geneid | 2638 |
---|---|
ensemblid | ENSG00000145321.13 |
hgncid | 4187 |
symbol | GC |
name | GC vitamin D binding protein |
refseq_nuc | NM_000583.4 |
refseq_prot | NP_000574.2 |
ensembl_nuc | ENST00000273951.13 |
ensembl_prot | ENSP00000273951.8 |
mane_status | MANE Select |
chr | chr4 |
start | 71741697 |
end | 71784079 |
strand | - |
ver | v1.2 |
region | chr4:71741697-71784079 |
region5000 | chr4:71736697-71789079 |
regionname0 | GC_chr4_71741697_71784079 |
regionname5000 | GC_chr4_71736697_71789079 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 474 | 191 | 75 | 17 | 91 | 0 | 8 | 74 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0002 | 0/1 | 474 | 101 | 10 | 21 | 48 | 7 | 14 | 34 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0003 | 0/0 | 474 | 81 | 9 | 14 | 47 | 1 | 10 | 39 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0004 | 0/0 | 474 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0005 | 0/0 | 474 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0006 | 0/0 | 474 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0007 | 1/0 | 474 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0008 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0009 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0010 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0011 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1425 | 121 | 35 | 12 | 66 | 0 | 8 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0002 | 0/1 | 1425 | 99 | 10 | 20 | 48 | 6 | 14 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0003 | 0/0 | 1425 | 81 | 9 | 14 | 47 | 1 | 10 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0004 | 0/0 | 1425 | 47 | 19 | 4 | 24 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0005 | 0/0 | 1425 | 14 | 13 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0006 | 0/0 | 1425 | 4 | 0 | 0 | 4 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0007 | 0/0 | 1425 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0008 | 0/0 | 1425 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0009 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0010 | 0/0 | 1425 | 2 | 0 | 1 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0011 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0012 | 1/0 | 1425 | 2 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0013 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0014 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0015 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0016 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0017 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0018 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0019 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
c0020 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 261 | 277 | 72 | 41 | 129 | 8 | 25 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
t0002 | 0/0 | 261 | 106 | 21 | 11 | 67 | 0 | 7 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
t0003 | 0/0 | 261 | 5 | 5 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0007 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0012 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1425 | 121 | 35 | 12 | 66 | 0 | 8 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0004 | 0/0 | 1425 | 47 | 19 | 4 | 24 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0005 | 0/0 | 1425 | 14 | 13 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0008 | 0/0 | 1425 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0009 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0011 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0015 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0020 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0002c0002 | 0/1 | 1425 | 99 | 10 | 20 | 48 | 6 | 14 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0002c0010 | 0/0 | 1425 | 2 | 0 | 1 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0003c0003 | 0/0 | 1425 | 81 | 9 | 14 | 47 | 1 | 10 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0004c0006 | 0/0 | 1425 | 4 | 0 | 0 | 4 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0005c0007 | 0/0 | 1425 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0006c0013 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0006c0014 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0007c0012 | 1/0 | 1425 | 2 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0008c0017 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0009c0016 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0010c0018 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0011c0019 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1685 | 38 | 21 | 2 | 13 | 0 | 2 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0001t0002 | 0/0 | 1685 | 83 | 14 | 10 | 53 | 0 | 6 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0004t0001 | 0/0 | 1685 | 46 | 18 | 4 | 24 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0004t0002 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0005t0001 | 0/0 | 1685 | 12 | 11 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0005t0002 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0005t0003 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0008t0001 | 0/0 | 1685 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0009t0001 | 0/0 | 1685 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0011t0002 | 0/0 | 1685 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0015t0001 | 0/0 | 1685 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0001c0020t0001 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0002c0002t0001 | 0/1 | 1685 | 87 | 8 | 19 | 39 | 6 | 14 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0002c0002t0002 | 0/0 | 1685 | 12 | 2 | 1 | 9 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0002c0010t0001 | 0/0 | 1685 | 2 | 0 | 1 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0003c0003t0001 | 0/0 | 1685 | 73 | 4 | 14 | 45 | 1 | 9 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0003c0003t0002 | 0/0 | 1685 | 4 | 1 | 0 | 2 | 0 | 1 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0003c0003t0003 | 0/0 | 1685 | 4 | 4 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0004c0006t0001 | 0/0 | 1685 | 4 | 0 | 0 | 4 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0005c0007t0001 | 0/0 | 1685 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0006c0013t0002 | 0/0 | 1685 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0006c0014t0002 | 0/0 | 1685 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0007c0012t0001 | 1/0 | 1685 | 2 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0008c0017t0001 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0009c0016t0001 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0010c0018t0002 | 0/0 | 1685 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
a0011c0019t0001 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | copy fasta | chr4 | 71736697 | 71789079 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0004t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0005t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0005t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0005t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0005t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0005t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0005t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0005t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0005t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0005t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0008t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0008t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0009t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0009t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0011t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0015t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0001c0020t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0012 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0010t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0002c0010t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0003c0003t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0004c0006t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0004c0006t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0004c0006t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0004c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0005c0007t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0005c0007t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0006c0013t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0006c0014t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0007c0012t0001g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0007c0012t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0008c0017t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0009c0016t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0010c0018t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
a0011c0019t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0003 | c0003 | t0001 | g0098 | EUR | GBR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00140 | hp2 | a0002 | c0010 | t0001 | g0151 | EUR | GBR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0237 | EUR | FIN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0175 | EUR | FIN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00408 | hp2 | a0005 | c0007 | t0001 | g0028 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00438 | hp1 | a0003 | c0003 | t0002 | g0292 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00438 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00544 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00558 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00558 | hp2 | a0001 | c0004 | t0001 | g0223 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0326 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00609 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0297 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00639 | hp1 | a0003 | c0003 | t0001 | g0077 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00642 | hp1 | a0003 | c0003 | t0001 | g0037 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG00741 | hp2 | a0003 | c0003 | t0001 | g0038 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01071 | hp2 | a0003 | c0003 | t0001 | g0072 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01109 | hp1 | a0003 | c0003 | t0001 | g0049 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01243 | hp1 | a0001 | c0005 | t0001 | g0125 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01243 | hp2 | a0001 | c0004 | t0001 | g0109 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0323 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01255 | hp2 | a0003 | c0003 | t0001 | g0010 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01258 | hp1 | a0002 | c0010 | t0001 | g0152 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01358 | hp2 | a0003 | c0003 | t0001 | g0099 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01361 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01496 | hp1 | a0003 | c0003 | t0001 | g0092 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0123 | EUR | IBS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0168 | EUR | IBS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0140 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01884 | hp2 | a0001 | c0008 | t0001 | g0105 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01928 | hp1 | a0003 | c0003 | t0001 | g0103 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01934 | hp2 | a0003 | c0003 | t0001 | g0153 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01943 | hp2 | a0003 | c0003 | t0001 | g0174 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01978 | hp1 | a0001 | c0004 | t0001 | g0216 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0185 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01981 | hp2 | a0003 | c0003 | t0001 | g0075 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02055 | hp1 | a0003 | c0003 | t0002 | g0285 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02074 | hp2 | a0003 | c0003 | t0001 | g0081 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02083 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02135 | hp1 | a0001 | c0004 | t0001 | g0214 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02145 | hp2 | a0001 | c0004 | t0001 | g0227 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02148 | hp2 | a0003 | c0003 | t0001 | g0076 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | CDX | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | CDX | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02165 | hp2 | a0003 | c0003 | t0001 | g0085 | EAS | CDX | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02257 | hp1 | a0003 | c0003 | t0001 | g0039 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02258 | hp2 | a0003 | c0003 | t0003 | g0048 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02273 | hp1 | a0001 | c0004 | t0001 | g0003 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02280 | hp1 | a0001 | c0004 | t0001 | g0235 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02280 | hp2 | a0001 | c0009 | t0001 | g0193 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0124 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02451 | hp2 | a0001 | c0005 | t0001 | g0014 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02572 | hp1 | a0001 | c0004 | t0001 | g0229 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02572 | hp2 | a0001 | c0005 | t0001 | g0127 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02615 | hp2 | a0003 | c0003 | t0003 | g0054 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0173 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02647 | hp1 | a0003 | c0003 | t0003 | g0114 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02647 | hp2 | a0009 | c0016 | t0001 | g0196 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02717 | hp1 | a0001 | c0008 | t0001 | g0018 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02717 | hp2 | a0001 | c0004 | t0001 | g0228 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02723 | hp1 | a0003 | c0003 | t0001 | g0240 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02723 | hp2 | a0001 | c0004 | t0001 | g0111 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02809 | hp2 | a0001 | c0005 | t0001 | g0142 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02818 | hp2 | a0001 | c0011 | t0002 | g0032 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02886 | hp2 | a0001 | c0004 | t0001 | g0019 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02896 | hp1 | a0001 | c0004 | t0001 | g0212 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02897 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02897 | hp2 | a0001 | c0004 | t0001 | g0211 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02970 | hp1 | a0001 | c0008 | t0001 | g0018 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02970 | hp2 | a0001 | c0005 | t0001 | g0014 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0252 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02976 | hp2 | a0001 | c0009 | t0001 | g0192 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0171 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0108 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03098 | hp1 | a0011 | c0019 | t0001 | g0116 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03098 | hp2 | a0001 | c0005 | t0003 | g0129 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03130 | hp1 | a0003 | c0003 | t0001 | g0058 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03195 | hp2 | a0001 | c0005 | t0001 | g0014 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03209 | hp2 | a0001 | c0011 | t0002 | g0032 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03453 | hp1 | a0001 | c0005 | t0001 | g0130 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03486 | hp1 | a0001 | c0005 | t0001 | g0021 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03486 | hp2 | a0001 | c0004 | t0001 | g0226 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0107 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03490 | hp2 | a0003 | c0003 | t0001 | g0071 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03516 | hp2 | a0001 | c0004 | t0001 | g0110 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03540 | hp1 | a0001 | c0004 | t0001 | g0221 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03579 | hp1 | a0001 | c0004 | t0001 | g0234 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03579 | hp2 | a0001 | c0005 | t0001 | g0128 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03654 | hp2 | a0003 | c0003 | t0001 | g0100 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0012 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03669 | hp2 | a0003 | c0003 | t0002 | g0288 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | STU | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03688 | hp2 | a0003 | c0003 | t0001 | g0191 | SAS | STU | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03704 | hp1 | a0003 | c0003 | t0001 | g0091 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0157 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03710 | hp2 | a0003 | c0003 | t0001 | g0065 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0188 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0307 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03834 | hp2 | a0003 | c0003 | t0001 | g0093 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03927 | hp2 | a0003 | c0003 | t0001 | g0121 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0164 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG04115 | hp1 | a0003 | c0003 | t0001 | g0060 | SAS | STU | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0172 | SAS | STU | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | STU | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG04199 | hp2 | a0003 | c0003 | t0001 | g0086 | SAS | STU | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18522 | hp1 | a0001 | c0004 | t0002 | g0251 | AFR | YRI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | YRI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | CHB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | CHB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18906 | hp2 | a0007 | c0012 | t0001 | g0199 | AFR | YRI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18940 | hp1 | a0006 | c0014 | t0002 | g0321 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18941 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18941 | hp2 | a0003 | c0003 | t0002 | g0259 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18943 | hp1 | a0005 | c0007 | t0001 | g0209 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18944 | hp1 | a0001 | c0004 | t0001 | g0215 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18944 | hp2 | a0003 | c0003 | t0001 | g0089 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18945 | hp1 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18945 | hp2 | a0004 | c0006 | t0001 | g0230 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18947 | hp1 | a0003 | c0003 | t0001 | g0064 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18949 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18950 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18951 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18954 | hp2 | a0003 | c0003 | t0001 | g0102 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18961 | hp1 | a0003 | c0003 | t0001 | g0079 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0312 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18962 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18965 | hp1 | a0004 | c0006 | t0001 | g0210 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18965 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18967 | hp1 | a0005 | c0007 | t0001 | g0028 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18967 | hp2 | a0003 | c0003 | t0001 | g0068 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18970 | hp1 | a0006 | c0013 | t0002 | g0320 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18970 | hp2 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18971 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18972 | hp1 | a0004 | c0006 | t0001 | g0133 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18973 | hp1 | a0003 | c0003 | t0001 | g0078 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18975 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18978 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18979 | hp2 | a0001 | c0004 | t0001 | g0232 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18982 | hp1 | a0010 | c0018 | t0002 | g0314 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18988 | hp1 | a0001 | c0004 | t0001 | g0205 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18988 | hp2 | a0003 | c0003 | t0001 | g0097 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18989 | hp2 | a0001 | c0004 | t0001 | g0204 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18991 | hp1 | a0001 | c0004 | t0001 | g0029 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18992 | hp2 | a0003 | c0003 | t0001 | g0070 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18994 | hp1 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18997 | hp1 | a0003 | c0003 | t0001 | g0095 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18997 | hp2 | a0001 | c0004 | t0001 | g0219 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18998 | hp1 | a0003 | c0003 | t0001 | g0087 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18998 | hp2 | a0001 | c0004 | t0001 | g0218 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19000 | hp2 | a0001 | c0004 | t0001 | g0222 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19001 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19002 | hp1 | a0003 | c0003 | t0001 | g0208 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19002 | hp2 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19010 | hp1 | a0003 | c0003 | t0001 | g0057 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19011 | hp1 | a0004 | c0006 | t0001 | g0181 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19012 | hp1 | a0001 | c0004 | t0001 | g0198 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19012 | hp2 | a0003 | c0003 | t0001 | g0082 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19030 | hp1 | a0001 | c0020 | t0001 | g0104 | AFR | LWK | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | LWK | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19054 | hp1 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19057 | hp1 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19059 | hp1 | a0003 | c0003 | t0001 | g0044 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19059 | hp2 | a0001 | c0004 | t0001 | g0233 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19062 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19065 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19066 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19074 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19074 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19076 | hp1 | a0001 | c0004 | t0001 | g0206 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19077 | hp1 | a0001 | c0004 | t0001 | g0029 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19078 | hp1 | a0001 | c0004 | t0001 | g0217 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19078 | hp2 | a0003 | c0003 | t0001 | g0056 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19080 | hp1 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19080 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19081 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19081 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19083 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19085 | hp2 | a0003 | c0003 | t0001 | g0084 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19086 | hp2 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19087 | hp2 | a0001 | c0015 | t0001 | g0088 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19088 | hp2 | a0001 | c0004 | t0001 | g0213 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19091 | hp1 | a0001 | c0004 | t0001 | g0231 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19091 | hp2 | a0003 | c0003 | t0001 | g0101 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | YRI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | ASW | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ASW | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0012 | EUR | TSI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0167 | EUR | TSI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0137 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG01123 | hp2 | a0003 | c0003 | t0001 | g0179 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02109 | hp1 | a0008 | c0017 | t0001 | g0106 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02109 | hp2 | a0001 | c0005 | t0002 | g0245 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02486 | hp1 | a0001 | c0004 | t0001 | g0224 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02486 | hp2 | a0001 | c0005 | t0001 | g0131 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02559 | hp1 | a0001 | c0004 | t0001 | g0019 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG02559 | hp2 | a0001 | c0004 | t0001 | g0207 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03471 | hp1 | a0001 | c0005 | t0001 | g0021 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG03471 | hp2 | a0003 | c0003 | t0003 | g0094 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | USA | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
HG06807 | hp2 | a0001 | c0005 | t0001 | g0126 | AFR | USA | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | USA | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0117 | AFR | USA | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA21309 | hp1 | a0001 | c0004 | t0001 | g0225 | AFR | LWK | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0324 | AFR | LWK | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0120 | REF | REF | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
homoSapiens_grch38 | hp1 | a0007 | c0012 | t0001 | g0138 | REF | REF | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:71752579
|
T | C | 10 | a0001a0002a0003others(7): Show | 386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
missense_variant | MODERATE | c.1334A>G | p.His445Arg | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/13 | 1395/1685 | 1334/1425 | 445/474 | chr4 | 71752579 | ||
chr4:71752580
|
G | A | 2 | a0004a0005 | 7 | HG00408.hp2 NA18943.hp1 NA18945.hp2 others(4): Show |
missense_variant | MODERATE | c.1333C>T | p.His445Tyr | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/13 | 1394/1685 | 1333/1425 | 445/474 | chr4 | 71752580 | ||
chr4:71752606
|
G | T | 1 | a0003 | 81 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
missense_variant | MODERATE | c.1307C>A | p.Thr436Lys | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/13 | 1368/1685 | 1307/1425 | 436/474 | chr4 | 71752606 | ||
chr4:71752617
|
A | C | 3 | a0002a0008a0010 | 103 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
missense_variant | MODERATE | c.1296T>G | p.Asp432Glu | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/13 | 1357/1685 | 1296/1425 | 432/474 | chr4 | 71752617 | ||
chr4:71754445
|
A | G | 1 | a0009 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1228T>C | p.Tyr410His | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/13 | 1289/1685 | 1228/1425 | 410/474 | chr4 | 71754445 | ||
chr4:71754495
|
T | C | 1 | a0010 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1178A>G | p.Lys393Arg | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/13 | 1239/1685 | 1178/1425 | 393/474 | chr4 | 71754495 | ||
chr4:71755091
|
T | C | 1 | a0004 | 4 | NA18945.hp2 NA18965.hp1 NA18972.hp1 others(1): Show |
missense_variant | MODERATE | c.1051A>G | p.Ser351Gly | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/13 | 1112/1685 | 1051/1425 | 351/474 | chr4 | 71755091 | ||
chr4:71756746
|
C | G | 1 | a0008 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1000G>C | p.Val334Leu | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/13 | 1061/1685 | 1000/1425 | 334/474 | chr4 | 71756746 | ||
chr4:71763435
|
G | C | 1 | a0011 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.674C>G | p.Ala225Gly | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/13 | 735/1685 | 674/1425 | 225/474 | chr4 | 71763435 | ||
chr4:71769397
|
C | T | 1 | a0006 | 2 | NA18940.hp1 NA18970.hp1 |
missense_variant | MODERATE | c.62G>A | p.Arg21Gln | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/13 | 123/1685 | 62/1425 | 21/474 | chr4 | 71769397 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:71752640
|
G | T | 1 | a0001c0011 | 2 | HG02818.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.1273C>A | p.Arg425Arg | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/13 | 1334/1685 | 1273/1425 | 425/474 | chr4 | 71752640 | ||
chr4:71755071
|
C | T | 1 | a0002c0010 | 2 | HG00140.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.1071G>A | p.Pro357Pro | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/13 | 1132/1685 | 1071/1425 | 357/474 | chr4 | 71755071 | ||
chr4:71756849
|
A | G | 7 | a0001c0004a0001c0008a0004c0006others(4): Show | 60 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(57): Show |
synonymous_variant | LOW | c.897T>C | p.Cys299Cys | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/13 | 958/1685 | 897/1425 | 299/474 | chr4 | 71756849 | ||
chr4:71756909
|
A | C | 1 | a0001c0015 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.837T>G | p.Pro279Pro | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/13 | 898/1685 | 837/1425 | 279/474 | chr4 | 71756909 | ||
chr4:71763912
|
A | G | 1 | a0001c0009 | 2 | HG02280.hp2 HG02976.hp2 |
synonymous_variant | LOW | c.498T>C | p.Asn166Asn | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 5/13 | 559/1685 | 498/1425 | 166/474 | chr4 | 71763912 | ||
chr4:71765497
|
G | A | 2 | a0001c0008a0001c0020 | 4 | HG01884.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.408C>T | p.Tyr136Tyr | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/13 | 469/1685 | 408/1425 | 136/474 | chr4 | 71765497 | ||
chr4:71765623
|
C | T | 1 | a0001c0005 | 14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
synonymous_variant | LOW | c.282G>A | p.Lys94Lys | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/13 | 343/1685 | 282/1425 | 94/474 | chr4 | 71765623 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:71741766
|
A | G | 2 | a0001c0005t0003a0003c0003t0003 | 5 | HG02258.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*130T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 13/13 | 4410 | chr4 | 71741766 | |||||
chr4:71784057
|
G | A | 9 | a0001c0001t0002a0001c0004t0002a0001c0005t0002others(6): Show | 106 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
5_prime_UTR_variant | MODIFIER | c.-39C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/13 | 39 | chr4 | 71784057 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:71741918
|
G | A | 1 | a0001c0008t0001g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.*26-48C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71741918 | ||||||
chr4:71741961
|
T | G | 46 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0051others(43): Show | 52 | HG00423.hp1 HG01106.hp2 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.*26-91A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71741961 | ||||||
chr4:71742240
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.*26-370T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742240 | ||||||
chr4:71742317
|
G | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0122others(4): Show | 8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*26-447C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742317 | ||||||
chr4:71742398
|
C | T | 144 | a0001c0001t0002g0254a0001c0001t0002g0302a0001c0004t0001g0218others(141): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.*26-528G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742398 | ||||||
chr4:71742604
|
T | C | 1 | a0003c0003t0001g0072 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.*26-734A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742604 | ||||||
chr4:71742647
|
C | T | 64 | a0001c0004t0001g0218a0001c0004t0001g0219a0001c0005t0001g0130others(61): Show | 77 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.*26-777G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742647 | ||||||
chr4:71742666
|
T | G | 63 | a0001c0004t0001g0218a0001c0004t0001g0219a0001c0005t0001g0130others(60): Show | 76 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.*26-796A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742666 | ||||||
chr4:71742699
|
G | A | 1 | a0005c0007t0001g0209 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.*26-829C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742699 | ||||||
chr4:71742712
|
C | CGCCTGTA others(1461): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | NA18951.hp2 NA18993.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.*26-843_*26-842ins others(1468): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742712 | ||||||
chr4:71742789
|
A | G | 1 | a0001c0001t0002g0305 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.*26-919T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742789 | ||||||
chr4:71742915
|
G | A | 67 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(64): Show | 76 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.*26-1045C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742915 | ||||||
chr4:71742952
|
C | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.*26-1082G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742952 | ||||||
chr4:71743075
|
A | G | 45 | a0001c0004t0001g0003a0001c0004t0001g0006a0001c0004t0001g0019others(42): Show | 57 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.*26-1205T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743075 | ||||||
chr4:71743099
|
T | C | 1 | a0003c0003t0001g0103 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.*26-1229A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743099 | ||||||
chr4:71743211
|
G | T | 12 | a0003c0003t0001g0002a0003c0003t0001g0004a0003c0003t0001g0009others(9): Show | 21 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.*26-1341C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743211 | ||||||
chr4:71743295
|
C | A | 11 | a0001c0001t0001g0145a0001c0001t0001g0197a0001c0001t0002g0256others(8): Show | 11 | HG03834.hp1 NA18957.hp2 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.*26-1425G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743295 | ||||||
chr4:71743377
|
A | C | 111 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(108): Show | 132 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.*26-1507T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743377 | ||||||
chr4:71743568
|
T | C | 7 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0122others(4): Show | 8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*26-1698A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743568 | ||||||
chr4:71743681
|
C | T | 64 | a0001c0004t0001g0218a0001c0004t0001g0219a0001c0005t0001g0130others(61): Show | 77 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.*26-1811G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743681 | ||||||
chr4:71743808
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.*26-1938C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743808 | ||||||
chr4:71743840
|
T | C | 1 | a0003c0003t0001g0153 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.*26-1970A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743840 | ||||||
chr4:71743972
|
G | A | 1 | a0003c0003t0003g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*26-2102C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743972 | ||||||
chr4:71744122
|
G | T | 50 | a0001c0004t0001g0003a0001c0004t0001g0006a0001c0004t0001g0019others(47): Show | 62 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.*25+2029C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744122 | ||||||
chr4:71744217
|
C | T | 45 | a0001c0004t0001g0003a0001c0004t0001g0006a0001c0004t0001g0019others(42): Show | 57 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.*25+1934G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744217 | ||||||
chr4:71744238
|
A | G | 1 | a0003c0003t0001g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.*25+1913T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744238 | ||||||
chr4:71744286
|
C | CA | 71 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0139others(68): Show | 87 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.*25+1864dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744286 | ||||||
chr4:71744286
|
C | CAA | 9 | a0001c0004t0001g0204a0001c0004t0001g0215a0001c0004t0001g0216others(6): Show | 9 | HG01978.hp1 HG01978.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.*25+1863_*25+1864d others(4): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744286 | ||||||
chr4:71744286
|
CA | C | 10 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0001g0195others(7): Show | 12 | HG01109.hp2 HG01167.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.*25+1864delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744286 | ||||||
chr4:71744297
|
A | C | 1 | a0001c0001t0002g0248 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*25+1854T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744297 | ||||||
chr4:71744303
|
A | C | 1 | a0001c0001t0002g0317 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.*25+1848T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744303 | ||||||
chr4:71744304
|
C | A | 79 | a0001c0001t0002g0302a0002c0002t0001g0005a0002c0002t0001g0012others(76): Show | 95 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.*25+1847G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744304 | ||||||
chr4:71744331
|
C | T | 1 | a0001c0005t0002g0245 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*25+1820G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744331 | ||||||
chr4:71744389
|
G | GCGGT | 4 | a0001c0001t0002g0253a0001c0001t0002g0291a0001c0001t0002g0294others(1): Show | 4 | HG02965.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.*25+1758_*25+1761d others(6): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744389 | ||||||
chr4:71744435
|
GGAGACAG others(3): Show |
G | 63 | a0001c0004t0001g0218a0001c0004t0001g0219a0001c0005t0001g0130others(60): Show | 76 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.*25+1706_*25+1715d others(12): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744435 | ||||||
chr4:71744458
|
C | CA | 177 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(174): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.*25+1692dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744458 | ||||||
chr4:71744458
|
C | CAA | 25 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0189others(22): Show | 30 | HG00408.hp1 HG01243.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.*25+1691_*25+1692d others(4): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744458 | ||||||
chr4:71744458
|
CA | C | 61 | a0001c0001t0002g0247a0001c0001t0002g0303a0001c0004t0001g0218others(58): Show | 74 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.*25+1692delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744458 | ||||||
chr4:71744491
|
C | A | 242 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(239): Show | 288 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.*25+1660G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744491 | ||||||
chr4:71744828
|
G | A | 45 | a0001c0004t0001g0003a0001c0004t0001g0006a0001c0004t0001g0019others(42): Show | 57 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.*25+1323C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744828 | ||||||
chr4:71744834
|
G | GA | 44 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0051others(41): Show | 50 | HG00423.hp1 HG01106.hp2 HG01943.hp1 others(47): Show |
intron_variant | MODIFIER | c.*25+1316dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744834 | ||||||
chr4:71744877
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.*25+1274G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744877 | ||||||
chr4:71745037
|
T | C | 3 | a0002c0002t0001g0016a0002c0002t0001g0173a0002c0002t0001g0220 | 5 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.*25+1114A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745037 | ||||||
chr4:71745113
|
C | T | 3 | a0001c0004t0001g0207a0001c0004t0001g0211a0001c0004t0001g0212 | 3 | HG02559.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.*25+1038G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745113 | ||||||
chr4:71745133
|
C | T | 13 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(10): Show | 18 | HG01167.hp1 HG01257.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.*25+1018G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745133 | ||||||
chr4:71745245
|
T | C | 3 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | NA18951.hp2 NA18993.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.*25+906A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745245 | ||||||
chr4:71745361
|
G | T | 1 | a0003c0003t0001g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.*25+790C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745361 | ||||||
chr4:71745465
|
T | C | 1 | a0011c0019t0001g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*25+686A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745465 | ||||||
chr4:71745498
|
A | G | 45 | a0001c0004t0001g0003a0001c0004t0001g0006a0001c0004t0001g0019others(42): Show | 57 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.*25+653T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745498 | ||||||
chr4:71745652
|
CTA | C | 18 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(15): Show | 23 | HG01167.hp1 HG01257.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.*25+497_*25+498del others(2): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745652 | ||||||
chr4:71745805
|
A | T | 2 | a0003c0003t0001g0078a0003c0003t0001g0079 | 2 | NA18961.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.*25+346T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745805 | ||||||
chr4:71745843
|
A | G | 1 | a0003c0003t0001g0091 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.*25+308T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745843 | ||||||
chr4:71745878
|
C | T | 325 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(322): Show | 387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.*25+273G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745878 | ||||||
chr4:71745941
|
C | T | 7 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0122others(4): Show | 8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*25+210G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745941 | ||||||
chr4:71745973
|
G | C | 78 | a0001c0001t0002g0302a0002c0002t0001g0005a0002c0002t0001g0012others(75): Show | 94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.*25+178C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745973 | ||||||
chr4:71745973
|
G | T | 1 | a0002c0002t0001g0168 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.*25+178C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745973 | ||||||
chr4:71745982
|
G | A | 13 | a0001c0001t0001g0050a0001c0001t0001g0112a0001c0001t0001g0182others(10): Show | 16 | HG01257.hp1 HG02258.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.*25+169C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745982 | ||||||
chr4:71746284
|
AAATCTTG others(19): Show |
A | 1 | a0001c0004t0001g0219 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1396-105_1396-80de others(27): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746284 | ||||||
chr4:71746501
|
A | T | 7 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0122others(4): Show | 8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396-296T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746501 | ||||||
chr4:71746517
|
G | A | 105 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(102): Show | 126 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1396-312C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746517 | ||||||
chr4:71746531
|
G | A | 1 | a0002c0002t0001g0183 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1396-326C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746531 | ||||||
chr4:71746576
|
T | G | 1 | a0002c0002t0002g0252 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1396-371A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746576 | ||||||
chr4:71746772
|
T | TA | 18 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0096others(15): Show | 19 | HG01167.hp1 HG02074.hp1 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.1396-568dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | ||||||
chr4:71746772
|
T | TAA | 103 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0051others(100): Show | 124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1396-569_1396-568d others(4): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | ||||||
chr4:71746772
|
T | TAAA | 79 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(76): Show | 92 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1396-570_1396-568d others(5): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | ||||||
chr4:71746772
|
T | TAAAA | 43 | a0001c0001t0001g0197a0001c0001t0002g0254a0001c0001t0002g0258others(40): Show | 53 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1396-571_1396-568d others(6): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | ||||||
chr4:71746772
|
T | TAAAAA | 9 | a0001c0004t0001g0204a0001c0004t0001g0205a0001c0004t0001g0214others(6): Show | 9 | HG01978.hp1 HG02135.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1396-572_1396-568d others(7): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | ||||||
chr4:71746772
|
T | TAAAAAAA others(9): Show |
1 | a0001c0009t0001g0192 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1396-583_1396-568d others(18): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | ||||||
chr4:71746772
|
T | TAAAAAAA others(10): Show |
2 | a0001c0001t0001g0194a0001c0009t0001g0193 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1396-584_1396-568d others(19): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | ||||||
chr4:71746772
|
T | TAAAAAAA others(11): Show |
1 | a0001c0001t0001g0195 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1396-585_1396-568d others(20): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | ||||||
chr4:71746772
|
TA | T | 54 | a0003c0003t0001g0002a0003c0003t0001g0004a0003c0003t0001g0009others(51): Show | 67 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1396-568delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | ||||||
chr4:71746899
|
G | A | 9 | a0001c0001t0001g0050a0001c0001t0001g0112a0001c0001t0001g0182others(6): Show | 12 | HG01257.hp1 HG02809.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396-694C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746899 | ||||||
chr4:71746926
|
GGGA | G | 104 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(101): Show | 123 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.1396-724_1396-722d others(5): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746926 | ||||||
chr4:71746970
|
C | A | 1 | a0001c0001t0002g0319 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1396-765G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746970 | ||||||
chr4:71746970
|
C | G | 42 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0051others(39): Show | 48 | HG00423.hp1 HG01106.hp2 HG01943.hp1 others(45): Show |
intron_variant | MODIFIER | c.1396-765G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746970 | ||||||
chr4:71746980
|
A | C | 2 | a0001c0004t0001g0211a0001c0004t0001g0212 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1396-775T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746980 | ||||||
chr4:71747114
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1396-909C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747114 | ||||||
chr4:71747185
|
T | G | 100 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(97): Show | 119 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1396-980A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747185 | ||||||
chr4:71747194
|
T | C | 43 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0051others(40): Show | 49 | HG00423.hp1 HG01106.hp2 HG01943.hp1 others(46): Show |
intron_variant | MODIFIER | c.1396-989A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747194 | ||||||
chr4:71747206
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1396-1001T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747206 | ||||||
chr4:71747258
|
T | A | 103 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(100): Show | 122 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1396-1053A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747258 | ||||||
chr4:71747319
|
A | C | 87 | a0001c0001t0002g0302a0002c0002t0001g0005a0002c0002t0001g0008others(84): Show | 105 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1396-1114T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747319 | ||||||
chr4:71747326
|
T | C | 1 | a0001c0004t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1396-1121A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747326 | ||||||
chr4:71747526
|
G | GGTATCAA others(19): Show |
1 | a0001c0004t0001g0219 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1396-1347_1396-132 others(30): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747526 | ||||||
chr4:71747770
|
A | G | 4 | a0003c0003t0003g0048a0003c0003t0003g0054a0003c0003t0003g0094others(1): Show | 4 | HG02258.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-1565T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747770 | ||||||
chr4:71747774
|
T | A | 11 | a0001c0001t0002g0243a0001c0001t0002g0325a0001c0005t0001g0014others(8): Show | 14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1396-1569A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747774 | ||||||
chr4:71747849
|
G | A | 43 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0051others(40): Show | 49 | HG00423.hp1 HG01106.hp2 HG01943.hp1 others(46): Show |
intron_variant | MODIFIER | c.1396-1644C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747849 | ||||||
chr4:71747914
|
A | G | 2 | a0003c0003t0001g0072a0003c0003t0001g0077 | 2 | HG00639.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1396-1709T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747914 | ||||||
chr4:71747976
|
A | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-1771T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747976 | ||||||
chr4:71748075
|
T | C | 190 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(187): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1396-1870A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748075 | ||||||
chr4:71748123
|
G | A | 51 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(48): Show | 58 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1396-1918C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748123 | ||||||
chr4:71748266
|
A | G | 1 | a0002c0002t0001g0169 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1396-2061T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748266 | ||||||
chr4:71748326
|
A | G | 1 | a0002c0002t0002g0252 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1396-2121T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748326 | ||||||
chr4:71748423
|
A | C | 186 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(183): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1396-2218T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748423 | ||||||
chr4:71748439
|
A | G | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-2234T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748439 | ||||||
chr4:71748550
|
G | C | 62 | a0003c0003t0001g0002a0003c0003t0001g0004a0003c0003t0001g0009others(59): Show | 75 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1396-2345C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748550 | ||||||
chr4:71748669
|
C | T | 1 | a0002c0002t0001g0155 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1396-2464G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748669 | ||||||
chr4:71748785
|
G | A | 1 | a0003c0003t0001g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1396-2580C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748785 | ||||||
chr4:71748870
|
A | G | 1 | a0001c0001t0002g0279 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1396-2665T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748870 | ||||||
chr4:71749051
|
A | C | 1 | a0002c0002t0001g0168 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1396-2846T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749051 | ||||||
chr4:71749054
|
G | A | 1 | a0003c0003t0001g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1396-2849C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749054 | ||||||
chr4:71749307
|
G | A | 1 | a0003c0003t0001g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1396-3102C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749307 | ||||||
chr4:71749488
|
T | C | 1 | a0001c0001t0002g0283 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1395+3030A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749488 | ||||||
chr4:71749645
|
A | G | 64 | a0003c0003t0001g0002a0003c0003t0001g0004a0003c0003t0001g0009others(61): Show | 77 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1395+2873T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749645 | ||||||
chr4:71749901
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1395+2617C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749901 | ||||||
chr4:71749904
|
T | C | 4 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0189others(1): Show | 5 | HG02622.hp1 HG02818.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395+2614A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749904 | ||||||
chr4:71749947
|
A | C | 1 | a0003c0003t0001g0075 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1395+2571T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749947 | ||||||
chr4:71750116
|
A | G | 186 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(183): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1395+2402T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750116 | ||||||
chr4:71750185
|
C | T | 1 | a0001c0005t0003g0129 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1395+2333G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750185 | ||||||
chr4:71750292
|
T | C | 1 | a0001c0001t0002g0242 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1395+2226A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750292 | ||||||
chr4:71750425
|
A | G | 7 | a0001c0004t0001g0019a0001c0004t0001g0020a0001c0004t0001g0109others(4): Show | 9 | HG01243.hp2 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1395+2093T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750425 | ||||||
chr4:71750597
|
C | G | 325 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(322): Show | 387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1395+1921G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750597 | ||||||
chr4:71750606
|
C | T | 3 | a0002c0002t0001g0143a0002c0002t0001g0144a0002c0002t0001g0175 | 3 | HG00280.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1395+1912G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750606 | ||||||
chr4:71750610
|
C | T | 135 | a0001c0001t0002g0302a0001c0004t0001g0003a0001c0004t0001g0006others(132): Show | 165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1395+1908G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750610 | ||||||
chr4:71750695
|
G | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+1823C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750695 | ||||||
chr4:71750809
|
C | A | 1 | a0001c0001t0002g0276 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1395+1709G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750809 | ||||||
chr4:71750872
|
G | C | 41 | a0001c0004t0001g0003a0001c0004t0001g0006a0001c0004t0001g0029others(38): Show | 51 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.1395+1646C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750872 | ||||||
chr4:71750900
|
CA | C | 131 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(128): Show | 156 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1395+1617delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750900 | ||||||
chr4:71750900
|
CAA | C | 190 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(187): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1395+1616_1395+161 others(6): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750900 | ||||||
chr4:71750901
|
A | C | 3 | a0003c0003t0001g0075a0003c0003t0001g0076a0003c0003t0001g0153 | 3 | HG01934.hp2 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1395+1617T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750901 | ||||||
chr4:71750912
|
G | A | 2 | a0003c0003t0001g0041a0003c0003t0001g0064 | 2 | NA18947.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1395+1606C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750912 | ||||||
chr4:71750912
|
G | C | 19 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(16): Show | 24 | HG01167.hp1 HG01257.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1395+1606C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750912 | ||||||
chr4:71750938
|
G | A | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1395+1580C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750938 | ||||||
chr4:71751007
|
T | C | 1 | a0003c0003t0001g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1395+1511A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751007 | ||||||
chr4:71751098
|
A | G | 1 | a0002c0002t0001g0236 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1395+1420T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751098 | ||||||
chr4:71751165
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0315a0001c0001t0002g0316others(2): Show | 8 | HG00639.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1395+1353G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751165 | ||||||
chr4:71751215
|
G | A | 135 | a0001c0001t0002g0302a0001c0004t0001g0003a0001c0004t0001g0006others(132): Show | 165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1395+1303C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751215 | ||||||
chr4:71751247
|
G | T | 1 | a0003c0003t0001g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1395+1271C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751247 | ||||||
chr4:71751296
|
A | G | 1 | a0002c0002t0002g0252 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1395+1222T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751296 | ||||||
chr4:71751421
|
C | G | 50 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(47): Show | 56 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1395+1097G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751421 | ||||||
chr4:71751495
|
T | C | 325 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(322): Show | 387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1395+1023A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751495 | ||||||
chr4:71751627
|
A | G | 2 | a0003c0003t0001g0056a0003c0003t0001g0070 | 2 | NA18992.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1395+891T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751627 | ||||||
chr4:71751675
|
G | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+843C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751675 | ||||||
chr4:71751840
|
T | TA | 62 | a0001c0020t0001g0104a0003c0003t0001g0002a0003c0003t0001g0004others(59): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1395+677dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751840 | ||||||
chr4:71752058
|
A | G | 63 | a0001c0001t0002g0242a0003c0003t0001g0002a0003c0003t0001g0004others(60): Show | 74 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1395+460T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71752058 | ||||||
chr4:71752077
|
C | T | 1 | a0001c0001t0002g0304 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1395+441G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71752077 | ||||||
chr4:71752107
|
C | T | 1 | a0001c0001t0002g0304 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1395+411G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71752107 | ||||||
chr4:71752341
|
A | G | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+177T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71752341 | ||||||
chr4:71752469
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1395+49G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71752469 | ||||||
chr4:71752484
|
C | G | 7 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0122others(4): Show | 8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395+34G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71752484 | ||||||
chr4:71752890
|
T | G | 3 | a0002c0002t0001g0143a0002c0002t0001g0144a0002c0002t0001g0175 | 3 | HG00280.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1263-240A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71752890 | ||||||
chr4:71753029
|
CT | C | 7 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0150others(4): Show | 8 | HG00609.hp2 HG02015.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1263-380delA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753029 | ||||||
chr4:71753194
|
A | T | 1 | a0002c0002t0001g0066 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1263-544T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753194 | ||||||
chr4:71753268
|
G | C | 8 | a0001c0001t0001g0050a0001c0001t0001g0112a0001c0001t0001g0182others(5): Show | 11 | HG01257.hp1 HG02809.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1263-618C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753268 | ||||||
chr4:71753431
|
T | C | 49 | a0001c0001t0002g0254a0001c0004t0001g0003a0001c0004t0001g0006others(46): Show | 61 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1263-781A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753431 | ||||||
chr4:71753448
|
G | T | 1 | a0001c0001t0001g0239 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1263-798C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753448 | ||||||
chr4:71753484
|
C | CA | 90 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0051others(87): Show | 108 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1263-835dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753484 | ||||||
chr4:71753484
|
CA | C | 9 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0122others(6): Show | 10 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1263-835delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753484 | ||||||
chr4:71753499
|
A | G | 11 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0122others(8): Show | 12 | HG02280.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1263-849T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753499 | ||||||
chr4:71753674
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1262+737A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753674 | ||||||
chr4:71753955
|
A | ATAT | 7 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0122others(4): Show | 8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1262+453_1262+455d others(5): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753955 | ||||||
chr4:71753957
|
ATTTTTAT others(6): Show |
A | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1262+441_1262+453d others(15): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753957 | ||||||
chr4:71754081
|
G | A | 47 | a0001c0004t0001g0003a0001c0004t0001g0006a0001c0004t0001g0019others(44): Show | 59 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1262+330C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71754081 | ||||||
chr4:71754279
|
A | C | 59 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(56): Show | 76 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1262+132T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71754279 | ||||||
chr4:71754537
|
A | C | 1 | a0001c0001t0001g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1165-29T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/12 | chr4 | 71754537 | ||||||
chr4:71754597
|
T | TCAGTATG others(11): Show |
1 | a0001c0001t0002g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1165-90_1165-89ins others(18): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/12 | chr4 | 71754597 | ||||||
chr4:71754831
|
TCCCAACA others(8): Show |
T | 1 | a0002c0002t0001g0200 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1164+132_1164+146d others(17): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/12 | chr4 | 71754831 | ||||||
chr4:71754840
|
T | C | 3 | a0002c0002t0001g0154a0002c0002t0001g0167a0002c0002t0001g0176 | 3 | HG00642.hp2 HG01192.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1164+138A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/12 | chr4 | 71754840 | ||||||
chr4:71754860
|
C | T | 1 | a0007c0012t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1164+118G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/12 | chr4 | 71754860 | ||||||
chr4:71755148
|
C | CTATT | 6 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0139others(3): Show | 8 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1035-45_1035-42dup others(4): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755148 | ||||||
chr4:71755148
|
C | CTATTTAT others(1): Show |
150 | a0001c0001t0001g0026a0001c0001t0001g0083a0001c0001t0001g0096others(147): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1035-49_1035-42dup others(8): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755148 | ||||||
chr4:71755148
|
C | CTATTTAT others(5): Show |
83 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0052others(80): Show | 98 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.1035-53_1035-42dup others(12): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755148 | ||||||
chr4:71755148
|
C | CTATTTAT others(9): Show |
30 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0182others(27): Show | 33 | HG00423.hp1 HG01106.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1035-57_1035-42dup others(16): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755148 | ||||||
chr4:71755148
|
C | CTATTTAT others(13): Show |
3 | a0001c0001t0001g0112a0001c0001t0002g0274a0001c0001t0002g0307 | 3 | HG03831.hp2 NA18946.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1035-61_1035-42dup others(20): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755148 | ||||||
chr4:71755222
|
G | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18951.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1035-115C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755222 | ||||||
chr4:71755245
|
C | G | 1 | a0002c0002t0002g0252 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1035-138G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755245 | ||||||
chr4:71755287
|
C | T | 3 | a0003c0003t0001g0098a0003c0003t0001g0099a0003c0003t0001g0103 | 3 | HG00140.hp1 HG01358.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.1035-180G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755287 | ||||||
chr4:71755324
|
G | A | 7 | a0001c0004t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(4): Show | 7 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1035-217C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755324 | ||||||
chr4:71755335
|
G | A | 2 | a0002c0002t0001g0154a0002c0002t0001g0176 | 2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1035-228C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755335 | ||||||
chr4:71755406
|
G | A | 1 | a0009c0016t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1035-299C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755406 | ||||||
chr4:71755678
|
T | C | 1 | a0002c0002t0001g0022 | 2 | HG01496.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1035-571A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755678 | ||||||
chr4:71755753
|
T | C | 3 | a0001c0001t0001g0051a0001c0001t0002g0307a0001c0001t0002g0308 | 3 | HG02602.hp1 HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1035-646A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755753 | ||||||
chr4:71755790
|
G | C | 1 | a0002c0002t0002g0252 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1035-683C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755790 | ||||||
chr4:71755896
|
A | G | 320 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(317): Show | 382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.1035-789T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755896 | ||||||
chr4:71755957
|
T | G | 84 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0012others(81): Show | 102 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1034+755A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755957 | ||||||
chr4:71755962
|
C | T | 61 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(58): Show | 78 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1034+750G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755962 | ||||||
chr4:71755972
|
G | T | 1 | a0004c0006t0001g0181 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1034+740C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755972 | ||||||
chr4:71756014
|
T | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1034+698A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756014 | ||||||
chr4:71756039
|
A | G | 48 | a0001c0004t0001g0003a0001c0004t0001g0006a0001c0004t0001g0019others(45): Show | 60 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1034+673T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756039 | ||||||
chr4:71756108
|
GA | G | 250 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0051others(247): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1034+603delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756108 | ||||||
chr4:71756116
|
T | A | 61 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(58): Show | 78 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1034+596A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756116 | ||||||
chr4:71756491
|
A | C | 325 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(322): Show | 387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1034+221T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756491 | ||||||
chr4:71756513
|
C | A | 1 | a0003c0003t0001g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1034+199G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756513 | ||||||
chr4:71756686
|
A | C | 324 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(321): Show | 386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.1034+26T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756686 | ||||||
chr4:71756929
|
G | T | 1 | a0007c0012t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.832-15C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71756929 | ||||||
chr4:71756942
|
T | C | 12 | a0001c0001t0002g0243a0001c0005t0001g0014a0001c0005t0001g0021others(9): Show | 15 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.832-28A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71756942 | ||||||
chr4:71756973
|
A | T | 1 | a0002c0002t0001g0160 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.832-59T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71756973 | ||||||
chr4:71757047
|
G | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-133C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757047 | ||||||
chr4:71757074
|
C | T | 1 | a0001c0001t0002g0269 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.832-160G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757074 | ||||||
chr4:71757200
|
A | T | 1 | a0003c0003t0001g0071 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.832-286T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757200 | ||||||
chr4:71757314
|
C | A | 2 | a0002c0002t0002g0296a0002c0002t0002g0297 | 2 | HG00621.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.832-400G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757314 | ||||||
chr4:71757358
|
C | T | 10 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0132others(7): Show | 12 | HG01071.hp1 HG01123.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-444G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757358 | ||||||
chr4:71757495
|
T | TA | 67 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(64): Show | 87 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.831+546dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757495 | ||||||
chr4:71757552
|
G | A | 1 | a0001c0004t0001g0218 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.831+490C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757552 | ||||||
chr4:71757607
|
A | AATG | 189 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0043others(186): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.831+432_831+434dup others(3): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757607 | ||||||
chr4:71757609
|
T | TGAC | 68 | a0002c0002t0001g0040a0002c0002t0001g0074a0002c0002t0001g0177others(65): Show | 81 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.831+432_831+433ins others(3): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757609 | ||||||
chr4:71757630
|
A | G | 60 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(57): Show | 77 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.831+412T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757630 | ||||||
chr4:71757667
|
G | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+375C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757667 | ||||||
chr4:71757915
|
C | T | 1 | a0001c0004t0001g0020 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.831+127G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757915 | ||||||
chr4:71757936
|
C | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+106G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757936 | ||||||
chr4:71758212
|
T | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.702-41A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758212 | ||||||
chr4:71758296
|
G | A | 1 | a0003c0003t0001g0065 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.702-125C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758296 | ||||||
chr4:71758418
|
C | T | 54 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0069others(51): Show | 61 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.702-247G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758418 | ||||||
chr4:71758448
|
A | C | 1 | a0001c0004t0001g0020 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.702-277T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758448 | ||||||
chr4:71758553
|
T | C | 1 | a0003c0003t0001g0089 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.702-382A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758553 | ||||||
chr4:71758624
|
A | G | 1 | a0003c0003t0001g0070 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.702-453T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758624 | ||||||
chr4:71758784
|
T | C | 56 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(53): Show | 73 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.702-613A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758784 | ||||||
chr4:71759013
|
C | T | 7 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0122others(4): Show | 8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.702-842G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759013 | ||||||
chr4:71759035
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.702-864A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759035 | ||||||
chr4:71759071
|
A | G | 2 | a0001c0001t0001g0241a0003c0003t0001g0240 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.702-900T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759071 | ||||||
chr4:71759135
|
A | G | 2 | a0001c0001t0001g0112a0001c0011t0002g0032 | 3 | HG02818.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.702-964T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759135 | ||||||
chr4:71759376
|
A | G | 1 | a0001c0020t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702-1205T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759376 | ||||||
chr4:71759380
|
A | C | 122 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(119): Show | 152 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.702-1209T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759380 | ||||||
chr4:71759545
|
A | G | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.702-1374T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759545 | ||||||
chr4:71759626
|
A | G | 1 | a0002c0002t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.702-1455T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759626 | ||||||
chr4:71759718
|
TACC | T | 55 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(52): Show | 72 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.702-1550_702-1548d others(5): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759718 | ||||||
chr4:71759759
|
C | G | 320 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(317): Show | 382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.702-1588G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759759 | ||||||
chr4:71759782
|
C | A | 1 | a0003c0003t0001g0084 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.702-1611G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759782 | ||||||
chr4:71760041
|
G | GT | 9 | a0001c0001t0001g0238a0001c0001t0002g0298a0001c0004t0001g0204others(6): Show | 10 | HG00408.hp2 HG02258.hp1 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.702-1871dupA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760041 | ||||||
chr4:71760041
|
GT | G | 246 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0043others(243): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.702-1871delA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760041 | ||||||
chr4:71760055
|
T | G | 7 | a0002c0002t0001g0040a0003c0003t0001g0002a0003c0003t0001g0004others(4): Show | 16 | HG02083.hp1 HG02165.hp2 NA18941.hp1 others(13): Show |
intron_variant | MODIFIER | c.702-1884A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760055 | ||||||
chr4:71760065
|
C | T | 1 | a0001c0001t0002g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.702-1894G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760065 | ||||||
chr4:71760183
|
A | C | 57 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(54): Show | 74 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.702-2012T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760183 | ||||||
chr4:71760191
|
C | G | 8 | a0002c0002t0001g0015a0002c0002t0001g0023a0002c0002t0001g0147others(5): Show | 11 | HG00408.hp1 HG02074.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.702-2020G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760191 | ||||||
chr4:71760210
|
A | AT | 58 | a0001c0001t0001g0036a0001c0001t0001g0194a0001c0001t0001g0195others(55): Show | 71 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.702-2040dupA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760210 | ||||||
chr4:71760210
|
AT | A | 8 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0122others(5): Show | 9 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.702-2040delA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760210 | ||||||
chr4:71760246
|
G | T | 261 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0043others(258): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.702-2075C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760246 | ||||||
chr4:71760327
|
C | A | 254 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0051others(251): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.702-2156G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760327 | ||||||
chr4:71760371
|
C | G | 260 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0043others(257): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.702-2200G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760371 | ||||||
chr4:71760377
|
C | T | 1 | a0002c0002t0001g0155 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.702-2206G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760377 | ||||||
chr4:71760386
|
A | T | 92 | a0001c0004t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(89): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.702-2215T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760386 | ||||||
chr4:71760397
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.702-2226G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760397 | ||||||
chr4:71760423
|
T | C | 1 | a0001c0020t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702-2252A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760423 | ||||||
chr4:71760490
|
G | A | 1 | a0002c0002t0001g0147 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.702-2319C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760490 | ||||||
chr4:71760522
|
G | A | 1 | a0001c0020t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702-2351C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760522 | ||||||
chr4:71760713
|
G | C | 1 | a0001c0015t0001g0088 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.702-2542C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760713 | ||||||
chr4:71760771
|
T | C | 58 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0051others(55): Show | 70 | HG00597.hp1 HG00621.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.702-2600A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760771 | ||||||
chr4:71760840
|
T | C | 2 | a0002c0002t0002g0323a0002c0002t0002g0324 | 2 | HG01255.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.701+2568A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760840 | ||||||
chr4:71760999
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0194others(4): Show | 9 | HG02145.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.701+2409G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760999 | ||||||
chr4:71761000
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.701+2408C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761000 | ||||||
chr4:71761061
|
G | C | 11 | a0001c0001t0001g0035a0001c0001t0001g0115a0001c0001t0001g0118others(8): Show | 13 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.701+2347C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761061 | ||||||
chr4:71761144
|
T | A | 17 | a0001c0001t0001g0035a0001c0001t0001g0115a0001c0001t0001g0118others(14): Show | 21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.701+2264A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761144 | ||||||
chr4:71761282
|
C | T | 23 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0194others(20): Show | 27 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.701+2126G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761282 | ||||||
chr4:71761411
|
G | A | 3 | a0001c0008t0001g0018a0001c0008t0001g0105a0001c0020t0001g0104 | 4 | HG01884.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.701+1997C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761411 | ||||||
chr4:71761610
|
G | A | 11 | a0001c0001t0001g0052a0001c0001t0002g0263a0001c0001t0002g0266others(8): Show | 11 | HG00423.hp1 HG02040.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.701+1798C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761610 | ||||||
chr4:71761967
|
A | T | 29 | a0001c0001t0001g0035a0001c0001t0001g0115a0001c0001t0001g0118others(26): Show | 36 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.701+1441T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761967 | ||||||
chr4:71762026
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.701+1382G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762026 | ||||||
chr4:71762080
|
G | C | 149 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0069others(146): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.701+1328C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762080 | ||||||
chr4:71762092
|
A | T | 1 | a0002c0002t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.701+1316T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762092 | ||||||
chr4:71762281
|
T | C | 1 | a0001c0004t0001g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.701+1127A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762281 | ||||||
chr4:71762286
|
C | T | 59 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0051others(56): Show | 71 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.701+1122G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762286 | ||||||
chr4:71762474
|
G | T | 1 | a0001c0005t0001g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.701+934C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762474 | ||||||
chr4:71762506
|
A | G | 18 | a0001c0001t0001g0035a0001c0001t0001g0115a0001c0001t0001g0118others(15): Show | 22 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.701+902T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762506 | ||||||
chr4:71762549
|
G | A | 1 | a0003c0003t0001g0044 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.701+859C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762549 | ||||||
chr4:71762588
|
T | C | 1 | a0002c0002t0001g0148 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.701+820A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762588 | ||||||
chr4:71762667
|
G | A | 1 | a0003c0003t0001g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.701+741C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762667 | ||||||
chr4:71762686
|
C | A | 2 | a0001c0015t0001g0088a0003c0003t0001g0087 | 2 | NA18998.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.701+722G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762686 | ||||||
chr4:71762731
|
C | T | 1 | a0001c0001t0002g0293 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.701+677G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762731 | ||||||
chr4:71762774
|
C | T | 11 | a0001c0005t0001g0014a0001c0005t0001g0021a0001c0005t0001g0125others(8): Show | 14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.701+634G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762774 | ||||||
chr4:71762940
|
T | G | 1 | a0001c0004t0001g0020 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.701+468A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762940 | ||||||
chr4:71763157
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701+251T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71763157 | ||||||
chr4:71763167
|
T | C | 17 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0002g0254others(14): Show | 21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.701+241A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71763167 | ||||||
chr4:71763169
|
T | A | 17 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0002g0254others(14): Show | 21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.701+239A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71763169 | ||||||
chr4:71763240
|
G | A | 3 | a0001c0008t0001g0018a0001c0008t0001g0105a0001c0020t0001g0104 | 4 | HG01884.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.701+168C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71763240 | ||||||
chr4:71763252
|
G | A | 103 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0036others(100): Show | 120 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.701+156C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71763252 | ||||||
chr4:71763257
|
C | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+151G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71763257 | ||||||
chr4:71763690
|
G | T | 6 | a0001c0001t0002g0247a0001c0001t0002g0248a0001c0001t0002g0249others(3): Show | 6 | HG01106.hp2 HG01943.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.606+114C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 5/12 | chr4 | 71763690 | ||||||
chr4:71763711
|
A | G | 3 | a0001c0008t0001g0018a0001c0008t0001g0105a0001c0020t0001g0104 | 4 | HG01884.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+93T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 5/12 | chr4 | 71763711 | ||||||
chr4:71763772
|
C | T | 1 | a0001c0001t0002g0266 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.606+32G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 5/12 | chr4 | 71763772 | ||||||
chr4:71763785
|
T | A | 2 | a0003c0003t0001g0089a0003c0003t0001g0102 | 2 | NA18944.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.606+19A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 5/12 | chr4 | 71763785 | ||||||
chr4:71763952
|
T | C | 2 | a0002c0002t0001g0236a0002c0002t0001g0237 | 2 | HG00280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.474-16A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71763952 | ||||||
chr4:71763960
|
G | T | 11 | a0001c0005t0001g0014a0001c0005t0001g0021a0001c0005t0001g0125others(8): Show | 14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.474-24C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71763960 | ||||||
chr4:71764010
|
T | A | 1 | a0002c0002t0001g0183 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.474-74A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764010 | ||||||
chr4:71764085
|
G | A | 2 | a0001c0004t0001g0221a0002c0002t0001g0184 | 2 | HG02735.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.474-149C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764085 | ||||||
chr4:71764192
|
G | A | 1 | a0003c0003t0001g0089 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.474-256C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764192 | ||||||
chr4:71764222
|
T | C | 11 | a0001c0005t0001g0014a0001c0005t0001g0021a0001c0005t0001g0125others(8): Show | 14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.474-286A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764222 | ||||||
chr4:71764345
|
G | A | 1 | a0002c0002t0001g0184 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.474-409C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764345 | ||||||
chr4:71764438
|
C | T | 1 | a0002c0002t0001g0157 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.474-502G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764438 | ||||||
chr4:71764493
|
A | C | 6 | a0001c0001t0002g0263a0001c0001t0002g0266a0001c0001t0002g0267others(3): Show | 6 | HG00423.hp1 NA18612.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-557T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764493 | ||||||
chr4:71764508
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0002g0307a0001c0001t0002g0308 | 3 | HG02602.hp1 HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.474-572C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764508 | ||||||
chr4:71764680
|
T | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 4 | HG00423.hp2 NA18954.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-744A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764680 | ||||||
chr4:71764699
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0112others(6): Show | 13 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.473+733C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764699 | ||||||
chr4:71764810
|
G | C | 44 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0052others(41): Show | 49 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.473+622C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764810 | ||||||
chr4:71764867
|
C | T | 11 | a0001c0005t0001g0014a0001c0005t0001g0021a0001c0005t0001g0125others(8): Show | 14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.473+565G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764867 | ||||||
chr4:71764925
|
C | A | 59 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0050others(56): Show | 68 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.473+507G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764925 | ||||||
chr4:71764936
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.473+496A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764936 | ||||||
chr4:71765258
|
G | A | 1 | a0003c0003t0001g0090 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.473+174C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71765258 | ||||||
chr4:71765831
|
T | A | 1 | a0003c0003t0001g0044 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.262-188A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71765831 | ||||||
chr4:71765851
|
C | A | 1 | a0003c0003t0001g0091 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.262-208G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71765851 | ||||||
chr4:71765922
|
A | G | 6 | a0001c0001t0001g0050a0001c0001t0001g0112a0001c0001t0002g0030others(3): Show | 8 | HG02809.hp1 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-279T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71765922 | ||||||
chr4:71765951
|
G | A | 44 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0052others(41): Show | 49 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.262-308C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71765951 | ||||||
chr4:71766018
|
T | C | 284 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(281): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.262-375A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766018 | ||||||
chr4:71766027
|
T | C | 225 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0043others(222): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.262-384A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766027 | ||||||
chr4:71766182
|
C | A | 18 | a0001c0001t0001g0035a0001c0001t0001g0115a0001c0001t0001g0118others(15): Show | 22 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.262-539G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766182 | ||||||
chr4:71766190
|
G | T | 18 | a0001c0001t0001g0035a0001c0001t0001g0115a0001c0001t0001g0118others(15): Show | 22 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.262-547C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766190 | ||||||
chr4:71766309
|
T | C | 1 | a0003c0003t0001g0092 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.262-666A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766309 | ||||||
chr4:71766491
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0238 | 5 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-848T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766491 | ||||||
chr4:71766568
|
T | C | 1 | a0002c0002t0001g0117 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.262-925A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766568 | ||||||
chr4:71766614
|
T | C | 11 | a0001c0005t0001g0014a0001c0005t0001g0021a0001c0005t0001g0125others(8): Show | 14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.262-971A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766614 | ||||||
chr4:71766689
|
C | T | 59 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0051others(56): Show | 71 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.262-1046G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766689 | ||||||
chr4:71766690
|
G | A | 44 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0052others(41): Show | 49 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.262-1047C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766690 | ||||||
chr4:71766794
|
C | A | 2 | a0001c0001t0002g0253a0001c0001t0002g0309 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.262-1151G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766794 | ||||||
chr4:71766924
|
C | T | 3 | a0001c0008t0001g0018a0001c0008t0001g0105a0001c0020t0001g0104 | 4 | HG01884.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-1281G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766924 | ||||||
chr4:71766925
|
C | T | 3 | a0003c0003t0001g0098a0003c0003t0001g0099a0003c0003t0001g0103 | 3 | HG00140.hp1 HG01358.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.262-1282G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766925 | ||||||
chr4:71766926
|
A | G | 266 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0036others(263): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.262-1283T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766926 | ||||||
chr4:71767065
|
C | G | 1 | a0003c0003t0001g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.261+1236G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767065 | ||||||
chr4:71767149
|
A | T | 11 | a0001c0005t0001g0014a0001c0005t0001g0021a0001c0005t0001g0125others(8): Show | 14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.261+1152T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767149 | ||||||
chr4:71767214
|
C | T | 17 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0002g0254others(14): Show | 21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.261+1087G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767214 | ||||||
chr4:71767215
|
A | G | 1 | a0002c0002t0001g0156 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.261+1086T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767215 | ||||||
chr4:71767255
|
G | A | 1 | a0001c0004t0001g0111 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.261+1046C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767255 | ||||||
chr4:71767608
|
G | GAT | 78 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0036others(75): Show | 93 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.261+691_261+692dup others(2): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767608 | ||||||
chr4:71767647
|
G | A | 2 | a0001c0004t0001g0206a0001c0004t0001g0222 | 2 | NA19000.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.261+654C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767647 | ||||||
chr4:71767678
|
T | A | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.261+623A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767678 | ||||||
chr4:71767696
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.261+605T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767696 | ||||||
chr4:71767714
|
T | C | 7 | a0001c0001t0001g0187a0002c0002t0001g0024a0002c0002t0001g0025others(4): Show | 9 | HG01071.hp1 HG01123.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+587A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767714 | ||||||
chr4:71767869
|
C | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+432G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767869 | ||||||
chr4:71767952
|
T | C | 59 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0051others(56): Show | 71 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.261+349A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767952 | ||||||
chr4:71768055
|
T | A | 43 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0052others(40): Show | 48 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.261+246A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71768055 | ||||||
chr4:71768116
|
A | G | 1 | a0002c0002t0001g0154 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.261+185T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71768116 | ||||||
chr4:71768117
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.261+184A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71768117 | ||||||
chr4:71768491
|
C | G | 1 | a0001c0005t0001g0014 | 3 | HG02451.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.129-58G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71768491 | ||||||
chr4:71768503
|
C | G | 3 | a0003c0003t0001g0041a0003c0003t0001g0064a0003c0003t0001g0097 | 3 | NA18947.hp1 NA18988.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.129-70G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71768503 | ||||||
chr4:71768559
|
C | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0112others(18): Show | 28 | HG01167.hp1 HG01243.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.129-126G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71768559 | ||||||
chr4:71768626
|
C | T | 56 | a0001c0001t0001g0036a0001c0001t0001g0051a0001c0001t0001g0096others(53): Show | 67 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.129-193G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71768626 | ||||||
chr4:71768666
|
A | G | 55 | a0001c0001t0001g0036a0001c0001t0001g0051a0001c0001t0001g0096others(52): Show | 66 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.129-233T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71768666 | ||||||
chr4:71768966
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.128+365C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71768966 | ||||||
chr4:71769001
|
C | T | 1 | a0001c0004t0001g0206 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.128+330G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71769001 | ||||||
chr4:71769081
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.128+250G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71769081 | ||||||
chr4:71769131
|
C | A | 1 | a0002c0002t0001g0134 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.128+200G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71769131 | ||||||
chr4:71769183
|
C | T | 1 | a0001c0001t0002g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.128+148G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71769183 | ||||||
chr4:71769253
|
G | A | 6 | a0001c0001t0001g0050a0001c0001t0001g0112a0001c0001t0002g0030others(3): Show | 8 | HG02809.hp1 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+78C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71769253 | ||||||
chr4:71769258
|
G | A | 193 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0043others(190): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.128+73C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71769258 | ||||||
chr4:71769645
|
C | T | 39 | a0001c0004t0001g0003a0001c0004t0001g0006a0001c0004t0001g0029others(36): Show | 48 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.59-245G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769645 | ||||||
chr4:71769646
|
G | A | 6 | a0001c0001t0001g0050a0001c0001t0001g0112a0001c0001t0002g0030others(3): Show | 8 | HG02809.hp1 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-246C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769646 | ||||||
chr4:71769668
|
G | A | 3 | a0001c0008t0001g0018a0001c0008t0001g0105a0001c0020t0001g0104 | 4 | HG01884.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-268C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769668 | ||||||
chr4:71769766
|
C | A | 1 | a0001c0004t0001g0223 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.59-366G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769766 | ||||||
chr4:71769795
|
A | T | 306 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(303): Show | 364 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.59-395T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769795 | ||||||
chr4:71769844
|
A | G | 1 | a0003c0003t0001g0153 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.59-444T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769844 | ||||||
chr4:71769978
|
TTCAGCTG others(76): Show |
T | 1 | a0001c0001t0002g0319 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.59-661_59-579delGG others(81): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769978 | ||||||
chr4:71770042
|
G | C | 34 | a0001c0001t0001g0052a0001c0001t0001g0197a0001c0001t0002g0033others(31): Show | 35 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.59-642C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770042 | ||||||
chr4:71770063
|
T | G | 1 | a0001c0001t0002g0319 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.59-663A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770063 | ||||||
chr4:71770222
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.59-822C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770222 | ||||||
chr4:71770440
|
A | G | 3 | a0001c0001t0002g0242a0001c0005t0001g0125a0001c0005t0001g0126 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.59-1040T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770440 | ||||||
chr4:71770555
|
C | T | 193 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0043others(190): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.59-1155G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770555 | ||||||
chr4:71770570
|
GC | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0238 | 5 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1171delG | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770570 | ||||||
chr4:71770589
|
T | G | 1 | a0002c0002t0001g0135 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.59-1189A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770589 | ||||||
chr4:71770907
|
G | A | 33 | a0001c0001t0001g0052a0001c0001t0001g0197a0001c0001t0002g0033others(30): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.59-1507C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770907 | ||||||
chr4:71771260
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18951.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.59-1860A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71771260 | ||||||
chr4:71771335
|
A | AT | 33 | a0001c0001t0001g0052a0001c0001t0001g0197a0001c0001t0002g0033others(30): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.59-1936dupA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71771335 | ||||||
chr4:71771363
|
A | G | 209 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0055others(206): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.59-1963T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71771363 | ||||||
chr4:71771627
|
C | T | 9 | a0001c0001t0001g0050a0001c0001t0001g0112a0001c0001t0002g0030others(6): Show | 11 | HG01167.hp1 HG01243.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-2227G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71771627 | ||||||
chr4:71771833
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.59-2433A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71771833 | ||||||
chr4:71772397
|
C | T | 1 | a0003c0003t0001g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.59-2997G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71772397 | ||||||
chr4:71772467
|
A | G | 3 | a0001c0004t0001g0006a0001c0004t0001g0204a0001c0004t0001g0205 | 6 | HG00438.hp2 NA18988.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3067T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71772467 | ||||||
chr4:71772797
|
T | A | 3 | a0001c0001t0002g0242a0001c0005t0001g0125a0001c0005t0001g0126 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.59-3397A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71772797 | ||||||
chr4:71773029
|
T | A | 1 | a0002c0002t0001g0188 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.59-3629A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773029 | ||||||
chr4:71773085
|
T | C | 1 | a0001c0004t0001g0233 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.59-3685A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773085 | ||||||
chr4:71773107
|
C | A | 58 | a0001c0001t0001g0036a0001c0001t0001g0051a0001c0001t0001g0096others(55): Show | 70 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.59-3707G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773107 | ||||||
chr4:71773107
|
C | T | 4 | a0001c0001t0002g0033a0001c0001t0002g0255a0001c0001t0002g0264others(1): Show | 5 | HG00597.hp2 HG00609.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3707G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773107 | ||||||
chr4:71773108
|
G | T | 9 | a0001c0005t0001g0014a0001c0005t0001g0021a0001c0005t0001g0127others(6): Show | 12 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-3708C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773108 | ||||||
chr4:71773285
|
G | A | 12 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0238others(9): Show | 17 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.59-3885C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773285 | ||||||
chr4:71773302
|
T | A | 1 | a0001c0001t0002g0277 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.59-3902A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773302 | ||||||
chr4:71773337
|
A | T | 1 | a0001c0001t0002g0263 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.59-3937T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773337 | ||||||
chr4:71773343
|
A | T | 1 | a0001c0001t0002g0262 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.59-3943T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773343 | ||||||
chr4:71773485
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.59-4085T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773485 | ||||||
chr4:71773490
|
T | G | 1 | a0003c0003t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.59-4090A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773490 | ||||||
chr4:71773565
|
C | T | 69 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0069others(66): Show | 84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.59-4165G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773565 | ||||||
chr4:71773673
|
C | T | 1 | a0003c0003t0001g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.59-4273G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773673 | ||||||
chr4:71773674
|
G | A | 9 | a0001c0001t0001g0050a0001c0001t0001g0112a0001c0001t0002g0030others(6): Show | 11 | HG01167.hp1 HG01243.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-4274C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773674 | ||||||
chr4:71773767
|
A | G | 1 | a0001c0020t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59-4367T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773767 | ||||||
chr4:71773872
|
C | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-4472G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773872 | ||||||
chr4:71774028
|
G | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-4628C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774028 | ||||||
chr4:71774226
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0002g0290 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.59-4826C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774226 | ||||||
chr4:71774255
|
A | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-4855T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774255 | ||||||
chr4:71774426
|
A | C | 1 | a0001c0005t0001g0014 | 3 | HG02451.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.59-5026T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774426 | ||||||
chr4:71774432
|
T | C | 323 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(320): Show | 385 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.59-5032A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774432 | ||||||
chr4:71774507
|
A | AG | 70 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(67): Show | 83 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.59-5108dupC | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774507 | ||||||
chr4:71774681
|
T | A | 1 | a0001c0001t0002g0278 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.59-5281A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774681 | ||||||
chr4:71774726
|
T | G | 17 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0002g0254others(14): Show | 21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-5326A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774726 | ||||||
chr4:71774859
|
AC | A | 9 | a0001c0005t0001g0014a0001c0005t0001g0021a0001c0005t0001g0127others(6): Show | 12 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-5460delG | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774859 | ||||||
chr4:71774861
|
T | A | 9 | a0001c0005t0001g0014a0001c0005t0001g0021a0001c0005t0001g0127others(6): Show | 12 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-5461A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774861 | ||||||
chr4:71774927
|
T | C | 1 | a0003c0003t0001g0095 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.59-5527A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774927 | ||||||
chr4:71774992
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.59-5592C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774992 | ||||||
chr4:71775032
|
CT | C | 289 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0036others(286): Show | 346 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.59-5633delA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775032 | ||||||
chr4:71775032
|
CTT | C | 9 | a0001c0001t0001g0035a0001c0001t0001g0203a0001c0001t0002g0278others(6): Show | 10 | HG03540.hp2 NA18963.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-5634_59-5633del others(2): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775032 | ||||||
chr4:71775033
|
T | C | 17 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0004t0001g0020others(14): Show | 20 | HG00735.hp2 HG01243.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-5633A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775033 | ||||||
chr4:71775034
|
T | C | 71 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0069others(68): Show | 86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.59-5634A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775034 | ||||||
chr4:71775119
|
C | T | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(4): Show | 9 | HG03834.hp1 NA18950.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-5719G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775119 | ||||||
chr4:71775155
|
T | C | 1 | a0003c0003t0002g0288 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.59-5755A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775155 | ||||||
chr4:71775261
|
T | A | 1 | a0001c0001t0002g0279 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.59-5861A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775261 | ||||||
chr4:71775557
|
A | AAACATAG others(45): Show |
1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.59-6209_59-6158dup others(52): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775557 | ||||||
chr4:71775559
|
A | C | 1 | a0001c0001t0002g0258 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.59-6159T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775559 | ||||||
chr4:71775562
|
T | C | 16 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0004t0001g0019others(13): Show | 20 | HG00735.hp2 HG01243.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-6162A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775562 | ||||||
chr4:71775647
|
G | T | 1 | a0001c0001t0002g0257 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.59-6247C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775647 | ||||||
chr4:71775701
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.59-6301T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775701 | ||||||
chr4:71775789
|
A | G | 58 | a0001c0001t0001g0036a0001c0001t0001g0051a0001c0001t0001g0096others(55): Show | 70 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.59-6389T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775789 | ||||||
chr4:71775824
|
G | A | 1 | a0001c0001t0002g0311 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.59-6424C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775824 | ||||||
chr4:71776331
|
A | G | 9 | a0001c0005t0001g0014a0001c0005t0001g0021a0001c0005t0001g0127others(6): Show | 12 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-6931T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776331 | ||||||
chr4:71776451
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.59-7051T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776451 | ||||||
chr4:71776586
|
G | A | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | NA18960.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.59-7186C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776586 | ||||||
chr4:71776650
|
C | T | 1 | a0002c0002t0001g0237 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.59-7250G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776650 | ||||||
chr4:71776718
|
A | G | 2 | a0002c0002t0001g0143a0002c0002t0001g0144 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.58+7243T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776718 | ||||||
chr4:71776766
|
T | C | 1 | a0003c0003t0001g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58+7195A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776766 | ||||||
chr4:71776931
|
T | C | 33 | a0001c0001t0001g0052a0001c0001t0001g0197a0001c0001t0002g0033others(30): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.58+7030A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776931 | ||||||
chr4:71777237
|
T | C | 17 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0002g0254others(14): Show | 21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.58+6724A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777237 | ||||||
chr4:71777313
|
C | G | 1 | a0001c0001t0002g0256 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.58+6648G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777313 | ||||||
chr4:71777380
|
C | T | 1 | a0002c0002t0001g0059 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.58+6581G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777380 | ||||||
chr4:71777762
|
AT | A | 9 | a0001c0004t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(6): Show | 9 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+6198delA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777762 | ||||||
chr4:71777771
|
T | C | 77 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0069others(74): Show | 93 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.58+6190A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777771 | ||||||
chr4:71777806
|
T | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.58+6155A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777806 | ||||||
chr4:71777830
|
G | A | 1 | a0002c0002t0002g0252 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58+6131C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777830 | ||||||
chr4:71777847
|
G | A | 3 | a0001c0001t0002g0242a0001c0005t0001g0125a0001c0005t0001g0126 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.58+6114C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777847 | ||||||
chr4:71777876
|
G | C | 1 | a0001c0001t0002g0280 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.58+6085C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777876 | ||||||
chr4:71778041
|
T | A | 1 | a0002c0002t0002g0252 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58+5920A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778041 | ||||||
chr4:71778041
|
TA | T | 64 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0051others(61): Show | 77 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.58+5919delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778041 | ||||||
chr4:71778043
|
A | T | 192 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0055others(189): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.58+5918T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778043 | ||||||
chr4:71778075
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.58+5886G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778075 | ||||||
chr4:71778319
|
T | C | 9 | a0001c0001t0001g0050a0001c0001t0001g0112a0001c0001t0002g0030others(6): Show | 11 | HG01167.hp1 HG01243.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+5642A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778319 | ||||||
chr4:71778580
|
A | G | 17 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0002g0254others(14): Show | 21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.58+5381T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778580 | ||||||
chr4:71778886
|
T | C | 321 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0036others(318): Show | 383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.58+5075A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778886 | ||||||
chr4:71778887
|
G | A | 33 | a0001c0001t0001g0052a0001c0001t0001g0197a0001c0001t0002g0033others(30): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.58+5074C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778887 | ||||||
chr4:71778891
|
G | GTTA | 42 | a0001c0001t0001g0052a0001c0001t0001g0112a0001c0001t0001g0197others(39): Show | 46 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.58+5067_58+5069dup others(3): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | ||||||
chr4:71778891
|
G | GTTATTA | 53 | a0001c0001t0001g0013a0001c0001t0001g0036a0001c0001t0001g0051others(50): Show | 65 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.58+5064_58+5069dup others(6): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | ||||||
chr4:71778891
|
G | GTTATTAT others(2): Show |
47 | a0001c0001t0001g0035a0001c0001t0002g0007a0001c0001t0002g0253others(44): Show | 59 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+5061_58+5069dup others(9): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | ||||||
chr4:71778891
|
G | GTTATTAT others(5): Show |
14 | a0001c0001t0002g0322a0001c0004t0001g0231a0001c0004t0001g0232others(11): Show | 16 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.58+5058_58+5069dup others(12): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | ||||||
chr4:71778891
|
G | GTTATTGT others(2): Show |
75 | a0001c0001t0001g0026a0001c0001t0001g0055a0001c0001t0001g0145others(72): Show | 86 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.58+5069_58+5070ins others(9): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | ||||||
chr4:71778891
|
G | GTTATTGT others(5): Show |
62 | a0001c0001t0001g0043a0001c0001t0001g0069a0001c0001t0001g0083others(59): Show | 78 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.58+5069_58+5070ins others(12): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | ||||||
chr4:71778891
|
G | GTTATTGT others(8): Show |
9 | a0002c0002t0001g0027a0002c0002t0002g0252a0003c0003t0001g0047others(6): Show | 10 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+5069_58+5070ins others(15): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | ||||||
chr4:71778891
|
G | GTTATTGT others(11): Show |
1 | a0003c0003t0001g0103 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.58+5069_58+5070ins others(18): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | ||||||
chr4:71778921
|
ATTG | A | 8 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0002g0242others(5): Show | 9 | HG01167.hp1 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+5037_58+5039del others(3): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778921 | ||||||
chr4:71778924
|
G | A | 313 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0036others(310): Show | 374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.58+5037C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778924 | ||||||
chr4:71779141
|
A | G | 38 | a0001c0001t0001g0052a0001c0001t0001g0194a0001c0001t0001g0195others(35): Show | 39 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.58+4820T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71779141 | ||||||
chr4:71779245
|
G | A | 229 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0052others(226): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.58+4716C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71779245 | ||||||
chr4:71779540
|
A | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+4421T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71779540 | ||||||
chr4:71779569
|
G | A | 51 | a0001c0001t0001g0122a0001c0001t0002g0001a0001c0001t0002g0007others(48): Show | 62 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.58+4392C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71779569 | ||||||
chr4:71779760
|
A | G | 1 | a0003c0003t0001g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.58+4201T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71779760 | ||||||
chr4:71779945
|
A | T | 1 | a0002c0002t0001g0141 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.58+4016T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71779945 | ||||||
chr4:71780021
|
C | G | 1 | a0003c0003t0003g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.58+3940G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780021 | ||||||
chr4:71780089
|
G | A | 92 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0030others(89): Show | 106 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.58+3872C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780089 | ||||||
chr4:71780170
|
T | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0009t0001g0192others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3791A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780170 | ||||||
chr4:71780423
|
A | G | 92 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0030others(89): Show | 106 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.58+3538T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780423 | ||||||
chr4:71780537
|
G | GAA | 48 | a0001c0001t0001g0197a0001c0001t0001g0201a0001c0001t0001g0202others(45): Show | 57 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.58+3422_58+3423dup others(2): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780537 | ||||||
chr4:71780693
|
T | A | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3268A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780693 | ||||||
chr4:71780724
|
G | A | 54 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0247others(51): Show | 65 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.58+3237C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780724 | ||||||
chr4:71780739
|
G | C | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3222C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780739 | ||||||
chr4:71780752
|
T | A | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3209A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780752 | ||||||
chr4:71780754
|
T | A | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3207A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780754 | ||||||
chr4:71780765
|
G | A | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3196C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780765 | ||||||
chr4:71780767
|
A | G | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3194T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780767 | ||||||
chr4:71780773
|
C | G | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3188G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780773 | ||||||
chr4:71780774
|
T | G | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3187A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780774 | ||||||
chr4:71780776
|
C | G | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3185G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780776 | ||||||
chr4:71780779
|
T | A | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3182A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780779 | ||||||
chr4:71780785
|
T | A | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3176A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780785 | ||||||
chr4:71780787
|
G | A | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3174C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780787 | ||||||
chr4:71780788
|
G | C | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3173C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780788 | ||||||
chr4:71780794
|
A | C | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3167T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780794 | ||||||
chr4:71780799
|
A | G | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3162T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780799 | ||||||
chr4:71780807
|
C | T | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3154G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780807 | ||||||
chr4:71780821
|
G | A | 8 | a0001c0005t0001g0021a0001c0005t0001g0125a0001c0005t0001g0126others(5): Show | 9 | HG01243.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+3140C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780821 | ||||||
chr4:71780829
|
A | C | 1 | a0003c0003t0001g0047 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.58+3132T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780829 | ||||||
chr4:71780844
|
AGAACTGG others(11): Show |
A | 1 | a0001c0001t0002g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3099_58+3116del others(18): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780844 | ||||||
chr4:71780876
|
T | C | 319 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0036others(316): Show | 379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.58+3085A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780876 | ||||||
chr4:71781008
|
G | A | 202 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0036others(199): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.58+2953C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781008 | ||||||
chr4:71781033
|
G | C | 325 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0035others(322): Show | 387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.58+2928C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781033 | ||||||
chr4:71781042
|
A | G | 1 | a0002c0002t0001g0137 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.58+2919T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781042 | ||||||
chr4:71781046
|
T | C | 49 | a0001c0001t0001g0197a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 58 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.58+2915A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781046 | ||||||
chr4:71781090
|
A | G | 5 | a0002c0002t0001g0132a0002c0002t0001g0134a0002c0002t0001g0135others(2): Show | 5 | NA18972.hp1 NA18982.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+2871T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781090 | ||||||
chr4:71781151
|
C | T | 1 | a0001c0001t0002g0253 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58+2810G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781151 | ||||||
chr4:71781290
|
C | T | 1 | a0002c0002t0001g0046 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2671G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781290 | ||||||
chr4:71781410
|
C | A | 2 | a0002c0002t0001g0236a0002c0002t0001g0237 | 2 | HG00280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.58+2551G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781410 | ||||||
chr4:71781410
|
C | T | 1 | a0002c0002t0002g0252 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58+2551G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781410 | ||||||
chr4:71781428
|
A | G | 2 | a0001c0004t0002g0251a0001c0011t0002g0032 | 3 | HG02818.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.58+2533T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781428 | ||||||
chr4:71781475
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.58+2486A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781475 | ||||||
chr4:71781718
|
G | C | 1 | a0001c0001t0001g0239 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.58+2243C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781718 | ||||||
chr4:71781871
|
C | G | 1 | a0003c0003t0001g0045 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.58+2090G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781871 | ||||||
chr4:71781925
|
A | G | 5 | a0001c0001t0002g0247a0001c0001t0002g0248a0001c0001t0002g0249others(2): Show | 5 | HG01106.hp2 HG01943.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+2036T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781925 | ||||||
chr4:71782031
|
A | T | 1 | a0001c0001t0002g0242 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.58+1930T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782031 | ||||||
chr4:71782032
|
C | T | 24 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(21): Show | 29 | HG00735.hp2 HG01243.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+1929G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782032 | ||||||
chr4:71782045
|
A | G | 117 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(114): Show | 136 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.58+1916T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782045 | ||||||
chr4:71782283
|
T | G | 1 | a0001c0004t0001g0020 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.58+1678A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782283 | ||||||
chr4:71782288
|
A | G | 5 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0243others(2): Show | 7 | HG02109.hp2 HG02809.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+1673T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782288 | ||||||
chr4:71782304
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.58+1657G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782304 | ||||||
chr4:71782571
|
A | G | 2 | a0001c0005t0001g0125a0001c0005t0001g0126 | 2 | HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.58+1390T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782571 | ||||||
chr4:71782723
|
T | G | 1 | a0003c0003t0001g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.58+1238A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782723 | ||||||
chr4:71782739
|
G | T | 1 | a0001c0005t0001g0125 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.58+1222C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782739 | ||||||
chr4:71782843
|
TGGCCTAT others(5): Show |
T | 6 | a0001c0001t0001g0043a0002c0002t0001g0040a0002c0002t0001g0042others(3): Show | 10 | NA18941.hp1 NA18943.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+1106_58+1117del others(12): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782843 | ||||||
chr4:71782848
|
T | C | 1 | a0002c0002t0001g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.58+1113A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782848 | ||||||
chr4:71783006
|
A | G | 8 | a0001c0005t0001g0021a0001c0005t0001g0125a0001c0005t0001g0126others(5): Show | 9 | HG01243.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+955T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783006 | ||||||
chr4:71783134
|
A | G | 117 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(114): Show | 136 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.58+827T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783134 | ||||||
chr4:71783215
|
C | A | 1 | a0001c0001t0001g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.58+746G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783215 | ||||||
chr4:71783222
|
A | G | 3 | a0003c0003t0001g0037a0003c0003t0001g0038a0003c0003t0001g0039 | 3 | HG00642.hp1 HG00741.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.58+739T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783222 | ||||||
chr4:71783331
|
A | G | 74 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0051others(71): Show | 90 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.58+630T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783331 | ||||||
chr4:71783345
|
A | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.58+616T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783345 | ||||||
chr4:71783682
|
G | A | 1 | a0002c0002t0002g0326 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.58+279C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783682 |