geneid | 137964 |
---|---|
ensemblid | ENSG00000158669.11 |
hgncid | 20880 |
symbol | GPAT4 |
name | glycerol-3-phosphate acyltransferase 4 |
refseq_nuc | NM_178819.4 |
refseq_prot | NP_848934.1 |
ensembl_nuc | ENST00000396987.7 |
ensembl_prot | ENSP00000380184.3 |
mane_status | MANE Select |
chr | chr8 |
start | 41578200 |
end | 41625001 |
strand | + |
ver | v1.2 |
region | chr8:41578200-41625001 |
region5000 | chr8:41573200-41630001 |
regionname0 | GPAT4_chr8_41578200_41625001 |
regionname5000 | GPAT4_chr8_41573200_41630001 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1371 | 405 | 86 | 62 | 196 | 12 | 47 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
c0002 | 0/0 | 1371 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
c0003 | 0/0 | 1371 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
c0004 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 4928 | 150 | 23 | 24 | 74 | 5 | 23 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0002 | 0/1 | 4937 | 55 | 1 | 11 | 32 | 3 | 7 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0003 | 0/0 | 4936 | 51 | 4 | 11 | 29 | 1 | 6 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0004 | 0/0 | 4937 | 32 | 12 | 1 | 19 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0005 | 0/0 | 4936 | 28 | 11 | 1 | 12 | 1 | 3 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0006 | 0/0 | 4937 | 13 | 6 | 5 | 0 | 0 | 2 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0007 | 0/0 | 4939 | 12 | 5 | 6 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0008 | 0/0 | 4937 | 8 | 8 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0009 | 0/0 | 4937 | 5 | 0 | 0 | 5 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0010 | 0/0 | 4936 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0011 | 0/0 | 4928 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0012 | 0/0 | 4937 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0013 | 0/0 | 4936 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0014 | 0/0 | 4937 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0015 | 0/0 | 4937 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0016 | 0/0 | 4936 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0017 | 0/0 | 4930 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0018 | 0/0 | 4937 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0019 | 0/0 | 4937 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0020 | 0/0 | 4939 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0021 | 0/0 | 4936 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0022 | 0/0 | 4936 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0023 | 0/0 | 4937 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0024 | 0/0 | 4937 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0025 | 0/0 | 4937 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0026 | 0/0 | 4937 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0027 | 0/0 | 4937 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0028 | 0/0 | 4936 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0029 | 0/0 | 4937 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0030 | 0/0 | 4937 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0031 | 0/0 | 4937 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0032 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0033 | 0/0 | 4928 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0034 | 0/0 | 4928 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0035 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0036 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0037 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0038 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0039 | 0/0 | 4937 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0040 | 0/0 | 4932 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0041 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0042 | 0/0 | 4927 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0043 | 0/0 | 4928 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0044 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0045 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0046 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0047 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0048 | 0/0 | 4928 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0049 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0050 | 0/0 | 4928 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0051 | 0/0 | 4935 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0052 | 0/0 | 4939 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0053 | 0/0 | 4939 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0054 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0055 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0056 | 0/0 | 4932 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0057 | 0/0 | 4932 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
t0058 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 3 | 3 | 0 | 3 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0002 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0005 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0031 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1371 | 405 | 86 | 62 | 196 | 12 | 47 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0003 | 0/0 | 1371 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0004 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0002c0002 | 0/0 | 1371 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 6298 | 150 | 23 | 24 | 74 | 5 | 23 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0002 | 0/1 | 6307 | 55 | 1 | 11 | 32 | 3 | 7 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0003 | 0/0 | 6306 | 50 | 4 | 11 | 29 | 1 | 5 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0004 | 0/0 | 6307 | 32 | 12 | 1 | 19 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0005 | 0/0 | 6306 | 28 | 11 | 1 | 12 | 1 | 3 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0006 | 0/0 | 6307 | 13 | 6 | 5 | 0 | 0 | 2 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0007 | 0/0 | 6309 | 11 | 5 | 5 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0008 | 0/0 | 6307 | 8 | 8 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0009 | 0/0 | 6307 | 5 | 0 | 0 | 5 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0010 | 0/0 | 6306 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0011 | 0/0 | 6298 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0012 | 0/0 | 6307 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0013 | 0/0 | 6306 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0015 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0016 | 0/0 | 6306 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0017 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0018 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0019 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0020 | 0/0 | 6309 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0021 | 0/0 | 6306 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0022 | 0/0 | 6306 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0023 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0024 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0025 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0026 | 0/0 | 6307 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0027 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0028 | 0/0 | 6306 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0029 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0030 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0031 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0032 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0033 | 0/0 | 6298 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0034 | 0/0 | 6298 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0035 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0036 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0037 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0038 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0039 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0040 | 0/0 | 6302 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0041 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0042 | 0/0 | 6297 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0043 | 0/0 | 6298 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0044 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0045 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0046 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0047 | 0/0 | 6298 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0048 | 0/0 | 6298 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0049 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0050 | 0/0 | 6298 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0052 | 0/0 | 6309 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0053 | 0/0 | 6309 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0054 | 0/0 | 6298 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0055 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0056 | 0/0 | 6302 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0057 | 0/0 | 6302 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0001t0058 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0003t0007 | 0/0 | 6309 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0003t0051 | 0/0 | 6305 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0001c0004t0003 | 0/0 | 6306 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
a0002c0002t0014 | 0/0 | 6307 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | copy fasta | chr8 | 41573200 | 41630001 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0001 | 0/0 | 9 | 0 | 3 | 3 | 0 | 3 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0006g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0006g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0006g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0006g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0007g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0007g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0007g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0007g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0007g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0007g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0008g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0009g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0009g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0009g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0010g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0011g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0012g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0012g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0013g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0013g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0015g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0016g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0017g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0018g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0019g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0020g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0021g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0022g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0023g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0024g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0025g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0026g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0027g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0028g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0029g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0030g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0031g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0032g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0033g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0034g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0035g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0036g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0037g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0038g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0039g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0040g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0041g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0042g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0043g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0044g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0045g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0046g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0047g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0048g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0049g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0050g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0052g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0053g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0054g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0055g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0056g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0057g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0001t0058g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0003t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0003t0051g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0001c0004t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0002c0002t0014g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
a0002c0002t0014g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | GBR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0283 | EUR | FIN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0340 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0316 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00621 | hp2 | a0001 | c0001 | t0011 | g0187 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0291 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00738 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG00741 | hp2 | a0001 | c0001 | t0024 | g0033 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01069 | hp1 | a0001 | c0003 | t0007 | g0002 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01069 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01070 | hp1 | a0001 | c0001 | t0007 | g0044 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01071 | hp1 | a0001 | c0001 | t0006 | g0275 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01074 | hp1 | a0001 | c0003 | t0051 | g0046 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01081 | hp2 | a0001 | c0001 | t0007 | g0045 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0294 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01106 | hp2 | a0001 | c0001 | t0007 | g0042 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0277 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0350 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01261 | hp2 | a0001 | c0001 | t0023 | g0293 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0274 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01361 | hp1 | a0001 | c0001 | t0006 | g0278 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01361 | hp2 | a0001 | c0001 | t0057 | g0047 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01496 | hp1 | a0001 | c0001 | t0033 | g0208 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0031 | EUR | IBS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01516 | hp2 | a0001 | c0001 | t0028 | g0086 | EUR | IBS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0327 | EUR | IBS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0344 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02004 | hp2 | a0001 | c0001 | t0005 | g0120 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0320 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02027 | hp2 | a0001 | c0001 | t0041 | g0256 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0096 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02074 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02083 | hp2 | a0001 | c0001 | t0039 | g0195 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02132 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02165 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | CDX | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CDX | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0099 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0113 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02523 | hp1 | a0001 | c0001 | t0049 | g0126 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0111 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0318 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02630 | hp1 | a0002 | c0002 | t0014 | g0095 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0107 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0097 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0273 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0349 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02698 | hp1 | a0001 | c0004 | t0003 | g0017 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0332 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02723 | hp1 | a0001 | c0001 | t0053 | g0040 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02723 | hp2 | a0001 | c0001 | t0047 | g0215 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02809 | hp2 | a0001 | c0001 | t0012 | g0269 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02818 | hp2 | a0001 | c0001 | t0056 | g0048 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0323 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0271 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0106 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02897 | hp2 | a0001 | c0001 | t0022 | g0272 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0052 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02965 | hp1 | a0001 | c0001 | t0019 | g0103 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0093 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03017 | hp2 | a0001 | c0001 | t0043 | g0144 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0110 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03098 | hp1 | a0001 | c0001 | t0015 | g0292 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0279 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03139 | hp1 | a0001 | c0001 | t0040 | g0268 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0331 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03195 | hp1 | a0001 | c0001 | t0010 | g0091 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03239 | hp1 | a0001 | c0001 | t0007 | g0002 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03239 | hp2 | a0001 | c0001 | t0026 | g0123 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03453 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03490 | hp1 | a0001 | c0001 | t0006 | g0012 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0021 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0012 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03516 | hp1 | a0001 | c0001 | t0029 | g0102 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03579 | hp2 | a0002 | c0002 | t0014 | g0094 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03654 | hp2 | a0001 | c0001 | t0048 | g0167 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0121 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0284 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03710 | hp1 | a0001 | c0001 | t0050 | g0209 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0109 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0065 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0321 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0325 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG04115 | hp2 | a0001 | c0001 | t0034 | g0193 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18522 | hp2 | a0001 | c0001 | t0054 | g0346 | AFR | YRI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | CHB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | CHB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18906 | hp2 | a0001 | c0001 | t0010 | g0092 | AFR | YRI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18942 | hp1 | a0001 | c0001 | t0032 | g0249 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18942 | hp2 | a0001 | c0001 | t0027 | g0305 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0317 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18944 | hp2 | a0001 | c0001 | t0058 | g0220 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18950 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18951 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18963 | hp2 | a0001 | c0001 | t0009 | g0348 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18966 | hp2 | a0001 | c0001 | t0013 | g0059 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18967 | hp2 | a0001 | c0001 | t0030 | g0281 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18969 | hp1 | a0001 | c0001 | t0038 | g0229 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18969 | hp2 | a0001 | c0001 | t0044 | g0183 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18970 | hp1 | a0001 | c0001 | t0035 | g0238 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18972 | hp1 | a0001 | c0001 | t0046 | g0171 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18972 | hp2 | a0001 | c0001 | t0009 | g0014 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18975 | hp1 | a0001 | c0001 | t0011 | g0186 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18978 | hp1 | a0001 | c0001 | t0004 | g0341 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0315 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18980 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18982 | hp1 | a0001 | c0001 | t0042 | g0176 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0339 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18984 | hp1 | a0001 | c0001 | t0021 | g0308 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18986 | hp1 | a0001 | c0001 | t0045 | g0146 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18986 | hp2 | a0001 | c0001 | t0009 | g0014 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18987 | hp1 | a0001 | c0001 | t0009 | g0296 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18999 | hp2 | a0001 | c0001 | t0009 | g0014 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19001 | hp2 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19011 | hp1 | a0001 | c0001 | t0013 | g0060 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19012 | hp2 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19043 | hp1 | a0001 | c0001 | t0031 | g0041 | AFR | LWK | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0043 | AFR | LWK | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19055 | hp1 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19060 | hp1 | a0001 | c0001 | t0011 | g0160 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19060 | hp2 | a0001 | c0001 | t0055 | g0151 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0351 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19074 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19077 | hp1 | a0001 | c0001 | t0017 | g0290 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19078 | hp2 | a0001 | c0001 | t0016 | g0066 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19080 | hp2 | a0001 | c0001 | t0037 | g0184 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19081 | hp2 | a0001 | c0001 | t0018 | g0302 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19085 | hp1 | a0001 | c0001 | t0036 | g0253 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | YRI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | YRI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ASW | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0068 | EUR | TSI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0021 | EUR | TSI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA20805 | hp1 | a0001 | c0001 | t0052 | g0002 | EUR | TSI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | TSI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA20905 | hp1 | a0001 | c0001 | t0020 | g0276 | SAS | GIH | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | GIH | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0324 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03471 | hp1 | a0001 | c0001 | t0025 | g0337 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0270 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | USA | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | USA | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | USA | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | USA | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | LWK | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
NA21309 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | LWK | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0286 | REF | REF | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0053 | REF | REF | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:41578276
|
T | G | 1 | a0001 | 207 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(204): Show |
splice_region_variant | LOW | c.-851T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/13 | chr8 | 41578276 | ||||||
chr8:41620928
|
C | G | 1 | a0002 | 2 | HG02630.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.1298C>G | p.Thr433Arg | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2225/6298 | 1298/1371 | 433/456 | chr8 | 41620928 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:41609665
|
A | G | 1 | a0001c0003 | 2 | HG01069.hp1 HG01074.hp1 |
synonymous_variant | LOW | c.246A>G | p.Ala82Ala | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/13 | 1173/6298 | 246/1371 | 82/456 | chr8 | 41609665 | ||
chr8:41609839
|
G | A | 1 | a0001c0004 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.420G>A | p.Leu140Leu | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/13 | 1347/6298 | 420/1371 | 140/456 | chr8 | 41609839 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:41598337
|
G | T | 1 | a0001c0001t0058 | 1 | NA18944.hp2 | 5_prime_UTR_variant | MODIFIER | c.-803G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | 803 | chr8 | 41598337 | |||||
chr8:41598365
|
G | C | 1 | a0001c0001t0031 | 1 | NA19043.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-775G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | chr8 | 41598365 | ||||||
chr8:41598557
|
C | A | 1 | a0001c0001t0032 | 1 | NA18942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-583C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | 583 | chr8 | 41598557 | |||||
chr8:41598607
|
C | T | 2 | a0001c0001t0056a0001c0001t0057 | 2 | HG01361.hp2 HG02818.hp2 |
5_prime_UTR_variant | MODIFIER | c.-533C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | 533 | chr8 | 41598607 | |||||
chr8:41598633
|
G | A | 1 | a0001c0001t0015 | 1 | HG03098.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-507G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | chr8 | 41598633 | ||||||
chr8:41598717
|
A | C | 1 | a0001c0001t0013 | 2 | NA18966.hp2 NA19011.hp1 |
5_prime_UTR_variant | MODIFIER | c.-423A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | 423 | chr8 | 41598717 | |||||
chr8:41598753
|
G | A | 1 | a0001c0001t0033 | 1 | HG01496.hp1 | 5_prime_UTR_variant | MODIFIER | c.-387G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | 387 | chr8 | 41598753 | |||||
chr8:41598791
|
A | T | 1 | a0001c0001t0055 | 1 | NA19060.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-349A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | chr8 | 41598791 | ||||||
chr8:41598819
|
G | A | 1 | a0001c0001t0034 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-321G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | 321 | chr8 | 41598819 | |||||
chr8:41621050
|
A | G | 6 | a0001c0001t0007a0001c0001t0052a0001c0001t0053others(3): Show | 16 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*49A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 49 | chr8 | 41621050 | |||||
chr8:41621068
|
G | A | 2 | a0001c0001t0056a0001c0001t0057 | 2 | HG01361.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*67G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 67 | chr8 | 41621068 | |||||
chr8:41621071
|
G | A | 1 | a0001c0001t0035 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*70G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 70 | chr8 | 41621071 | |||||
chr8:41621154
|
G | A | 1 | a0001c0001t0031 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*153G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 153 | chr8 | 41621154 | |||||
chr8:41621165
|
G | A | 1 | a0001c0001t0036 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*164G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 164 | chr8 | 41621165 | |||||
chr8:41621183
|
A | C | 1 | a0001c0001t0010 | 3 | HG02970.hp2 HG03195.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*182A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 182 | chr8 | 41621183 | |||||
chr8:41621201
|
G | A | 1 | a0001c0001t0016 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*200G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 200 | chr8 | 41621201 | |||||
chr8:41621220
|
G | A | 1 | a0001c0001t0017 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*219G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 219 | chr8 | 41621220 | |||||
chr8:41621307
|
G | A | 1 | a0001c0001t0031 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*306G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 306 | chr8 | 41621307 | |||||
chr8:41621373
|
T | G | 1 | a0001c0001t0018 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 372 | chr8 | 41621373 | |||||
chr8:41621467
|
C | T | 1 | a0001c0001t0030 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*466C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 466 | chr8 | 41621467 | |||||
chr8:41621774
|
T | C | 5 | a0001c0001t0007a0001c0001t0052a0001c0001t0053others(2): Show | 15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*773T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 773 | chr8 | 41621774 | |||||
chr8:41621797
|
A | G | 1 | a0001c0001t0053 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*796A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 796 | chr8 | 41621797 | |||||
chr8:41621837
|
G | A | 1 | a0001c0001t0037 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*836G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 836 | chr8 | 41621837 | |||||
chr8:41621862
|
C | T | 1 | a0001c0001t0029 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*861C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 861 | chr8 | 41621862 | |||||
chr8:41621887
|
G | A | 3 | a0001c0001t0009a0001c0001t0017a0001c0001t0038 | 7 | NA18963.hp2 NA18969.hp1 NA18972.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*886G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 886 | chr8 | 41621887 | |||||
chr8:41621918
|
G | A | 2 | a0001c0001t0019a0001c0001t0029 | 2 | HG02965.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*917G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 917 | chr8 | 41621918 | |||||
chr8:41621922
|
A | G | 1 | a0001c0001t0050 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*921A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 921 | chr8 | 41621922 | |||||
chr8:41622175
|
A | G | 6 | a0001c0001t0003a0001c0001t0010a0001c0001t0013others(3): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1174A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1174 | chr8 | 41622175 | |||||
chr8:41622286
|
A | AGGAACAG | 34 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(31): Show | 233 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*1287_*1288insAACA others(3): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1288 | INFO_REALIGN_3_PRIME | chr8 | 41622286 | ||||
chr8:41622387
|
C | T | 1 | a0001c0001t0052 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1386C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1386 | chr8 | 41622387 | |||||
chr8:41622396
|
G | T | 1 | a0001c0001t0049 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1395G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1395 | chr8 | 41622396 | |||||
chr8:41622579
|
C | T | 1 | a0001c0001t0005 | 28 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1578C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1578 | chr8 | 41622579 | |||||
chr8:41622810
|
TA | T | 6 | a0001c0001t0003a0001c0001t0010a0001c0001t0013others(3): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1812delA | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1812 | INFO_REALIGN_3_PRIME | chr8 | 41622810 | ||||
chr8:41622861
|
C | T | 1 | a0001c0001t0048 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1860C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1860 | chr8 | 41622861 | |||||
chr8:41622943
|
C | T | 1 | a0001c0001t0027 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1942C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1942 | chr8 | 41622943 | |||||
chr8:41622990
|
G | A | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(27): Show | 219 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1989G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1989 | chr8 | 41622990 | |||||
chr8:41623027
|
TAC | T | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(26): Show | 218 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*2038_*2039delCA | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2038 | INFO_REALIGN_3_PRIME | chr8 | 41623027 | ||||
chr8:41623067
|
A | C | 2 | a0001c0001t0008a0002c0002t0014 | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2066A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2066 | chr8 | 41623067 | |||||
chr8:41623153
|
C | T | 2 | a0001c0001t0008a0002c0002t0014 | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2152C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2152 | chr8 | 41623153 | |||||
chr8:41623317
|
C | T | 1 | a0001c0001t0047 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2316C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2316 | chr8 | 41623317 | |||||
chr8:41623517
|
A | T | 16 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(13): Show | 105 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2516A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2516 | chr8 | 41623517 | |||||
chr8:41623518
|
G | T | 16 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(13): Show | 105 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2517G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2517 | chr8 | 41623518 | |||||
chr8:41623577
|
G | A | 35 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(32): Show | 234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*2576G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2576 | chr8 | 41623577 | |||||
chr8:41623705
|
G | A | 17 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(14): Show | 119 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*2704G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2704 | chr8 | 41623705 | |||||
chr8:41623785
|
T | TCAGA | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | 236 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*2788_*2791dupACAG | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2792 | INFO_REALIGN_3_PRIME | chr8 | 41623785 | ||||
chr8:41623819
|
C | A | 1 | a0001c0001t0041 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2818C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2818 | chr8 | 41623819 | |||||
chr8:41623838
|
CT | C | 4 | a0001c0001t0005a0001c0001t0021a0001c0001t0022others(1): Show | 31 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2852delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2852 | INFO_REALIGN_3_PRIME | chr8 | 41623838 | ||||
chr8:41623859
|
C | T | 1 | a0001c0001t0046 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2858C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2858 | chr8 | 41623859 | |||||
chr8:41623879
|
C | T | 1 | a0001c0001t0019 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2878C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2878 | chr8 | 41623879 | |||||
chr8:41623887
|
G | T | 1 | a0001c0001t0025 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2886G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2886 | chr8 | 41623887 | |||||
chr8:41623931
|
C | T | 1 | a0001c0001t0040 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2930C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2930 | chr8 | 41623931 | |||||
chr8:41623983
|
A | G | 1 | a0001c0001t0045 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2982A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2982 | chr8 | 41623983 | |||||
chr8:41624117
|
G | A | 1 | a0001c0001t0008 | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3116G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3116 | chr8 | 41624117 | |||||
chr8:41624121
|
G | C | 1 | a0001c0001t0056 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3120G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3120 | chr8 | 41624121 | |||||
chr8:41624266
|
G | A | 1 | a0001c0001t0023 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3265G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3265 | chr8 | 41624266 | |||||
chr8:41624433
|
C | G | 1 | a0001c0001t0044 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3432C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3432 | chr8 | 41624433 | |||||
chr8:41624529
|
C | T | 1 | a0001c0001t0029 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3528C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3528 | chr8 | 41624529 | |||||
chr8:41624561
|
T | C | 1 | a0001c0001t0028 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3560T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3560 | chr8 | 41624561 | |||||
chr8:41624582
|
G | A | 2 | a0001c0001t0026a0001c0001t0043 | 2 | HG03017.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3581G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3581 | chr8 | 41624582 | |||||
chr8:41624717
|
A | T | 1 | a0001c0001t0012 | 2 | HG02809.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3716A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3716 | chr8 | 41624717 | |||||
chr8:41624749
|
C | T | 4 | a0001c0001t0006a0001c0001t0012a0001c0001t0020others(1): Show | 17 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3748C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3748 | chr8 | 41624749 | |||||
chr8:41624802
|
G | A | 1 | a0001c0001t0024 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3801G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3801 | chr8 | 41624802 | |||||
chr8:41624835
|
G | A | 1 | a0001c0001t0011 | 3 | HG00621.hp2 NA18975.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3834G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3834 | chr8 | 41624835 | |||||
chr8:41624842
|
G | C | 10 | a0001c0001t0002a0001c0001t0009a0001c0001t0017others(7): Show | 68 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3841G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3841 | chr8 | 41624842 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:41578330
|
G | C | 4 | a0001c0001t0005g0034a0001c0001t0005g0035a0001c0001t0005g0036others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+52G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578330 | ||||||
chr8:41578350
|
G | A | 1 | a0001c0001t0004g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-849+72G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578350 | ||||||
chr8:41578350
|
G | C | 1 | a0001c0001t0004g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-849+72G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578350 | ||||||
chr8:41578388
|
A | G | 1 | a0001c0001t0003g0351 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-849+110A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578388 | ||||||
chr8:41578530
|
C | T | 1 | a0001c0001t0007g0350 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-849+252C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578530 | ||||||
chr8:41578566
|
T | A | 14 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(11): Show | 17 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-849+288T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578566 | ||||||
chr8:41578595
|
C | T | 2 | a0001c0001t0056g0048a0001c0001t0057g0047 | 2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-849+317C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578595 | ||||||
chr8:41578612
|
G | A | 5 | a0001c0001t0004g0008a0001c0001t0004g0038a0001c0001t0004g0049others(2): Show | 7 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-849+334G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578612 | ||||||
chr8:41578659
|
C | T | 1 | a0001c0001t0001g0349 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-849+381C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578659 | ||||||
chr8:41578930
|
G | C | 1 | a0001c0001t0006g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-849+652G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578930 | ||||||
chr8:41578980
|
G | T | 354 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0023others(351): Show | 409 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(406): Show |
intron_variant | MODIFIER | c.-849+702G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578980 | ||||||
chr8:41579016
|
G | A | 49 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(46): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-849+738G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579016 | ||||||
chr8:41579223
|
T | C | 7 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(4): Show | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-849+945T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579223 | ||||||
chr8:41579320
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-849+1042T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579320 | ||||||
chr8:41579360
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-849+1082G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579360 | ||||||
chr8:41579503
|
G | A | 2 | a0001c0001t0019g0103a0001c0001t0029g0102 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-849+1225G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579503 | ||||||
chr8:41579557
|
G | T | 1 | a0001c0001t0009g0348 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-849+1279G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579557 | ||||||
chr8:41579576
|
G | GC | 40 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(37): Show | 48 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-849+1300dupC | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41579576 | |||||
chr8:41579657
|
G | A | 2 | a0001c0001t0006g0104a0001c0001t0006g0105 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-849+1379G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579657 | ||||||
chr8:41579665
|
C | T | 4 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0007g0344others(1): Show | 4 | HG01884.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+1387C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579665 | ||||||
chr8:41579694
|
C | T | 2 | a0001c0001t0002g0342a0001c0001t0002g0343 | 2 | HG00408.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.-849+1416C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579694 | ||||||
chr8:41579720
|
C | G | 40 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(37): Show | 48 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-849+1442C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579720 | ||||||
chr8:41579794
|
C | G | 95 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(92): Show | 118 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-849+1516C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579794 | ||||||
chr8:41579798
|
G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.-849+1520G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579798 | ||||||
chr8:41579831
|
C | T | 2 | a0001c0001t0002g0033a0001c0001t0024g0033 | 2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-849+1553C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579831 | ||||||
chr8:41579836
|
C | CA | 15 | a0001c0001t0006g0012a0001c0001t0006g0052a0001c0001t0006g0104others(12): Show | 17 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.-849+1569dupA | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41579836 | |||||
chr8:41579858
|
A | G | 4 | a0001c0001t0004g0338a0001c0001t0004g0339a0001c0001t0004g0340others(1): Show | 4 | HG00438.hp1 NA18978.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+1580A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579858 | ||||||
chr8:41579963
|
C | G | 1 | a0001c0001t0006g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-849+1685C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579963 | ||||||
chr8:41580001
|
G | C | 192 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(189): Show | 234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.-849+1723G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580001 | ||||||
chr8:41580054
|
G | A | 2 | a0001c0001t0002g0280a0001c0001t0030g0281 | 2 | NA18967.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-849+1776G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580054 | ||||||
chr8:41580124
|
C | A | 2 | a0002c0002t0014g0094a0002c0002t0014g0095 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-849+1846C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580124 | ||||||
chr8:41580185
|
G | A | 1 | a0001c0001t0004g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-849+1907G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580185 | ||||||
chr8:41580209
|
G | A | 95 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(92): Show | 118 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-849+1931G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580209 | ||||||
chr8:41580226
|
C | T | 2 | a0001c0001t0006g0104a0001c0001t0006g0105 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-849+1948C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580226 | ||||||
chr8:41580264
|
C | T | 1 | a0002c0002t0014g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-849+1986C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580264 | ||||||
chr8:41580385
|
A | C | 1 | a0001c0001t0003g0085 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-849+2107A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580385 | ||||||
chr8:41580403
|
T | C | 1 | a0001c0001t0053g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-849+2125T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580403 | ||||||
chr8:41580805
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 5 | HG02135.hp2 HG02523.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-849+2527G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580805 | ||||||
chr8:41580850
|
T | G | 1 | a0001c0001t0002g0282 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-849+2572T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580850 | ||||||
chr8:41580859
|
T | C | 192 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(189): Show | 234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.-849+2581T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580859 | ||||||
chr8:41580879
|
G | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 5 | HG02135.hp2 HG02523.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-849+2601G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580879 | ||||||
chr8:41580948
|
C | T | 1 | a0001c0001t0004g0051 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-849+2670C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580948 | ||||||
chr8:41581051
|
A | G | 1 | a0001c0001t0025g0337 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-849+2773A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581051 | ||||||
chr8:41581105
|
A | C | 171 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(168): Show | 207 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.-849+2827A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581105 | ||||||
chr8:41581109
|
A | G | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.-849+2831A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581109 | ||||||
chr8:41581111
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-849+2833A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581111 | ||||||
chr8:41581160
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-849+2882A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581160 | ||||||
chr8:41581163
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-849+2885G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581163 | ||||||
chr8:41581170
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-849+2892A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581170 | ||||||
chr8:41581367
|
C | T | 1 | a0001c0001t0004g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-849+3089C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581367 | ||||||
chr8:41581555
|
G | A | 192 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(189): Show | 234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.-849+3277G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581555 | ||||||
chr8:41581584
|
C | T | 49 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(46): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-849+3306C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581584 | ||||||
chr8:41581625
|
C | CT | 25 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0251others(22): Show | 25 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.-849+3368dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581625 | |||||
chr8:41581625
|
CT | C | 11 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0003g0351others(8): Show | 11 | HG01243.hp2 HG01361.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-849+3368delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581625 | |||||
chr8:41581626
|
T | C | 4 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0003g0056others(1): Show | 4 | HG00639.hp2 HG01175.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-849+3348T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581626 | ||||||
chr8:41581774
|
G | A | 12 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(9): Show | 12 | HG02071.hp1 NA18954.hp2 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.-849+3496G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581774 | ||||||
chr8:41581817
|
T | C | 1 | a0001c0001t0029g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-849+3539T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581817 | ||||||
chr8:41581855
|
G | A | 80 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(77): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-849+3577G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581855 | ||||||
chr8:41581939
|
T | C | 1 | a0001c0001t0002g0283 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-849+3661T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581939 | ||||||
chr8:41581945
|
T | C | 1 | a0001c0001t0002g0284 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-849+3667T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581945 | ||||||
chr8:41581946
|
T | TAA | 47 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(44): Show | 56 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-849+3679_-849+368 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581946 | |||||
chr8:41581989
|
A | T | 1 | a0001c0001t0001g0199 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-849+3711A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581989 | ||||||
chr8:41581993
|
A | AT | 87 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0125others(84): Show | 95 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-849+3747dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41581993
|
A | ATT | 24 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0140others(21): Show | 29 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-849+3746_-849+374 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41581993
|
A | ATTT | 9 | a0001c0001t0001g0129a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.-849+3745_-849+374 others(7): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41581993
|
A | ATTTT | 6 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(3): Show | 6 | HG01099.hp1 HG02015.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.-849+3744_-849+374 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41581993
|
A | ATTTTT | 5 | a0001c0001t0001g0030a0001c0001t0001g0198a0001c0001t0001g0245others(2): Show | 6 | HG01358.hp1 HG01952.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-849+3743_-849+374 others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41581993
|
ATTTTTT | A | 5 | a0001c0001t0002g0332a0001c0001t0004g0008a0001c0001t0004g0331others(2): Show | 7 | HG02109.hp2 HG02630.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.-849+3742_-849+374 others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41581993
|
ATTTTTTT | A | 32 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0280others(29): Show | 34 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-849+3741_-849+374 others(11): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41581993
|
ATTTTTTT others(1): Show |
A | 65 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0033others(62): Show | 84 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-849+3740_-849+374 others(12): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41581993
|
ATTTTTTT others(2): Show |
A | 18 | a0001c0001t0005g0010a0001c0001t0005g0021a0001c0001t0005g0022others(15): Show | 22 | HG02074.hp2 HG02132.hp1 HG02165.hp1 others(19): Show |
intron_variant | MODIFIER | c.-849+3739_-849+374 others(13): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41581993
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0257 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-849+3736_-849+374 others(16): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41581993
|
ATTTTTTT others(6): Show |
A | 4 | a0001c0001t0001g0200a0001c0001t0002g0287a0001c0001t0056g0048others(1): Show | 4 | HG01361.hp2 HG02040.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+3735_-849+374 others(17): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41581993
|
ATTTTTTT others(7): Show |
A | 13 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0007g0002others(10): Show | 16 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.-849+3734_-849+374 others(18): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41581993
|
ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0031g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-849+3733_-849+374 others(19): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | |||||
chr8:41582005
|
T | A | 4 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0007g0344others(1): Show | 4 | HG01884.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+3727T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582005 | ||||||
chr8:41582018
|
T | A | 4 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0007g0344others(1): Show | 4 | HG01884.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+3740T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582018 | ||||||
chr8:41582122
|
A | G | 2 | a0001c0001t0003g0019a0001c0001t0003g0079 | 3 | HG00621.hp1 HG02083.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-849+3844A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582122 | ||||||
chr8:41582154
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-849+3876C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582154 | ||||||
chr8:41582241
|
T | G | 1 | a0001c0001t0041g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-849+3963T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582241 | ||||||
chr8:41582304
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-849+4026G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582304 | ||||||
chr8:41582337
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-849+4059T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582337 | ||||||
chr8:41582358
|
A | G | 1 | a0001c0001t0038g0229 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-849+4080A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582358 | ||||||
chr8:41582444
|
T | TAC | 28 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0147others(25): Show | 31 | HG00642.hp2 HG01081.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-849+4198_-849+419 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582444 | |||||
chr8:41582444
|
T | TACAC | 65 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0189others(62): Show | 84 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.-849+4196_-849+419 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582444 | |||||
chr8:41582444
|
T | TACACAC | 15 | a0001c0001t0001g0163a0001c0001t0002g0285a0001c0001t0002g0321others(12): Show | 16 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-849+4194_-849+419 others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582444 | |||||
chr8:41582444
|
T | TACACACA others(1): Show |
13 | a0001c0001t0004g0013a0001c0001t0004g0288a0001c0001t0004g0289others(10): Show | 15 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.-849+4192_-849+419 others(12): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582444 | |||||
chr8:41582444
|
T | TACACACA others(3): Show |
4 | a0001c0001t0004g0316a0001c0001t0004g0317a0001c0001t0004g0336others(1): Show | 4 | HG00544.hp1 NA18944.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+4190_-849+419 others(14): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582444 | |||||
chr8:41582444
|
TACAC | T | 3 | a0001c0001t0040g0268a0002c0002t0014g0094a0002c0002t0014g0095 | 3 | HG02630.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-849+4196_-849+419 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582444 | |||||
chr8:41582472
|
CACACAT | C | 48 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(45): Show | 57 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.-849+4195_-849+420 others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582472 | ||||||
chr8:41582474
|
CACAT | C | 21 | a0001c0001t0003g0058a0001c0001t0004g0315a0001c0001t0005g0010others(18): Show | 25 | HG02004.hp2 HG02055.hp2 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.-849+4197_-849+420 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582474 | ||||||
chr8:41582476
|
CAT | C | 4 | a0001c0001t0005g0108a0001c0001t0005g0109a0001c0001t0005g0110others(1): Show | 4 | HG02074.hp2 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+4199_-849+420 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582476 | ||||||
chr8:41582478
|
T | C | 98 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(95): Show | 121 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.-849+4200T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582478 | ||||||
chr8:41582674
|
A | AGT | 10 | a0001c0001t0006g0012a0001c0001t0006g0052a0001c0001t0006g0273others(7): Show | 12 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.-849+4416_-849+441 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582674 | |||||
chr8:41582674
|
A | AGTGT | 11 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(8): Show | 14 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-849+4414_-849+441 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582674 | |||||
chr8:41582674
|
A | AGTGTGT | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(48): Show | 68 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-849+4412_-849+441 others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582674 | |||||
chr8:41582674
|
A | AGTGTGTG others(1): Show |
32 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(29): Show | 36 | HG00408.hp2 HG02004.hp2 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.-849+4410_-849+441 others(12): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582674 | |||||
chr8:41582674
|
A | AGTGTGTG others(3): Show |
1 | a0001c0001t0029g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-849+4408_-849+441 others(14): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582674 | |||||
chr8:41582674
|
A | T | 3 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0266 | 3 | NA18984.hp2 NA18988.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-849+4396A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582674 | ||||||
chr8:41582676
|
T | A | 2 | a0002c0002t0014g0094a0002c0002t0014g0095 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-849+4398T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582676 | ||||||
chr8:41582684
|
T | TGTGTGTG others(8): Show |
1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-849+4417_-849+441 others(19): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582684 | |||||
chr8:41582688
|
T | TGTGTGG | 49 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(46): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-849+4415_-849+441 others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582688 | |||||
chr8:41582694
|
T | TGTGTGG | 4 | a0001c0001t0004g0294a0001c0001t0004g0318a0001c0001t0015g0292others(1): Show | 4 | HG01106.hp1 HG02622.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-849+4417_-849+441 others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582694 | |||||
chr8:41582694
|
T | TGTGTGTG others(1): Show |
14 | a0001c0001t0004g0013a0001c0001t0004g0015a0001c0001t0004g0288others(11): Show | 18 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-849+4417_-849+441 others(12): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582694 | |||||
chr8:41582694
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0004g0291 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-849+4417_-849+441 others(14): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582694 | |||||
chr8:41582696
|
G | C | 1 | a0001c0001t0029g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-849+4418G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582696 | ||||||
chr8:41582696
|
G | T | 1 | a0001c0001t0001g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-849+4418G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582696 | ||||||
chr8:41582814
|
T | G | 3 | a0001c0001t0001g0149a0001c0001t0001g0168a0001c0001t0048g0167 | 3 | HG01109.hp2 HG01496.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-849+4536T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582814 | ||||||
chr8:41582948
|
C | T | 171 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(168): Show | 207 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.-849+4670C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582948 | ||||||
chr8:41583044
|
G | A | 5 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(2): Show | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-849+4766G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583044 | ||||||
chr8:41583087
|
G | A | 19 | a0001c0001t0005g0010a0001c0001t0005g0021a0001c0001t0005g0022others(16): Show | 23 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-849+4809G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583087 | ||||||
chr8:41583232
|
AT | A | 5 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(2): Show | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-849+4955delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583232 | ||||||
chr8:41583330
|
A | C | 2 | a0001c0001t0003g0081a0001c0001t0003g0083 | 2 | HG01433.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-849+5052A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583330 | ||||||
chr8:41583341
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-849+5063A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583341 | ||||||
chr8:41583456
|
T | A | 191 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(188): Show | 233 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.-849+5178T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583456 | ||||||
chr8:41583561
|
A | G | 1 | a0001c0003t0051g0046 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-849+5283A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583561 | ||||||
chr8:41583985
|
C | T | 9 | a0001c0001t0006g0012a0001c0001t0006g0052a0001c0001t0006g0273others(6): Show | 11 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-849+5707C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583985 | ||||||
chr8:41584022
|
A | G | 2 | a0001c0001t0005g0117a0001c0001t0005g0122 | 2 | NA18946.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.-849+5744A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584022 | ||||||
chr8:41584160
|
A | G | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.-849+5882A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584160 | ||||||
chr8:41584189
|
G | A | 4 | a0001c0001t0001g0191a0001c0001t0007g0007a0001c0001t0007g0350others(1): Show | 6 | HG00735.hp2 HG01243.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-849+5911G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584189 | ||||||
chr8:41584507
|
G | A | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-849+6229G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584507 | ||||||
chr8:41584647
|
G | A | 4 | a0001c0001t0003g0016a0001c0001t0003g0084a0001c0001t0013g0059others(1): Show | 5 | HG02080.hp2 NA18747.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.-849+6369G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584647 | ||||||
chr8:41584670
|
G | A | 1 | a0001c0001t0007g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-849+6392G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584670 | ||||||
chr8:41584688
|
G | T | 1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-849+6410G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584688 | ||||||
chr8:41584794
|
C | CT | 7 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(4): Show | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-849+6519dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41584794 | |||||
chr8:41584920
|
G | T | 7 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(4): Show | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-849+6642G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584920 | ||||||
chr8:41584938
|
G | A | 14 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(11): Show | 17 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-849+6660G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584938 | ||||||
chr8:41585209
|
T | G | 7 | a0001c0001t0001g0024a0001c0001t0001g0150a0001c0001t0001g0169others(4): Show | 8 | HG00408.hp1 HG02523.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.-849+6931T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585209 | ||||||
chr8:41585285
|
C | T | 2 | a0001c0001t0005g0022a0001c0001t0005g0116 | 3 | HG02132.hp1 NA19001.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-849+7007C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585285 | ||||||
chr8:41585333
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-849+7055G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585333 | ||||||
chr8:41585362
|
T | C | 1 | a0001c0001t0004g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-849+7084T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585362 | ||||||
chr8:41585376
|
G | A | 7 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(4): Show | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-849+7098G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585376 | ||||||
chr8:41585381
|
TCCGTA | T | 24 | a0001c0001t0005g0010a0001c0001t0005g0021a0001c0001t0005g0022others(21): Show | 28 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-849+7104_-849+710 others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585381 | ||||||
chr8:41585412
|
C | T | 7 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(4): Show | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-849+7134C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585412 | ||||||
chr8:41585457
|
A | G | 52 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(49): Show | 67 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.-849+7179A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585457 | ||||||
chr8:41585487
|
T | C | 1 | a0001c0001t0007g0007 | 3 | HG02258.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-849+7209T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585487 | ||||||
chr8:41585563
|
T | G | 2 | a0001c0001t0001g0200a0001c0001t0001g0257 | 2 | HG02040.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-849+7285T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585563 | ||||||
chr8:41585634
|
G | A | 1 | a0001c0001t0007g0007 | 3 | HG02258.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-849+7356G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585634 | ||||||
chr8:41585676
|
T | G | 79 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(76): Show | 100 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-849+7398T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585676 | ||||||
chr8:41585845
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-849+7567A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585845 | ||||||
chr8:41585917
|
G | A | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.-849+7639G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585917 | ||||||
chr8:41586007
|
G | C | 49 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(46): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-849+7729G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586007 | ||||||
chr8:41586128
|
C | T | 1 | a0001c0001t0005g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-849+7850C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586128 | ||||||
chr8:41586206
|
G | C | 1 | a0001c0001t0047g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-849+7928G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586206 | ||||||
chr8:41586505
|
C | G | 256 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0101others(253): Show | 300 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(297): Show |
intron_variant | MODIFIER | c.-849+8227C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586505 | ||||||
chr8:41586524
|
T | G | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-849+8246T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586524 | ||||||
chr8:41586736
|
C | A | 1 | a0001c0001t0046g0171 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-849+8458C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586736 | ||||||
chr8:41586768
|
G | A | 5 | a0001c0001t0005g0106a0001c0001t0005g0107a0001c0001t0005g0110others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-849+8490G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586768 | ||||||
chr8:41586868
|
C | A | 192 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(189): Show | 234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.-849+8590C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586868 | ||||||
chr8:41586880
|
C | T | 1 | a0001c0001t0055g0151 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-849+8602C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586880 | ||||||
chr8:41586891
|
G | C | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.-849+8613G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586891 | ||||||
chr8:41587191
|
G | C | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-849+8913G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587191 | ||||||
chr8:41587368
|
A | G | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.-849+9090A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587368 | ||||||
chr8:41587382
|
TCTC | T | 5 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(2): Show | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-849+9107_-849+910 others(7): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41587382 | |||||
chr8:41587511
|
T | C | 1 | a0001c0001t0004g0316 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-849+9233T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587511 | ||||||
chr8:41587518
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-849+9240T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587518 | ||||||
chr8:41587537
|
C | T | 9 | a0001c0001t0006g0012a0001c0001t0006g0052a0001c0001t0006g0273others(6): Show | 11 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-849+9259C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587537 | ||||||
chr8:41587617
|
A | C | 1 | a0001c0001t0007g0045 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-849+9339A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587617 | ||||||
chr8:41587737
|
C | G | 1 | a0001c0001t0031g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-849+9459C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587737 | ||||||
chr8:41587754
|
G | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0002g0283others(5): Show | 12 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.-849+9476G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587754 | ||||||
chr8:41587859
|
G | A | 1 | a0001c0001t0008g0096 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-849+9581G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587859 | ||||||
chr8:41587990
|
A | G | 9 | a0001c0001t0006g0012a0001c0001t0006g0052a0001c0001t0006g0273others(6): Show | 11 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-849+9712A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587990 | ||||||
chr8:41588339
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-848-9953G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588339 | ||||||
chr8:41588341
|
C | T | 1 | a0001c0001t0004g0316 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-848-9951C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588341 | ||||||
chr8:41588442
|
A | AGTTCT | 169 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(166): Show | 205 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.-848-9834_-848-983 others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41588442 | |||||
chr8:41588463
|
T | G | 1 | a0001c0001t0002g0342 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-848-9829T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588463 | ||||||
chr8:41588466
|
T | C | 1 | a0001c0001t0002g0342 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-848-9826T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588466 | ||||||
chr8:41588473
|
C | T | 1 | a0001c0001t0002g0342 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-848-9819C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588473 | ||||||
chr8:41588756
|
G | C | 2 | a0002c0002t0014g0094a0002c0002t0014g0095 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-848-9536G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588756 | ||||||
chr8:41588907
|
G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.-848-9385G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588907 | ||||||
chr8:41588912
|
C | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0216 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-848-9380C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588912 | ||||||
chr8:41589124
|
T | C | 192 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(189): Show | 234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.-848-9168T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41589124 | ||||||
chr8:41589206
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-848-9086C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41589206 | ||||||
chr8:41589360
|
CGGGAT | C | 176 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(173): Show | 215 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-848-8923_-848-891 others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41589360 | |||||
chr8:41589466
|
G | T | 1 | a0001c0001t0001g0202 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-848-8826G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41589466 | ||||||
chr8:41589751
|
C | T | 5 | a0001c0001t0005g0106a0001c0001t0005g0107a0001c0001t0005g0110others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-848-8541C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41589751 | ||||||
chr8:41589925
|
G | C | 1 | a0001c0001t0001g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-848-8367G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41589925 | ||||||
chr8:41589951
|
T | G | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.-848-8341T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41589951 | ||||||
chr8:41590032
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-848-8260G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590032 | ||||||
chr8:41590070
|
A | G | 1 | a0001c0001t0003g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-848-8222A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590070 | ||||||
chr8:41590142
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-848-8150A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590142 | ||||||
chr8:41590158
|
T | C | 95 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(92): Show | 118 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-848-8134T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590158 | ||||||
chr8:41590227
|
C | T | 1 | a0001c0001t0015g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-848-8065C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590227 | ||||||
chr8:41590235
|
C | T | 171 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(168): Show | 207 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.-848-8057C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590235 | ||||||
chr8:41590261
|
A | T | 19 | a0001c0001t0004g0013a0001c0001t0004g0015a0001c0001t0004g0288others(16): Show | 23 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.-848-8031A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590261 | ||||||
chr8:41590618
|
T | G | 1 | a0001c0001t0002g0285 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-848-7674T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590618 | ||||||
chr8:41590633
|
G | C | 1 | a0001c0001t0002g0285 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-848-7659G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590633 | ||||||
chr8:41590664
|
A | T | 2 | a0002c0002t0014g0094a0002c0002t0014g0095 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-848-7628A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590664 | ||||||
chr8:41590706
|
G | C | 2 | a0001c0001t0001g0172a0001c0001t0046g0171 | 2 | HG02071.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.-848-7586G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590706 | ||||||
chr8:41590747
|
T | G | 2 | a0001c0001t0002g0295a0001c0001t0002g0333 | 2 | NA18975.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-848-7545T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590747 | ||||||
chr8:41590803
|
A | G | 3 | a0001c0001t0011g0160a0001c0001t0011g0186a0001c0001t0011g0187 | 3 | HG00621.hp2 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-848-7489A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590803 | ||||||
chr8:41590877
|
G | T | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-848-7415G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590877 | ||||||
chr8:41590894
|
TAAAC | T | 24 | a0001c0001t0005g0010a0001c0001t0005g0021a0001c0001t0005g0022others(21): Show | 28 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-848-7393_-848-739 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41590894 | |||||
chr8:41591082
|
T | C | 1 | a0001c0001t0031g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-848-7210T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591082 | ||||||
chr8:41591103
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0239 | 2 | NA18988.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-848-7189C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591103 | ||||||
chr8:41591279
|
G | A | 94 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(91): Show | 117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-848-7013G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591279 | ||||||
chr8:41591420
|
C | T | 171 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(168): Show | 207 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.-848-6872C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591420 | ||||||
chr8:41591596
|
G | A | 95 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(92): Show | 118 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-848-6696G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591596 | ||||||
chr8:41591944
|
A | G | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.-848-6348A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591944 | ||||||
chr8:41591980
|
A | C | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.-848-6312A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591980 | ||||||
chr8:41592055
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-848-6237A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592055 | ||||||
chr8:41592244
|
T | G | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.-848-6048T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592244 | ||||||
chr8:41592265
|
C | T | 4 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0007g0344others(1): Show | 4 | HG01884.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-848-6027C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592265 | ||||||
chr8:41592404
|
A | T | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.-848-5888A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592404 | ||||||
chr8:41592585
|
C | G | 1 | a0001c0001t0001g0139 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-848-5707C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592585 | ||||||
chr8:41592640
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-848-5652A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592640 | ||||||
chr8:41592777
|
T | C | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.-848-5515T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592777 | ||||||
chr8:41592826
|
A | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0185a0001c0001t0001g0252 | 3 | HG03669.hp2 HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-848-5466A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592826 | ||||||
chr8:41592968
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-848-5324C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592968 | ||||||
chr8:41593014
|
A | G | 1 | a0001c0001t0004g0289 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-848-5278A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593014 | ||||||
chr8:41593052
|
A | G | 1 | a0001c0001t0005g0021 | 2 | HG03490.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-848-5240A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593052 | ||||||
chr8:41593141
|
G | A | 2 | a0001c0001t0004g0015a0001c0001t0004g0315 | 4 | HG02080.hp1 NA18970.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.-848-5151G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593141 | ||||||
chr8:41593343
|
A | T | 1 | a0001c0001t0001g0254 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-848-4949A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593343 | ||||||
chr8:41593410
|
A | C | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.-848-4882A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593410 | ||||||
chr8:41593512
|
G | A | 5 | a0001c0001t0009g0014a0001c0001t0009g0296a0001c0001t0009g0348others(2): Show | 7 | HG03239.hp2 NA18963.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.-848-4780G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593512 | ||||||
chr8:41593593
|
G | C | 3 | a0001c0001t0002g0297a0001c0001t0002g0321a0001c0001t0002g0325 | 3 | HG00735.hp1 HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-848-4699G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593593 | ||||||
chr8:41593649
|
A | G | 14 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(11): Show | 17 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-848-4643A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593649 | ||||||
chr8:41593713
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-848-4579C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593713 | ||||||
chr8:41593908
|
A | G | 1 | a0001c0001t0002g0314 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-848-4384A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593908 | ||||||
chr8:41594097
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0138 | 3 | NA18954.hp2 NA19057.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-848-4195A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594097 | ||||||
chr8:41594110
|
C | A | 2 | a0001c0001t0019g0103a0001c0001t0029g0102 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-848-4182C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594110 | ||||||
chr8:41594169
|
T | C | 2 | a0001c0001t0004g0294a0001c0001t0004g0318 | 2 | HG01106.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-848-4123T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594169 | ||||||
chr8:41594218
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-848-4074C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594218 | ||||||
chr8:41594262
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-848-4030A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594262 | ||||||
chr8:41594438
|
A | G | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-848-3854A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594438 | ||||||
chr8:41594546
|
C | CT | 40 | a0001c0001t0001g0192a0001c0001t0002g0298a0001c0001t0004g0336others(37): Show | 47 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.-848-3729dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41594546 | |||||
chr8:41594546
|
C | CTT | 146 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(143): Show | 181 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.-848-3730_-848-372 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41594546 | |||||
chr8:41594546
|
C | CTTT | 7 | a0001c0001t0002g0329a0001c0001t0003g0077a0001c0001t0003g0079others(4): Show | 7 | HG00544.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-848-3731_-848-372 others(7): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41594546 | |||||
chr8:41594568
|
T | C | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-848-3724T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594568 | ||||||
chr8:41594600
|
C | G | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | NA18954.hp2 NA19057.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-848-3692C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594600 | ||||||
chr8:41594606
|
T | C | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-848-3686T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594606 | ||||||
chr8:41594607
|
C | G | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-848-3685C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594607 | ||||||
chr8:41594608
|
C | G | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-848-3684C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594608 | ||||||
chr8:41594639
|
G | A | 2 | a0001c0001t0002g0282a0001c0001t0002g0329 | 2 | NA18949.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-848-3653G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594639 | ||||||
chr8:41594693
|
C | A | 1 | a0001c0001t0005g0108 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-848-3599C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594693 | ||||||
chr8:41594747
|
G | T | 72 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(69): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.-848-3545G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594747 | ||||||
chr8:41594796
|
C | T | 93 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(90): Show | 116 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-848-3496C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594796 | ||||||
chr8:41594827
|
A | G | 92 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(89): Show | 115 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-848-3465A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594827 | ||||||
chr8:41594980
|
A | G | 1 | a0001c0001t0009g0348 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-848-3312A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594980 | ||||||
chr8:41595077
|
C | T | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.-848-3215C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595077 | ||||||
chr8:41595156
|
G | GT | 120 | a0001c0001t0001g0129a0001c0001t0001g0148a0001c0001t0001g0158others(117): Show | 143 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.-848-3117dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595156 | |||||
chr8:41595156
|
G | GTT | 17 | a0001c0001t0003g0018a0001c0001t0003g0076a0001c0001t0003g0081others(14): Show | 18 | HG00597.hp2 HG01433.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-848-3118_-848-311 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595156 | |||||
chr8:41595325
|
C | CT | 29 | a0001c0001t0001g0101a0001c0001t0001g0125a0001c0001t0001g0127others(26): Show | 29 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-848-2939dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595325 | |||||
chr8:41595325
|
CT | C | 14 | a0001c0001t0001g0153a0001c0001t0001g0204a0001c0001t0001g0219others(11): Show | 17 | HG00738.hp1 HG01069.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.-848-2939delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595325 | |||||
chr8:41595325
|
CTTTT | C | 33 | a0001c0001t0002g0311a0001c0001t0003g0057a0001c0001t0003g0074others(30): Show | 37 | HG01106.hp1 HG01243.hp1 HG02004.hp2 others(34): Show |
intron_variant | MODIFIER | c.-848-2942_-848-293 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595325 | |||||
chr8:41595325
|
CTTTTT | C | 139 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(136): Show | 174 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.-848-2943_-848-293 others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595325 | |||||
chr8:41595434
|
G | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0002g0283others(5): Show | 12 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.-848-2858G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595434 | ||||||
chr8:41595573
|
G | A | 94 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(91): Show | 117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-848-2719G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595573 | ||||||
chr8:41595687
|
A | G | 2 | a0002c0002t0014g0094a0002c0002t0014g0095 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-848-2605A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595687 | ||||||
chr8:41595691
|
CTCTT | C | 3 | a0001c0001t0001g0198a0001c0001t0011g0160a0001c0001t0011g0186 | 3 | NA18975.hp1 NA19060.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-848-2593_-848-259 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595691 | |||||
chr8:41595811
|
TCTCTTTT others(1): Show |
T | 40 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(37): Show | 48 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-848-2468_-848-246 others(12): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595811 | |||||
chr8:41595871
|
G | A | 2 | a0002c0002t0014g0094a0002c0002t0014g0095 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-848-2421G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595871 | ||||||
chr8:41595959
|
A | G | 12 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(9): Show | 15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-848-2333A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595959 | ||||||
chr8:41595974
|
G | T | 5 | a0001c0001t0005g0106a0001c0001t0005g0107a0001c0001t0005g0110others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-848-2318G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595974 | ||||||
chr8:41595987
|
C | T | 25 | a0001c0001t0002g0298a0001c0001t0005g0010a0001c0001t0005g0021others(22): Show | 29 | HG01169.hp1 HG02004.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.-848-2305C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595987 | ||||||
chr8:41596061
|
A | G | 5 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(2): Show | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-848-2231A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596061 | ||||||
chr8:41596146
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-848-2146C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596146 | ||||||
chr8:41596247
|
C | T | 1 | a0001c0001t0002g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-848-2045C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596247 | ||||||
chr8:41596338
|
A | C | 1 | a0001c0001t0001g0267 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-848-1954A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596338 | ||||||
chr8:41596425
|
C | G | 192 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(189): Show | 234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.-848-1867C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596425 | ||||||
chr8:41596614
|
A | G | 1 | a0001c0001t0002g0322 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-848-1678A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596614 | ||||||
chr8:41596704
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-848-1588C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596704 | ||||||
chr8:41596731
|
A | C | 8 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0002g0283others(5): Show | 12 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.-848-1561A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596731 | ||||||
chr8:41596752
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0046g0171 | 2 | HG02071.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.-848-1540G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596752 | ||||||
chr8:41596779
|
C | T | 1 | a0001c0001t0003g0020 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-848-1513C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596779 | ||||||
chr8:41596787
|
A | C | 1 | a0001c0001t0053g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-848-1505A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596787 | ||||||
chr8:41596845
|
G | A | 1 | a0001c0001t0058g0220 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-848-1447G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596845 | ||||||
chr8:41597013
|
G | A | 5 | a0001c0001t0005g0106a0001c0001t0005g0107a0001c0001t0005g0110others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-848-1279G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597013 | ||||||
chr8:41597027
|
C | T | 12 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(9): Show | 15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-848-1265C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597027 | ||||||
chr8:41597028
|
G | A | 1 | a0001c0001t0041g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-848-1264G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597028 | ||||||
chr8:41597060
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-848-1232G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597060 | ||||||
chr8:41597268
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-848-1024A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597268 | ||||||
chr8:41597472
|
G | C | 1 | a0001c0001t0040g0268 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-848-820G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597472 | ||||||
chr8:41597485
|
A | G | 16 | a0001c0001t0004g0039a0001c0001t0006g0012a0001c0001t0006g0052others(13): Show | 18 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-848-807A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597485 | ||||||
chr8:41597824
|
G | A | 7 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(4): Show | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-848-468G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597824 | ||||||
chr8:41598060
|
C | T | 171 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(168): Show | 207 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.-848-232C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41598060 | ||||||
chr8:41598133
|
G | A | 7 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(4): Show | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-848-159G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41598133 | ||||||
chr8:41598136
|
C | G | 1 | a0001c0001t0008g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-848-156C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41598136 | ||||||
chr8:41599321
|
C | A | 2 | a0001c0001t0004g0015a0001c0001t0004g0315 | 4 | HG02080.hp1 NA18970.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+17C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41599321 | ||||||
chr8:41599353
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.165+49G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41599353 | ||||||
chr8:41599575
|
C | T | 59 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0101others(56): Show | 61 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.165+271C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41599575 | ||||||
chr8:41599620
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.165+316G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41599620 | ||||||
chr8:41599629
|
G | A | 2 | a0001c0001t0003g0019a0001c0001t0003g0079 | 3 | HG00621.hp1 HG02083.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.165+325G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41599629 | ||||||
chr8:41599784
|
A | G | 2 | a0001c0001t0019g0103a0001c0001t0029g0102 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.165+480A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41599784 | ||||||
chr8:41600036
|
C | CT | 14 | a0001c0001t0001g0192a0001c0001t0007g0002a0001c0001t0007g0007others(11): Show | 17 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+750dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | |||||
chr8:41600036
|
C | CTTTT | 4 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0098others(1): Show | 7 | HG02055.hp1 HG02280.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+747_165+750dup others(4): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | |||||
chr8:41600036
|
C | CTTTTTT | 74 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(71): Show | 95 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.165+745_165+750dup others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | |||||
chr8:41600036
|
C | CTTTTTTT | 31 | a0001c0001t0002g0282a0001c0001t0002g0303a0001c0001t0002g0313others(28): Show | 38 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.165+744_165+750dup others(7): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | |||||
chr8:41600036
|
C | CTTTTTTT others(1): Show |
46 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(43): Show | 54 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.165+743_165+750dup others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | |||||
chr8:41600036
|
C | CTTTTTTT others(2): Show |
11 | a0001c0001t0003g0017a0001c0001t0003g0058a0001c0001t0003g0065others(8): Show | 11 | HG00597.hp2 HG01099.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.165+742_165+750dup others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | |||||
chr8:41600036
|
CT | C | 6 | a0001c0001t0001g0174a0001c0001t0001g0207a0001c0001t0001g0222others(3): Show | 6 | HG01496.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+750delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | |||||
chr8:41600054
|
TC | T | 3 | a0001c0001t0004g0323a0001c0001t0004g0324a0001c0001t0004g0331 | 3 | HG02559.hp2 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.165+751delC | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600054 | ||||||
chr8:41600055
|
C | T | 174 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(171): Show | 213 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.165+751C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600055 | ||||||
chr8:41600100
|
G | T | 2 | a0001c0001t0056g0048a0001c0001t0057g0047 | 2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.165+796G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600100 | ||||||
chr8:41600178
|
A | G | 14 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(11): Show | 17 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+874A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600178 | ||||||
chr8:41600289
|
A | T | 1 | a0002c0002t0014g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.165+985A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600289 | ||||||
chr8:41600334
|
ACCTGGCC others(10): Show |
A | 1 | a0001c0001t0002g0282 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.165+1032_165+1048d others(19): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600334 | |||||
chr8:41600476
|
A | T | 1 | a0001c0001t0002g0282 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.165+1172A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600476 | ||||||
chr8:41600540
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.165+1236C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600540 | ||||||
chr8:41600552
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.165+1248C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600552 | ||||||
chr8:41600553
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.165+1249T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600553 | ||||||
chr8:41600588
|
G | GT | 20 | a0001c0001t0001g0129a0001c0001t0002g0282a0001c0001t0003g0054others(17): Show | 23 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.165+1296dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600588 | |||||
chr8:41600660
|
G | C | 1 | a0001c0001t0001g0241 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.165+1356G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600660 | ||||||
chr8:41600668
|
G | A | 3 | a0001c0001t0011g0160a0001c0001t0011g0186a0001c0001t0011g0187 | 3 | HG00621.hp2 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.165+1364G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600668 | ||||||
chr8:41600688
|
G | C | 1 | a0001c0001t0029g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.165+1384G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600688 | ||||||
chr8:41600915
|
T | G | 12 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0100others(9): Show | 14 | HG04115.hp2 NA18945.hp2 NA18955.hp2 others(11): Show |
intron_variant | MODIFIER | c.165+1611T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600915 | ||||||
chr8:41601087
|
G | A | 192 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(189): Show | 234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.165+1783G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601087 | ||||||
chr8:41601134
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.165+1830A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601134 | ||||||
chr8:41601140
|
TA | T | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.165+1838delA | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41601140 | |||||
chr8:41601167
|
C | T | 2 | a0002c0002t0014g0094a0002c0002t0014g0095 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.165+1863C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601167 | ||||||
chr8:41601434
|
G | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0251a0001c0001t0001g0255 | 3 | HG00642.hp2 HG03540.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.165+2130G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601434 | ||||||
chr8:41601767
|
T | C | 7 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(4): Show | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+2463T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601767 | ||||||
chr8:41601902
|
C | T | 12 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(9): Show | 15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+2598C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601902 | ||||||
chr8:41601954
|
C | T | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.165+2650C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601954 | ||||||
chr8:41601955
|
C | G | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.165+2651C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601955 | ||||||
chr8:41601956
|
C | T | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.165+2652C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601956 | ||||||
chr8:41601957
|
A | ATG | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.165+2653_165+2654i others(4): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601957 | ||||||
chr8:41601958
|
A | T | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.165+2654A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601958 | ||||||
chr8:41602014
|
G | A | 2 | a0001c0001t0010g0092a0001c0001t0010g0093 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.165+2710G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602014 | ||||||
chr8:41602015
|
C | T | 2 | a0001c0001t0010g0092a0001c0001t0010g0093 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.165+2711C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602015 | ||||||
chr8:41602084
|
A | AGCTGGGA others(7): Show |
1 | a0001c0001t0002g0282 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.165+2781_165+2794d others(16): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41602084 | |||||
chr8:41602201
|
C | T | 1 | a0001c0001t0005g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.165+2897C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602201 | ||||||
chr8:41602231
|
T | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.165+2927T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602231 | ||||||
chr8:41602485
|
G | T | 12 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(9): Show | 15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+3181G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602485 | ||||||
chr8:41602495
|
T | C | 1 | a0001c0001t0037g0184 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.165+3191T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602495 | ||||||
chr8:41602504
|
A | C | 192 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(189): Show | 234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.165+3200A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602504 | ||||||
chr8:41602564
|
G | C | 11 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(8): Show | 14 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+3260G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602564 | ||||||
chr8:41602668
|
C | T | 95 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(92): Show | 118 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.165+3364C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602668 | ||||||
chr8:41602756
|
T | G | 14 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(11): Show | 17 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+3452T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602756 | ||||||
chr8:41602780
|
A | G | 1 | a0001c0001t0029g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.165+3476A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602780 | ||||||
chr8:41602868
|
T | A | 1 | a0001c0001t0002g0326 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.165+3564T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602868 | ||||||
chr8:41602893
|
C | T | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.165+3589C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602893 | ||||||
chr8:41603075
|
G | A | 3 | a0001c0001t0011g0160a0001c0001t0011g0186a0001c0001t0011g0187 | 3 | HG00621.hp2 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.165+3771G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603075 | ||||||
chr8:41603151
|
G | C | 1 | a0001c0001t0004g0339 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.165+3847G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603151 | ||||||
chr8:41603270
|
T | C | 171 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(168): Show | 207 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.165+3966T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603270 | ||||||
chr8:41603292
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.165+3988C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603292 | ||||||
chr8:41603525
|
CA | C | 157 | a0001c0001t0001g0124a0001c0001t0001g0133a0001c0001t0001g0154others(154): Show | 193 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.165+4242delA | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603525 | |||||
chr8:41603525
|
CAA | C | 12 | a0001c0001t0002g0033a0001c0001t0003g0064a0001c0001t0003g0072others(9): Show | 12 | HG00741.hp2 HG01192.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.165+4241_165+4242d others(4): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603525 | |||||
chr8:41603525
|
CAAAAAAA | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(2): Show | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+4236_165+4242d others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603525 | |||||
chr8:41603539
|
A | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.165+4235A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603539 | ||||||
chr8:41603586
|
T | A | 5 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(2): Show | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+4282T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603586 | ||||||
chr8:41603896
|
A | AGAAT | 46 | a0001c0001t0001g0030a0001c0001t0001g0127a0001c0001t0001g0182others(43): Show | 52 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.165+4618_165+4621d others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603896 | |||||
chr8:41603896
|
A | AGAATGAA others(1): Show |
52 | a0001c0001t0001g0029a0001c0001t0001g0101a0001c0001t0001g0129others(49): Show | 53 | HG00099.hp2 HG00673.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.165+4614_165+4621d others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603896 | |||||
chr8:41603896
|
A | AGAATGAA others(5): Show |
61 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(58): Show | 69 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.165+4610_165+4621d others(14): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603896 | |||||
chr8:41603896
|
A | AGAATGAA others(9): Show |
15 | a0001c0001t0001g0125a0001c0001t0001g0156a0001c0001t0001g0161others(12): Show | 15 | HG00642.hp2 HG00735.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+4606_165+4621d others(18): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603896 | |||||
chr8:41603896
|
A | AGAATGAA others(13): Show |
5 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0214others(2): Show | 5 | HG00323.hp1 HG02109.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+4602_165+4621d others(22): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603896 | |||||
chr8:41603904
|
T | A | 1 | a0002c0002t0014g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.165+4600T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603904 | ||||||
chr8:41604036
|
A | AT | 9 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0166others(6): Show | 9 | HG00323.hp1 HG01952.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+4749dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41604036 | |||||
chr8:41604036
|
AT | A | 21 | a0001c0001t0002g0282a0001c0001t0007g0002a0001c0001t0007g0007others(18): Show | 27 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.165+4749delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41604036 | |||||
chr8:41604036
|
ATT | A | 146 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(143): Show | 178 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.165+4748_165+4749d others(4): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41604036 | |||||
chr8:41604036
|
ATTTT | A | 24 | a0001c0001t0005g0010a0001c0001t0005g0021a0001c0001t0005g0022others(21): Show | 28 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.165+4746_165+4749d others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41604036 | |||||
chr8:41604284
|
C | G | 1 | a0001c0001t0004g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.165+4980C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41604284 | ||||||
chr8:41604463
|
G | C | 2 | a0001c0001t0004g0294a0001c0001t0004g0318 | 2 | HG01106.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.166-4953G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41604463 | ||||||
chr8:41604588
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-4828A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41604588 | ||||||
chr8:41604655
|
T | G | 1 | a0001c0001t0002g0309 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.166-4761T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41604655 | ||||||
chr8:41605119
|
T | C | 95 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(92): Show | 118 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.166-4297T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605119 | ||||||
chr8:41605201
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.166-4215A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605201 | ||||||
chr8:41605206
|
C | T | 1 | a0001c0001t0004g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166-4210C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605206 | ||||||
chr8:41605239
|
G | T | 2 | a0001c0001t0056g0048a0001c0001t0057g0047 | 2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.166-4177G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605239 | ||||||
chr8:41605249
|
C | T | 2 | a0001c0001t0056g0048a0001c0001t0057g0047 | 2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.166-4167C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605249 | ||||||
chr8:41605294
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.166-4122G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605294 | ||||||
chr8:41605379
|
A | G | 49 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(46): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.166-4037A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605379 | ||||||
chr8:41605390
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.166-4026G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605390 | ||||||
chr8:41605436
|
A | C | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.166-3980A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605436 | ||||||
chr8:41605454
|
A | G | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.166-3962A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605454 | ||||||
chr8:41605546
|
TTTTG | T | 67 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(64): Show | 75 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.166-3830_166-3827d others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41605546 | |||||
chr8:41605546
|
TTTTGTTT others(1): Show |
T | 84 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0101others(81): Show | 86 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.166-3834_166-3827d others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41605546 | |||||
chr8:41605546
|
TTTTGTTT others(5): Show |
T | 51 | a0001c0001t0001g0200a0001c0001t0001g0235a0001c0001t0003g0003others(48): Show | 60 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.166-3838_166-3827d others(14): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41605546 | |||||
chr8:41605546
|
TTTTGTTT others(9): Show |
T | 127 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(124): Show | 157 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.166-3842_166-3827d others(18): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41605546 | |||||
chr8:41605546
|
TTTTGTTT others(17): Show |
T | 15 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(12): Show | 18 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.166-3850_166-3827d others(26): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41605546 | |||||
chr8:41605558
|
G | T | 6 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG02071.hp1 NA18959.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-3858G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605558 | ||||||
chr8:41605697
|
C | T | 2 | a0001c0001t0056g0048a0001c0001t0057g0047 | 2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.166-3719C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605697 | ||||||
chr8:41605698
|
G | A | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.166-3718G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605698 | ||||||
chr8:41605800
|
G | A | 1 | a0001c0001t0001g0347 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.166-3616G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605800 | ||||||
chr8:41605840
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0049g0126 | 2 | HG02135.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.166-3576G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605840 | ||||||
chr8:41605901
|
G | A | 2 | a0001c0001t0005g0117a0001c0001t0005g0122 | 2 | NA18946.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.166-3515G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605901 | ||||||
chr8:41606007
|
G | T | 1 | a0001c0001t0003g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.166-3409G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606007 | ||||||
chr8:41606045
|
G | A | 1 | a0001c0001t0029g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.166-3371G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606045 | ||||||
chr8:41606201
|
C | G | 73 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(70): Show | 86 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.166-3215C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606201 | ||||||
chr8:41606301
|
A | G | 5 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0164others(2): Show | 5 | HG01081.hp1 HG01109.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-3115A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606301 | ||||||
chr8:41606572
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.166-2844A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606572 | ||||||
chr8:41606580
|
C | T | 1 | a0001c0001t0019g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.166-2836C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606580 | ||||||
chr8:41606628
|
A | G | 1 | a0001c0001t0031g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.166-2788A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606628 | ||||||
chr8:41607213
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.166-2203G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607213 | ||||||
chr8:41607238
|
G | T | 1 | a0001c0001t0004g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166-2178G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607238 | ||||||
chr8:41607284
|
G | A | 1 | a0001c0001t0003g0061 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.166-2132G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607284 | ||||||
chr8:41607352
|
G | A | 73 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(70): Show | 86 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.166-2064G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607352 | ||||||
chr8:41607453
|
A | G | 1 | a0001c0001t0005g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.166-1963A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607453 | ||||||
chr8:41607461
|
G | C | 1 | a0001c0001t0040g0268 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.166-1955G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607461 | ||||||
chr8:41607540
|
C | CT | 38 | a0001c0001t0001g0028a0001c0001t0001g0225a0001c0001t0002g0333others(35): Show | 46 | HG00423.hp1 HG02004.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.166-1860dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41607540 | |||||
chr8:41607540
|
CT | C | 8 | a0001c0001t0001g0153a0001c0001t0001g0175a0001c0001t0001g0244others(5): Show | 8 | HG00323.hp2 HG01099.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-1860delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41607540 | |||||
chr8:41607608
|
C | T | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.166-1808C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607608 | ||||||
chr8:41607658
|
A | G | 1 | a0001c0001t0003g0057 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.166-1758A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607658 | ||||||
chr8:41607662
|
G | A | 1 | a0001c0001t0005g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.166-1754G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607662 | ||||||
chr8:41607881
|
C | T | 2 | a0001c0001t0003g0081a0001c0001t0003g0083 | 2 | HG01433.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.166-1535C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607881 | ||||||
chr8:41607982
|
G | A | 1 | a0001c0001t0023g0293 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.166-1434G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607982 | ||||||
chr8:41608046
|
C | T | 15 | a0001c0001t0004g0013a0001c0001t0004g0015a0001c0001t0004g0288others(12): Show | 19 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.166-1370C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41608046 | ||||||
chr8:41608074
|
A | G | 7 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(4): Show | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-1342A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41608074 | ||||||
chr8:41608200
|
G | A | 24 | a0001c0001t0005g0010a0001c0001t0005g0021a0001c0001t0005g0022others(21): Show | 28 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.166-1216G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41608200 | ||||||
chr8:41608293
|
C | T | 12 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(9): Show | 15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.166-1123C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41608293 | ||||||
chr8:41608819
|
GT | G | 194 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(191): Show | 236 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.166-586delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41608819 | |||||
chr8:41608879
|
C | T | 1 | a0001c0001t0003g0081 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.166-537C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41608879 | ||||||
chr8:41608955
|
G | T | 1 | a0001c0001t0002g0310 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.166-461G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41608955 | ||||||
chr8:41609049
|
C | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0002g0283others(5): Show | 12 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-367C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41609049 | ||||||
chr8:41609270
|
T | C | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.166-146T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41609270 | ||||||
chr8:41609560
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.235+75C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 3/12 | chr8 | 41609560 | ||||||
chr8:41609610
|
G | T | 1 | a0001c0001t0015g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.236-45G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 3/12 | chr8 | 41609610 | ||||||
chr8:41610070
|
G | A | 1 | a0001c0001t0005g0108 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.536+115G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610070 | ||||||
chr8:41610245
|
G | A | 1 | a0001c0001t0031g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.536+290G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610245 | ||||||
chr8:41610300
|
T | C | 5 | a0001c0001t0004g0008a0001c0001t0004g0038a0001c0001t0004g0049others(2): Show | 7 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.536+345T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610300 | ||||||
chr8:41610308
|
C | T | 12 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(9): Show | 15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.536+353C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610308 | ||||||
chr8:41610457
|
A | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0206a0001c0001t0001g0216others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.537-279A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610457 | ||||||
chr8:41610488
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.537-248C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610488 | ||||||
chr8:41610541
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0164others(2): Show | 5 | HG01081.hp1 HG01109.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.537-195C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610541 | ||||||
chr8:41610943
|
G | A | 1 | a0001c0001t0003g0067 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.611+133G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41610943 | ||||||
chr8:41611047
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.611+237C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611047 | ||||||
chr8:41611051
|
A | AC | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.611+243dupC | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 41611051 | |||||
chr8:41611087
|
A | G | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.611+277A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611087 | ||||||
chr8:41611089
|
G | A | 97 | a0001c0001t0001g0194a0001c0001t0002g0001a0001c0001t0002g0006others(94): Show | 120 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.611+279G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611089 | ||||||
chr8:41611290
|
T | A | 165 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(162): Show | 201 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.611+480T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611290 | ||||||
chr8:41611303
|
G | C | 1 | a0001c0001t0001g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.611+493G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611303 | ||||||
chr8:41611332
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.611+522T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611332 | ||||||
chr8:41611376
|
T | G | 2 | a0001c0001t0003g0068a0001c0001t0003g0073 | 2 | HG01099.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.612-527T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611376 | ||||||
chr8:41611523
|
C | T | 15 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(12): Show | 18 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.612-380C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611523 | ||||||
chr8:41612000
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0252 | 2 | HG03710.hp2 HG03831.hp2 |
splice_region_variant&intron_variant | LOW | c.701+8C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 6/12 | chr8 | 41612000 | ||||||
chr8:41612001
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.701+9G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 6/12 | chr8 | 41612001 | ||||||
chr8:41612028
|
C | T | 7 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(4): Show | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.701+36C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 6/12 | chr8 | 41612028 | ||||||
chr8:41612061
|
C | T | 15 | a0001c0001t0006g0012a0001c0001t0006g0052a0001c0001t0006g0104others(12): Show | 17 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.701+69C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 6/12 | chr8 | 41612061 | ||||||
chr8:41612284
|
T | C | 2 | a0001c0001t0001g0168a0001c0001t0048g0167 | 2 | HG01109.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.795+11T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 7/12 | chr8 | 41612284 | ||||||
chr8:41612288
|
C | T | 15 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0100others(12): Show | 17 | HG04115.hp2 NA18945.hp2 NA18955.hp2 others(14): Show |
intron_variant | MODIFIER | c.795+15C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 7/12 | chr8 | 41612288 | ||||||
chr8:41612984
|
C | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | NA18959.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.911+24C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41612984 | ||||||
chr8:41613080
|
A | T | 2 | a0001c0001t0003g0069a0001c0001t0003g0085 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.911+120A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613080 | ||||||
chr8:41613172
|
G | A | 171 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(168): Show | 207 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.911+212G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613172 | ||||||
chr8:41613244
|
A | C | 1 | a0001c0001t0007g0007 | 3 | HG02258.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.911+284A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613244 | ||||||
chr8:41613259
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.911+299A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613259 | ||||||
chr8:41613299
|
T | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(2): Show | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.911+339T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613299 | ||||||
chr8:41613365
|
G | A | 62 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0101others(59): Show | 64 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.911+405G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613365 | ||||||
chr8:41613386
|
A | G | 1 | a0001c0001t0019g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.911+426A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613386 | ||||||
chr8:41613481
|
T | C | 171 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(168): Show | 207 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.911+521T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613481 | ||||||
chr8:41613647
|
G | A | 13 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(10): Show | 16 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.911+687G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613647 | ||||||
chr8:41613730
|
C | T | 1 | a0001c0001t0002g0322 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.912-656C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613730 | ||||||
chr8:41613802
|
G | C | 2 | a0002c0002t0014g0094a0002c0002t0014g0095 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.912-584G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613802 | ||||||
chr8:41613855
|
T | G | 178 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(175): Show | 217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.912-531T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613855 | ||||||
chr8:41613878
|
C | T | 2 | a0001c0001t0006g0271a0001c0001t0022g0272 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.912-508C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613878 | ||||||
chr8:41614014
|
C | T | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.912-372C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41614014 | ||||||
chr8:41614124
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.912-262C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41614124 | ||||||
chr8:41614159
|
C | T | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.912-227C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41614159 | ||||||
chr8:41614267
|
A | G | 74 | a0001c0001t0002g0298a0001c0001t0003g0003a0001c0001t0003g0009others(71): Show | 87 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.912-119A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41614267 | ||||||
chr8:41614683
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.967+242T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 9/12 | chr8 | 41614683 | ||||||
chr8:41614713
|
A | G | 8 | a0001c0001t0007g0002a0001c0001t0007g0042a0001c0001t0007g0043others(5): Show | 9 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.968-250A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 9/12 | chr8 | 41614713 | ||||||
chr8:41614718
|
G | A | 1 | a0001c0001t0037g0184 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.968-245G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 9/12 | chr8 | 41614718 | ||||||
chr8:41614856
|
G | A | 95 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(92): Show | 118 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.968-107G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 9/12 | chr8 | 41614856 | ||||||
chr8:41615093
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1053+45G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615093 | ||||||
chr8:41615115
|
A | C | 1 | a0001c0001t0004g0318 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1053+67A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615115 | ||||||
chr8:41615165
|
G | A | 1 | a0001c0001t0002g0295 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1053+117G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615165 | ||||||
chr8:41615167
|
G | C | 1 | a0001c0001t0046g0171 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1053+119G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615167 | ||||||
chr8:41615278
|
C | T | 4 | a0001c0001t0002g0313a0001c0001t0002g0314a0001c0001t0002g0330others(1): Show | 4 | NA18943.hp2 NA18981.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+230C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615278 | ||||||
chr8:41615326
|
C | T | 94 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(91): Show | 117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1053+278C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615326 | ||||||
chr8:41615363
|
G | C | 1 | a0001c0001t0003g0020 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1053+315G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615363 | ||||||
chr8:41615389
|
T | C | 1 | a0001c0001t0013g0060 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1053+341T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615389 | ||||||
chr8:41615449
|
AT | A | 144 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(141): Show | 176 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.1053+403delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 41615449 | |||||
chr8:41615450
|
T | TG | 6 | a0001c0001t0006g0274a0001c0001t0006g0279a0001c0001t0007g0344others(3): Show | 6 | HG01243.hp2 HG01346.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053+402_1053+403i others(3): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615450 | ||||||
chr8:41615450
|
TTG | T | 13 | a0001c0001t0002g0284a0001c0001t0004g0008a0001c0001t0004g0038others(10): Show | 18 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1053+403_1053+404d others(4): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615450 | ||||||
chr8:41615451
|
T | G | 36 | a0001c0001t0002g0330a0001c0001t0004g0319a0001c0001t0006g0012others(33): Show | 41 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1053+403T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615451 | ||||||
chr8:41615630
|
G | T | 1 | a0001c0001t0005g0120 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1053+582G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615630 | ||||||
chr8:41615768
|
G | A | 1 | a0001c0001t0003g0057 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1053+720G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615768 | ||||||
chr8:41615898
|
G | A | 171 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(168): Show | 207 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.1053+850G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615898 | ||||||
chr8:41616265
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1053+1217T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616265 | ||||||
chr8:41616495
|
G | T | 2 | a0001c0001t0007g0007a0001c0001t0053g0040 | 4 | HG02258.hp1 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+1447G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616495 | ||||||
chr8:41616592
|
G | C | 1 | a0001c0001t0031g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1053+1544G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616592 | ||||||
chr8:41616710
|
C | T | 7 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(4): Show | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1053+1662C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616710 | ||||||
chr8:41616735
|
AGTAAAAT others(2): Show |
A | 5 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(2): Show | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1053+1688_1053+169 others(13): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616735 | ||||||
chr8:41616771
|
T | C | 194 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(191): Show | 236 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.1053+1723T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616771 | ||||||
chr8:41616827
|
G | T | 1 | a0001c0001t0003g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1053+1779G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616827 | ||||||
chr8:41616851
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1053+1803A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616851 | ||||||
chr8:41617095
|
T | C | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.1054-1589T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617095 | ||||||
chr8:41617225
|
G | A | 1 | a0001c0001t0045g0146 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1054-1459G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617225 | ||||||
chr8:41617294
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1054-1390G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617294 | ||||||
chr8:41617338
|
T | C | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1054-1346T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617338 | ||||||
chr8:41617343
|
G | A | 5 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(2): Show | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054-1341G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617343 | ||||||
chr8:41617556
|
T | C | 5 | a0001c0001t0004g0008a0001c0001t0004g0038a0001c0001t0004g0049others(2): Show | 7 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054-1128T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617556 | ||||||
chr8:41617587
|
A | T | 193 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(190): Show | 235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.1054-1097A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617587 | ||||||
chr8:41617674
|
G | T | 1 | a0001c0001t0019g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1054-1010G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617674 | ||||||
chr8:41617704
|
G | A | 1 | a0001c0001t0043g0144 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1054-980G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617704 | ||||||
chr8:41617779
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1054-905C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617779 | ||||||
chr8:41618133
|
T | G | 1 | a0001c0001t0003g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1054-551T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618133 | ||||||
chr8:41618162
|
A | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0265 | 2 | HG00099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1054-522A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618162 | ||||||
chr8:41618169
|
T | C | 97 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(94): Show | 121 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1054-515T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618169 | ||||||
chr8:41618231
|
T | C | 1 | a0001c0001t0003g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1054-453T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618231 | ||||||
chr8:41618370
|
T | C | 1 | a0001c0001t0006g0278 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1054-314T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618370 | ||||||
chr8:41618443
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0261a0001c0001t0001g0263 | 3 | HG00609.hp2 HG02129.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1054-241G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618443 | ||||||
chr8:41618466
|
T | C | 5 | a0001c0001t0003g0062a0001c0001t0003g0065a0001c0001t0003g0076others(2): Show | 5 | HG00544.hp2 HG00597.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-218T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618466 | ||||||
chr8:41618484
|
G | A | 12 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(9): Show | 15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1054-200G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618484 | ||||||
chr8:41618509
|
GC | G | 3 | a0001c0001t0004g0323a0001c0001t0004g0324a0001c0001t0004g0331 | 3 | HG02559.hp2 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1054-174delC | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618509 | ||||||
chr8:41618538
|
G | C | 1 | a0001c0001t0008g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1054-146G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618538 | ||||||
chr8:41618630
|
G | A | 1 | a0001c0001t0005g0120 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1054-54G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618630 | ||||||
chr8:41618864
|
G | A | 1 | a0001c0001t0004g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1183-34G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 11/12 | chr8 | 41618864 | ||||||
chr8:41619025
|
T | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(2): Show | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1262+48T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619025 | ||||||
chr8:41619152
|
GGGAACCT others(15): Show |
G | 1 | a0001c0001t0003g0063 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1262+179_1262+200d others(24): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 41619152 | |||||
chr8:41619300
|
G | C | 1 | a0001c0001t0006g0104 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1262+323G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619300 | ||||||
chr8:41619472
|
A | G | 12 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(9): Show | 15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1262+495A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619472 | ||||||
chr8:41619530
|
T | C | 2 | a0001c0001t0008g0098a0001c0001t0008g0099 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1262+553T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619530 | ||||||
chr8:41619572
|
A | G | 5 | a0001c0001t0005g0010a0001c0001t0005g0108a0001c0001t0005g0112others(2): Show | 7 | HG02074.hp2 HG02165.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1262+595A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619572 | ||||||
chr8:41619919
|
C | T | 1 | a0001c0001t0017g0290 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1262+942C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619919 | ||||||
chr8:41619921
|
C | G | 5 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(2): Show | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1262+944C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619921 | ||||||
chr8:41620161
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1263-732G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620161 | ||||||
chr8:41620165
|
C | T | 12 | a0001c0001t0007g0002a0001c0001t0007g0007a0001c0001t0007g0042others(9): Show | 15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1263-728C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620165 | ||||||
chr8:41620273
|
T | C | 342 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(339): Show | 394 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(391): Show |
intron_variant | MODIFIER | c.1263-620T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620273 | ||||||
chr8:41620283
|
C | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0247 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1263-610C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620283 | ||||||
chr8:41620314
|
C | CAGGG | 98 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0031others(95): Show | 122 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1263-575_1263-572d others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 41620314 | |||||
chr8:41620420
|
C | T | 1 | a0001c0001t0023g0293 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1263-473C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620420 | ||||||
chr8:41620515
|
G | A | 7 | a0001c0001t0008g0004a0001c0001t0008g0096a0001c0001t0008g0097others(4): Show | 10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1263-378G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620515 | ||||||
chr8:41620842
|
G | A | 49 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0016others(46): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1263-51G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620842 |