geneid | 441054 |
---|---|
ensemblid | ENSG00000205129.9 |
hgncid | 34346 |
symbol | C4orf47 |
name | cilia and flagella associated protein 96 |
refseq_nuc | NM_001114357.3 |
refseq_prot | NP_001107829.1 |
ensembl_nuc | ENST00000378850.5 |
ensembl_prot | ENSP00000368127.4 |
mane_status | MANE Select |
chr | chr4 |
start | 185426254 |
end | 185449826 |
strand | + |
ver | v1.2 |
region | chr4:185426254-185449826 |
region5000 | chr4:185421254-185454826 |
regionname0 | C4orf47_chr4_185426254_185449826 |
regionname5000 | C4orf47_chr4_185421254_185454826 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 309 | 321 | 79 | 56 | 137 | 14 | 34 | 99 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0002 | 0/1 | 309 | 25 | 5 | 10 | 1 | 0 | 8 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0003 | 0/0 | 309 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0004 | 0/0 | 309 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0005 | 0/0 | 309 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0006 | 0/0 | 309 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0007 | 0/0 | 309 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 930 | 313 | 73 | 55 | 136 | 14 | 34 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
c0002 | 0/1 | 930 | 25 | 5 | 10 | 1 | 0 | 8 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
c0003 | 0/0 | 930 | 8 | 8 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
c0004 | 0/0 | 930 | 5 | 4 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
c0005 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
c0006 | 0/0 | 930 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
c0007 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
c0008 | 0/0 | 930 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
c0009 | 0/0 | 930 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
c0010 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
c0011 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 404 | 255 | 48 | 47 | 118 | 9 | 32 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
t0002 | 0/0 | 404 | 40 | 24 | 1 | 8 | 1 | 6 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
t0003 | 0/0 | 404 | 38 | 3 | 14 | 14 | 4 | 3 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
t0004 | 0/0 | 404 | 17 | 13 | 3 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
t0005 | 1/0 | 404 | 3 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
t0006 | 0/0 | 404 | 3 | 2 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
t0007 | 0/0 | 404 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0014 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0034 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 930 | 313 | 73 | 55 | 136 | 14 | 34 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0004 | 0/0 | 930 | 5 | 4 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0007 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0009 | 0/0 | 930 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0010 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0002c0002 | 0/1 | 930 | 25 | 5 | 10 | 1 | 0 | 8 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0003c0003 | 0/0 | 930 | 8 | 8 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0004c0006 | 0/0 | 930 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0005c0008 | 0/0 | 930 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0006c0011 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0007c0005 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1333 | 218 | 33 | 36 | 116 | 9 | 24 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0001t0002 | 0/0 | 1333 | 36 | 20 | 1 | 8 | 1 | 6 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0001t0003 | 0/0 | 1333 | 36 | 3 | 14 | 12 | 4 | 3 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0001t0004 | 0/0 | 1333 | 17 | 13 | 3 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0001t0005 | 1/0 | 1333 | 3 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0001t0006 | 0/0 | 1333 | 3 | 2 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0004t0001 | 0/0 | 1333 | 3 | 2 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0004t0007 | 0/0 | 1333 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0007t0002 | 0/0 | 1333 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0009t0003 | 0/0 | 1333 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0001c0010t0001 | 0/0 | 1333 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0002c0002t0001 | 0/1 | 1333 | 25 | 5 | 10 | 1 | 0 | 8 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0003c0003t0001 | 0/0 | 1333 | 5 | 5 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0003c0003t0002 | 0/0 | 1333 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0004c0006t0003 | 0/0 | 1333 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0005c0008t0001 | 0/0 | 1333 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0006c0011t0001 | 0/0 | 1333 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
a0007c0005t0001 | 0/0 | 1333 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | copy fasta | chr4 | 185421254 | 185454826 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0005g0001 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0001t0006g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0004t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0004t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0004t0007g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0007t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0009t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0001c0010t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0014 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0003c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0003c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0003c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0003c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0003c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0003c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0003c0003t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0004c0006t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0005c0008t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0006c0011t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
a0007c0005t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | GBR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | GBR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0019 | EUR | GBR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0117 | EUR | FIN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | FIN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0079 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0110 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00733 | hp2 | a0001 | c0004 | t0001 | g0224 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0065 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0295 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0081 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0047 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0028 | EUR | IBS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0210 | EUR | IBS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01884 | hp1 | a0001 | c0004 | t0007 | g0030 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0111 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0063 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02129 | hp2 | a0004 | c0006 | t0003 | g0003 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CDX | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | CDX | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02257 | hp1 | a0003 | c0003 | t0001 | g0043 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0314 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0303 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02280 | hp1 | a0007 | c0005 | t0001 | g0070 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02615 | hp2 | a0001 | c0010 | t0001 | g0045 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02622 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02647 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0053 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0304 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0222 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02809 | hp2 | a0001 | c0007 | t0002 | g0256 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02896 | hp1 | a0003 | c0003 | t0002 | g0076 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02976 | hp1 | a0003 | c0003 | t0002 | g0060 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03486 | hp1 | a0001 | c0004 | t0001 | g0104 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0040 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0122 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0082 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0078 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0316 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0013 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0106 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0243 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0271 | AFR | YRI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | YRI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | CHB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0083 | AFR | YRI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18906 | hp2 | a0003 | c0003 | t0001 | g0048 | AFR | YRI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18975 | hp1 | a0001 | c0009 | t0003 | g0003 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18981 | hp1 | a0005 | c0008 | t0001 | g0134 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | LWK | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | LWK | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA19240 | hp2 | a0001 | c0004 | t0007 | g0030 | AFR | YRI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | ASW | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | ASW | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | TSI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | GIH | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | GIH | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02109 | hp2 | a0006 | c0011 | t0001 | g0305 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02559 | hp1 | a0003 | c0003 | t0002 | g0049 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0223 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | USA | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | USA | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | LWK | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | LWK | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0014 | REF | REF | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0001 | REF | REF | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:185432078
|
T | C | 1 | a0007 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.197T>C | p.Phe66Ser | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/8 | 418/1333 | 197/930 | 66/309 | chr4 | 185432078 | ||
chr4:185432131
|
C | T | 1 | a0006 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.250C>T | p.Arg84Trp | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/8 | 471/1333 | 250/930 | 84/309 | chr4 | 185432131 | ||
chr4:185436101
|
G | A | 1 | a0003 | 8 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
missense_variant | MODERATE | c.376G>A | p.Ala126Thr | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 4/8 | 597/1333 | 376/930 | 126/309 | chr4 | 185436101 | ||
chr4:185440597
|
C | T | 1 | a0005 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.592C>T | p.His198Tyr | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/8 | 813/1333 | 592/930 | 198/309 | chr4 | 185440597 | ||
chr4:185445027
|
G | A | 1 | a0002 | 25 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(22): Show |
missense_variant | MODERATE | c.778G>A | p.Ala260Thr | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/8 | 999/1333 | 778/930 | 260/309 | chr4 | 185445027 | ||
chr4:185445118
|
T | C | 1 | a0004 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.869T>C | p.Leu290Ser | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/8 | 1090/1333 | 869/930 | 290/309 | chr4 | 185445118 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:185436178
|
A | G | 1 | a0001c0010 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.453A>G | p.Gly151Gly | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 4/8 | 674/1333 | 453/930 | 151/309 | chr4 | 185436178 | ||
chr4:185436350
|
A | G | 1 | a0001c0009 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.525A>G | p.Leu175Leu | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/8 | 746/1333 | 525/930 | 175/309 | chr4 | 185436350 | ||
chr4:185440617
|
C | T | 1 | a0001c0007 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.612C>T | p.Asp204Asp | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/8 | 833/1333 | 612/930 | 204/309 | chr4 | 185440617 | ||
chr4:185440701
|
G | A | 1 | a0001c0004 | 5 | HG00733.hp2 HG01884.hp1 HG03471.hp2 others(2): Show |
synonymous_variant | LOW | c.696G>A | p.Pro232Pro | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/8 | 917/1333 | 696/930 | 232/309 | chr4 | 185440701 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:185426254
|
A | G | 1 | a0001c0001t0006 | 3 | HG01099.hp1 HG03516.hp1 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-221A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/8 | 3158 | chr4 | 185426254 | |||||
chr4:185426289
|
G | A | 1 | a0001c0004t0007 | 2 | HG01884.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-186G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/8 | 3123 | chr4 | 185426289 | |||||
chr4:185429405
|
C | T | 4 | a0001c0001t0003a0001c0001t0004a0001c0009t0003others(1): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/8 | chr4 | 185429405 | ||||||
chr4:185449692
|
C | T | 4 | a0001c0001t0002a0001c0001t0004a0001c0007t0002others(1): Show | 57 | HG00642.hp1 HG01109.hp2 HG01934.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*48C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 8/8 | 48 | chr4 | 185449692 | |||||
chr4:185449802
|
G | C | 17 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*158G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 8/8 | 158 | chr4 | 185449802 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:185426481
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-79+85T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185426481 | ||||||
chr4:185426539
|
T | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | NA18964.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-79+143T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185426539 | ||||||
chr4:185426811
|
C | T | 1 | a0001c0001t0001g0318 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-79+415C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185426811 | ||||||
chr4:185426879
|
CAAA | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0046others(13): Show | 18 | HG01243.hp1 HG01433.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-79+517_-79+519del others(3): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | |||||
chr4:185426879
|
CAAAA | C | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0062others(18): Show | 24 | HG00741.hp1 HG01081.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.-79+516_-79+519del others(4): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | |||||
chr4:185426879
|
CAAAAA | C | 17 | a0001c0001t0001g0015a0001c0001t0001g0085a0001c0001t0001g0086others(14): Show | 23 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-79+515_-79+519del others(5): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | |||||
chr4:185426879
|
CAAAAAAA others(3): Show |
C | 15 | a0001c0001t0001g0017a0001c0001t0001g0091a0001c0001t0001g0092others(12): Show | 16 | HG00597.hp2 HG00642.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.-79+510_-79+519del others(10): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | |||||
chr4:185426879
|
CAAAAAAA others(4): Show |
C | 134 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(131): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-79+509_-79+519del others(11): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | |||||
chr4:185426879
|
CAAAAAAA others(5): Show |
C | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0032others(90): Show | 102 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.-79+508_-79+519del others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | |||||
chr4:185426879
|
CAAAAAAA others(6): Show |
C | 9 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-79+507_-79+519del others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | |||||
chr4:185426879
|
CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0315a0001c0001t0002g0006a0001c0001t0002g0314 | 5 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+506_-79+519del others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | |||||
chr4:185426879
|
CAAAAAAA others(10): Show |
C | 1 | a0002c0002t0001g0316 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-79+503_-79+519del others(17): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | |||||
chr4:185426879
|
CAAAAAAA others(13): Show |
C | 1 | a0001c0001t0003g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-79+500_-79+519del others(20): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | |||||
chr4:185426918
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-79+522G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185426918 | ||||||
chr4:185426962
|
G | A | 3 | a0001c0001t0002g0007a0001c0001t0002g0038a0001c0001t0002g0039 | 4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-79+566G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185426962 | ||||||
chr4:185427048
|
G | C | 1 | a0001c0004t0001g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-79+652G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427048 | ||||||
chr4:185427064
|
C | CA | 17 | a0001c0001t0001g0105a0001c0001t0002g0080a0001c0001t0002g0090others(14): Show | 18 | HG00639.hp1 HG00733.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.-79+683dupA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185427064 | |||||
chr4:185427064
|
CA | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(165): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.-79+683delA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185427064 | |||||
chr4:185427289
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-79+893G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427289 | ||||||
chr4:185427356
|
A | G | 1 | a0002c0002t0001g0061 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-79+960A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427356 | ||||||
chr4:185427433
|
T | C | 18 | a0001c0001t0001g0121a0001c0001t0001g0270a0001c0001t0003g0230others(15): Show | 20 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-79+1037T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427433 | ||||||
chr4:185427481
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-79+1085C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427481 | ||||||
chr4:185427663
|
G | A | 202 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(199): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-79+1267G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427663 | ||||||
chr4:185427668
|
GAGAATTC others(319): Show |
G | 14 | a0002c0002t0001g0002a0002c0002t0001g0010a0002c0002t0001g0013others(11): Show | 19 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-79+1278_-78-1335d others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185427668 | |||||
chr4:185427970
|
C | T | 18 | a0001c0001t0001g0121a0001c0001t0001g0270a0001c0001t0003g0230others(15): Show | 20 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-78-1364C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427970 | ||||||
chr4:185428029
|
T | A | 2 | a0001c0001t0006g0122a0001c0001t0006g0271 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-78-1305T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428029 | ||||||
chr4:185428086
|
CA | C | 219 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(216): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.-78-1232delA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185428086 | |||||
chr4:185428086
|
CAA | C | 55 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0268others(52): Show | 64 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.-78-1233_-78-1232d others(4): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185428086 | |||||
chr4:185428109
|
T | G | 3 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0007g0030 | 4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78-1225T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428109 | ||||||
chr4:185428111
|
A | T | 3 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0007g0030 | 4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78-1223A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428111 | ||||||
chr4:185428162
|
A | G | 202 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(199): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-78-1172A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428162 | ||||||
chr4:185428165
|
T | A | 2 | a0001c0001t0003g0019a0001c0001t0003g0127 | 3 | HG00140.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-78-1169T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428165 | ||||||
chr4:185428295
|
C | A | 4 | a0001c0001t0002g0007a0001c0001t0002g0038a0001c0001t0002g0039others(1): Show | 5 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78-1039C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428295 | ||||||
chr4:185428398
|
A | G | 18 | a0001c0001t0001g0121a0001c0001t0001g0270a0001c0001t0003g0230others(15): Show | 20 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-78-936A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428398 | ||||||
chr4:185428446
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | NA18998.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-78-888G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428446 | ||||||
chr4:185428556
|
TA | T | 78 | a0001c0001t0001g0005a0001c0001t0001g0088a0001c0001t0001g0121others(75): Show | 92 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.-78-764delA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185428556 | |||||
chr4:185428556
|
TAA | T | 200 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(197): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.-78-765_-78-764del others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185428556 | |||||
chr4:185428561
|
A | G | 37 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0268others(34): Show | 43 | HG00544.hp1 HG01109.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.-78-773A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428561 | ||||||
chr4:185428582
|
AC | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0112others(19): Show | 25 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.-78-751delC | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428582 | ||||||
chr4:185428583
|
C | A | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | NA19064.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-78-751C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428583 | ||||||
chr4:185428583
|
CA | C | 291 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(288): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-78-741delA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185428583 | |||||
chr4:185428587
|
A | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0312 | 3 | HG02647.hp2 NA18948.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-78-747A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428587 | ||||||
chr4:185428611
|
C | A | 280 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(277): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-78-723C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428611 | ||||||
chr4:185428802
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0270 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-78-532T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428802 | ||||||
chr4:185428878
|
T | G | 20 | a0001c0001t0001g0088a0001c0010t0001g0045a0002c0002t0001g0002others(17): Show | 25 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.-78-456T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428878 | ||||||
chr4:185428909
|
C | T | 195 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(192): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-78-425C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428909 | ||||||
chr4:185429033
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-78-301G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185429033 | ||||||
chr4:185429044
|
A | C | 1 | a0001c0001t0003g0220 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-78-290A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185429044 | ||||||
chr4:185429075
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-78-259G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185429075 | ||||||
chr4:185429081
|
G | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0268others(33): Show | 42 | HG00544.hp1 HG01109.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.-78-253G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185429081 | ||||||
chr4:185429086
|
G | C | 1 | a0001c0001t0001g0252 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-78-248G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185429086 | ||||||
chr4:185429181
|
C | A | 17 | a0002c0002t0001g0002a0002c0002t0001g0010a0002c0002t0001g0013others(14): Show | 22 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-78-153C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185429181 | ||||||
chr4:185429286
|
C | CT | 54 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0265others(51): Show | 62 | HG00544.hp1 HG00642.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.-78-42dupT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185429286 | |||||
chr4:185429705
|
G | A | 23 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0092others(20): Show | 24 | HG00438.hp1 HG00597.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.100+194G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429705 | ||||||
chr4:185429744
|
A | G | 1 | a0002c0002t0001g0078 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.100+233A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429744 | ||||||
chr4:185429760
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.100+249C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429760 | ||||||
chr4:185429814
|
T | A | 1 | a0001c0010t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.100+303T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429814 | ||||||
chr4:185429850
|
TA | T | 3 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0007g0030 | 4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+340delA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429850 | ||||||
chr4:185429853
|
G | A | 1 | a0001c0001t0002g0257 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.100+342G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429853 | ||||||
chr4:185429853
|
G | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0314 | 4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+342G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429853 | ||||||
chr4:185429854
|
G | A | 27 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0105others(24): Show | 30 | HG00408.hp1 HG00544.hp2 HG02523.hp2 others(27): Show |
intron_variant | MODIFIER | c.100+343G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429854 | ||||||
chr4:185429854
|
G | C | 18 | a0001c0001t0001g0121a0001c0001t0001g0270a0001c0001t0003g0230others(15): Show | 20 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.100+343G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429854 | ||||||
chr4:185429855
|
C | A | 174 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.100+344C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429855 | ||||||
chr4:185429855
|
C | G | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0032others(98): Show | 118 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+344C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429855 | ||||||
chr4:185429919
|
A | C | 225 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(222): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.100+408A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429919 | ||||||
chr4:185429919
|
A | G | 51 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0265others(48): Show | 57 | HG00544.hp1 HG00642.hp1 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.100+408A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429919 | ||||||
chr4:185429926
|
G | T | 10 | a0001c0001t0003g0119a0001c0001t0003g0126a0001c0001t0003g0212others(7): Show | 10 | HG01123.hp2 HG01255.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+415G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429926 | ||||||
chr4:185430139
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100+628G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430139 | ||||||
chr4:185430243
|
A | G | 3 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0007g0030 | 4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+732A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430243 | ||||||
chr4:185430293
|
C | T | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.100+782C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430293 | ||||||
chr4:185430458
|
C | T | 174 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.100+947C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430458 | ||||||
chr4:185430738
|
A | G | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02027.hp2 HG02602.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+1227A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430738 | ||||||
chr4:185430949
|
C | T | 18 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0233others(15): Show | 18 | HG02698.hp1 HG02738.hp1 HG04184.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-1033C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430949 | ||||||
chr4:185430982
|
T | C | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.101-1000T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430982 | ||||||
chr4:185430983
|
G | A | 276 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(273): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.101-999G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430983 | ||||||
chr4:185431039
|
G | A | 1 | a0001c0010t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.101-943G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185431039 | ||||||
chr4:185431124
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.101-858C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185431124 | ||||||
chr4:185431125
|
G | A | 16 | a0001c0001t0003g0230a0001c0001t0004g0018a0001c0001t0004g0031others(13): Show | 18 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-857G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185431125 | ||||||
chr4:185431165
|
G | A | 1 | a0001c0004t0001g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.101-817G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185431165 | ||||||
chr4:185431209
|
CA | C | 246 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(243): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.101-752delA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 185431209 | |||||
chr4:185431209
|
CAA | C | 23 | a0001c0001t0001g0209a0001c0001t0001g0211a0001c0001t0001g0302others(20): Show | 28 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.101-753_101-752del others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 185431209 | |||||
chr4:185431322
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.101-660A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185431322 | ||||||
chr4:185432202
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02922.hp2 | splice_donor_variant&intron_variant | HIGH | c.320+1G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432202 | ||||||
chr4:185432261
|
A | G | 1 | a0001c0010t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.320+60A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432261 | ||||||
chr4:185432516
|
G | T | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.320+315G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432516 | ||||||
chr4:185432614
|
G | A | 6 | a0001c0001t0001g0092a0001c0001t0001g0128a0001c0001t0001g0131others(3): Show | 6 | NA18966.hp2 NA18979.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.320+413G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432614 | ||||||
chr4:185432628
|
C | T | 1 | a0002c0002t0001g0065 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.320+427C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432628 | ||||||
chr4:185432712
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.320+511A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432712 | ||||||
chr4:185432712
|
A | T | 1 | a0001c0001t0001g0254 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.320+511A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432712 | ||||||
chr4:185432810
|
C | G | 4 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0001g0224others(1): Show | 5 | HG00733.hp2 HG01884.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+609C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432810 | ||||||
chr4:185432861
|
T | TA | 254 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(251): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.320+672dupA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185432861 | |||||
chr4:185432861
|
T | TAA | 19 | a0001c0001t0001g0147a0002c0002t0001g0002a0002c0002t0001g0010others(16): Show | 24 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.320+671_320+672dup others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185432861 | |||||
chr4:185432932
|
T | C | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.320+731T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432932 | ||||||
chr4:185432967
|
T | G | 1 | a0001c0001t0002g0090 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.320+766T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432967 | ||||||
chr4:185433203
|
G | A | 2 | a0002c0002t0001g0079a0002c0002t0001g0089 | 2 | HG00639.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.320+1002G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433203 | ||||||
chr4:185433248
|
A | T | 1 | a0001c0001t0001g0270 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.320+1047A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433248 | ||||||
chr4:185433254
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.320+1053G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433254 | ||||||
chr4:185433265
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.320+1064T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433265 | ||||||
chr4:185433307
|
A | G | 1 | a0003c0003t0002g0049 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.320+1106A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433307 | ||||||
chr4:185433408
|
AAAAAAGA others(4): Show |
A | 7 | a0001c0001t0001g0118a0001c0001t0001g0142a0001c0001t0001g0206others(4): Show | 7 | HG01167.hp2 HG02273.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.320+1212_320+1222d others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185433408 | |||||
chr4:185433409
|
AAAAAG | A | 18 | a0001c0001t0001g0062a0001c0001t0001g0121a0001c0001t0001g0270others(15): Show | 20 | HG01167.hp1 HG01975.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.320+1219_320+1223d others(7): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185433409 | |||||
chr4:185433409
|
AAAAAGAA others(3): Show |
A | 190 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(187): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.320+1214_320+1223d others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185433409 | |||||
chr4:185433410
|
AAAAG | A | 55 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0268others(52): Show | 66 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.320+1213_320+1216d others(6): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185433410 | |||||
chr4:185433414
|
G | A | 5 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0001g0224others(2): Show | 6 | HG00733.hp2 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.320+1213G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433414 | ||||||
chr4:185433532
|
A | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0265others(70): Show | 86 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.320+1331A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433532 | ||||||
chr4:185433535
|
C | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0265others(70): Show | 86 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.320+1334C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433535 | ||||||
chr4:185433538
|
C | CTAGTA | 73 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0265others(70): Show | 86 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.320+1338_320+1339i others(7): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185433538 | |||||
chr4:185433540
|
T | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0265others(70): Show | 86 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.320+1339T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433540 | ||||||
chr4:185433541
|
T | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0265others(70): Show | 86 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.320+1340T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433541 | ||||||
chr4:185433542
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.320+1341G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433542 | ||||||
chr4:185433603
|
T | TAAGAGTG others(348): Show |
1 | a0001c0001t0002g0259 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.320+1417_320+1418i others(357): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185433603 | |||||
chr4:185433646
|
A | C | 1 | a0002c0002t0001g0047 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.320+1445A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433646 | ||||||
chr4:185433722
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.320+1521C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433722 | ||||||
chr4:185433763
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.320+1562G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433763 | ||||||
chr4:185433784
|
C | A | 1 | a0001c0001t0001g0123 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.320+1583C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433784 | ||||||
chr4:185433833
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.320+1632C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433833 | ||||||
chr4:185433938
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.320+1737G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433938 | ||||||
chr4:185434018
|
T | C | 315 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(312): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.320+1817T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434018 | ||||||
chr4:185434128
|
A | G | 315 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(312): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.321-1918A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434128 | ||||||
chr4:185434153
|
A | T | 1 | a0001c0010t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.321-1893A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434153 | ||||||
chr4:185434381
|
A | AT | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.321-1658dupT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185434381 | |||||
chr4:185434413
|
A | G | 2 | a0001c0001t0002g0007a0001c0001t0002g0038 | 3 | HG02486.hp2 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.321-1633A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434413 | ||||||
chr4:185434462
|
C | T | 5 | a0003c0003t0001g0016a0003c0003t0001g0048a0003c0003t0002g0049others(2): Show | 6 | HG02559.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.321-1584C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434462 | ||||||
chr4:185434486
|
G | C | 1 | a0001c0004t0007g0030 | 2 | HG01884.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.321-1560G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434486 | ||||||
chr4:185434626
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.321-1420A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434626 | ||||||
chr4:185434641
|
C | T | 1 | a0001c0001t0003g0203 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.321-1405C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434641 | ||||||
chr4:185434688
|
C | CT | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.321-1357dupT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185434688 | |||||
chr4:185434692
|
A | AC | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.321-1354_321-1353i others(3): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434692 | ||||||
chr4:185434793
|
C | T | 193 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(190): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.321-1253C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434793 | ||||||
chr4:185434800
|
G | A | 1 | a0002c0002t0001g0081 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.321-1246G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434800 | ||||||
chr4:185434937
|
C | A | 1 | a0001c0001t0004g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.321-1109C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434937 | ||||||
chr4:185434939
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.321-1107C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434939 | ||||||
chr4:185434966
|
C | T | 1 | a0001c0001t0003g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.321-1080C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434966 | ||||||
chr4:185435273
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0242 | 2 | HG02698.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.321-773G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435273 | ||||||
chr4:185435290
|
A | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0314 | 4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.321-756A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435290 | ||||||
chr4:185435355
|
G | T | 315 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(312): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.321-691G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435355 | ||||||
chr4:185435418
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0085 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.321-628G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435418 | ||||||
chr4:185435440
|
A | G | 14 | a0002c0002t0001g0002a0002c0002t0001g0010a0002c0002t0001g0013others(11): Show | 19 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.321-606A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435440 | ||||||
chr4:185435569
|
T | G | 1 | a0001c0004t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.321-477T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435569 | ||||||
chr4:185435880
|
ATATCT | A | 271 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(268): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.321-162_321-158del others(5): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185435880 | |||||
chr4:185435992
|
A | C | 1 | a0001c0001t0002g0258 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.321-54A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435992 | ||||||
chr4:185436369
|
C | G | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.534+10C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436369 | ||||||
chr4:185436494
|
G | A | 1 | a0001c0010t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.534+135G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436494 | ||||||
chr4:185436552
|
T | G | 14 | a0002c0002t0001g0002a0002c0002t0001g0010a0002c0002t0001g0013others(11): Show | 19 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.534+193T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436552 | ||||||
chr4:185436579
|
G | A | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.534+220G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436579 | ||||||
chr4:185436664
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.534+305C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436664 | ||||||
chr4:185436665
|
G | A | 1 | a0001c0001t0003g0093 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.534+306G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436665 | ||||||
chr4:185436709
|
C | CAATAATA others(2): Show |
4 | a0001c0001t0001g0035a0001c0001t0001g0141a0001c0001t0001g0201others(1): Show | 4 | HG00323.hp1 HG01071.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+352_534+353ins others(9): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436709 | |||||
chr4:185436709
|
C | CTAATAAT others(3): Show |
1 | a0001c0001t0001g0274 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.534+350_534+351ins others(10): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436709 | ||||||
chr4:185436712
|
A | AAAT | 51 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0032others(48): Show | 57 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.534+384_534+386dup others(3): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | |||||
chr4:185436712
|
A | AAATAAT | 40 | a0001c0001t0001g0020a0001c0001t0001g0091a0001c0001t0001g0092others(37): Show | 42 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.534+381_534+386dup others(6): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | |||||
chr4:185436712
|
A | AAATAATA others(2): Show |
44 | a0001c0001t0001g0029a0001c0001t0001g0088a0001c0001t0001g0130others(41): Show | 53 | HG00438.hp2 HG00733.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.534+378_534+386dup others(9): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | |||||
chr4:185436712
|
A | AAATAATA others(5): Show |
33 | a0001c0001t0001g0027a0001c0001t0001g0097a0001c0001t0001g0116others(30): Show | 35 | HG01071.hp2 HG01074.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.534+375_534+386dup others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | |||||
chr4:185436712
|
A | AAATAATA others(8): Show |
77 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(74): Show | 84 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.534+372_534+386dup others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | |||||
chr4:185436712
|
A | AAATAATA others(11): Show |
4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0278others(1): Show | 4 | HG02080.hp2 HG02486.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+369_534+386dup others(18): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | |||||
chr4:185436712
|
A | AAATAATA others(14): Show |
1 | a0001c0001t0001g0151 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.534+366_534+386dup others(21): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | |||||
chr4:185436712
|
A | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0141a0001c0001t0001g0201others(2): Show | 5 | HG00323.hp1 HG01071.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+353A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436712 | ||||||
chr4:185436712
|
AAAT | A | 18 | a0001c0001t0001g0121a0001c0001t0001g0268a0001c0001t0001g0270others(15): Show | 20 | HG00544.hp1 HG00642.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.534+384_534+386del others(3): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | |||||
chr4:185436746
|
T | A | 2 | a0001c0004t0001g0223a0001c0004t0007g0030 | 3 | HG01884.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.534+387T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436746 | ||||||
chr4:185436747
|
C | T | 2 | a0001c0004t0001g0223a0001c0004t0007g0030 | 3 | HG01884.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.534+388C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436747 | ||||||
chr4:185436749
|
C | A | 3 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0007g0030 | 4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+390C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436749 | ||||||
chr4:185436775
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.534+416A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436775 | ||||||
chr4:185436903
|
C | T | 1 | a0001c0001t0004g0109 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.534+544C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436903 | ||||||
chr4:185436998
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.534+639G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436998 | ||||||
chr4:185437103
|
G | A | 5 | a0002c0002t0001g0040a0002c0002t0001g0061a0002c0002t0001g0078others(2): Show | 5 | HG00639.hp1 HG01106.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+744G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437103 | ||||||
chr4:185437157
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.534+798T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437157 | ||||||
chr4:185437163
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.534+804C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437163 | ||||||
chr4:185437231
|
A | T | 14 | a0002c0002t0001g0002a0002c0002t0001g0010a0002c0002t0001g0013others(11): Show | 19 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.534+872A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437231 | ||||||
chr4:185437307
|
C | T | 1 | a0001c0010t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.534+948C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437307 | ||||||
chr4:185437308
|
G | A | 10 | a0001c0001t0001g0105a0001c0001t0001g0233a0001c0001t0001g0234others(7): Show | 11 | HG00733.hp2 HG01884.hp1 HG03471.hp2 others(8): Show |
intron_variant | MODIFIER | c.534+949G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437308 | ||||||
chr4:185437360
|
A | G | 18 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0233others(15): Show | 18 | HG02698.hp1 HG02738.hp1 HG04184.hp2 others(15): Show |
intron_variant | MODIFIER | c.534+1001A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437360 | ||||||
chr4:185437449
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.534+1090C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437449 | ||||||
chr4:185437481
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.534+1122A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437481 | ||||||
chr4:185437714
|
T | C | 1 | a0001c0010t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.534+1355T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437714 | ||||||
chr4:185437716
|
T | A | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.534+1357T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437716 | ||||||
chr4:185437717
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.534+1358G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437717 | ||||||
chr4:185437976
|
C | T | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.534+1617C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437976 | ||||||
chr4:185437988
|
C | T | 4 | a0001c0001t0001g0105a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | NA18998.hp2 NA19000.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+1629C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437988 | ||||||
chr4:185438003
|
C | CT | 25 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0237others(22): Show | 33 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.534+1653dupT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185438003 | |||||
chr4:185438067
|
T | G | 1 | a0001c0001t0001g0219 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.534+1708T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438067 | ||||||
chr4:185438341
|
A | G | 4 | a0001c0001t0002g0007a0001c0001t0002g0038a0001c0001t0002g0039others(1): Show | 5 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+1982A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438341 | ||||||
chr4:185438353
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.534+1994G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438353 | ||||||
chr4:185438418
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.534+2059C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438418 | ||||||
chr4:185438435
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0270 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.534+2076T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438435 | ||||||
chr4:185438480
|
G | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0155a0001c0001t0001g0279 | 3 | NA18612.hp2 NA18966.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.535-2060G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438480 | ||||||
chr4:185438491
|
T | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0237others(22): Show | 33 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.535-2049T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438491 | ||||||
chr4:185438647
|
G | A | 1 | a0001c0010t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.535-1893G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438647 | ||||||
chr4:185438659
|
A | G | 4 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0001g0224others(1): Show | 5 | HG00733.hp2 HG01884.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.535-1881A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438659 | ||||||
chr4:185438681
|
A | G | 175 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(172): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.535-1859A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438681 | ||||||
chr4:185438703
|
G | T | 54 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0265others(51): Show | 62 | HG00544.hp1 HG00642.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.535-1837G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438703 | ||||||
chr4:185438732
|
C | T | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.535-1808C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438732 | ||||||
chr4:185438736
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.535-1804T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438736 | ||||||
chr4:185438739
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0176 | 2 | HG00597.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.535-1801A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438739 | ||||||
chr4:185438741
|
T | G | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.535-1799T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438741 | ||||||
chr4:185438807
|
C | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0058 | 3 | HG02922.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.535-1733C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438807 | ||||||
chr4:185438837
|
G | A | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.535-1703G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438837 | ||||||
chr4:185438966
|
T | G | 1 | a0001c0001t0001g0156 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.535-1574T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438966 | ||||||
chr4:185439005
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.535-1535C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185439005 | ||||||
chr4:185439012
|
G | C | 32 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0268others(29): Show | 36 | HG00544.hp1 HG01109.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.535-1528G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185439012 | ||||||
chr4:185439221
|
G | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0268others(15): Show | 21 | HG00544.hp1 HG02040.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.535-1319G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185439221 | ||||||
chr4:185439520
|
T | C | 174 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.535-1020T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185439520 | ||||||
chr4:185439724
|
A | T | 1 | a0001c0010t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.535-816A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185439724 | ||||||
chr4:185439727
|
CAT | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0314 | 4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-812_535-811del others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185439727 | ||||||
chr4:185439813
|
A | ACT | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.535-725_535-724dup others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185439813 | |||||
chr4:185439945
|
CAT | C | 19 | a0002c0002t0001g0002a0002c0002t0001g0010a0002c0002t0001g0013others(16): Show | 24 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.535-588_535-587del others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185439945 | |||||
chr4:185439989
|
TATATACA others(1): Show |
T | 2 | a0001c0001t0001g0012a0001c0001t0002g0075 | 3 | HG02055.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.535-546_535-539del others(8): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185439989 | |||||
chr4:185440006
|
TATAG | T | 7 | a0003c0003t0001g0016a0003c0003t0001g0043a0003c0003t0001g0048others(4): Show | 8 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.535-530_535-527del others(4): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185440006 | |||||
chr4:185440010
|
G | GATAC | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.535-527_535-526ins others(4): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185440010 | |||||
chr4:185440243
|
C | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0268others(15): Show | 21 | HG00544.hp1 HG02040.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.535-297C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185440243 | ||||||
chr4:185440720
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02145.hp2 | splice_donor_variant&intron_variant | HIGH | c.714+1G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185440720 | ||||||
chr4:185440722
|
A | G | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
splice_region_variant&intron_variant | LOW | c.714+3A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185440722 | ||||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
5 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG01123.hp1 HG01192.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(295): Show |
17 | a0001c0001t0001g0121a0001c0001t0001g0270a0001c0001t0003g0230others(14): Show | 19 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(300): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(295): Show |
1 | a0001c0001t0004g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(300): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
9 | a0002c0002t0001g0002a0002c0002t0001g0040a0002c0002t0001g0061others(6): Show | 11 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(295): Show |
33 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0268others(30): Show | 39 | HG00544.hp1 HG01109.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(300): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
1 | a0001c0001t0002g0263 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
3 | a0001c0001t0006g0122a0001c0001t0006g0271a0001c0001t0006g0295 | 3 | HG01099.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(295): Show |
1 | a0006c0011t0001g0305 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.714+51_714+52insGC others(300): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
1 | a0001c0001t0002g0313 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0278 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
3 | a0001c0001t0001g0118a0001c0001t0001g0155a0001c0001t0001g0279 | 3 | NA18612.hp2 NA18966.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
1 | a0005c0008t0001g0134 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
145 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(142): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0206 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0209 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0142 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0025 | 2 | HG00621.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(295): Show |
24 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0105others(21): Show | 27 | HG00408.hp1 HG00544.hp2 HG02523.hp2 others(24): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(300): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
5 | a0001c0001t0001g0092a0001c0001t0001g0128a0001c0001t0001g0131others(2): Show | 5 | NA18966.hp2 NA19007.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
4 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0001g0150others(1): Show | 4 | HG01081.hp1 HG02055.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
1 | a0002c0002t0001g0014 | 2 | HG03831.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
9 | a0002c0002t0001g0010a0002c0002t0001g0013a0002c0002t0001g0047others(6): Show | 11 | HG01081.hp2 HG01255.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0269 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440758
|
T | TAAAGAAA others(295): Show |
1 | a0001c0001t0002g0267 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(300): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | |||||
chr4:185440765
|
A | G | 1 | a0001c0010t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.714+46A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185440765 | ||||||
chr4:185440818
|
T | C | 1 | a0003c0003t0001g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.714+99T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185440818 | ||||||
chr4:185440822
|
T | C | 315 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(312): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.714+103T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185440822 | ||||||
chr4:185440956
|
AT | A | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.714+249delT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440956 | |||||
chr4:185441079
|
T | C | 3 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0007g0030 | 4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+360T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441079 | ||||||
chr4:185441311
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.714+592T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441311 | ||||||
chr4:185441333
|
T | C | 1 | a0002c0002t0001g0078 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+614T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441333 | ||||||
chr4:185441340
|
G | A | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.714+621G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441340 | ||||||
chr4:185441380
|
ATATCT | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0268others(31): Show | 38 | HG00544.hp1 HG00733.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.714+665_714+669del others(5): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185441380 | |||||
chr4:185441419
|
CTTGTT | C | 23 | a0001c0001t0001g0025a0001c0001t0001g0124a0001c0001t0001g0125others(20): Show | 24 | HG00423.hp1 HG00621.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.714+706_714+710del others(5): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185441419 | |||||
chr4:185441510
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.714+791A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441510 | ||||||
chr4:185441514
|
A | C | 1 | a0001c0001t0001g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.714+795A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441514 | ||||||
chr4:185441565
|
G | A | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.714+846G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441565 | ||||||
chr4:185441609
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0197a0001c0001t0001g0207 | 3 | HG02602.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.714+890C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441609 | ||||||
chr4:185442418
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.714+1699T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442418 | ||||||
chr4:185442423
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.714+1704T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442423 | ||||||
chr4:185442545
|
C | T | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.714+1826C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442545 | ||||||
chr4:185442560
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.714+1841C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442560 | ||||||
chr4:185442738
|
C | A | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.714+2019C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442738 | ||||||
chr4:185442864
|
A | G | 54 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0265others(51): Show | 62 | HG00544.hp1 HG00642.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.715-2100A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442864 | ||||||
chr4:185442946
|
G | A | 7 | a0001c0001t0003g0119a0001c0001t0003g0126a0001c0001t0003g0212others(4): Show | 7 | HG01123.hp2 HG01255.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-2018G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442946 | ||||||
chr4:185443017
|
A | G | 23 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0105others(20): Show | 26 | HG00408.hp1 HG00544.hp2 HG02523.hp2 others(23): Show |
intron_variant | MODIFIER | c.715-1947A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443017 | ||||||
chr4:185443138
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.715-1826G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443138 | ||||||
chr4:185443192
|
A | G | 271 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(268): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.715-1772A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443192 | ||||||
chr4:185443320
|
G | GTATATAT others(3): Show |
1 | a0001c0010t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.715-1630_715-1621d others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | |||||
chr4:185443320
|
G | GTATATAT others(5): Show |
4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0202others(1): Show | 4 | HG02155.hp1 NA19007.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1632_715-1621d others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | |||||
chr4:185443320
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0004g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.715-1638_715-1621d others(20): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | |||||
chr4:185443320
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0004g0109 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.715-1640_715-1621d others(22): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | |||||
chr4:185443320
|
G | GTATATAT others(17): Show |
1 | a0001c0001t0004g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(26): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | |||||
chr4:185443320
|
GTATA | G | 10 | a0001c0001t0001g0025a0001c0001t0001g0124a0001c0001t0001g0125others(7): Show | 11 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.715-1624_715-1621d others(6): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | |||||
chr4:185443320
|
GTATATA | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0278a0001c0001t0001g0285others(1): Show | 4 | HG02132.hp2 NA18612.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-1626_715-1621d others(8): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | |||||
chr4:185443322
|
A | G | 6 | a0002c0002t0001g0040a0002c0002t0001g0061a0002c0002t0001g0078others(3): Show | 6 | HG00639.hp1 HG01106.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-1642A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443322 | ||||||
chr4:185443332
|
A | T | 1 | a0001c0001t0001g0251 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.715-1632A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443332 | ||||||
chr4:185443333
|
TATATA | T | 8 | a0001c0001t0001g0277a0001c0001t0001g0281a0001c0001t0001g0282others(5): Show | 8 | HG01123.hp1 HG01192.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-1630_715-1626d others(7): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443333 | ||||||
chr4:185443334
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0240 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.715-1629_715-1628i others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443334 | |||||
chr4:185443334
|
A | T | 1 | a0001c0001t0001g0251 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.715-1630A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443334 | ||||||
chr4:185443336
|
A | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0251 | 2 | HG02523.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.715-1628A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443336 | ||||||
chr4:185443338
|
A | T | 8 | a0001c0001t0001g0147a0001c0001t0001g0183a0001c0001t0001g0240others(5): Show | 8 | HG00621.hp2 HG00735.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-1626A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443338 | ||||||
chr4:185443338
|
ATATATT | A | 11 | a0002c0002t0001g0002a0002c0002t0001g0010a0002c0002t0001g0013others(8): Show | 16 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.715-1624_715-1619d others(8): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443338 | |||||
chr4:185443340
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0250 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.715-1623_715-1622i others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443340 | |||||
chr4:185443340
|
A | T | 26 | a0001c0001t0001g0025a0001c0001t0001g0124a0001c0001t0001g0125others(23): Show | 27 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.715-1624A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443340 | ||||||
chr4:185443340
|
ATATTTT | A | 6 | a0002c0002t0001g0040a0002c0002t0001g0061a0002c0002t0001g0078others(3): Show | 6 | HG00639.hp1 HG01106.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-1622_715-1617d others(8): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443340 | |||||
chr4:185443342
|
A | ATATATAT others(4): Show |
6 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG01358.hp2 HG02129.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0189 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0004g0232 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(27): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0004g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(31): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0004g0222 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(35): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(36): Show |
1 | a0001c0001t0001g0241 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(45): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(35): Show |
1 | a0001c0001t0001g0244 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(44): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0245 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(46): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0004g0107 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(31): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0246 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(40): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(42): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0004g0018 | 2 | HG01975.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(27): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0004g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(29): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0242 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(37): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0248 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(38): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(33): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0254 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(36): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0253 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(38): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(14): Show |
1 | a0001c0004t0001g0224 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(23): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0236 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(24): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0252 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(36): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(28): Show |
2 | a0001c0001t0001g0105a0001c0001t0001g0233 | 2 | NA18998.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(37): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0003g0230a0001c0001t0004g0031 | 3 | HG02572.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(20): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0160 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(22): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0234 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(37): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0298 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(19): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0102 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(17): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0021a0001c0001t0001g0142a0001c0001t0001g0190 | 4 | HG00408.hp2 HG00741.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(18): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0191a0001c0001t0001g0274 | 2 | NA18999.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0291a0001c0001t0003g0212 | 2 | HG01975.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(7): Show |
9 | a0001c0001t0001g0035a0001c0001t0001g0138a0001c0001t0001g0141others(6): Show | 9 | HG00099.hp2 HG01099.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(16): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0161a0001c0001t0001g0192 | 2 | HG00738.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(17): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0103a0001c0001t0006g0295 | 2 | HG01099.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(18): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0095a0001c0001t0001g0153a0001c0001t0006g0122others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(19): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0237 | 4 | NA18952.hp1 NA18959.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(28): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(29): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0133 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(4): Show |
12 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0139others(9): Show | 12 | HG00639.hp2 HG01071.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(5): Show |
37 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0027others(34): Show | 43 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0148a0001c0001t0001g0289 | 2 | NA19056.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(7): Show |
8 | a0001c0001t0001g0100a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01258.hp2 HG01433.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(16): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0101a0001c0001t0001g0130 | 2 | HG01081.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(17): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(9): Show |
1 | a0001c0004t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(18): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0032 | 2 | NA18955.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(28): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(3): Show |
5 | a0001c0001t0001g0140a0001c0001t0002g0264a0001c0001t0002g0267others(2): Show | 5 | HG00438.hp1 HG01071.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(4): Show |
9 | a0001c0001t0001g0115a0001c0001t0001g0123a0001c0001t0001g0143others(6): Show | 9 | HG01256.hp1 HG01496.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(5): Show |
8 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0088others(5): Show | 11 | HG00423.hp2 HG02280.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(6): Show |
4 | a0001c0001t0001g0137a0001c0001t0001g0144a0001c0001t0001g0167others(1): Show | 4 | HG02738.hp2 HG04184.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(7): Show |
5 | a0001c0001t0001g0118a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01074.hp2 HG01516.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(16): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(8): Show |
1 | a0001c0004t0001g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(17): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(9): Show |
1 | a0001c0004t0007g0030 | 2 | HG01884.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(18): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0239 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(24): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATTT others(1): Show |
8 | a0001c0001t0001g0268a0001c0001t0001g0318a0001c0001t0002g0036others(5): Show | 8 | HG00544.hp1 HG03654.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(10): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATTT others(3): Show |
1 | a0001c0001t0003g0170 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATTT others(4): Show |
5 | a0001c0001t0001g0151a0001c0001t0001g0171a0001c0001t0001g0180others(2): Show | 5 | HG00735.hp1 HG04228.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATTT others(5): Show |
6 | a0001c0001t0001g0024a0001c0001t0001g0152a0001c0001t0001g0173others(3): Show | 7 | HG00738.hp2 HG02040.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATATTT others(6): Show |
1 | a0001c0001t0001g0175 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATGTAT others(54): Show |
1 | a0001c0001t0001g0249 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(63): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATTTTT others(3): Show |
1 | a0001c0001t0001g0290 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATTTTT others(4): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0270 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATTTTT others(5): Show |
4 | a0001c0001t0001g0155a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | NA18612.hp2 NA18966.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATATTTTT others(6): Show |
1 | a0001c0001t0001g0096 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATTTTT | 6 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(3): Show | 7 | HG01884.hp2 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-1607_715-1603d others(7): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | ATTTTTTT others(3): Show |
1 | a0006c0011t0001g0305 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.715-1612_715-1603d others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
A | T | 31 | a0001c0001t0001g0025a0001c0001t0001g0124a0001c0001t0001g0125others(28): Show | 32 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.715-1622A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443342 | ||||||
chr4:185443342
|
AT | A | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(17): Show | 24 | HG00140.hp2 HG00741.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.715-1603delT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443342
|
ATT | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0051others(3): Show | 8 | HG02145.hp1 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-1604_715-1603d others(4): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | |||||
chr4:185443343
|
T | TA | 5 | a0001c0001t0001g0058a0001c0001t0001g0068a0001c0001t0001g0086others(2): Show | 5 | HG01192.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(3): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443343 | ||||||
chr4:185443343
|
T | TATATATA others(14): Show |
1 | a0001c0001t0004g0111 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(23): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443343 | ||||||
chr4:185443343
|
T | TATATATA others(16): Show |
3 | a0001c0001t0004g0106a0001c0001t0004g0110a0001c0001t0004g0228 | 3 | HG00642.hp1 HG03209.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(25): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443343 | ||||||
chr4:185443343
|
T | TATATATA others(18): Show |
1 | a0001c0001t0004g0227 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(27): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443343 | ||||||
chr4:185443344
|
T | A | 5 | a0001c0001t0001g0055a0001c0001t0004g0229a0003c0003t0001g0043others(2): Show | 5 | HG02257.hp1 HG02976.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-1620T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443344 | ||||||
chr4:185443345
|
T | A | 7 | a0001c0001t0001g0058a0001c0001t0001g0067a0001c0001t0001g0068others(4): Show | 7 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-1619T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443345 | ||||||
chr4:185443346
|
T | A | 1 | a0001c0001t0002g0006 | 3 | HG02145.hp1 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.715-1618T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443346 | ||||||
chr4:185443347
|
T | A | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.715-1617T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443347 | ||||||
chr4:185443374
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.715-1590T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443374 | ||||||
chr4:185443451
|
C | T | 16 | a0001c0001t0003g0230a0001c0001t0004g0018a0001c0001t0004g0031others(13): Show | 18 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.715-1513C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443451 | ||||||
chr4:185443589
|
T | C | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.715-1375T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443589 | ||||||
chr4:185443593
|
C | T | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.715-1371C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443593 | ||||||
chr4:185443597
|
A | C | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.715-1367A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443597 | ||||||
chr4:185443598
|
T | C | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.715-1366T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443598 | ||||||
chr4:185443601
|
G | A | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.715-1363G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443601 | ||||||
chr4:185443676
|
G | A | 175 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(172): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.715-1288G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443676 | ||||||
chr4:185443739
|
T | C | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.715-1225T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443739 | ||||||
chr4:185443776
|
A | G | 1 | a0001c0001t0003g0093 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.715-1188A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443776 | ||||||
chr4:185443913
|
A | G | 275 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(272): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.715-1051A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443913 | ||||||
chr4:185443921
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.715-1010_715-1000d others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0071a0001c0001t0001g0087 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.715-1016_715-1000d others(19): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.715-1017_715-1000d others(20): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTT | C | 6 | a0001c0001t0001g0046a0001c0001t0001g0057a0001c0001t0001g0073others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-1004_715-1000d others(7): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.715-1009_715-1000d others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.715-1010_715-1000d others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0001g0224 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.715-1011_715-1000d others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0069a0001c0010t0001g0045a0003c0003t0001g0043others(1): Show | 4 | HG00741.hp1 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1012_715-1000d others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(7): Show |
C | 26 | a0001c0001t0001g0132a0001c0001t0001g0140a0001c0001t0001g0141others(23): Show | 27 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.715-1013_715-1000d others(16): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(8): Show |
C | 143 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(140): Show | 154 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.715-1014_715-1000d others(17): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(9): Show |
C | 8 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0143others(5): Show | 8 | HG00099.hp2 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-1015_715-1000d others(18): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(10): Show |
C | 19 | a0001c0001t0001g0270a0001c0001t0003g0230a0001c0001t0004g0018others(16): Show | 21 | HG00642.hp1 HG01433.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.715-1016_715-1000d others(19): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(11): Show |
C | 24 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0032others(21): Show | 33 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.715-1017_715-1000d others(20): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(12): Show |
C | 5 | a0001c0001t0001g0237a0001c0001t0002g0006a0001c0001t0002g0258others(2): Show | 7 | HG01109.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-1018_715-1000d others(21): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(13): Show |
C | 32 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0268others(29): Show | 37 | HG00544.hp1 HG01884.hp2 HG02040.hp1 others(34): Show |
intron_variant | MODIFIER | c.715-1019_715-1000d others(22): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0001g0318 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.715-1020_715-1000d others(23): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(15): Show |
C | 4 | a0001c0001t0001g0247a0001c0004t0001g0104a0001c0004t0001g0223others(1): Show | 5 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-1021_715-1000d others(24): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(16): Show |
C | 14 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0233others(11): Show | 14 | HG02698.hp1 HG02738.hp1 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.715-1022_715-1000d others(25): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(17): Show |
C | 2 | a0001c0001t0001g0248a0001c0001t0001g0252 | 2 | NA18973.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.715-1023_715-1000d others(26): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443921
|
CTTTTTTT others(18): Show |
C | 3 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0059 | 4 | HG01243.hp1 NA18990.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-1024_715-1000d others(27): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | |||||
chr4:185443925
|
T | C | 2 | a0003c0003t0001g0048a0003c0003t0002g0060 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.715-1039T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443925 | ||||||
chr4:185443927
|
T | C | 1 | a0003c0003t0002g0049 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.715-1037T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443927 | ||||||
chr4:185443928
|
T | C | 1 | a0003c0003t0002g0076 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.715-1036T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443928 | ||||||
chr4:185443944
|
T | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0314 | 4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1020T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443944 | ||||||
chr4:185443978
|
G | T | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.715-986G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443978 | ||||||
chr4:185443985
|
T | C | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(274): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.715-979T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443985 | ||||||
chr4:185443995
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.715-969G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443995 | ||||||
chr4:185444039
|
C | T | 2 | a0001c0004t0001g0224a0001c0010t0001g0045 | 2 | HG00733.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.715-925C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444039 | ||||||
chr4:185444047
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0058a0001c0001t0004g0106 | 4 | HG02922.hp1 HG03453.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-917G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444047 | ||||||
chr4:185444110
|
C | T | 1 | a0001c0001t0004g0109 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.715-854C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444110 | ||||||
chr4:185444143
|
C | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0085 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.715-821C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444143 | ||||||
chr4:185444155
|
T | G | 2 | a0002c0002t0001g0065a0002c0002t0001g0316 | 2 | HG01081.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.715-809T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444155 | ||||||
chr4:185444205
|
G | A | 6 | a0001c0001t0001g0105a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | NA18954.hp1 NA18998.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-759G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444205 | ||||||
chr4:185444340
|
C | G | 1 | a0001c0001t0001g0244 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.715-624C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444340 | ||||||
chr4:185444454
|
T | C | 3 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0007g0030 | 4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-510T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444454 | ||||||
chr4:185444495
|
A | C | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.715-469A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444495 | ||||||
chr4:185444510
|
T | A | 1 | a0001c0004t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.715-454T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444510 | ||||||
chr4:185444569
|
GACTGGCA others(8): Show |
G | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.715-391_715-377del others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185444569 | |||||
chr4:185444688
|
A | G | 315 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(312): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.715-276A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444688 | ||||||
chr4:185444844
|
G | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0268others(33): Show | 42 | HG00544.hp1 HG01109.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.715-120G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444844 | ||||||
chr4:185444871
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.715-93C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444871 | ||||||
chr4:185444947
|
C | T | 14 | a0002c0002t0001g0002a0002c0002t0001g0010a0002c0002t0001g0013others(11): Show | 19 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.715-17C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444947 | ||||||
chr4:185445161
|
T | C | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.881+31T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445161 | ||||||
chr4:185445199
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.881+69A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445199 | ||||||
chr4:185445228
|
T | C | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.881+98T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445228 | ||||||
chr4:185445264
|
T | G | 3 | a0001c0001t0001g0091a0001c0001t0001g0197a0001c0001t0001g0207 | 3 | HG02602.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.881+134T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445264 | ||||||
chr4:185445461
|
G | T | 36 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0268others(33): Show | 42 | HG00544.hp1 HG01109.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.881+331G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445461 | ||||||
chr4:185445517
|
A | G | 17 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0233others(14): Show | 17 | HG02698.hp1 HG02738.hp1 HG04199.hp1 others(14): Show |
intron_variant | MODIFIER | c.881+387A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445517 | ||||||
chr4:185445655
|
C | T | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.881+525C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445655 | ||||||
chr4:185445864
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.881+734G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445864 | ||||||
chr4:185445878
|
A | T | 3 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0007g0030 | 4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+748A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445878 | ||||||
chr4:185446040
|
C | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0298 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.881+910C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446040 | ||||||
chr4:185446065
|
T | G | 1 | a0001c0001t0003g0170 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.881+935T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446065 | ||||||
chr4:185446075
|
A | G | 3 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0007g0030 | 4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+945A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446075 | ||||||
chr4:185446121
|
G | A | 2 | a0003c0003t0001g0043a0003c0003t0001g0053 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.881+991G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446121 | ||||||
chr4:185446297
|
A | T | 1 | a0002c0002t0001g0050 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.881+1167A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446297 | ||||||
chr4:185446358
|
A | G | 1 | a0002c0002t0001g0079 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.881+1228A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446358 | ||||||
chr4:185446588
|
C | G | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.881+1458C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446588 | ||||||
chr4:185446711
|
A | G | 26 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0237others(23): Show | 34 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.881+1581A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446711 | ||||||
chr4:185446721
|
CACA | C | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.881+1595_881+1597d others(5): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 185446721 | |||||
chr4:185446932
|
C | G | 1 | a0001c0001t0001g0300 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.881+1802C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446932 | ||||||
chr4:185446956
|
A | G | 198 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(195): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.881+1826A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446956 | ||||||
chr4:185447136
|
G | A | 17 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0233others(14): Show | 17 | HG02698.hp1 HG02738.hp1 HG04199.hp1 others(14): Show |
intron_variant | MODIFIER | c.881+2006G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447136 | ||||||
chr4:185447186
|
CT | C | 192 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(189): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.881+2069delT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 185447186 | |||||
chr4:185447187
|
T | C | 18 | a0001c0001t0001g0121a0001c0001t0001g0270a0001c0001t0003g0230others(15): Show | 20 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.881+2057T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447187 | ||||||
chr4:185447212
|
C | G | 1 | a0001c0001t0001g0282 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.881+2082C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447212 | ||||||
chr4:185447213
|
A | G | 278 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(275): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.881+2083A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447213 | ||||||
chr4:185447233
|
A | G | 6 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0259others(3): Show | 6 | HG00639.hp1 HG01106.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+2103A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447233 | ||||||
chr4:185447268
|
A | G | 6 | a0001c0001t0001g0154a0001c0001t0001g0180a0001c0001t0001g0291others(3): Show | 6 | HG00423.hp1 HG00639.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+2138A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447268 | ||||||
chr4:185447272
|
G | C | 6 | a0001c0001t0001g0154a0001c0001t0001g0180a0001c0001t0001g0291others(3): Show | 6 | HG00423.hp1 HG00639.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+2142G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447272 | ||||||
chr4:185447331
|
G | A | 2 | a0001c0001t0006g0122a0001c0001t0006g0271 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.881+2201G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447331 | ||||||
chr4:185447338
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.881+2208C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447338 | ||||||
chr4:185447381
|
T | C | 273 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(270): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.882-2215T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447381 | ||||||
chr4:185447388
|
G | T | 1 | a0001c0001t0001g0287 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.882-2208G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447388 | ||||||
chr4:185447393
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0298 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.882-2203G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447393 | ||||||
chr4:185447398
|
A | T | 3 | a0001c0001t0001g0291a0001c0001t0001g0298a0001c0001t0003g0157 | 3 | HG01981.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.882-2198A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447398 | ||||||
chr4:185447401
|
T | C | 3 | a0001c0001t0001g0291a0001c0001t0001g0298a0001c0001t0003g0157 | 3 | HG01981.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.882-2195T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447401 | ||||||
chr4:185447416
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.882-2180G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447416 | ||||||
chr4:185447539
|
C | T | 3 | a0001c0001t0001g0072a0002c0002t0001g0064a0002c0002t0001g0082 | 3 | HG03195.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.882-2057C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447539 | ||||||
chr4:185447655
|
T | TG | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(40): Show | 51 | HG00140.hp2 HG00741.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.882-1940dupG | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 185447655 | |||||
chr4:185447964
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0265a0001c0001t0001g0310 | 5 | HG02074.hp2 HG02083.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.882-1632A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447964 | ||||||
chr4:185448015
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0298 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.882-1581G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448015 | ||||||
chr4:185448024
|
T | G | 3 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0007g0030 | 4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-1572T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448024 | ||||||
chr4:185448089
|
C | T | 1 | a0002c0002t0001g0050 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.882-1507C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448089 | ||||||
chr4:185448227
|
G | C | 1 | a0001c0010t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882-1369G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448227 | ||||||
chr4:185448255
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.882-1341A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448255 | ||||||
chr4:185448263
|
C | T | 1 | a0001c0001t0003g0212 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.882-1333C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448263 | ||||||
chr4:185448426
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.882-1170A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448426 | ||||||
chr4:185448544
|
C | G | 1 | a0002c0002t0001g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.882-1052C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448544 | ||||||
chr4:185448691
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.882-905C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448691 | ||||||
chr4:185448864
|
G | GCATAT | 44 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(41): Show | 52 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.882-732_882-731ins others(5): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448864 | ||||||
chr4:185448866
|
A | T | 44 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(41): Show | 52 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.882-730A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448866 | ||||||
chr4:185448867
|
C | G | 44 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(41): Show | 52 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.882-729C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448867 | ||||||
chr4:185448955
|
G | A | 3 | a0001c0004t0001g0104a0001c0004t0001g0223a0001c0004t0007g0030 | 4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-641G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448955 | ||||||
chr4:185448962
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.882-634C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448962 | ||||||
chr4:185448962
|
CTT | C | 44 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(41): Show | 52 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.882-632_882-631del others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 185448962 | |||||
chr4:185449210
|
T | C | 121 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0035others(118): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.882-386T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185449210 | ||||||
chr4:185449413
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.882-183T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185449413 | ||||||
chr4:185449522
|
T | TA | 177 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(174): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.882-62dupA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 185449522 | |||||
chr4:185449573
|
G | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0051others(11): Show | 17 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.882-23G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185449573 |