
chr4:71001535
|
A | G | 5 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(2): Show | 5 | HG01884.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+3353A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001535 | ||||||
chr4:71001586
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.207+3404G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001586 | ||||||
chr4:71001669
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0085others(1): Show | 8 | HG01192.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+3487T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001669 | ||||||
chr4:71001694
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.207+3512C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001694 | ||||||
chr4:71001714
|
A | C | 4 | a0001c0001t0003g0005a0001c0001t0003g0048a0001c0001t0003g0049others(1): Show | 8 | HG02055.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+3532A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001714 | ||||||
chr4:71001855
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | NA18968.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.207+3673C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001855 | ||||||
chr4:71001964
|
A | G | 2 | a0001c0001t0002g0064a0001c0001t0002g0191 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.207+3782A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001964 | ||||||
chr4:71002220
|
C | T | 3 | a0001c0001t0004g0004a0001c0001t0004g0062a0001c0001t0004g0063 | 8 | HG02615.hp2 HG02965.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+4038C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002220 | ||||||
chr4:71002239
|
A | C | 1 | a0001c0001t0002g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.207+4057A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002239 | ||||||
chr4:71002402
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.207+4220G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002402 | ||||||
chr4:71002411
|
C | T | 4 | a0001c0001t0006g0162a0001c0001t0013g0173a0003c0004t0006g0171others(1): Show | 4 | HG01109.hp2 HG01884.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+4229C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002411 | ||||||
chr4:71002462
|
C | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.207+4280C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002462 | ||||||
chr4:71002654
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.207+4472G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002654 | ||||||
chr4:71002669
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.207+4487A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002669 | ||||||
chr4:71002716
|
C | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | NA18968.hp2 NA18977.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+4534C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002716 | ||||||
chr4:71002868
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.207+4686C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002868 | ||||||
chr4:71002934
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0150others(1): Show | 4 | HG00423.hp2 NA19056.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+4752C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002934 | ||||||
chr4:71002985
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.207+4803T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002985 | ||||||
chr4:71003082
|
C | T | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+4900C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003082 | ||||||
chr4:71003193
|
T | C | 1 | a0006c0007t0001g0089 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.207+5011T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003193 | ||||||
chr4:71003264
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.207+5082T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003264 | ||||||
chr4:71003348
|
C | A | 1 | a0001c0001t0001g0029 | 2 | HG01261.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.207+5166C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003348 | ||||||
chr4:71003428
|
A | G | 3 | a0001c0001t0013g0173a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+5246A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003428 | ||||||
chr4:71003440
|
G | A | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+5258G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003440 | ||||||
chr4:71003457
|
C | G | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.207+5275C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003457 | ||||||
chr4:71003697
|
A | T | 9 | a0001c0001t0002g0021a0001c0001t0002g0167a0001c0001t0002g0168others(6): Show | 11 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.207+5515A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003697 | ||||||
chr4:71003724
|
C | G | 1 | a0001c0001t0001g0028 | 2 | HG01192.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.207+5542C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003724 | ||||||
chr4:71003802
|
C | A | 1 | a0001c0001t0002g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.207+5620C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003802 | ||||||
chr4:71003901
|
T | A | 1 | a0001c0001t0001g0037 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.207+5719T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003901 | ||||||
chr4:71004010
|
T | C | 2 | a0001c0001t0005g0052a0001c0001t0005g0053 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+5828T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004010 | ||||||
chr4:71004036
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.207+5854A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004036 | ||||||
chr4:71004169
|
A | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0085others(1): Show | 8 | HG01192.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+5987A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004169 | ||||||
chr4:71004235
|
A | G | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+6053A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004235 | ||||||
chr4:71004254
|
G | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.207+6072G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004254 | ||||||
chr4:71004484
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.207+6302G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004484 | ||||||
chr4:71004564
|
C | G | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+6382C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004564 | ||||||
chr4:71004815
|
A | T | 1 | a0001c0001t0002g0065 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.207+6633A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004815 | ||||||
chr4:71004906
|
G | GGGATCTG others(20): Show |
1 | a0002c0002t0002g0184 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.207+6725_207+6751d others(29): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71004906 | |||||
chr4:71004926
|
ACTTGGCT others(16): Show |
A | 6 | a0001c0001t0002g0021a0001c0001t0005g0043a0001c0001t0005g0052others(3): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+6771_207+6793d others(25): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71004926 | |||||
chr4:71005067
|
A | G | 13 | a0001c0001t0002g0057a0002c0002t0002g0020a0002c0002t0002g0175others(10): Show | 15 | HG00673.hp1 HG01123.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+6885A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005067 | ||||||
chr4:71005170
|
T | C | 1 | a0001c0001t0001g0015 | 3 | HG01167.hp1 HG01169.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.207+6988T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005170 | ||||||
chr4:71005171
|
C | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.207+6989C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005171 | ||||||
chr4:71005211
|
A | G | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+7029A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005211 | ||||||
chr4:71005240
|
C | T | 3 | a0001c0001t0013g0173a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+7058C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005240 | ||||||
chr4:71005490
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.207+7308C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005490 | ||||||
chr4:71005599
|
C | T | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+7417C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005599 | ||||||
chr4:71005827
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0002g0067 | 2 | HG02258.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.207+7645T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005827 | ||||||
chr4:71005861
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.207+7679C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005861 | ||||||
chr4:71005960
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.207+7778C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005960 | ||||||
chr4:71006051
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.207+7869G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006051 | ||||||
chr4:71006100
|
C | CA | 4 | a0001c0001t0004g0004a0001c0001t0004g0061a0001c0001t0004g0062others(1): Show | 9 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.207+7932dupA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71006100 | |||||
chr4:71006114
|
A | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.207+7932A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006114 | ||||||
chr4:71006133
|
C | CA | 15 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0064others(12): Show | 20 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.207+7969dupA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71006133 | |||||
chr4:71006133
|
CAA | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.207+7968_207+7969d others(4): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71006133 | |||||
chr4:71006133
|
CAAA | C | 5 | a0001c0001t0002g0021a0001c0001t0004g0004a0001c0001t0004g0062others(2): Show | 11 | HG02145.hp1 HG02615.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+7967_207+7969d others(5): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71006133 | |||||
chr4:71006153
|
C | T | 1 | a0001c0001t0003g0024 | 2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.207+7971C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006153 | ||||||
chr4:71006246
|
G | T | 1 | a0002c0002t0002g0174 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.207+8064G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006246 | ||||||
chr4:71006262
|
G | T | 5 | a0001c0001t0002g0064a0001c0001t0002g0164a0001c0001t0002g0165others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+8080G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006262 | ||||||
chr4:71006293
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.207+8111C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006293 | ||||||
chr4:71006462
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.207+8280T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006462 | ||||||
chr4:71006478
|
T | G | 7 | a0001c0001t0002g0022a0001c0001t0002g0025a0001c0001t0002g0040others(4): Show | 9 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+8296T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006478 | ||||||
chr4:71006637
|
G | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.207+8455G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006637 | ||||||
chr4:71006697
|
A | T | 3 | a0001c0001t0013g0173a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+8515A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006697 | ||||||
chr4:71006768
|
A | G | 13 | a0002c0002t0002g0020a0002c0002t0002g0175a0002c0002t0002g0176others(10): Show | 15 | HG00673.hp1 HG01123.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+8586A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006768 | ||||||
chr4:71006809
|
G | GA | 5 | a0001c0001t0001g0030a0001c0001t0001g0055a0001c0001t0001g0094others(2): Show | 6 | HG00438.hp1 HG00438.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+8634dupA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71006809 | |||||
chr4:71006866
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.207+8684A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006866 | ||||||
chr4:71007011
|
T | C | 1 | a0002c0002t0002g0176 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.207+8829T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007011 | ||||||
chr4:71007025
|
A | G | 1 | a0001c0001t0003g0049 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.207+8843A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007025 | ||||||
chr4:71007106
|
C | T | 2 | a0003c0004t0006g0171a0003c0004t0006g0172 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+8924C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007106 | ||||||
chr4:71007300
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | NA19002.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.207+9118A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007300 | ||||||
chr4:71007459
|
G | T | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.207+9277G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007459 | ||||||
chr4:71007470
|
G | A | 2 | a0003c0004t0006g0171a0003c0004t0006g0172 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+9288G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007470 | ||||||
chr4:71007661
|
A | G | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+9479A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007661 | ||||||
chr4:71007776
|
C | T | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+9594C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007776 | ||||||
chr4:71007846
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.207+9664A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007846 | ||||||
chr4:71008028
|
A | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(63): Show | 105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.207+9846A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008028 | ||||||
chr4:71008047
|
G | A | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+9865G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008047 | ||||||
chr4:71008413
|
AT | A | 2 | a0001c0001t0002g0021a0001c0001t0010g0021 | 3 | HG02145.hp1 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.207+10236delT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71008413 | |||||
chr4:71008421
|
A | G | 2 | a0002c0002t0002g0020a0002c0002t0002g0183 | 4 | HG03834.hp1 NA18962.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+10239A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008421 | ||||||
chr4:71008500
|
C | T | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+10318C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008500 | ||||||
chr4:71008614
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.207+10432A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008614 | ||||||
chr4:71008842
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.207+10660C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008842 | ||||||
chr4:71008893
|
A | G | 1 | a0001c0001t0002g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.207+10711A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008893 | ||||||
chr4:71008972
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.207+10790G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008972 | ||||||
chr4:71009257
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.207+11075C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009257 | ||||||
chr4:71009393
|
A | C | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.207+11211A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009393 | ||||||
chr4:71009476
|
A | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0061a0001c0001t0004g0062others(1): Show | 9 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.207+11294A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009476 | ||||||
chr4:71009520
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.207+11338A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009520 | ||||||
chr4:71009622
|
C | T | 1 | a0001c0001t0003g0049 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.207+11440C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009622 | ||||||
chr4:71009853
|
A | C | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+11671A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009853 | ||||||
chr4:71009967
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0118others(5): Show | 17 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.207+11785A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009967 | ||||||
chr4:71010033
|
T | G | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0059others(1): Show | 4 | HG01167.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+11851T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010033 | ||||||
chr4:71010166
|
C | CT | 59 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(56): Show | 78 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.207+12001dupT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71010166 | |||||
chr4:71010166
|
C | CTT | 42 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0021others(39): Show | 53 | HG00099.hp1 HG00323.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.207+12000_207+1200 others(6): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71010166 | |||||
chr4:71010183
|
T | A | 2 | a0003c0004t0006g0171a0003c0004t0006g0172 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+12001T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010183 | ||||||
chr4:71010232
|
T | C | 4 | a0001c0001t0006g0162a0001c0001t0013g0173a0003c0004t0006g0171others(1): Show | 4 | HG01109.hp2 HG01884.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+12050T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010232 | ||||||
chr4:71010524
|
A | T | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-11843A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010524 | ||||||
chr4:71010569
|
T | A | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.208-11798T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010569 | ||||||
chr4:71010638
|
C | A | 2 | a0003c0004t0006g0171a0003c0004t0006g0172 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-11729C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010638 | ||||||
chr4:71010648
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.208-11719G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010648 | ||||||
chr4:71010719
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.208-11648A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010719 | ||||||
chr4:71010722
|
A | G | 3 | a0001c0001t0002g0022a0001c0001t0002g0040a0001c0001t0002g0041 | 4 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-11645A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010722 | ||||||
chr4:71011204
|
AAGGGCTG others(7): Show |
A | 1 | a0001c0001t0002g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.208-11159_208-1114 others(18): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71011204 | |||||
chr4:71011232
|
CT | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.208-11111delT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71011232 | |||||
chr4:71011232
|
CTT | C | 8 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0075others(5): Show | 8 | HG00738.hp1 HG01070.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.208-11112_208-1111 others(6): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71011232 | |||||
chr4:71011232
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-11120_208-1111 others(14): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71011232 | |||||
chr4:71011234
|
T | C | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-11133T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011234 | ||||||
chr4:71011235
|
T | C | 2 | a0003c0004t0006g0171a0003c0004t0006g0172 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-11132T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011235 | ||||||
chr4:71011288
|
T | C | 4 | a0001c0003t0001g0033a0001c0003t0001g0127a0001c0003t0007g0019others(1): Show | 7 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-11079T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011288 | ||||||
chr4:71011351
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.208-11016T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011351 | ||||||
chr4:71011443
|
G | A | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.208-10924G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011443 | ||||||
chr4:71011460
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0069a0001c0001t0001g0070others(7): Show | 13 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.208-10907G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011460 | ||||||
chr4:71011475
|
G | A | 31 | a0001c0001t0002g0021a0001c0001t0002g0056a0001c0001t0002g0057others(28): Show | 40 | HG00673.hp1 HG01123.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.208-10892G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011475 | ||||||
chr4:71011506
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.208-10861A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011506 | ||||||
chr4:71011515
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.208-10852C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011515 | ||||||
chr4:71011569
|
A | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.208-10798A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011569 | ||||||
chr4:71011606
|
C | T | 7 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0044others(4): Show | 12 | HG02055.hp1 HG02602.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.208-10761C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011606 | ||||||
chr4:71011717
|
A | T | 1 | a0002c0002t0002g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.208-10650A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011717 | ||||||
chr4:71011722
|
A | G | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-10645A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011722 | ||||||
chr4:71011872
|
ATATAT | A | 14 | a0002c0002t0002g0020a0002c0002t0002g0174a0002c0002t0002g0175others(11): Show | 16 | HG00673.hp1 HG01123.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.208-10490_208-1048 others(9): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71011872 | |||||
chr4:71011912
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.208-10455A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011912 | ||||||
chr4:71011913
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.208-10454C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011913 | ||||||
chr4:71011955
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.208-10412A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011955 | ||||||
chr4:71012019
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.208-10348C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012019 | ||||||
chr4:71012201
|
C | T | 5 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0059others(2): Show | 5 | HG01167.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-10166C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012201 | ||||||
chr4:71012377
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.208-9990A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012377 | ||||||
chr4:71012625
|
CA | C | 1 | a0001c0001t0001g0017 | 3 | HG00099.hp2 HG00323.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.208-9741delA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012625 | ||||||
chr4:71012709
|
G | T | 7 | a0001c0001t0002g0022a0001c0001t0002g0025a0001c0001t0002g0040others(4): Show | 9 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-9658G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012709 | ||||||
chr4:71012762
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.208-9605C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012762 | ||||||
chr4:71012809
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0115 | 2 | NA18982.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.208-9558A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012809 | ||||||
chr4:71012988
|
C | A | 1 | a0001c0001t0001g0144 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.208-9379C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012988 | ||||||
chr4:71012993
|
G | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.208-9374G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012993 | ||||||
chr4:71013077
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.208-9290G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013077 | ||||||
chr4:71013129
|
C | T | 2 | a0003c0004t0006g0171a0003c0004t0006g0172 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-9238C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013129 | ||||||
chr4:71013168
|
G | C | 5 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(2): Show | 6 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-9199G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013168 | ||||||
chr4:71013201
|
T | A | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-9166T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013201 | ||||||
chr4:71013402
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208-8965C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013402 | ||||||
chr4:71013599
|
A | G | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-8768A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013599 | ||||||
chr4:71013622
|
C | A | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-8745C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013622 | ||||||
chr4:71013629
|
G | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.208-8738G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013629 | ||||||
chr4:71013634
|
C | A | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-8733C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013634 | ||||||
chr4:71013641
|
A | T | 5 | a0001c0001t0001g0151a0001c0001t0005g0043a0001c0001t0005g0052others(2): Show | 5 | HG00423.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-8726A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013641 | ||||||
chr4:71013642
|
T | A | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-8725T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013642 | ||||||
chr4:71013661
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.208-8706A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013661 | ||||||
chr4:71013670
|
G | C | 3 | a0001c0001t0013g0173a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-8697G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013670 | ||||||
chr4:71013725
|
C | T | 1 | a0001c0001t0002g0025 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.208-8642C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013725 | ||||||
chr4:71013755
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(28): Show | 51 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.208-8612G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013755 | ||||||
chr4:71013783
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.208-8584C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013783 | ||||||
chr4:71013827
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.208-8540G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013827 | ||||||
chr4:71013833
|
A | G | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.208-8534A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013833 | ||||||
chr4:71013873
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0001g0072others(2): Show | 7 | HG01106.hp2 HG01175.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-8494A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013873 | ||||||
chr4:71013890
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.208-8477A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013890 | ||||||
chr4:71013942
|
C | A | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.208-8425C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013942 | ||||||
chr4:71014072
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.208-8295G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014072 | ||||||
chr4:71014257
|
A | G | 1 | a0001c0003t0001g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.208-8110A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014257 | ||||||
chr4:71014278
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.208-8089A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014278 | ||||||
chr4:71014484
|
T | C | 1 | a0002c0002t0002g0175 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.208-7883T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014484 | ||||||
chr4:71014486
|
G | A | 1 | a0002c0002t0002g0175 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.208-7881G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014486 | ||||||
chr4:71014592
|
AC | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.208-7773delC | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71014592 | |||||
chr4:71014605
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0015g0129 | 2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.208-7762G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014605 | ||||||
chr4:71014728
|
C | A | 3 | a0002c0002t0002g0177a0002c0002t0002g0178a0002c0002t0002g0179 | 3 | NA18995.hp1 NA18997.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.208-7639C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014728 | ||||||
chr4:71014845
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.208-7522A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014845 | ||||||
chr4:71014970
|
A | G | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-7397A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014970 | ||||||
chr4:71015054
|
A | C | 7 | a0001c0001t0002g0022a0001c0001t0002g0025a0001c0001t0002g0040others(4): Show | 9 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-7313A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015054 | ||||||
chr4:71015083
|
G | C | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-7284G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015083 | ||||||
chr4:71015136
|
TAAACACC others(5): Show |
T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.208-7218_208-7207d others(14): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71015136 | |||||
chr4:71015160
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.208-7207C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015160 | ||||||
chr4:71015350
|
C | A | 3 | a0001c0001t0013g0173a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-7017C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015350 | ||||||
chr4:71015351
|
A | G | 3 | a0001c0001t0013g0173a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-7016A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015351 | ||||||
chr4:71015399
|
T | C | 3 | a0002c0002t0002g0177a0002c0002t0002g0178a0002c0002t0002g0179 | 3 | NA18995.hp1 NA18997.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.208-6968T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015399 | ||||||
chr4:71015705
|
C | A | 7 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0064others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-6662C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015705 | ||||||
chr4:71015879
|
C | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0121 | 9 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-6488C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015879 | ||||||
chr4:71015879
|
C | T | 1 | a0001c0001t0001g0016 | 3 | HG02717.hp1 HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.208-6488C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015879 | ||||||
chr4:71015946
|
T | G | 4 | a0001c0001t0006g0162a0001c0001t0013g0173a0003c0004t0006g0171others(1): Show | 4 | HG01109.hp2 HG01884.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-6421T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015946 | ||||||
chr4:71015969
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-6398A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015969 | ||||||
chr4:71015982
|
G | A | 3 | a0001c0001t0013g0173a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-6385G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015982 | ||||||
chr4:71016022
|
A | T | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG02109.hp1 HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.208-6345A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016022 | ||||||
chr4:71016024
|
T | C | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG02109.hp1 HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.208-6343T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016024 | ||||||
chr4:71016039
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.208-6328G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016039 | ||||||
chr4:71016137
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.208-6230T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016137 | ||||||
chr4:71016230
|
T | C | 7 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0044others(4): Show | 12 | HG02055.hp1 HG02602.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.208-6137T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016230 | ||||||
chr4:71016242
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.208-6125C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016242 | ||||||
chr4:71016365
|
A | C | 1 | a0001c0001t0002g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.208-6002A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016365 | ||||||
chr4:71016517
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.208-5850T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016517 | ||||||
chr4:71016518
|
A | G | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-5849A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016518 | ||||||
chr4:71016631
|
A | G | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0059others(1): Show | 4 | HG01167.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-5736A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016631 | ||||||
chr4:71016706
|
G | A | 9 | a0001c0001t0002g0021a0001c0001t0002g0167a0001c0001t0002g0168others(6): Show | 11 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-5661G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016706 | ||||||
chr4:71016718
|
A | C | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-5649A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016718 | ||||||
chr4:71016721
|
G | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0170others(1): Show | 4 | HG02602.hp2 HG03490.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-5646G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016721 | ||||||
chr4:71016747
|
T | A | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.208-5620T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016747 | ||||||
chr4:71016840
|
A | T | 1 | a0001c0001t0002g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208-5527A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016840 | ||||||
chr4:71016878
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.208-5489G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016878 | ||||||
chr4:71016887
|
T | A | 5 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(2): Show | 6 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-5480T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016887 | ||||||
chr4:71016910
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.208-5457A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016910 | ||||||
chr4:71016918
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0006g0162 | 2 | HG01884.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.208-5449C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016918 | ||||||
chr4:71016933
|
G | C | 7 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0044others(4): Show | 12 | HG02055.hp1 HG02602.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.208-5434G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016933 | ||||||
chr4:71016968
|
A | G | 2 | a0003c0004t0006g0171a0003c0004t0006g0172 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-5399A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016968 | ||||||
chr4:71016974
|
A | G | 2 | a0001c0001t0002g0167a0001c0001t0002g0168 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.208-5393A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016974 | ||||||
chr4:71017004
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.208-5363G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017004 | ||||||
chr4:71017008
|
G | A | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-5359G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017008 | ||||||
chr4:71017134
|
C | T | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-5233C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017134 | ||||||
chr4:71017135
|
T | G | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-5232T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017135 | ||||||
chr4:71017322
|
A | G | 2 | a0001c0001t0005g0043a0001c0001t0005g0054 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.208-5045A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017322 | ||||||
chr4:71017392
|
C | G | 1 | a0001c0001t0001g0082 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.208-4975C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017392 | ||||||
chr4:71017409
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208-4958C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017409 | ||||||
chr4:71017424
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | NA18986.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.208-4943A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017424 | ||||||
chr4:71017468
|
A | G | 3 | a0001c0001t0013g0173a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-4899A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017468 | ||||||
chr4:71017762
|
C | T | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0059others(1): Show | 4 | HG01167.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-4605C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017762 | ||||||
chr4:71017777
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.208-4590T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017777 | ||||||
chr4:71017790
|
G | A | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-4577G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017790 | ||||||
chr4:71017836
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208-4531A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017836 | ||||||
chr4:71017875
|
A | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0140 | 2 | HG02056.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.208-4492A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017875 | ||||||
chr4:71018072
|
C | G | 1 | a0001c0001t0001g0126 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.208-4295C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018072 | ||||||
chr4:71018126
|
C | CT | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.208-4223dupT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71018126 | |||||
chr4:71018251
|
C | G | 5 | a0001c0001t0002g0064a0001c0001t0002g0164a0001c0001t0002g0165others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-4116C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018251 | ||||||
chr4:71018374
|
C | T | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-3993C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018374 | ||||||
chr4:71018423
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG01243.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.208-3944C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018423 | ||||||
chr4:71018488
|
T | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.208-3879T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018488 | ||||||
chr4:71018497
|
T | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0001g0072others(2): Show | 7 | HG01106.hp2 HG01175.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-3870T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018497 | ||||||
chr4:71018666
|
AT | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(158): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.208-3679delT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71018666 | |||||
chr4:71018666
|
ATT | A | 10 | a0001c0001t0001g0107a0001c0001t0001g0153a0001c0001t0002g0021others(7): Show | 11 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-3680_208-3679d others(4): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71018666 | |||||
chr4:71018911
|
A | G | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-3456A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018911 | ||||||
chr4:71018911
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.208-3456A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018911 | ||||||
chr4:71018915
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.208-3452G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018915 | ||||||
chr4:71018923
|
C | T | 3 | a0001c0003t0001g0033a0001c0003t0007g0019a0006c0007t0001g0089 | 6 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-3444C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018923 | ||||||
chr4:71019021
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0121 | 9 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-3346T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019021 | ||||||
chr4:71019043
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.208-3324T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019043 | ||||||
chr4:71019150
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.208-3217A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019150 | ||||||
chr4:71019192
|
A | G | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.208-3175A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019192 | ||||||
chr4:71019258
|
G | A | 1 | a0002c0002t0002g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.208-3109G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019258 | ||||||
chr4:71019392
|
G | T | 1 | a0001c0001t0002g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.208-2975G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019392 | ||||||
chr4:71019592
|
C | G | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0059others(1): Show | 4 | HG01167.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-2775C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019592 | ||||||
chr4:71019782
|
A | AT | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.208-2576dupT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71019782 | |||||
chr4:71019791
|
T | TA | 1 | a0001c0001t0001g0016 | 3 | HG02717.hp1 HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.208-2573dupA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71019791 | |||||
chr4:71019792
|
A | T | 2 | a0001c0001t0002g0067a0001c0001t0016g0095 | 2 | HG02083.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.208-2575A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019792 | ||||||
chr4:71019932
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.208-2435G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019932 | ||||||
chr4:71019980
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.208-2387G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019980 | ||||||
chr4:71020343
|
A | G | 1 | a0002c0002t0002g0174 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208-2024A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71020343 | ||||||
chr4:71020347
|
G | T | 9 | a0001c0001t0002g0021a0001c0001t0002g0167a0001c0001t0002g0168others(6): Show | 11 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-2020G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71020347 | ||||||
chr4:71020355
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.208-2012T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71020355 | ||||||
chr4:71020377
|
T | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.208-1990T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71020377 | ||||||
chr4:71020695
|
T | TTTTG | 3 | a0001c0001t0013g0173a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-1660_208-1657d others(6): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71020695 | |||||
chr4:71020844
|
C | T | 2 | a0003c0004t0006g0171a0003c0004t0006g0172 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-1523C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71020844 | ||||||
chr4:71020858
|
A | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0115 | 2 | NA18982.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.208-1509A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71020858 | ||||||
chr4:71021038
|
A | G | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-1329A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021038 | ||||||
chr4:71021066
|
CT | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.208-1281delT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71021066 | |||||
chr4:71021066
|
CTT | C | 14 | a0001c0001t0001g0105a0001c0001t0001g0134a0001c0001t0001g0156others(11): Show | 14 | HG01243.hp2 HG02109.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.208-1282_208-1281d others(4): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71021066 | |||||
chr4:71021069
|
T | C | 1 | a0002c0002t0002g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.208-1298T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021069 | ||||||
chr4:71021099
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.208-1268C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021099 | ||||||
chr4:71021107
|
C | T | 1 | a0001c0001t0002g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.208-1260C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021107 | ||||||
chr4:71021108
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.208-1259G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021108 | ||||||
chr4:71021124
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.208-1243G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021124 | ||||||
chr4:71021124
|
G | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | NA18968.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.208-1243G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021124 | ||||||
chr4:71021136
|
C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0078others(2): Show | 9 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-1231C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021136 | ||||||
chr4:71021177
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.208-1190G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021177 | ||||||
chr4:71021232
|
C | T | 1 | a0001c0001t0015g0129 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.208-1135C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021232 | ||||||
chr4:71021280
|
T | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.208-1087T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021280 | ||||||
chr4:71021366
|
C | T | 4 | a0001c0001t0001g0096a0001c0001t0001g0139a0001c0001t0001g0160others(1): Show | 4 | HG00438.hp2 HG03195.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1001C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021366 | ||||||
chr4:71021542
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.208-825A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021542 | ||||||
chr4:71021744
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.208-623C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021744 | ||||||
chr4:71021769
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.208-598A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021769 | ||||||
chr4:71021784
|
TGAGGTCA others(1): Show |
T | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-579_208-572del others(8): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71021784 | |||||
chr4:71021798
|
G | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.208-569G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021798 | ||||||
chr4:71021799
|
G | A | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-568G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021799 | ||||||
chr4:71021829
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.208-538C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021829 | ||||||
chr4:71021929
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.208-438T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021929 | ||||||
chr4:71021953
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.208-414A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021953 | ||||||
chr4:71022163
|
G | T | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-204G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71022163 | ||||||
chr4:71022613
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.401+53G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71022613 | ||||||
chr4:71022650
|
T | G | 2 | a0003c0004t0006g0171a0003c0004t0006g0172 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.401+90T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71022650 | ||||||
chr4:71022775
|
G | C | 1 | a0001c0001t0002g0022 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.401+215G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71022775 | ||||||
chr4:71022846
|
C | T | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.401+286C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71022846 | ||||||
chr4:71022921
|
G | A | 1 | a0002c0002t0002g0180 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.401+361G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71022921 | ||||||
chr4:71023075
|
A | G | 1 | a0001c0001t0001g0035 | 2 | HG01255.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.402-484A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71023075 | ||||||
chr4:71023212
|
C | T | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-347C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71023212 | ||||||
chr4:71023394
|
A | C | 2 | a0003c0004t0006g0171a0003c0004t0006g0172 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.402-165A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71023394 | ||||||
chr4:71023718
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.549+12T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71023718 | ||||||
chr4:71023746
|
G | T | 1 | a0001c0001t0001g0152 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.549+40G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71023746 | ||||||
chr4:71023913
|
T | G | 1 | a0001c0001t0001g0034 | 2 | NA18950.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.549+207T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71023913 | ||||||
chr4:71023953
|
C | T | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.549+247C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71023953 | ||||||
chr4:71024069
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.549+363T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71024069 | ||||||
chr4:71024242
|
G | A | 4 | a0001c0001t0002g0022a0001c0001t0002g0040a0001c0001t0002g0041others(1): Show | 5 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.549+536G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71024242 | ||||||
chr4:71024395
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.549+689C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71024395 | ||||||
chr4:71024448
|
C | T | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.549+742C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71024448 | ||||||
chr4:71024596
|
C | T | 38 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0025others(35): Show | 49 | HG00323.hp2 HG00673.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.549+890C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71024596 | ||||||
chr4:71024683
|
A | G | 1 | a0001c0001t0008g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.549+977A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71024683 | ||||||
chr4:71025003
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.550-813A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025003 | ||||||
chr4:71025057
|
T | C | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.550-759T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025057 | ||||||
chr4:71025239
|
T | G | 1 | a0001c0001t0002g0047 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.550-577T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025239 | ||||||
chr4:71025330
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0104a0001c0001t0001g0155others(4): Show | 9 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.550-486G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025330 | ||||||
chr4:71025380
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0006g0162 | 2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.550-436T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025380 | ||||||
chr4:71025466
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.550-350A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025466 | ||||||
chr4:71025777
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0008g0073a0001c0001t0008g0074 | 5 | HG02647.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-39C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025777 | ||||||
chr4:71026258
|
G | A | 1 | a0001c0001t0006g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.665+327G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026258 | ||||||
chr4:71026312
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.666-353T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026312 | ||||||
chr4:71026319
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.666-346T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026319 | ||||||
chr4:71026418
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.666-247T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026418 | ||||||
chr4:71026441
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-224G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026441 | ||||||
chr4:71026443
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-222T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026443 | ||||||
chr4:71026444
|
A | ATTCTCTT others(7): Show |
1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-221_666-220ins others(14): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026444 | ||||||
chr4:71026445
|
C | A | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-220C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026445 | ||||||
chr4:71026450
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-215C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026450 | ||||||
chr4:71026452
|
C | A | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-213C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026452 | ||||||
chr4:71026453
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-212A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026453 | ||||||
chr4:71026454
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-211G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026454 | ||||||
chr4:71026456
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-209T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026456 | ||||||
chr4:71026457
|
G | C | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-208G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026457 | ||||||
chr4:71026462
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-203T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026462 | ||||||
chr4:71026464
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-201T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026464 | ||||||
chr4:71026471
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-194C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026471 | ||||||
chr4:71026473
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-192T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026473 | ||||||
chr4:71026493
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-172G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026493 | ||||||
chr4:71026494
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-171G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026494 | ||||||
chr4:71026498
|
A | C | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-167A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026498 | ||||||
chr4:71026796
|
A | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.756+41A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71026796 | ||||||
chr4:71026892
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.756+137A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71026892 | ||||||
chr4:71026912
|
T | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0061a0001c0001t0004g0062others(1): Show | 9 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.756+157T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71026912 | ||||||
chr4:71026935
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG01243.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.756+180C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71026935 | ||||||
chr4:71027037
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.756+282G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027037 | ||||||
chr4:71027092
|
T | C | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.756+337T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027092 | ||||||
chr4:71027112
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.756+357A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027112 | ||||||
chr4:71027124
|
C | T | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.756+369C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027124 | ||||||
chr4:71027206
|
A | G | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.756+451A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027206 | ||||||
chr4:71027304
|
A | G | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.756+549A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027304 | ||||||
chr4:71027394
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.756+639A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027394 | ||||||
chr4:71027486
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.756+731T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027486 | ||||||
chr4:71027688
|
G | A | 1 | a0001c0003t0001g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.756+933G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027688 | ||||||
chr4:71027745
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0009g0097a0001c0001t0009g0163 | 3 | HG01891.hp1 HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.756+990A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027745 | ||||||
chr4:71027782
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.756+1027G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027782 | ||||||
chr4:71028075
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.757-1277A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028075 | ||||||
chr4:71028110
|
A | G | 9 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0003g0005others(6): Show | 14 | HG01243.hp2 HG02055.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.757-1242A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028110 | ||||||
chr4:71028147
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(74): Show | 121 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.757-1205C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028147 | ||||||
chr4:71028178
|
A | G | 3 | a0001c0001t0004g0063a0003c0004t0006g0171a0003c0004t0006g0172 | 3 | HG02886.hp2 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.757-1174A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028178 | ||||||
chr4:71028350
|
G | C | 4 | a0001c0001t0005g0043a0001c0001t0005g0052a0001c0001t0005g0053others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.757-1002G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028350 | ||||||
chr4:71028604
|
C | CTTTT | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.757-743_757-740dup others(4): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 71028604 | |||||
chr4:71028759
|
A | AT | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.757-578dupT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 71028759 | |||||
chr4:71028837
|
A | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0029others(11): Show | 25 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.757-515A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028837 | ||||||
chr4:71028846
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(74): Show | 121 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.757-506C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028846 | ||||||
chr4:71028856
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(74): Show | 121 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.757-496C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028856 | ||||||
chr4:71028976
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.757-376C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028976 | ||||||
chr4:71028989
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.757-363G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028989 | ||||||
chr4:71029105
|
G | A | 1 | a0001c0001t0013g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.757-247G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71029105 | ||||||
chr4:71029189
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.757-163C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71029189 | ||||||
chr4:71029224
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.757-128A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71029224 | ||||||
chr4:71029286
|
G | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.757-66G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71029286 |