geneid | 2645 |
---|---|
ensemblid | ENSG00000106633.18 |
hgncid | 4195 |
symbol | GCK |
name | glucokinase |
refseq_nuc | NM_000162.5 |
refseq_prot | NP_000153.1 |
ensembl_nuc | ENST00000403799.8 |
ensembl_prot | ENSP00000384247.3 |
mane_status | MANE Select |
chr | chr7 |
start | 44144275 |
end | 44189439 |
strand | - |
ver | v1.2 |
region | chr7:44144275-44189439 |
region5000 | chr7:44139275-44194439 |
regionname0 | GCK_chr7_44144275_44189439 |
regionname5000 | GCK_chr7_44139275_44194439 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1398 | 384 | 84 | 62 | 180 | 18 | 38 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
c0002 | 0/0 | 1398 | 3 | 3 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
c0003 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
c0004 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
c0005 | 0/0 | 1398 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
c0006 | 0/0 | 1398 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
c0007 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1348 | 137 | 16 | 21 | 69 | 7 | 23 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0002 | 0/0 | 1347 | 136 | 42 | 15 | 64 | 4 | 11 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0003 | 0/1 | 1348 | 51 | 1 | 22 | 19 | 5 | 3 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0004 | 0/0 | 1347 | 17 | 16 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0005 | 0/0 | 1347 | 11 | 9 | 2 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0006 | 0/0 | 1347 | 6 | 0 | 0 | 6 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0007 | 0/0 | 1348 | 6 | 0 | 2 | 4 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0008 | 0/0 | 1348 | 6 | 0 | 1 | 5 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0009 | 0/0 | 1348 | 4 | 0 | 0 | 4 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0010 | 0/0 | 1347 | 3 | 0 | 0 | 3 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0011 | 0/0 | 1347 | 3 | 0 | 0 | 3 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0012 | 0/0 | 1348 | 3 | 3 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0013 | 0/0 | 1347 | 2 | 2 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0014 | 0/0 | 1348 | 2 | 0 | 0 | 0 | 2 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0015 | 0/0 | 1348 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0016 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0017 | 0/0 | 1348 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0018 | 0/0 | 1348 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
t0019 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1398 | 384 | 84 | 62 | 180 | 18 | 38 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0003 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0004 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0005 | 0/0 | 1398 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0006 | 0/0 | 1398 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0007 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0002c0002 | 0/0 | 1398 | 3 | 3 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2745 | 136 | 16 | 20 | 69 | 7 | 23 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0002 | 0/0 | 2744 | 131 | 38 | 14 | 64 | 4 | 11 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0003 | 0/1 | 2745 | 51 | 1 | 22 | 19 | 5 | 3 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0004 | 0/0 | 2744 | 16 | 15 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0005 | 0/0 | 2744 | 11 | 9 | 2 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0006 | 0/0 | 2744 | 6 | 0 | 0 | 6 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0007 | 0/0 | 2745 | 6 | 0 | 2 | 4 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0008 | 0/0 | 2745 | 6 | 0 | 1 | 5 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0009 | 0/0 | 2745 | 4 | 0 | 0 | 4 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0010 | 0/0 | 2744 | 3 | 0 | 0 | 3 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0011 | 0/0 | 2744 | 3 | 0 | 0 | 3 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0012 | 0/0 | 2745 | 3 | 3 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0013 | 0/0 | 2744 | 2 | 2 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0014 | 0/0 | 2745 | 2 | 0 | 0 | 0 | 2 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0015 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0017 | 0/0 | 2745 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0018 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0001t0019 | 0/0 | 2744 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0003t0002 | 0/0 | 2744 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0004t0004 | 0/0 | 2744 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0005t0001 | 0/0 | 2745 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0006t0002 | 0/0 | 2744 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0001c0007t0016 | 0/0 | 2744 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
a0002c0002t0002 | 0/0 | 2744 | 3 | 3 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | copy fasta | chr7 | 44139275 | 44194439 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0007g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0007g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0007g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0007g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0007g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0008g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0008g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0008g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0008g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0008g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0008g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0009g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0009g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0009g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0010g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0010g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0010g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0011g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0011g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0011g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0012g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0012g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0012g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0013g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0013g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0014g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0015g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0017g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0018g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0001t0019g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0003t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0004t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0005t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0006t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0001c0007t0016g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
a0002c0002t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | GBR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0028 | EUR | GBR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0294 | EUR | GBR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0172 | EUR | FIN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0223 | EUR | FIN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | FIN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00423 | hp1 | a0001 | c0001 | t0007 | g0023 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00597 | hp1 | a0001 | c0001 | t0008 | g0341 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00639 | hp2 | a0001 | c0006 | t0002 | g0068 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00733 | hp1 | a0001 | c0001 | t0007 | g0336 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0325 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0237 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0147 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01169 | hp2 | a0001 | c0001 | t0008 | g0338 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0150 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | IBS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0292 | EUR | IBS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01516 | hp1 | a0001 | c0001 | t0014 | g0025 | EUR | IBS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0327 | EUR | IBS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01517 | hp1 | a0001 | c0001 | t0014 | g0025 | EUR | IBS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | IBS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0321 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02293 | hp2 | a0001 | c0005 | t0001 | g0228 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0145 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0113 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0215 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02717 | hp1 | a0001 | c0003 | t0002 | g0288 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0170 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0318 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02922 | hp1 | a0001 | c0001 | t0013 | g0360 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0275 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0315 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03041 | hp2 | a0001 | c0004 | t0004 | g0262 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03130 | hp2 | a0001 | c0001 | t0012 | g0357 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0274 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0114 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0146 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03579 | hp1 | a0001 | c0001 | t0013 | g0359 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03831 | hp2 | a0001 | c0001 | t0017 | g0073 | SAS | BEB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0322 | SAS | BEB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | BEB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0225 | AFR | YRI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0312 | AFR | YRI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18747 | hp1 | a0001 | c0001 | t0006 | g0179 | EAS | CHB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | YRI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18939 | hp2 | a0001 | c0001 | t0019 | g0350 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18941 | hp1 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18954 | hp1 | a0001 | c0001 | t0010 | g0344 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18966 | hp2 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18967 | hp1 | a0001 | c0001 | t0008 | g0347 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18969 | hp1 | a0001 | c0001 | t0009 | g0355 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18969 | hp2 | a0001 | c0001 | t0011 | g0352 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18977 | hp1 | a0001 | c0001 | t0007 | g0342 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18981 | hp1 | a0001 | c0001 | t0009 | g0353 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18983 | hp2 | a0001 | c0001 | t0018 | g0343 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18988 | hp2 | a0001 | c0001 | t0008 | g0340 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18997 | hp1 | a0001 | c0001 | t0006 | g0257 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19002 | hp1 | a0001 | c0001 | t0007 | g0023 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | LWK | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | LWK | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0258 | AFR | LWK | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19056 | hp2 | a0001 | c0001 | t0011 | g0354 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19057 | hp2 | a0001 | c0001 | t0010 | g0348 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19058 | hp2 | a0001 | c0001 | t0008 | g0346 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19063 | hp1 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19077 | hp1 | a0001 | c0001 | t0008 | g0345 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19077 | hp2 | a0001 | c0001 | t0015 | g0282 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19079 | hp1 | a0001 | c0001 | t0011 | g0351 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19079 | hp2 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19084 | hp1 | a0001 | c0001 | t0007 | g0339 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19086 | hp1 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19089 | hp1 | a0001 | c0001 | t0010 | g0349 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | YRI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA19240 | hp2 | a0001 | c0001 | t0012 | g0358 | AFR | YRI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | TSI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | TSI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | TSI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0253 | EUR | TSI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | GIH | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | GIH | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG01123 | hp2 | a0001 | c0001 | t0007 | g0337 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0144 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02109 | hp2 | a0001 | c0007 | t0016 | g0222 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0311 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0141 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0356 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | USA | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | USA | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18955 | hp1 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | USA | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | USA | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | LWK | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | LWK | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0277 | REF | REF | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0027 | REF | REF | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:44188923
|
C | T | 1 | a0002 | 3 | HG02257.hp1 HG03139.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.31G>A | p.Ala11Thr | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | 517/2745 | 31/1398 | 11/465 | chr7 | 44188923 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:44146528
|
C | G | 1 | a0001c0004 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.954G>C | p.Gly318Gly | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/10 | 1440/2745 | 954/1398 | 318/465 | chr7 | 44146528 | ||
chr7:44149794
|
G | A | 1 | a0001c0005 | 1 | HG02293.hp2 | synonymous_variant | LOW | c.645C>T | p.Tyr215Tyr | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/10 | 1131/2745 | 645/1398 | 215/465 | chr7 | 44149794 | ||
chr7:44149821
|
C | T | 1 | a0001c0003 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.618G>A | p.Thr206Thr | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/10 | 1104/2745 | 618/1398 | 206/465 | chr7 | 44149821 | ||
chr7:44152295
|
G | A | 1 | a0001c0006 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.339C>T | p.Asp113Asp | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/10 | 825/2745 | 339/1398 | 113/465 | chr7 | 44152295 | ||
chr7:44152301
|
G | A | 1 | a0001c0007 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.333C>T | p.Pro111Pro | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/10 | 819/2745 | 333/1398 | 111/465 | chr7 | 44152301 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:44144289
|
C | T | 1 | a0001c0001t0006 | 6 | NA18747.hp1 NA18941.hp1 NA18955.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*847G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 847 | chr7 | 44144289 | |||||
chr7:44144339
|
G | A | 1 | a0001c0001t0005 | 11 | HG00741.hp2 HG01109.hp1 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*797C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 797 | chr7 | 44144339 | |||||
chr7:44144376
|
TG | T | 13 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(10): Show | 180 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*759delC | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 759 | chr7 | 44144376 | |||||
chr7:44144626
|
G | A | 2 | a0001c0001t0015a0001c0001t0018 | 2 | NA18983.hp2 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*510C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 510 | chr7 | 44144626 | |||||
chr7:44144659
|
G | A | 4 | a0001c0001t0004a0001c0001t0005a0001c0004t0004others(1): Show | 29 | HG00741.hp2 HG01109.hp1 HG01433.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*477C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 477 | chr7 | 44144659 | |||||
chr7:44144761
|
A | G | 1 | a0001c0001t0017 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*375T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 375 | chr7 | 44144761 | |||||
chr7:44144780
|
C | T | 1 | a0001c0007t0016 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*356G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 356 | chr7 | 44144780 | |||||
chr7:44144804
|
C | T | 4 | a0001c0001t0003a0001c0001t0007a0001c0001t0015others(1): Show | 59 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*332G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 332 | chr7 | 44144804 | |||||
chr7:44189037
|
G | C | 6 | a0001c0001t0007a0001c0001t0008a0001c0001t0010others(3): Show | 21 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-84C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | 84 | chr7 | 44189037 | |||||
chr7:44189152
|
G | A | 1 | a0001c0001t0019 | 1 | NA18939.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-199C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | chr7 | 44189152 | ||||||
chr7:44189168
|
T | C | 2 | a0001c0001t0009a0001c0001t0011 | 7 | NA18966.hp2 NA18969.hp1 NA18969.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-215A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | 215 | chr7 | 44189168 | |||||
chr7:44189170
|
G | C | 2 | a0001c0001t0012a0001c0001t0013 | 5 | HG02922.hp1 HG03130.hp2 HG03471.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-217C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | 217 | chr7 | 44189170 | |||||
chr7:44189220
|
C | A | 2 | a0001c0001t0012a0001c0001t0013 | 5 | HG02922.hp1 HG03130.hp2 HG03471.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-267G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | 267 | chr7 | 44189220 | |||||
chr7:44189406
|
G | A | 1 | a0001c0001t0014 | 2 | HG01516.hp1 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-453C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | 453 | chr7 | 44189406 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:44145448
|
C | T | 24 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0064others(21): Show | 25 | HG01074.hp2 HG01256.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.1253+49G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 9/9 | chr7 | 44145448 | ||||||
chr7:44145449
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1253+48C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 9/9 | chr7 | 44145449 | ||||||
chr7:44145489
|
G | A | 167 | a0001c0001t0001g0259a0001c0001t0002g0001a0001c0001t0002g0006others(164): Show | 181 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(178): Show |
splice_region_variant&intron_variant | LOW | c.1253+8C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 9/9 | chr7 | 44145489 | ||||||
chr7:44145784
|
C | T | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1020-54G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44145784 | ||||||
chr7:44145825
|
C | T | 1 | a0001c0003t0002g0288 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1020-95G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44145825 | ||||||
chr7:44146057
|
G | T | 52 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0009others(49): Show | 59 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1020-327C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146057 | ||||||
chr7:44146141
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1019+322G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146141 | ||||||
chr7:44146159
|
C | G | 104 | a0001c0001t0001g0259a0001c0001t0002g0001a0001c0001t0002g0006others(101): Show | 114 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1019+304G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146159 | ||||||
chr7:44146187
|
GC | G | 79 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0061others(76): Show | 87 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1019+275delG | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146187 | ||||||
chr7:44146206
|
C | G | 56 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0319others(53): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.1019+257G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146206 | ||||||
chr7:44146218
|
G | T | 1 | a0001c0001t0004g0219 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1019+245C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146218 | ||||||
chr7:44146289
|
C | A | 54 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0003g0004others(51): Show | 61 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.1019+174G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146289 | ||||||
chr7:44146315
|
C | T | 1 | a0001c0007t0016g0222 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1019+148G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146315 | ||||||
chr7:44146334
|
C | A | 1 | a0001c0001t0008g0341 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1019+129G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146334 | ||||||
chr7:44146344
|
C | T | 1 | a0001c0001t0003g0280 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1019+119G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146344 | ||||||
chr7:44146356
|
A | G | 58 | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0039others(55): Show | 60 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1019+107T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146356 | ||||||
chr7:44146708
|
A | G | 1 | a0001c0001t0003g0321 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.864-90T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44146708 | ||||||
chr7:44146723
|
C | T | 1 | a0001c0001t0014g0025 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.864-105G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44146723 | ||||||
chr7:44146729
|
C | T | 5 | a0001c0001t0001g0094a0001c0001t0001g0159a0001c0001t0008g0341others(2): Show | 6 | HG00597.hp1 HG02040.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.864-111G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44146729 | ||||||
chr7:44146752
|
C | A | 1 | a0001c0001t0003g0176 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.864-134G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44146752 | ||||||
chr7:44147058
|
G | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.864-440C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44147058 | ||||||
chr7:44147408
|
G | A | 2 | a0001c0001t0001g0319a0001c0001t0001g0320 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.863+242C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44147408 | ||||||
chr7:44147569
|
A | T | 1 | a0001c0001t0002g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.863+81T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44147569 | ||||||
chr7:44147853
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.680-20C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44147853 | ||||||
chr7:44147879
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.680-46G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44147879 | ||||||
chr7:44148005
|
C | G | 1 | a0001c0001t0002g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.680-172G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44148005 | ||||||
chr7:44148510
|
GT | G | 164 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(161): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.680-678delA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44148510 | ||||||
chr7:44148621
|
T | C | 240 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(237): Show | 260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.680-788A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44148621 | ||||||
chr7:44148802
|
G | A | 1 | a0001c0001t0003g0202 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.679+958C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44148802 | ||||||
chr7:44148810
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.679+950G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44148810 | ||||||
chr7:44149168
|
A | G | 1 | a0001c0001t0002g0260 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.679+592T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149168 | ||||||
chr7:44149275
|
C | T | 1 | a0001c0001t0005g0145 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.679+485G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149275 | ||||||
chr7:44149411
|
C | T | 74 | a0001c0001t0001g0083a0001c0001t0001g0166a0001c0001t0001g0233others(71): Show | 78 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.679+349G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149411 | ||||||
chr7:44149424
|
T | C | 240 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(237): Show | 260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.679+336A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149424 | ||||||
chr7:44149484
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.679+276T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149484 | ||||||
chr7:44149591
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.679+169C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149591 | ||||||
chr7:44149675
|
T | C | 76 | a0001c0001t0001g0083a0001c0001t0001g0166a0001c0001t0001g0233others(73): Show | 80 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.679+85A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149675 | ||||||
chr7:44149722
|
A | G | 240 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(237): Show | 260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.679+38T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149722 | ||||||
chr7:44149940
|
C | A | 5 | a0001c0001t0001g0156a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | NA18949.hp2 NA18962.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+29G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 5/9 | chr7 | 44149940 | ||||||
chr7:44150093
|
C | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0169a0001c0001t0001g0227others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-29G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 4/9 | chr7 | 44150093 | ||||||
chr7:44150298
|
T | C | 1 | a0001c0001t0010g0348 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.484-234A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 4/9 | chr7 | 44150298 | ||||||
chr7:44150538
|
T | C | 1 | a0001c0001t0003g0272 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.483+418A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 4/9 | chr7 | 44150538 | ||||||
chr7:44150869
|
T | G | 242 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(239): Show | 262 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.483+87A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 4/9 | chr7 | 44150869 | ||||||
chr7:44150898
|
T | A | 15 | a0001c0001t0002g0022a0001c0001t0002g0115a0001c0001t0002g0167others(12): Show | 16 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.483+58A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 4/9 | chr7 | 44150898 | ||||||
chr7:44151113
|
G | C | 1 | a0001c0001t0001g0293 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.364-38C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151113 | ||||||
chr7:44151453
|
A | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0078 | 3 | NA18983.hp1 NA19062.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.364-378T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151453 | ||||||
chr7:44151525
|
G | A | 1 | a0001c0001t0002g0249 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.364-450C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151525 | ||||||
chr7:44151581
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.364-506G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151581 | ||||||
chr7:44151591
|
T | A | 69 | a0001c0001t0001g0166a0001c0001t0001g0259a0001c0001t0001g0304others(66): Show | 73 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.364-516A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151591 | ||||||
chr7:44151591
|
T | G | 46 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0230others(43): Show | 52 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.364-516A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151591 | ||||||
chr7:44151710
|
C | T | 106 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(103): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.363+561G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151710 | ||||||
chr7:44151747
|
T | C | 119 | a0001c0001t0001g0042a0001c0001t0001g0166a0001c0001t0001g0173others(116): Show | 129 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.363+524A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151747 | ||||||
chr7:44151763
|
T | C | 120 | a0001c0001t0001g0094a0001c0001t0001g0166a0001c0001t0001g0173others(117): Show | 130 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.363+508A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151763 | ||||||
chr7:44151953
|
C | T | 11 | a0001c0001t0002g0115a0001c0001t0002g0140a0001c0001t0005g0113others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.363+318G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151953 | ||||||
chr7:44151954
|
G | A | 1 | a0001c0001t0003g0202 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.363+317C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151954 | ||||||
chr7:44152106
|
G | A | 7 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0081others(4): Show | 7 | HG02015.hp1 NA18956.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+165C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44152106 | ||||||
chr7:44152201
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.363+70G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44152201 | ||||||
chr7:44152604
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(125): Show | 144 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.209-179T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152604 | ||||||
chr7:44152661
|
C | A | 118 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(115): Show | 128 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.209-236G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152661 | ||||||
chr7:44152758
|
C | CT | 269 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(266): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.209-334dupA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152758 | ||||||
chr7:44152758
|
C | CTT | 77 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 88 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.209-335_209-334dup others(2): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152758 | ||||||
chr7:44152794
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.209-369G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152794 | ||||||
chr7:44152950
|
G | A | 6 | a0001c0001t0002g0022a0001c0001t0002g0167a0001c0001t0002g0168others(3): Show | 7 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+351C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152950 | ||||||
chr7:44152953
|
G | A | 126 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(123): Show | 137 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.208+348C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152953 | ||||||
chr7:44153079
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.208+222C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44153079 | ||||||
chr7:44153525
|
G | T | 1 | a0001c0004t0004g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.46-62C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44153525 | ||||||
chr7:44153805
|
C | T | 126 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(123): Show | 137 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.46-342G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44153805 | ||||||
chr7:44153863
|
G | T | 107 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(104): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.46-400C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44153863 | ||||||
chr7:44153952
|
T | G | 13 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0002g0048others(10): Show | 15 | HG00639.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.46-489A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44153952 | ||||||
chr7:44153986
|
C | T | 1 | a0001c0001t0006g0177 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.46-523G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44153986 | ||||||
chr7:44154142
|
G | A | 1 | a0001c0001t0002g0208 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.46-679C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154142 | ||||||
chr7:44154248
|
T | G | 1 | a0001c0001t0002g0129 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.46-785A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154248 | ||||||
chr7:44154323
|
G | T | 1 | a0001c0001t0002g0017 | 2 | HG02074.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.46-860C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154323 | ||||||
chr7:44154638
|
GA | G | 3 | a0001c0001t0002g0014a0001c0001t0002g0028a0001c0001t0002g0223 | 4 | HG00099.hp2 HG00323.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-1176delT | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154638 | ||||||
chr7:44154883
|
G | A | 47 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0061others(44): Show | 53 | HG00140.hp1 HG00741.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.46-1420C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154883 | ||||||
chr7:44154924
|
T | G | 357 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(354): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.46-1461A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154924 | ||||||
chr7:44154952
|
G | A | 125 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(122): Show | 136 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.46-1489C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154952 | ||||||
chr7:44154952
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.46-1489C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154952 | ||||||
chr7:44154987
|
A | G | 13 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0002g0048others(10): Show | 15 | HG00639.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.46-1524T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154987 | ||||||
chr7:44155112
|
T | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0078 | 3 | NA18983.hp1 NA19062.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.46-1649A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155112 | ||||||
chr7:44155152
|
C | A | 1 | a0001c0001t0005g0237 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.46-1689G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155152 | ||||||
chr7:44155222
|
C | T | 1 | a0001c0001t0002g0132 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.46-1759G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155222 | ||||||
chr7:44155239
|
C | A | 30 | a0001c0001t0001g0195a0001c0001t0002g0001a0001c0001t0002g0026others(27): Show | 35 | HG00741.hp2 HG01109.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.46-1776G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155239 | ||||||
chr7:44155351
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.46-1888C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155351 | ||||||
chr7:44155397
|
G | A | 8 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0037others(5): Show | 11 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.46-1934C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155397 | ||||||
chr7:44155410
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.46-1947G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155410 | ||||||
chr7:44155477
|
G | A | 1 | a0001c0001t0007g0342 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-2014C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155477 | ||||||
chr7:44155516
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.46-2053T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155516 | ||||||
chr7:44155635
|
A | C | 1 | a0001c0001t0001g0293 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.46-2172T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155635 | ||||||
chr7:44155820
|
G | A | 10 | a0001c0001t0001g0083a0001c0001t0001g0233a0001c0001t0001g0234others(7): Show | 10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-2357C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155820 | ||||||
chr7:44155855
|
G | A | 1 | a0001c0001t0003g0184 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.46-2392C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155855 | ||||||
chr7:44155927
|
T | C | 1 | a0001c0001t0012g0358 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.46-2464A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155927 | ||||||
chr7:44156167
|
G | A | 1 | a0001c0001t0018g0343 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.46-2704C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156167 | ||||||
chr7:44156312
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.46-2849C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156312 | ||||||
chr7:44156342
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.46-2879G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156342 | ||||||
chr7:44156381
|
GT | G | 3 | a0001c0001t0001g0196a0001c0001t0001g0203a0001c0001t0001g0334 | 3 | HG01255.hp1 HG01952.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.46-2919delA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156381 | ||||||
chr7:44156435
|
A | G | 1 | a0001c0001t0002g0036 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.46-2972T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156435 | ||||||
chr7:44156470
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0018others(171): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.46-3007G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156470 | ||||||
chr7:44156949
|
G | C | 3 | a0001c0001t0002g0140a0001c0001t0005g0146a0001c0001t0005g0147 | 3 | HG01109.hp1 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.46-3486C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156949 | ||||||
chr7:44156983
|
A | G | 1 | a0001c0001t0017g0073 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.46-3520T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156983 | ||||||
chr7:44157214
|
A | G | 2 | a0001c0001t0002g0057a0001c0001t0003g0056 | 2 | NA18979.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.46-3751T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157214 | ||||||
chr7:44157241
|
C | T | 1 | a0001c0001t0002g0226 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.46-3778G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157241 | ||||||
chr7:44157276
|
T | C | 1 | a0001c0001t0002g0232 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.46-3813A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157276 | ||||||
chr7:44157377
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.46-3914C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157377 | ||||||
chr7:44157464
|
C | G | 5 | a0001c0001t0002g0006a0001c0001t0002g0031a0001c0001t0002g0033others(2): Show | 6 | NA18940.hp2 NA18944.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-4001G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157464 | ||||||
chr7:44157560
|
G | A | 1 | a0001c0001t0002g0133 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.46-4097C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157560 | ||||||
chr7:44157631
|
G | A | 1 | a0001c0001t0004g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46-4168C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157631 | ||||||
chr7:44157678
|
A | G | 1 | a0002c0002t0002g0003 | 3 | HG02257.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.46-4215T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157678 | ||||||
chr7:44157824
|
C | T | 1 | a0001c0001t0002g0089 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.46-4361G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157824 | ||||||
chr7:44157854
|
A | G | 3 | a0001c0001t0013g0359a0001c0001t0013g0360a0002c0002t0002g0003 | 5 | HG02257.hp1 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-4391T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157854 | ||||||
chr7:44157901
|
G | A | 4 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0003g0150others(1): Show | 4 | HG01496.hp1 HG02293.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-4438C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157901 | ||||||
chr7:44157929
|
G | A | 3 | a0001c0001t0002g0133a0001c0001t0002g0289a0001c0001t0003g0180 | 3 | HG00544.hp1 HG02293.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.46-4466C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157929 | ||||||
chr7:44157968
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0241 | 2 | NA18949.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.46-4505G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157968 | ||||||
chr7:44157984
|
G | T | 100 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(97): Show | 110 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.46-4521C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157984 | ||||||
chr7:44158080
|
T | C | 1 | a0001c0001t0005g0145 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.46-4617A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158080 | ||||||
chr7:44158167
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.46-4704A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158167 | ||||||
chr7:44158176
|
C | T | 11 | a0001c0001t0001g0083a0001c0001t0001g0233a0001c0001t0001g0234others(8): Show | 11 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.46-4713G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158176 | ||||||
chr7:44158360
|
G | C | 1 | a0001c0001t0001g0055 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.46-4897C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158360 | ||||||
chr7:44158451
|
C | G | 2 | a0001c0001t0012g0357a0001c0001t0012g0358 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.46-4988G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158451 | ||||||
chr7:44158495
|
G | A | 2 | a0001c0001t0002g0092a0001c0001t0002g0139 | 2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.46-5032C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158495 | ||||||
chr7:44158558
|
A | G | 1 | a0001c0001t0017g0073 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.46-5095T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158558 | ||||||
chr7:44158679
|
C | T | 4 | a0001c0001t0004g0051a0001c0001t0004g0085a0001c0001t0004g0215others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-5216G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158679 | ||||||
chr7:44158733
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.46-5270G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158733 | ||||||
chr7:44159021
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.46-5558G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159021 | ||||||
chr7:44159057
|
T | C | 1 | a0002c0002t0002g0003 | 3 | HG02257.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.46-5594A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159057 | ||||||
chr7:44159061
|
T | A | 1 | a0001c0001t0001g0105 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.46-5598A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159061 | ||||||
chr7:44159144
|
A | G | 2 | a0001c0001t0002g0057a0001c0001t0003g0056 | 2 | NA18979.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.46-5681T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159144 | ||||||
chr7:44159164
|
G | A | 10 | a0001c0001t0001g0083a0001c0001t0001g0233a0001c0001t0001g0234others(7): Show | 10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-5701C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159164 | ||||||
chr7:44159345
|
G | GC | 359 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(356): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.46-5883dupG | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159345 | ||||||
chr7:44159362
|
G | GC | 359 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(356): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.46-5900dupG | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159362 | ||||||
chr7:44159368
|
T | TG | 359 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(356): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.46-5906dupC | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159368 | ||||||
chr7:44159402
|
C | A | 1 | a0001c0001t0001g0241 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.46-5939G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159402 | ||||||
chr7:44159413
|
C | T | 1 | a0001c0001t0003g0280 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.46-5950G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159413 | ||||||
chr7:44159543
|
C | T | 95 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(92): Show | 104 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.46-6080G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159543 | ||||||
chr7:44159693
|
G | A | 2 | a0001c0001t0013g0359a0001c0001t0013g0360 | 2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46-6230C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159693 | ||||||
chr7:44159852
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.46-6389G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159852 | ||||||
chr7:44159930
|
C | A | 1 | a0001c0001t0002g0186 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.46-6467G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159930 | ||||||
chr7:44160350
|
C | T | 1 | a0001c0001t0005g0275 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.46-6887G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160350 | ||||||
chr7:44160487
|
C | T | 1 | a0001c0003t0002g0288 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.46-7024G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160487 | ||||||
chr7:44160500
|
G | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0041others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.46-7037C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160500 | ||||||
chr7:44160637
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.46-7174C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160637 | ||||||
chr7:44160666
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.46-7203G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160666 | ||||||
chr7:44160727
|
T | C | 1 | a0001c0001t0002g0033 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.46-7264A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160727 | ||||||
chr7:44160798
|
T | G | 1 | a0001c0001t0002g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.46-7335A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160798 | ||||||
chr7:44160884
|
A | G | 1 | a0001c0001t0001g0326 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.46-7421T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160884 | ||||||
chr7:44160929
|
G | A | 5 | a0001c0001t0001g0220a0001c0001t0002g0014a0001c0001t0002g0223others(2): Show | 6 | HG00323.hp1 HG01256.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-7466C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160929 | ||||||
chr7:44161079
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.46-7616G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161079 | ||||||
chr7:44161080
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.46-7617C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161080 | ||||||
chr7:44161116
|
T | TTAATTA | 123 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0055others(120): Show | 133 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.46-7654_46-7653ins others(6): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161116 | ||||||
chr7:44161157
|
G | A | 6 | a0001c0001t0001g0083a0001c0001t0001g0234a0001c0001t0001g0324others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-7694C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161157 | ||||||
chr7:44161285
|
T | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0015others(240): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.46-7822A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161285 | ||||||
chr7:44161323
|
T | C | 3 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0003g0172 | 3 | HG00280.hp1 HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.46-7860A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161323 | ||||||
chr7:44161403
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.46-7940C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161403 | ||||||
chr7:44161550
|
C | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0041others(45): Show | 57 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.46-8087G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161550 | ||||||
chr7:44161716
|
T | A | 2 | a0001c0001t0002g0278a0001c0001t0002g0309 | 2 | NA18950.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.46-8253A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161716 | ||||||
chr7:44161943
|
G | C | 7 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(4): Show | 7 | HG02258.hp1 HG02630.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-8480C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161943 | ||||||
chr7:44162283
|
C | T | 1 | a0001c0007t0016g0222 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.46-8820G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44162283 | ||||||
chr7:44162634
|
A | C | 1 | a0001c0001t0002g0133 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.46-9171T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44162634 | ||||||
chr7:44162790
|
T | C | 15 | a0001c0001t0002g0022a0001c0001t0002g0065a0001c0001t0002g0066others(12): Show | 16 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.46-9327A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44162790 | ||||||
chr7:44163117
|
C | T | 7 | a0001c0001t0002g0022a0001c0001t0002g0167a0001c0001t0002g0168others(4): Show | 8 | HG00639.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-9654G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44163117 | ||||||
chr7:44163223
|
A | T | 1 | a0001c0001t0001g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.46-9760T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44163223 | ||||||
chr7:44163295
|
G | A | 1 | a0001c0001t0002g0226 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.46-9832C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44163295 | ||||||
chr7:44163334
|
T | C | 1 | a0001c0001t0002g0060 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.46-9871A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44163334 | ||||||
chr7:44163407
|
C | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(241): Show | 273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.46-9944G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44163407 | ||||||
chr7:44163619
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.46-10156C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44163619 | ||||||
chr7:44164135
|
T | C | 6 | a0001c0001t0002g0022a0001c0001t0002g0167a0001c0001t0002g0168others(3): Show | 7 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-10672A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164135 | ||||||
chr7:44164150
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.46-10687C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164150 | ||||||
chr7:44164163
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.46-10700T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164163 | ||||||
chr7:44164313
|
A | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.46-10850T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164313 | ||||||
chr7:44164349
|
A | G | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46-10886T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164349 | ||||||
chr7:44164419
|
A | G | 4 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0002g0104others(1): Show | 6 | HG02257.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-10956T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164419 | ||||||
chr7:44164708
|
G | A | 1 | a0001c0001t0003g0277 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.46-11245C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164708 | ||||||
chr7:44164723
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.46-11260C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164723 | ||||||
chr7:44164827
|
C | T | 62 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0142others(59): Show | 67 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.46-11364G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164827 | ||||||
chr7:44164927
|
G | T | 1 | a0001c0001t0001g0303 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.46-11464C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164927 | ||||||
chr7:44165078
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0241 | 2 | NA18949.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.46-11615G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165078 | ||||||
chr7:44165133
|
A | G | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.46-11670T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165133 | ||||||
chr7:44165135
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.46-11672C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165135 | ||||||
chr7:44165236
|
C | T | 2 | a0001c0001t0003g0009a0001c0001t0004g0221 | 3 | HG01070.hp1 HG01071.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.46-11773G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165236 | ||||||
chr7:44165253
|
A | G | 5 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0181others(2): Show | 5 | HG01934.hp1 NA18967.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-11790T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165253 | ||||||
chr7:44165345
|
A | AAAT | 59 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0142others(56): Show | 63 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.46-11885_46-11883d others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165345 | ||||||
chr7:44165345
|
A | AAATAAT | 4 | a0001c0001t0002g0010a0001c0001t0002g0086a0001c0001t0002g0155others(1): Show | 5 | HG00423.hp2 NA18943.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-11888_46-11883d others(8): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165345 | ||||||
chr7:44165345
|
A | AAATAATA others(2): Show |
51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.46-11891_46-11883d others(11): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165345 | ||||||
chr7:44165345
|
A | AAATAATA others(5): Show |
1 | a0001c0001t0003g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.46-11894_46-11883d others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165345 | ||||||
chr7:44165345
|
A | AAATAATA others(8): Show |
1 | a0001c0001t0003g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.46-11897_46-11883d others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165345 | ||||||
chr7:44165395
|
G | A | 241 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(238): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.46-11932C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165395 | ||||||
chr7:44165550
|
T | C | 62 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0054others(59): Show | 66 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.46-12087A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165550 | ||||||
chr7:44165915
|
A | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.46-12452T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165915 | ||||||
chr7:44166006
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.46-12543C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166006 | ||||||
chr7:44166147
|
T | C | 1 | a0001c0001t0003g0116 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.46-12684A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166147 | ||||||
chr7:44166211
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.46-12748G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166211 | ||||||
chr7:44166296
|
C | T | 5 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(2): Show | 5 | HG00558.hp2 HG00673.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-12833G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166296 | ||||||
chr7:44166307
|
A | C | 184 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(181): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.46-12844T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166307 | ||||||
chr7:44166387
|
G | A | 2 | a0001c0001t0003g0170a0001c0001t0003g0171 | 2 | HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.46-12924C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166387 | ||||||
chr7:44166535
|
TA | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(224): Show | 252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.46-13073delT | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166535 | ||||||
chr7:44166592
|
C | T | 1 | a0001c0003t0002g0288 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.46-13129G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166592 | ||||||
chr7:44166749
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.46-13286T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166749 | ||||||
chr7:44166756
|
GAT | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.46-13295_46-13294d others(4): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166756 | ||||||
chr7:44166795
|
T | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.46-13332A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166795 | ||||||
chr7:44166862
|
T | TA | 325 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(322): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.46-13400dupT | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166862 | ||||||
chr7:44167004
|
C | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0002g0104 | 3 | HG02818.hp1 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.46-13541G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167004 | ||||||
chr7:44167083
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.46-13620G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167083 | ||||||
chr7:44167225
|
T | C | 3 | a0001c0001t0001g0164a0001c0001t0001g0209a0001c0001t0001g0331 | 3 | HG00280.hp2 HG01109.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.46-13762A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167225 | ||||||
chr7:44167344
|
C | G | 7 | a0001c0001t0002g0022a0001c0001t0002g0167a0001c0001t0002g0168others(4): Show | 10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-13881G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167344 | ||||||
chr7:44167346
|
G | A | 3 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0019g0350 | 3 | NA18939.hp2 NA18978.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.46-13883C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167346 | ||||||
chr7:44167497
|
G | A | 11 | a0001c0001t0001g0083a0001c0001t0001g0233a0001c0001t0001g0234others(8): Show | 11 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.46-14034C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167497 | ||||||
chr7:44167510
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.46-14047G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167510 | ||||||
chr7:44167567
|
T | C | 1 | a0001c0001t0002g0036 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.46-14104A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167567 | ||||||
chr7:44167642
|
T | C | 3 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0003g0172 | 3 | HG00280.hp1 HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.46-14179A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167642 | ||||||
chr7:44167889
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.46-14426G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167889 | ||||||
chr7:44167895
|
T | C | 105 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0038others(102): Show | 115 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.46-14432A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167895 | ||||||
chr7:44167956
|
G | A | 4 | a0001c0001t0012g0357a0001c0001t0012g0358a0001c0001t0013g0359others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-14493C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167956 | ||||||
chr7:44168012
|
C | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0195 | 2 | HG02647.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.46-14549G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168012 | ||||||
chr7:44168408
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.46-14945C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168408 | ||||||
chr7:44168431
|
C | A | 1 | a0001c0001t0001g0295 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.46-14968G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168431 | ||||||
chr7:44168448
|
C | CT | 8 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0247others(5): Show | 9 | HG01433.hp1 HG02145.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.46-14986dupA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168448 | ||||||
chr7:44168448
|
CT | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0295a0001c0001t0001g0296others(4): Show | 7 | HG01099.hp2 HG01257.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-14986delA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168448 | ||||||
chr7:44168487
|
C | T | 4 | a0001c0001t0002g0022a0001c0001t0002g0310a0001c0001t0002g0316others(1): Show | 5 | HG02055.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-15024G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168487 | ||||||
chr7:44168637
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.46-15174C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168637 | ||||||
chr7:44169023
|
T | C | 1 | a0001c0001t0005g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.46-15560A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44169023 | ||||||
chr7:44169028
|
T | C | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46-15565A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44169028 | ||||||
chr7:44169464
|
C | A | 4 | a0001c0001t0012g0357a0001c0001t0012g0358a0001c0001t0013g0359others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-16001G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44169464 | ||||||
chr7:44169723
|
G | A | 64 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0142others(61): Show | 69 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.46-16260C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44169723 | ||||||
chr7:44169912
|
A | T | 1 | a0001c0001t0001g0011 | 2 | NA18948.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.46-16449T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44169912 | ||||||
chr7:44170275
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0002g0104 | 3 | HG02818.hp1 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.46-16812C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44170275 | ||||||
chr7:44170306
|
C | A | 2 | a0001c0001t0002g0129a0001c0001t0019g0350 | 2 | NA18939.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.46-16843G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44170306 | ||||||
chr7:44170482
|
C | T | 1 | a0001c0001t0002g0052 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.46-17019G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44170482 | ||||||
chr7:44170681
|
T | C | 1 | a0001c0001t0003g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.46-17218A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44170681 | ||||||
chr7:44170881
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.46-17418C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44170881 | ||||||
chr7:44171111
|
C | T | 74 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0083others(71): Show | 79 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.46-17648G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171111 | ||||||
chr7:44171422
|
A | AAAAT | 64 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0142others(61): Show | 69 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.45+17483_45+17486d others(6): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171422 | ||||||
chr7:44171422
|
A | AAAATAAA others(1): Show |
104 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0038others(101): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.45+17479_45+17486d others(10): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171422 | ||||||
chr7:44171422
|
A | AAAATAAA others(5): Show |
1 | a0001c0001t0001g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.45+17475_45+17486d others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171422 | ||||||
chr7:44171470
|
C | T | 1 | a0001c0001t0003g0158 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.45+17439G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171470 | ||||||
chr7:44171498
|
A | T | 3 | a0001c0001t0003g0044a0001c0001t0003g0292a0001c0001t0003g0294 | 3 | HG00140.hp2 HG01361.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.45+17411T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171498 | ||||||
chr7:44171568
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.45+17341G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171568 | ||||||
chr7:44171694
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.45+17215T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171694 | ||||||
chr7:44171738
|
T | C | 74 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0083others(71): Show | 79 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.45+17171A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171738 | ||||||
chr7:44171808
|
T | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.45+17101A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171808 | ||||||
chr7:44171844
|
G | GT | 50 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(47): Show | 60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+17064dupA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171844 | ||||||
chr7:44171851
|
G | GT | 10 | a0001c0001t0001g0156a0001c0001t0001g0206a0001c0001t0001g0241others(7): Show | 11 | HG00140.hp2 HG01361.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+17057dupA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171851 | ||||||
chr7:44171851
|
G | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.45+17058C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171851 | ||||||
chr7:44171862
|
T | G | 1 | a0001c0001t0002g0040 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.45+17047A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171862 | ||||||
chr7:44172019
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.45+16890G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172019 | ||||||
chr7:44172135
|
G | A | 1 | a0001c0001t0003g0325 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.45+16774C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172135 | ||||||
chr7:44172196
|
G | A | 6 | a0001c0001t0002g0022a0001c0001t0002g0167a0001c0001t0002g0168others(3): Show | 7 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+16713C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172196 | ||||||
chr7:44172302
|
C | G | 1 | a0001c0001t0002g0109 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.45+16607G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172302 | ||||||
chr7:44172332
|
C | G | 1 | a0001c0001t0001g0335 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.45+16577G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172332 | ||||||
chr7:44172332
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.45+16577G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172332 | ||||||
chr7:44172526
|
G | C | 1 | a0001c0001t0005g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.45+16383C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172526 | ||||||
chr7:44172677
|
A | C | 1 | a0001c0001t0008g0346 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.45+16232T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172677 | ||||||
chr7:44172686
|
G | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.45+16223C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172686 | ||||||
chr7:44172826
|
C | A | 1 | a0001c0001t0002g0036 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.45+16083G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172826 | ||||||
chr7:44172894
|
T | A | 1 | a0001c0001t0002g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+16015A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172894 | ||||||
chr7:44172967
|
C | T | 6 | a0001c0001t0002g0022a0001c0001t0002g0167a0001c0001t0002g0168others(3): Show | 7 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+15942G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172967 | ||||||
chr7:44172985
|
C | T | 10 | a0001c0001t0001g0083a0001c0001t0001g0233a0001c0001t0001g0234others(7): Show | 10 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+15924G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172985 | ||||||
chr7:44173346
|
C | T | 2 | a0001c0001t0010g0349a0001c0001t0018g0343 | 2 | NA18983.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.45+15563G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173346 | ||||||
chr7:44173494
|
T | C | 1 | a0001c0004t0004g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.45+15415A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173494 | ||||||
chr7:44173623
|
A | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(227): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.45+15286T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173623 | ||||||
chr7:44173699
|
G | A | 4 | a0001c0001t0001g0264a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG01099.hp2 HG01261.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+15210C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173699 | ||||||
chr7:44173760
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0002g0104 | 3 | HG02818.hp1 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.45+15149A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173760 | ||||||
chr7:44173777
|
T | C | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.45+15132A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173777 | ||||||
chr7:44173833
|
G | A | 10 | a0001c0001t0001g0083a0001c0001t0001g0233a0001c0001t0001g0234others(7): Show | 10 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+15076C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173833 | ||||||
chr7:44173943
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.45+14966C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173943 | ||||||
chr7:44174029
|
G | A | 10 | a0001c0001t0001g0083a0001c0001t0001g0233a0001c0001t0001g0234others(7): Show | 10 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+14880C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174029 | ||||||
chr7:44174275
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(51): Show | 64 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.45+14634G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174275 | ||||||
chr7:44174531
|
G | C | 1 | a0001c0001t0001g0075 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.45+14378C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174531 | ||||||
chr7:44174557
|
C | CCTT | 246 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(243): Show | 274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.45+14349_45+14351d others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174557 | ||||||
chr7:44174641
|
T | C | 7 | a0001c0001t0002g0022a0001c0001t0002g0167a0001c0001t0002g0168others(4): Show | 10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+14268A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174641 | ||||||
chr7:44174643
|
C | A | 4 | a0001c0001t0004g0021a0001c0001t0004g0258a0001c0001t0004g0311others(1): Show | 5 | HG01433.hp2 HG02257.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+14266G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174643 | ||||||
chr7:44174676
|
CT | C | 11 | a0001c0001t0001g0165a0001c0001t0002g0095a0001c0001t0003g0116others(8): Show | 12 | HG00423.hp1 HG00597.hp2 NA18954.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+14232delA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174676 | ||||||
chr7:44174695
|
TTCC | T | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0038others(99): Show | 112 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.45+14211_45+14213d others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174695 | ||||||
chr7:44174725
|
T | C | 1 | a0001c0001t0004g0020 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.45+14184A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174725 | ||||||
chr7:44174774
|
T | A | 1 | a0001c0001t0004g0215 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.45+14135A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174774 | ||||||
chr7:44174842
|
T | C | 1 | a0001c0001t0002g0236 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.45+14067A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174842 | ||||||
chr7:44174844
|
G | C | 1 | a0001c0001t0002g0236 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.45+14065C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174844 | ||||||
chr7:44174844
|
G | GTTCCTC | 10 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(7): Show | 15 | NA18942.hp2 NA18948.hp1 NA18950.hp1 others(12): Show |
intron_variant | MODIFIER | c.45+14059_45+14064d others(8): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174844 | ||||||
chr7:44174848
|
C | CTCTTCTT others(2): Show |
3 | a0001c0001t0001g0264a0001c0001t0002g0168a0001c0001t0002g0317 | 3 | HG02280.hp1 HG02622.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.45+14060_45+14061i others(11): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174848 | ||||||
chr7:44174848
|
C | CTCTTCTT others(5): Show |
1 | a0001c0001t0002g0022 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.45+14060_45+14061i others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174848 | ||||||
chr7:44174848
|
C | CTCTTCTT others(8): Show |
1 | a0001c0001t0002g0316 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.45+14060_45+14061i others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174848 | ||||||
chr7:44174848
|
C | CTCTTCTT others(11): Show |
2 | a0001c0001t0002g0167a0001c0001t0002g0310 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.45+14060_45+14061i others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174848 | ||||||
chr7:44174848
|
C | CTCTTCTT others(17): Show |
1 | a0001c0001t0003g0280 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.45+14060_45+14061i others(26): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174848 | ||||||
chr7:44174848
|
CTCTTCCT others(14): Show |
C | 1 | a0001c0001t0002g0254 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.45+14040_45+14060d others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174848 | ||||||
chr7:44174854
|
C | CTCCTCTT others(11): Show |
1 | a0001c0001t0004g0051 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.45+14054_45+14055i others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCCTCTT others(20): Show |
2 | a0001c0001t0001g0286a0001c0001t0008g0347 | 2 | NA18967.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.45+14054_45+14055i others(29): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCT | 13 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0206others(10): Show | 13 | HG01109.hp2 HG01255.hp1 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+14052_45+14054d others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCCT others(11): Show |
1 | a0001c0001t0002g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.45+14054_45+14055i others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCCT others(14): Show |
1 | a0001c0001t0001g0319 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.45+14054_45+14055i others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCCT others(17): Show |
1 | a0001c0001t0001g0320 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+14054_45+14055i others(26): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCCT others(2): Show |
10 | a0001c0001t0001g0265a0001c0001t0002g0151a0001c0001t0002g0189others(7): Show | 12 | HG00733.hp1 HG00738.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+14054_45+14055i others(11): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCCT others(8): Show |
1 | a0001c0001t0003g0116 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.45+14054_45+14055i others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCCT others(5): Show |
7 | a0001c0001t0001g0165a0001c0001t0001g0181a0001c0001t0001g0188others(4): Show | 7 | HG00280.hp1 HG00609.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+14054_45+14055i others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCCT others(8): Show |
4 | a0001c0001t0001g0190a0001c0001t0003g0277a0001c0001t0007g0339others(1): Show | 4 | NA19074.hp2 NA19077.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+14054_45+14055i others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCCT others(11): Show |
6 | a0001c0001t0002g0084a0001c0001t0003g0117a0001c0001t0003g0276others(3): Show | 7 | HG00423.hp1 HG02559.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+14054_45+14055i others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCCT others(14): Show |
1 | a0001c0001t0007g0342 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.45+14054_45+14055i others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCCT others(20): Show |
1 | a0001c0001t0003g0102 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.45+14054_45+14055i others(29): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCT | 24 | a0001c0001t0001g0029a0001c0001t0001g0093a0001c0001t0001g0121others(21): Show | 25 | HG01099.hp1 HG01106.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.45+14049_45+14054d others(8): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCTT others(2): Show |
15 | a0001c0001t0001g0101a0001c0001t0001g0120a0001c0001t0001g0164others(12): Show | 15 | HG00597.hp1 HG01074.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+14046_45+14054d others(11): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCTT others(5): Show |
11 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0201others(8): Show | 11 | HG00140.hp2 HG00733.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+14043_45+14054d others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCTT others(8): Show |
14 | a0001c0001t0001g0098a0001c0001t0001g0119a0001c0001t0001g0198others(11): Show | 14 | HG00544.hp2 HG00673.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.45+14040_45+14054d others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCTT others(11): Show |
7 | a0001c0001t0001g0149a0001c0001t0001g0197a0001c0001t0001g0293others(4): Show | 8 | HG00621.hp2 HG01358.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+14037_45+14054d others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCTT others(14): Show |
2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | NA18946.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.45+14054_45+14055i others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCTT others(23): Show |
1 | a0001c0001t0002g0216 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.45+14054_45+14055i others(32): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCTT others(14): Show |
3 | a0001c0001t0001g0112a0001c0001t0001g0200a0001c0001t0001g0335 | 3 | HG02080.hp1 NA18956.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.45+14034_45+14054d others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | CTCTTCTT others(17): Show |
1 | a0001c0001t0003g0292 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.45+14031_45+14054d others(26): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
C | T | 13 | a0001c0001t0001g0264a0001c0001t0002g0022a0001c0001t0002g0065others(10): Show | 16 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+14055G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
CTCT | C | 16 | a0001c0001t0001g0016a0001c0001t0001g0238a0001c0001t0001g0255others(13): Show | 18 | HG00438.hp2 HG01099.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.45+14052_45+14054d others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
CTCTTCT | C | 19 | a0001c0001t0001g0209a0001c0001t0001g0279a0001c0001t0002g0010others(16): Show | 22 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.45+14049_45+14054d others(8): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
CTCTTCTT others(2): Show |
C | 23 | a0001c0001t0001g0269a0001c0001t0001g0290a0001c0001t0001g0304others(20): Show | 23 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.45+14046_45+14054d others(11): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
CTCTTCTT others(5): Show |
C | 4 | a0001c0001t0001g0094a0001c0001t0001g0166a0001c0001t0002g0226others(1): Show | 4 | HG01071.hp2 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+14043_45+14054d others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
CTCTTCTT others(8): Show |
C | 4 | a0001c0001t0001g0064a0001c0001t0001g0142a0001c0001t0005g0113others(1): Show | 4 | HG01256.hp1 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+14040_45+14054d others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
CTCTTCTT others(11): Show |
C | 8 | a0001c0001t0002g0115a0001c0001t0002g0143a0001c0001t0005g0114others(5): Show | 8 | HG00741.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+14037_45+14054d others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174854
|
CTCTTCTT others(14): Show |
C | 2 | a0001c0001t0001g0210a0001c0001t0005g0147 | 2 | HG01109.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.45+14034_45+14054d others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | ||||||
chr7:44174857
|
T | TTCC | 5 | a0001c0001t0001g0192a0001c0001t0002g0186a0001c0001t0003g0185others(2): Show | 5 | HG01123.hp1 HG01981.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+14051_45+14052i others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174857 | ||||||
chr7:44174860
|
T | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0001t0003g0009others(1): Show | 6 | HG01070.hp1 HG01071.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+14049A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174860 | ||||||
chr7:44174863
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.45+14046A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174863 | ||||||
chr7:44174914
|
T | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(47): Show | 60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+13995A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174914 | ||||||
chr7:44174915
|
T | C | 73 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0142others(70): Show | 78 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.45+13994A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174915
|
T | TCTC | 5 | a0001c0001t0002g0035a0001c0001t0002g0058a0001c0001t0002g0063others(2): Show | 5 | HG01255.hp2 HG01891.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174915
|
T | TCTTCTC | 5 | a0001c0001t0002g0034a0001c0001t0002g0043a0001c0001t0002g0057others(2): Show | 5 | HG02071.hp2 HG02895.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(8): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174915
|
T | TCTTCTTC others(2): Show |
7 | a0001c0001t0002g0006a0001c0001t0002g0033a0001c0001t0002g0089others(4): Show | 8 | HG00558.hp2 HG02135.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(11): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174915
|
T | TCTTCTTC others(5): Show |
13 | a0001c0001t0001g0234a0001c0001t0002g0019a0001c0001t0002g0028others(10): Show | 14 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174915
|
T | TCTTCTTC others(8): Show |
13 | a0001c0001t0001g0007a0001c0001t0001g0054a0001c0001t0001g0055others(10): Show | 17 | HG00323.hp1 HG01891.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174915
|
T | TCTTCTTC others(11): Show |
15 | a0001c0001t0001g0062a0001c0001t0001g0079a0001c0001t0001g0105others(12): Show | 17 | HG00140.hp1 HG00673.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174915
|
T | TCTTCTTC others(14): Show |
14 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(11): Show | 14 | HG02015.hp1 HG02647.hp1 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174915
|
T | TCTTCTTC others(17): Show |
12 | a0001c0001t0001g0061a0001c0001t0001g0247a0001c0001t0001g0261others(9): Show | 12 | HG01884.hp1 HG02615.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(26): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174915
|
T | TCTTCTTC others(20): Show |
9 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0076others(6): Show | 11 | HG01433.hp2 HG01934.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(29): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174915
|
T | TCTTCTTC others(23): Show |
6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0002g0070others(3): Show | 6 | HG01257.hp2 NA18522.hp2 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(32): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174915
|
T | TCTTCTTC others(26): Show |
4 | a0001c0001t0002g0037a0001c0001t0002g0289a0001c0001t0004g0311others(1): Show | 4 | HG00544.hp1 HG02486.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(35): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174915
|
T | TCTTCTTC others(29): Show |
1 | a0001c0001t0001g0306 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.45+13993_45+13994i others(38): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | ||||||
chr7:44174937
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.45+13972G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174937 | ||||||
chr7:44175056
|
T | G | 2 | a0001c0001t0002g0316a0001c0001t0002g0317 | 2 | HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.45+13853A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175056 | ||||||
chr7:44175168
|
G | A | 4 | a0001c0001t0012g0357a0001c0001t0012g0358a0001c0001t0013g0359others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+13741C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175168 | ||||||
chr7:44175310
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.45+13599T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175310 | ||||||
chr7:44175349
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.45+13560A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175349 | ||||||
chr7:44175415
|
T | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(51): Show | 64 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.45+13494A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175415 | ||||||
chr7:44175467
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.45+13442A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175467 | ||||||
chr7:44175551
|
G | A | 1 | a0001c0001t0005g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.45+13358C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175551 | ||||||
chr7:44175789
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+13120G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175789 | ||||||
chr7:44176062
|
C | A | 1 | a0001c0001t0002g0148 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.45+12847G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176062 | ||||||
chr7:44176272
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.45+12637C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176272 | ||||||
chr7:44176398
|
C | T | 3 | a0001c0001t0004g0273a0001c0001t0004g0274a0001c0001t0005g0275 | 3 | HG02895.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.45+12511G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176398 | ||||||
chr7:44176417
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.45+12492C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176417 | ||||||
chr7:44176513
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.45+12396C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176513 | ||||||
chr7:44176538
|
G | A | 180 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(177): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.45+12371C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176538 | ||||||
chr7:44176575
|
C | T | 6 | a0001c0001t0002g0022a0001c0001t0002g0167a0001c0001t0002g0168others(3): Show | 7 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+12334G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176575 | ||||||
chr7:44176625
|
C | A | 2 | a0001c0001t0009g0353a0001c0001t0011g0352 | 2 | NA18969.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.45+12284G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176625 | ||||||
chr7:44176681
|
G | A | 63 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0054others(60): Show | 67 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.45+12228C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176681 | ||||||
chr7:44176698
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.45+12211G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176698 | ||||||
chr7:44176800
|
C | T | 11 | a0001c0001t0001g0105a0001c0001t0002g0006a0001c0001t0002g0017others(8): Show | 13 | HG00609.hp1 HG02074.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+12109G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176800 | ||||||
chr7:44176808
|
C | T | 3 | a0001c0001t0004g0273a0001c0001t0004g0274a0001c0001t0005g0275 | 3 | HG02895.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.45+12101G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176808 | ||||||
chr7:44176941
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.45+11968G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176941 | ||||||
chr7:44176947
|
G | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0050others(65): Show | 72 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.45+11962C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176947 | ||||||
chr7:44176999
|
T | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(52): Show | 67 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.45+11910A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176999 | ||||||
chr7:44177010
|
C | T | 7 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0002g0104others(4): Show | 7 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+11899G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177010 | ||||||
chr7:44177057
|
C | A | 4 | a0001c0001t0002g0048a0001c0001t0002g0069a0001c0001t0004g0047others(1): Show | 4 | HG00639.hp2 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+11852G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177057 | ||||||
chr7:44177155
|
C | T | 236 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(233): Show | 263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.45+11754G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177155 | ||||||
chr7:44177229
|
C | G | 2 | a0001c0001t0002g0013a0001c0001t0003g0199 | 3 | HG01070.hp2 HG01081.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.45+11680G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177229 | ||||||
chr7:44177342
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0002g0104 | 3 | HG02818.hp1 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.45+11567C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177342 | ||||||
chr7:44177412
|
T | C | 1 | a0001c0001t0002g0329 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+11497A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177412 | ||||||
chr7:44177527
|
C | T | 242 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.45+11382G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177527 | ||||||
chr7:44177595
|
A | C | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG00544.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.45+11314T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177595 | ||||||
chr7:44177617
|
C | CA | 236 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(233): Show | 263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.45+11291dupT | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177617 | ||||||
chr7:44177680
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.45+11229C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177680 | ||||||
chr7:44177762
|
A | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(52): Show | 67 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.45+11147T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177762 | ||||||
chr7:44177765
|
T | C | 1 | a0001c0001t0003g0212 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.45+11144A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177765 | ||||||
chr7:44177842
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.45+11067A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177842 | ||||||
chr7:44177847
|
A | C | 1 | a0001c0001t0001g0290 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.45+11062T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177847 | ||||||
chr7:44177976
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.45+10933G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177976 | ||||||
chr7:44177977
|
T | C | 5 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0072others(2): Show | 8 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+10932A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177977 | ||||||
chr7:44178062
|
GT | G | 4 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0002g0104others(1): Show | 6 | HG02257.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+10846delA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178062 | ||||||
chr7:44178224
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.45+10685C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178224 | ||||||
chr7:44178250
|
A | C | 1 | a0001c0001t0001g0196 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.45+10659T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178250 | ||||||
chr7:44178261
|
G | A | 1 | a0001c0001t0002g0232 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.45+10648C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178261 | ||||||
chr7:44178409
|
A | T | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.45+10500T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178409 | ||||||
chr7:44178453
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.45+10456C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178453 | ||||||
chr7:44178742
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(51): Show | 64 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.45+10167C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178742 | ||||||
chr7:44178746
|
C | A | 1 | a0001c0001t0003g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.45+10163G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178746 | ||||||
chr7:44179195
|
T | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(48): Show | 61 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.45+9714A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179195 | ||||||
chr7:44179257
|
G | A | 98 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0038others(95): Show | 108 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.45+9652C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179257 | ||||||
chr7:44179330
|
C | T | 1 | a0001c0001t0008g0340 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.45+9579G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179330 | ||||||
chr7:44179436
|
T | C | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.45+9473A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179436 | ||||||
chr7:44179475
|
T | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.45+9434A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179475 | ||||||
chr7:44179498
|
T | C | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9411A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179498 | ||||||
chr7:44179502
|
C | G | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9407G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179502 | ||||||
chr7:44179505
|
A | C | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9404T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179505 | ||||||
chr7:44179506
|
T | G | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9403A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179506 | ||||||
chr7:44179507
|
T | C | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9402A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179507 | ||||||
chr7:44179509
|
G | T | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9400C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179509 | ||||||
chr7:44179511
|
C | T | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9398G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179511 | ||||||
chr7:44179512
|
A | T | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9397T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179512 | ||||||
chr7:44179602
|
G | T | 1 | a0001c0001t0004g0315 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+9307C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179602 | ||||||
chr7:44179683
|
G | A | 11 | a0001c0001t0001g0083a0001c0001t0001g0233a0001c0001t0001g0234others(8): Show | 11 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+9226C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179683 | ||||||
chr7:44179739
|
A | G | 65 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0142others(62): Show | 70 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.45+9170T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179739 | ||||||
chr7:44179835
|
T | C | 1 | a0001c0001t0002g0289 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.45+9074A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179835 | ||||||
chr7:44179970
|
T | A | 4 | a0001c0001t0012g0357a0001c0001t0012g0358a0001c0001t0013g0359others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+8939A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179970 | ||||||
chr7:44179973
|
C | T | 1 | a0001c0001t0005g0225 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.45+8936G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179973 | ||||||
chr7:44180004
|
A | T | 1 | a0001c0001t0001g0195 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.45+8905T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180004 | ||||||
chr7:44180005
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.45+8904G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180005 | ||||||
chr7:44180006
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.45+8903C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180006 | ||||||
chr7:44180106
|
T | C | 64 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0142others(61): Show | 69 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.45+8803A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180106 | ||||||
chr7:44180143
|
C | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(47): Show | 60 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+8766G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180143 | ||||||
chr7:44180220
|
G | C | 1 | a0001c0001t0003g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.45+8689C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180220 | ||||||
chr7:44180226
|
G | T | 1 | a0001c0001t0002g0097 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.45+8683C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180226 | ||||||
chr7:44180251
|
G | A | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.45+8658C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180251 | ||||||
chr7:44180314
|
G | A | 3 | a0001c0001t0002g0270a0001c0001t0002g0291a0001c0001t0002g0333 | 3 | HG02148.hp1 NA18939.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.45+8595C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180314 | ||||||
chr7:44180320
|
A | G | 1 | a0001c0001t0005g0237 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.45+8589T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180320 | ||||||
chr7:44180352
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0002g0043 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.45+8557C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180352 | ||||||
chr7:44180396
|
G | T | 2 | a0001c0001t0002g0189a0001c0001t0002g0236 | 2 | NA18948.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.45+8513C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180396 | ||||||
chr7:44180590
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.45+8319A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180590 | ||||||
chr7:44180628
|
G | A | 1 | a0001c0001t0004g0315 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+8281C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180628 | ||||||
chr7:44180812
|
A | G | 2 | a0001c0001t0003g0163a0001c0001t0003g0174 | 2 | NA18941.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.45+8097T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180812 | ||||||
chr7:44180822
|
A | G | 11 | a0001c0001t0001g0083a0001c0001t0001g0233a0001c0001t0001g0234others(8): Show | 11 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+8087T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180822 | ||||||
chr7:44181001
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.45+7908A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181001 | ||||||
chr7:44181006
|
A | T | 1 | a0001c0001t0002g0249 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.45+7903T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181006 | ||||||
chr7:44181074
|
C | G | 3 | a0001c0001t0002g0087a0001c0001t0002g0278a0001c0001t0002g0309 | 3 | NA18950.hp2 NA18970.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.45+7835G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181074 | ||||||
chr7:44181320
|
C | A | 7 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 7 | HG01496.hp1 HG02293.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+7589G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181320 | ||||||
chr7:44181394
|
G | C | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.45+7515C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181394 | ||||||
chr7:44181483
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.45+7426C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181483 | ||||||
chr7:44181696
|
G | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(47): Show | 60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+7213C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181696 | ||||||
chr7:44181703
|
A | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(47): Show | 60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+7206T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181703 | ||||||
chr7:44181806
|
G | A | 23 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0165others(20): Show | 28 | HG00423.hp2 HG00609.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+7103C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181806 | ||||||
chr7:44181944
|
C | G | 2 | a0001c0001t0009g0353a0001c0001t0011g0352 | 2 | NA18969.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.45+6965G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181944 | ||||||
chr7:44181982
|
A | C | 315 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(312): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.45+6927T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181982 | ||||||
chr7:44182176
|
G | C | 2 | a0001c0001t0002g0070a0001c0001t0002g0071 | 2 | NA18978.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.45+6733C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182176 | ||||||
chr7:44182294
|
A | G | 4 | a0001c0001t0002g0115a0001c0001t0004g0273a0001c0001t0004g0274others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6615T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182294 | ||||||
chr7:44182326
|
A | G | 8 | a0001c0001t0001g0319a0001c0001t0002g0022a0001c0001t0002g0316others(5): Show | 9 | HG02280.hp1 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+6583T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182326 | ||||||
chr7:44182343
|
C | A | 1 | a0001c0001t0001g0235 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.45+6566G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182343 | ||||||
chr7:44182389
|
C | T | 2 | a0001c0001t0007g0337a0001c0001t0008g0338 | 2 | HG01123.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.45+6520G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182389 | ||||||
chr7:44182404
|
G | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.45+6505C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182404 | ||||||
chr7:44182405
|
A | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.45+6504T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182405 | ||||||
chr7:44182470
|
A | G | 4 | a0001c0001t0001g0038a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | NA18965.hp1 NA18985.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6439T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182470 | ||||||
chr7:44182621
|
C | G | 40 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0101others(37): Show | 45 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.45+6288G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182621 | ||||||
chr7:44182626
|
G | C | 289 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(286): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.45+6283C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182626 | ||||||
chr7:44182854
|
G | A | 3 | a0001c0001t0002g0084a0001c0001t0002g0310a0001c0001t0004g0085 | 3 | HG02055.hp1 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.45+6055C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182854 | ||||||
chr7:44182872
|
A | G | 298 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(295): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.45+6037T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182872 | ||||||
chr7:44183155
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+5754G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183155 | ||||||
chr7:44183189
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.45+5720C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183189 | ||||||
chr7:44183197
|
C | T | 1 | a0001c0004t0004g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.45+5712G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183197 | ||||||
chr7:44183203
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0015others(110): Show | 126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.45+5706G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183203 | ||||||
chr7:44183246
|
C | A | 1 | a0001c0001t0002g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.45+5663G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183246 | ||||||
chr7:44183399
|
C | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | HG01109.hp2 HG01358.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.45+5510G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183399 | ||||||
chr7:44183433
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.45+5476G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183433 | ||||||
chr7:44183693
|
T | TA | 19 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(16): Show | 20 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.45+5215_45+5216ins others(1): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183693 | ||||||
chr7:44183696
|
G | A | 14 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(11): Show | 15 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.45+5213C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183696 | ||||||
chr7:44183837
|
T | G | 1 | a0001c0001t0002g0157 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.45+5072A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183837 | ||||||
chr7:44183880
|
G | A | 267 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(264): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.45+5029C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183880 | ||||||
chr7:44183909
|
C | A | 4 | a0001c0001t0004g0021a0001c0001t0004g0311a0001c0001t0004g0312others(1): Show | 7 | HG01433.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+5000G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183909 | ||||||
chr7:44183959
|
C | T | 18 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(15): Show | 19 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.45+4950G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183959 | ||||||
chr7:44184122
|
G | A | 77 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0098others(74): Show | 81 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.45+4787C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184122 | ||||||
chr7:44184259
|
G | A | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.45+4650C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184259 | ||||||
chr7:44184343
|
G | A | 82 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0098others(79): Show | 87 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.45+4566C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184343 | ||||||
chr7:44184356
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.45+4553C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184356 | ||||||
chr7:44184377
|
T | C | 2 | a0001c0001t0001g0314a0001c0001t0002g0313 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.45+4532A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184377 | ||||||
chr7:44184499
|
C | T | 12 | a0001c0001t0001g0169a0001c0001t0002g0006a0001c0001t0002g0031others(9): Show | 13 | HG00280.hp1 HG01074.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+4410G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184499 | ||||||
chr7:44184551
|
C | T | 5 | a0001c0001t0002g0092a0001c0001t0012g0357a0001c0001t0012g0358others(2): Show | 5 | HG02602.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+4358G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184551 | ||||||
chr7:44184569
|
C | G | 1 | a0002c0002t0002g0003 | 3 | HG02257.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.45+4340G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184569 | ||||||
chr7:44184840
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.45+4069C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184840 | ||||||
chr7:44184845
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.45+4064A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184845 | ||||||
chr7:44184933
|
GAT | G | 18 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(15): Show | 19 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.45+3974_45+3975del others(2): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184933 | ||||||
chr7:44184937
|
T | TAC | 4 | a0001c0001t0001g0308a0001c0001t0001g0314a0001c0001t0002g0017others(1): Show | 5 | HG01099.hp1 HG02074.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+3970_45+3971dup others(2): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184937 | ||||||
chr7:44184939
|
C | T | 2 | a0001c0001t0002g0167a0001c0001t0002g0168 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.45+3970G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184939 | ||||||
chr7:44185003
|
G | A | 4 | a0001c0001t0012g0357a0001c0001t0012g0358a0001c0001t0013g0359others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+3906C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185003 | ||||||
chr7:44185015
|
T | TAC | 267 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(264): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.45+3892_45+3893dup others(2): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185015 | ||||||
chr7:44185015
|
T | TACAC | 5 | a0001c0001t0001g0159a0001c0001t0001g0166a0001c0001t0003g0158others(2): Show | 5 | HG01106.hp2 HG01981.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+3890_45+3893dup others(4): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185015 | ||||||
chr7:44185031
|
C | CACAG | 5 | a0001c0001t0001g0259a0001c0001t0001g0261a0001c0001t0002g0260others(2): Show | 5 | HG01257.hp1 HG02615.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+3877_45+3878ins others(4): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185031 | ||||||
chr7:44185031
|
CAG | C | 18 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(15): Show | 19 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.45+3876_45+3877del others(2): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185031 | ||||||
chr7:44185087
|
C | G | 2 | a0001c0001t0001g0319a0001c0001t0001g0320 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.45+3822G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185087 | ||||||
chr7:44185252
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0015others(111): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.45+3657C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185252 | ||||||
chr7:44185322
|
G | T | 1 | a0001c0001t0006g0257 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.45+3587C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185322 | ||||||
chr7:44185657
|
A | G | 4 | a0001c0001t0012g0357a0001c0001t0012g0358a0001c0001t0013g0359others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+3252T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185657 | ||||||
chr7:44185699
|
G | GC | 359 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(356): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.45+3209dupG | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185699 | ||||||
chr7:44185741
|
T | A | 1 | a0001c0001t0006g0257 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.45+3168A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185741 | ||||||
chr7:44185887
|
G | C | 15 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(12): Show | 16 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+3022C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185887 | ||||||
chr7:44185938
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.45+2971C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185938 | ||||||
chr7:44185948
|
C | T | 2 | a0001c0001t0012g0357a0001c0001t0012g0358 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.45+2961G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185948 | ||||||
chr7:44185957
|
C | T | 4 | a0001c0001t0012g0357a0001c0001t0012g0358a0001c0001t0013g0359others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+2952G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185957 | ||||||
chr7:44186106
|
G | T | 1 | a0001c0001t0002g0162 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.45+2803C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186106 | ||||||
chr7:44186161
|
G | A | 1 | a0001c0001t0002g0318 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.45+2748C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186161 | ||||||
chr7:44186209
|
G | A | 4 | a0001c0001t0012g0357a0001c0001t0012g0358a0001c0001t0013g0359others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+2700C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186209 | ||||||
chr7:44186217
|
C | A | 1 | a0001c0001t0002g0082 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+2692G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186217 | ||||||
chr7:44186230
|
A | G | 19 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(16): Show | 20 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.45+2679T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186230 | ||||||
chr7:44186320
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.45+2589C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186320 | ||||||
chr7:44186384
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.45+2525G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186384 | ||||||
chr7:44186388
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.45+2521C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186388 | ||||||
chr7:44186412
|
C | T | 4 | a0001c0001t0012g0357a0001c0001t0012g0358a0001c0001t0013g0359others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+2497G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186412 | ||||||
chr7:44186491
|
C | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0015others(116): Show | 132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.45+2418G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186491 | ||||||
chr7:44186502
|
C | T | 74 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0098others(71): Show | 78 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.45+2407G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186502 | ||||||
chr7:44186757
|
A | G | 6 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0088others(3): Show | 6 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+2152T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186757 | ||||||
chr7:44187089
|
C | G | 15 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(12): Show | 16 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+1820G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187089 | ||||||
chr7:44187114
|
G | A | 5 | a0001c0001t0002g0022a0001c0001t0002g0316a0001c0001t0002g0317others(2): Show | 6 | HG02280.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+1795C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187114 | ||||||
chr7:44187266
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.45+1643G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187266 | ||||||
chr7:44187345
|
G | A | 19 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(16): Show | 20 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.45+1564C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187345 | ||||||
chr7:44187357
|
T | G | 15 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(12): Show | 16 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+1552A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187357 | ||||||
chr7:44187358
|
G | T | 2 | a0001c0001t0002g0084a0001c0001t0004g0085 | 2 | HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.45+1551C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187358 | ||||||
chr7:44187421
|
G | T | 60 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0038others(57): Show | 66 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.45+1488C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187421 | ||||||
chr7:44187495
|
T | C | 2 | a0001c0001t0001g0319a0001c0001t0001g0320 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.45+1414A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187495 | ||||||
chr7:44187523
|
T | C | 2 | a0001c0001t0003g0321a0001c0001t0003g0322 | 2 | HG02145.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.45+1386A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187523 | ||||||
chr7:44187686
|
A | C | 20 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(17): Show | 21 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.45+1223T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187686 | ||||||
chr7:44187697
|
G | A | 1 | a0001c0001t0002g0323 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.45+1212C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187697 | ||||||
chr7:44187774
|
C | T | 1 | a0001c0001t0011g0351 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.45+1135G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187774 | ||||||
chr7:44187790
|
T | A | 5 | a0001c0001t0012g0356a0001c0001t0012g0357a0001c0001t0012g0358others(2): Show | 5 | HG02922.hp1 HG03130.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+1119A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187790 | ||||||
chr7:44187874
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.45+1035C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187874 | ||||||
chr7:44187941
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.45+968G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187941 | ||||||
chr7:44188037
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.45+872G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188037 | ||||||
chr7:44188039
|
T | G | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG00738.hp1 HG01358.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+870A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188039 | ||||||
chr7:44188061
|
G | GC | 359 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(356): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.45+847dupG | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188061 | ||||||
chr7:44188293
|
T | C | 1 | a0001c0001t0002g0329 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+616A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188293 | ||||||
chr7:44188298
|
C | T | 15 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(12): Show | 16 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+611G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188298 | ||||||
chr7:44188321
|
C | A | 1 | a0001c0001t0002g0330 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.45+588G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188321 | ||||||
chr7:44188380
|
C | A | 2 | a0001c0001t0001g0331a0001c0001t0001g0332 | 2 | HG01109.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.45+529G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188380 | ||||||
chr7:44188480
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.45+429G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188480 | ||||||
chr7:44188512
|
G | A | 1 | a0001c0001t0002g0333 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.45+397C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188512 | ||||||
chr7:44188548
|
GC | G | 15 | a0001c0001t0007g0023a0001c0001t0007g0336a0001c0001t0007g0337others(12): Show | 16 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+360delG | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188548 | ||||||
chr7:44188608
|
G | C | 1 | a0001c0001t0001g0334 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.45+301C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188608 | ||||||
chr7:44188737
|
G | C | 1 | a0001c0001t0001g0335 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.45+172C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188737 |