geneid | 84649 |
---|---|
ensemblid | ENSG00000062282.15 |
hgncid | 16940 |
symbol | DGAT2 |
name | diacylglycerol O-acyltransferase 2 |
refseq_nuc | NM_032564.5 |
refseq_prot | NP_115953.2 |
ensembl_nuc | ENST00000228027.12 |
ensembl_prot | ENSP00000228027.6 |
mane_status | MANE Select |
chr | chr11 |
start | 75768778 |
end | 75801534 |
strand | + |
ver | v1.2 |
region | chr11:75768778-75801534 |
region5000 | chr11:75763778-75806534 |
regionname0 | DGAT2_chr11_75768778_75801534 |
regionname5000 | DGAT2_chr11_75763778_75806534 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 388 | 309 | 78 | 46 | 142 | 8 | 33 | 104 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0002 | 0/0 | 388 | 9 | 8 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0003 | 0/0 | 388 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0004 | 0/0 | 388 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0005 | 0/0 | 388 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0006 | 0/0 | 388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1167 | 295 | 70 | 45 | 138 | 7 | 33 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
c0002 | 0/0 | 1167 | 9 | 8 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
c0003 | 0/0 | 1167 | 8 | 7 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
c0004 | 0/0 | 1167 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
c0005 | 0/0 | 1167 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
c0006 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
c0007 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
c0008 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
c0009 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
c0010 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
c0011 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1241 | 192 | 38 | 33 | 88 | 6 | 25 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0002 | 0/0 | 1241 | 111 | 37 | 11 | 55 | 1 | 7 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0003 | 0/0 | 1241 | 8 | 7 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0004 | 0/0 | 1241 | 2 | 0 | 1 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0005 | 0/0 | 1241 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0006 | 0/0 | 1241 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0007 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0008 | 0/0 | 1241 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0009 | 0/0 | 1241 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0010 | 0/0 | 1241 | 1 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0011 | 0/0 | 1241 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0012 | 0/0 | 1241 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0013 | 0/0 | 1241 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
t0014 | 0/0 | 1241 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 35 | 3 | 2 | 27 | 1 | 2 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0002 | 0/0 | 28 | 1 | 5 | 18 | 0 | 4 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0003 | 0/0 | 19 | 0 | 4 | 4 | 3 | 8 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0006 | 0/0 | 5 | 2 | 1 | 0 | 0 | 2 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0036 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0037 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1167 | 295 | 70 | 45 | 138 | 7 | 33 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0003 | 0/0 | 1167 | 8 | 7 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0005 | 0/0 | 1167 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0006 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0008 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0011 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0002c0002 | 0/0 | 1167 | 9 | 8 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0003c0004 | 0/0 | 1167 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0004c0010 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0005c0009 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0006c0007 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2407 | 181 | 37 | 33 | 80 | 6 | 23 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0001t0002 | 0/0 | 2407 | 102 | 29 | 10 | 55 | 1 | 7 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0001t0004 | 0/0 | 2407 | 2 | 0 | 1 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0001t0005 | 0/0 | 2407 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0001t0006 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0001t0007 | 0/0 | 2407 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0001t0008 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0001t0009 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0001t0011 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0001t0012 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0001t0013 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0001t0014 | 0/0 | 2407 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0003t0002 | 0/0 | 2407 | 8 | 7 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0005t0001 | 0/0 | 2407 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0006t0001 | 0/0 | 2407 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0008t0010 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0001c0011t0001 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0002c0002t0002 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0002c0002t0003 | 0/0 | 2407 | 8 | 7 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0003c0004t0001 | 0/0 | 2407 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0004c0010t0001 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0005c0009t0001 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
a0006c0007t0001 | 0/0 | 2407 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | copy fasta | chr11 | 75763778 | 75806534 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 32 | 3 | 1 | 25 | 1 | 2 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0003 | 0/0 | 17 | 0 | 4 | 4 | 3 | 6 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0006 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0036 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0037 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0002 | 0/0 | 28 | 1 | 5 | 18 | 0 | 4 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0009g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0011g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0012g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0013g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0001t0014g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0003t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0003t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0003t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0005t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0008t0010g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0001c0011t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0002c0002t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0002c0002t0003g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0002c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0002c0002t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0002c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0002c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0003c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0003c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0003c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0004c0010t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0005c0009t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
a0006c0007t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | GBR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00621 | hp2 | a0001 | c0005 | t0001 | g0016 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00639 | hp2 | a0001 | c0001 | t0014 | g0082 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00673 | hp2 | a0001 | c0001 | t0005 | g0133 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01074 | hp1 | a0001 | c0003 | t0002 | g0067 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01884 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02080 | hp1 | a0001 | c0001 | t0007 | g0170 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02145 | hp2 | a0002 | c0002 | t0003 | g0064 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CDX | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02523 | hp2 | a0001 | c0005 | t0001 | g0016 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02572 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02622 | hp2 | a0002 | c0002 | t0003 | g0062 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02630 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02698 | hp1 | a0005 | c0009 | t0001 | g0003 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02896 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02976 | hp1 | a0002 | c0002 | t0003 | g0065 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03041 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03209 | hp2 | a0002 | c0002 | t0003 | g0063 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03486 | hp1 | a0001 | c0003 | t0002 | g0068 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03491 | hp1 | a0001 | c0001 | t0011 | g0003 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0112 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG04115 | hp1 | a0002 | c0002 | t0003 | g0026 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG04199 | hp1 | a0001 | c0001 | t0009 | g0006 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG04228 | hp1 | a0004 | c0010 | t0001 | g0116 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CHB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | YRI | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18906 | hp2 | a0001 | c0001 | t0013 | g0091 | AFR | YRI | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18939 | hp1 | a0006 | c0007 | t0001 | g0018 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18942 | hp1 | a0003 | c0004 | t0001 | g0111 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18971 | hp2 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18984 | hp2 | a0003 | c0004 | t0001 | g0139 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18994 | hp1 | a0003 | c0004 | t0001 | g0104 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19002 | hp1 | a0001 | c0005 | t0001 | g0016 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0088 | AFR | LWK | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19030 | hp2 | a0002 | c0002 | t0003 | g0026 | AFR | LWK | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19043 | hp1 | a0001 | c0011 | t0001 | g0008 | AFR | LWK | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19240 | hp1 | a0001 | c0001 | t0012 | g0146 | AFR | YRI | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | YRI | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ASW | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ASW | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA20752 | hp1 | a0001 | c0008 | t0010 | g0147 | EUR | TSI | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0066 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03471 | hp1 | a0001 | c0003 | t0002 | g0011 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | USA | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
HG06807 | hp2 | a0001 | c0003 | t0002 | g0011 | AFR | USA | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | USA | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
NA20300 | hp2 | a0001 | c0003 | t0002 | g0011 | AFR | USA | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0119 | REF | REF | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0036 | REF | REF | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:75769052
|
G | A | 1 | a0003 | 3 | NA18942.hp1 NA18984.hp2 NA18994.hp1 |
missense_variant | MODERATE | c.61G>A | p.Asp21Asn | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/8 | 275/2407 | 61/1167 | 21/388 | chr11 | 75769052 | ||
chr11:75796340
|
C | G | 1 | a0004 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.442C>G | p.His148Asp | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 5/8 | 656/2407 | 442/1167 | 148/388 | chr11 | 75796340 | ||
chr11:75797224
|
T | C | 1 | a0006 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.701T>C | p.Ile234Thr | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/8 | 915/2407 | 701/1167 | 234/388 | chr11 | 75797224 | ||
chr11:75798267
|
G | A | 1 | a0005 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.850G>A | p.Val284Met | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/8 | 1064/2407 | 850/1167 | 284/388 | chr11 | 75798267 | ||
chr11:75800424
|
G | A | 1 | a0002 | 9 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
missense_variant | MODERATE | c.1083G>A | p.Met361Ile | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 1297/2407 | 1083/1167 | 361/388 | chr11 | 75800424 | ||
chr11:75801533
|
T | C | 1 | a0001 | 1 | HG03491.hp1 | splice_region_variant | LOW | c.*1025T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | chr11 | 75801533 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:75769063
|
G | A | 1 | a0001c0003 | 8 | HG01074.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
synonymous_variant | LOW | c.72G>A | p.Gln24Gln | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/8 | 286/2407 | 72/1167 | 24/388 | chr11 | 75769063 | ||
chr11:75790210
|
C | T | 1 | a0001c0011 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.273C>T | p.Leu91Leu | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 3/8 | 487/2407 | 273/1167 | 91/388 | chr11 | 75790210 | ||
chr11:75790710
|
T | C | 1 | a0001c0006 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.408T>C | p.Phe136Phe | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/8 | 622/2407 | 408/1167 | 136/388 | chr11 | 75790710 | ||
chr11:75797288
|
C | A | 1 | a0001c0008 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.765C>A | p.Thr255Thr | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/8 | 979/2407 | 765/1167 | 255/388 | chr11 | 75797288 | ||
chr11:75798344
|
C | T | 1 | a0001c0005 | 3 | HG00621.hp2 HG02523.hp2 NA19002.hp1 |
synonymous_variant | LOW | c.927C>T | p.Phe309Phe | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/8 | 1141/2407 | 927/1167 | 309/388 | chr11 | 75798344 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:75768789
|
C | T | 1 | a0001c0001t0014 | 1 | HG00639.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-203C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/8 | chr11 | 75768789 | ||||||
chr11:75768817
|
C | G | 1 | a0001c0001t0005 | 2 | HG00673.hp2 HG02083.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-175C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/8 | chr11 | 75768817 | ||||||
chr11:75768819
|
C | T | 2 | a0001c0001t0013a0002c0002t0003 | 9 | HG02145.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-173C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/8 | chr11 | 75768819 | ||||||
chr11:75768845
|
G | C | 1 | a0001c0001t0006 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-147G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/8 | 147 | chr11 | 75768845 | |||||
chr11:75800527
|
T | C | 8 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(5): Show | 123 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*19T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 19 | chr11 | 75800527 | |||||
chr11:75800707
|
C | A | 1 | a0001c0001t0013 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*199C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 199 | chr11 | 75800707 | |||||
chr11:75800882
|
C | G | 1 | a0001c0001t0007 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*374C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 374 | chr11 | 75800882 | |||||
chr11:75800917
|
T | C | 1 | a0001c0001t0004 | 2 | HG01175.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*409T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 409 | chr11 | 75800917 | |||||
chr11:75801072
|
C | T | 1 | a0001c0001t0012 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 564 | chr11 | 75801072 | |||||
chr11:75801224
|
T | C | 1 | a0001c0001t0008 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*716T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 716 | chr11 | 75801224 | |||||
chr11:75801425
|
G | A | 1 | a0001c0001t0009 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*917G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 917 | chr11 | 75801425 | |||||
chr11:75801488
|
T | C | 1 | a0001c0008t0010 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*980T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 980 | chr11 | 75801488 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:75769152
|
A | G | 1 | a0001c0001t0001g0042 | 2 | NA18943.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.121+40A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769152 | ||||||
chr11:75769325
|
T | C | 6 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+213T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769325 | ||||||
chr11:75769375
|
C | G | 5 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(2): Show | 5 | HG02055.hp1 HG02280.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+263C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769375 | ||||||
chr11:75769410
|
A | G | 1 | a0001c0001t0001g0041 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.121+298A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769410 | ||||||
chr11:75769637
|
G | T | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.121+525G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769637 | ||||||
chr11:75769815
|
C | G | 1 | a0001c0001t0002g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.121+703C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769815 | ||||||
chr11:75769819
|
A | T | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.121+707A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769819 | ||||||
chr11:75770085
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.121+973A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75770085 | ||||||
chr11:75770141
|
A | G | 1 | a0001c0001t0002g0172 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.121+1029A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75770141 | ||||||
chr11:75770286
|
G | A | 1 | a0001c0001t0001g0022 | 2 | HG00642.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.121+1174G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75770286 | ||||||
chr11:75770488
|
G | C | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.121+1376G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75770488 | ||||||
chr11:75770619
|
G | C | 76 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(73): Show | 132 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.121+1507G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75770619 | ||||||
chr11:75770799
|
CT | C | 18 | a0001c0001t0001g0053a0001c0001t0001g0094a0001c0001t0001g0095others(15): Show | 22 | HG00438.hp1 HG01243.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.121+1699delT | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 75770799 | |||||
chr11:75770997
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.121+1885G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75770997 | ||||||
chr11:75771053
|
G | A | 1 | a0001c0001t0001g0033 | 2 | NA18988.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.121+1941G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771053 | ||||||
chr11:75771221
|
G | A | 1 | a0001c0001t0001g0014 | 3 | HG00323.hp2 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.121+2109G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771221 | ||||||
chr11:75771249
|
T | C | 2 | a0001c0001t0002g0024a0001c0001t0002g0057 | 3 | HG00642.hp2 HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.121+2137T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771249 | ||||||
chr11:75771272
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.121+2160C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771272 | ||||||
chr11:75771465
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.121+2353A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771465 | ||||||
chr11:75771793
|
A | G | 1 | a0001c0001t0013g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.121+2681A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771793 | ||||||
chr11:75771882
|
A | G | 1 | a0001c0001t0002g0090 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.121+2770A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771882 | ||||||
chr11:75772040
|
C | G | 1 | a0001c0001t0002g0089 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.121+2928C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772040 | ||||||
chr11:75772044
|
T | G | 1 | a0001c0001t0002g0010 | 3 | HG01891.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.121+2932T>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772044 | ||||||
chr11:75772087
|
G | A | 1 | a0001c0001t0013g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.121+2975G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772087 | ||||||
chr11:75772099
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.121+2987G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772099 | ||||||
chr11:75772166
|
C | T | 2 | a0001c0001t0002g0171a0001c0001t0007g0170 | 2 | HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.121+3054C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772166 | ||||||
chr11:75772518
|
C | G | 16 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.121+3406C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772518 | ||||||
chr11:75772521
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.121+3409C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772521 | ||||||
chr11:75772527
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.121+3415A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772527 | ||||||
chr11:75772578
|
A | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(32): Show | 65 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.121+3466A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772578 | ||||||
chr11:75772623
|
A | G | 1 | a0001c0001t0001g0040 | 2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.121+3511A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772623 | ||||||
chr11:75772682
|
A | G | 1 | a0001c0001t0013g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.121+3570A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772682 | ||||||
chr11:75772706
|
G | A | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060 | 3 | HG02055.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.121+3594G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772706 | ||||||
chr11:75772860
|
T | C | 59 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(56): Show | 108 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.121+3748T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772860 | ||||||
chr11:75772967
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121+3855G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772967 | ||||||
chr11:75773224
|
C | A | 16 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.121+4112C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75773224 | ||||||
chr11:75773388
|
C | G | 1 | a0001c0001t0013g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.121+4276C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75773388 | ||||||
chr11:75773734
|
C | T | 6 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+4622C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75773734 | ||||||
chr11:75773805
|
A | G | 35 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(32): Show | 82 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.121+4693A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75773805 | ||||||
chr11:75773884
|
C | G | 28 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(25): Show | 71 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.121+4772C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75773884 | ||||||
chr11:75774150
|
T | G | 1 | a0001c0001t0002g0069 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.121+5038T>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774150 | ||||||
chr11:75774186
|
G | A | 31 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(28): Show | 74 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.121+5074G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774186 | ||||||
chr11:75774265
|
C | T | 6 | a0001c0001t0002g0005a0001c0001t0002g0078a0001c0001t0002g0079others(3): Show | 10 | HG02040.hp1 HG02071.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.121+5153C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774265 | ||||||
chr11:75774293
|
C | G | 1 | a0001c0001t0002g0069 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.121+5181C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774293 | ||||||
chr11:75774321
|
C | T | 1 | a0001c0008t0010g0147 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.121+5209C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774321 | ||||||
chr11:75774427
|
T | C | 1 | a0001c0001t0002g0078 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.121+5315T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774427 | ||||||
chr11:75774452
|
T | G | 1 | a0001c0001t0002g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.121+5340T>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774452 | ||||||
chr11:75774494
|
C | T | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.121+5382C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774494 | ||||||
chr11:75774644
|
G | T | 1 | a0001c0001t0012g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.121+5532G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774644 | ||||||
chr11:75774758
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.121+5646C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774758 | ||||||
chr11:75775195
|
C | T | 1 | a0001c0001t0001g0033 | 2 | NA18988.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.121+6083C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75775195 | ||||||
chr11:75775239
|
GAAGAGGC others(9): Show |
G | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.121+6128_121+6143d others(18): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75775239 | ||||||
chr11:75775251
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.121+6139C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75775251 | ||||||
chr11:75775427
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG02818.hp1 HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.121+6315T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75775427 | ||||||
chr11:75775542
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.121+6430G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75775542 | ||||||
chr11:75776001
|
C | A | 1 | a0001c0001t0002g0070 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.121+6889C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776001 | ||||||
chr11:75776100
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121+6988C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776100 | ||||||
chr11:75776101
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.121+6989G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776101 | ||||||
chr11:75776111
|
A | G | 2 | a0001c0001t0001g0008a0001c0011t0001g0008 | 4 | HG02258.hp2 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+6999A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776111 | ||||||
chr11:75776243
|
A | C | 2 | a0001c0003t0002g0067a0001c0003t0002g0068 | 2 | HG01074.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.121+7131A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776243 | ||||||
chr11:75776277
|
C | T | 24 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0039others(21): Show | 29 | HG00597.hp1 HG00642.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.121+7165C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776277 | ||||||
chr11:75776281
|
C | T | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(29): Show | 75 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.121+7169C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776281 | ||||||
chr11:75776429
|
A | G | 2 | a0001c0001t0002g0171a0001c0001t0007g0170 | 2 | HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.121+7317A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776429 | ||||||
chr11:75776566
|
A | G | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.121+7454A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776566 | ||||||
chr11:75776601
|
C | G | 2 | a0001c0001t0002g0028a0001c0001t0002g0092 | 3 | HG02451.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.121+7489C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776601 | ||||||
chr11:75777006
|
G | A | 16 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.122-7612G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777006 | ||||||
chr11:75777009
|
C | A | 25 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(22): Show | 67 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.122-7609C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777009 | ||||||
chr11:75777115
|
G | C | 1 | a0001c0001t0001g0040 | 2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.122-7503G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777115 | ||||||
chr11:75777141
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.122-7477C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777141 | ||||||
chr11:75777294
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.122-7324G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777294 | ||||||
chr11:75777312
|
CAG | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0095 | 4 | NA18939.hp2 NA18956.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-7305_122-7304d others(4): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777312 | ||||||
chr11:75777723
|
G | C | 1 | a0001c0001t0014g0082 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.122-6895G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777723 | ||||||
chr11:75777802
|
C | T | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.122-6816C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777802 | ||||||
chr11:75778045
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-6573T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778045 | ||||||
chr11:75778076
|
T | G | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-6542T>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778076 | ||||||
chr11:75778185
|
A | G | 1 | a0001c0001t0002g0027 | 2 | NA18955.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.122-6433A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778185 | ||||||
chr11:75778283
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.122-6335C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778283 | ||||||
chr11:75778284
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0102a0001c0001t0001g0103 | 5 | HG01123.hp2 HG01192.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-6334G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778284 | ||||||
chr11:75778310
|
A | T | 1 | a0001c0001t0013g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122-6308A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778310 | ||||||
chr11:75778359
|
C | A | 31 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(28): Show | 74 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.122-6259C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778359 | ||||||
chr11:75778364
|
C | T | 1 | a0002c0002t0002g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.122-6254C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778364 | ||||||
chr11:75778525
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-6093C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778525 | ||||||
chr11:75778527
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-6091T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778527 | ||||||
chr11:75778561
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.122-6057G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778561 | ||||||
chr11:75778675
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.122-5943A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778675 | ||||||
chr11:75778681
|
A | T | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-5937A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778681 | ||||||
chr11:75778704
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.122-5914G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778704 | ||||||
chr11:75778767
|
G | A | 3 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051 | 3 | HG00438.hp1 NA18951.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.122-5851G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778767 | ||||||
chr11:75778833
|
C | CA | 39 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(36): Show | 50 | HG00438.hp1 HG00438.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.122-5763dupA | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 75778833 | |||||
chr11:75778833
|
C | CAA | 26 | a0001c0001t0001g0083a0001c0001t0002g0002a0001c0001t0002g0004others(23): Show | 67 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.122-5764_122-5763d others(4): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 75778833 | |||||
chr11:75778833
|
CA | C | 22 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0144others(19): Show | 24 | HG01255.hp1 HG01255.hp2 HG02132.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-5763delA | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 75778833 | |||||
chr11:75778985
|
C | T | 1 | a0002c0002t0003g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.122-5633C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778985 | ||||||
chr11:75779093
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122-5525G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779093 | ||||||
chr11:75779109
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.122-5509G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779109 | ||||||
chr11:75779154
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG00741.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.122-5464C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779154 | ||||||
chr11:75779256
|
A | T | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-5362A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779256 | ||||||
chr11:75779260
|
G | T | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-5358G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779260 | ||||||
chr11:75779263
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.122-5355G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779263 | ||||||
chr11:75779551
|
C | A | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.122-5067C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779551 | ||||||
chr11:75779572
|
C | A | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-5046C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779572 | ||||||
chr11:75779597
|
C | T | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.122-5021C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779597 | ||||||
chr11:75779606
|
C | A | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-5012C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779606 | ||||||
chr11:75779660
|
A | T | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-4958A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779660 | ||||||
chr11:75779775
|
C | A | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-4843C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779775 | ||||||
chr11:75779843
|
C | T | 1 | a0001c0001t0013g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122-4775C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779843 | ||||||
chr11:75779881
|
C | CCCAGTCT others(10): Show |
1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-4736_122-4720d others(19): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 75779881 | |||||
chr11:75779906
|
C | A | 3 | a0001c0001t0002g0056a0001c0001t0002g0086a0001c0001t0002g0087 | 3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.122-4712C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779906 | ||||||
chr11:75779906
|
C | G | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.122-4712C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779906 | ||||||
chr11:75780215
|
T | A | 1 | a0002c0002t0002g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.122-4403T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780215 | ||||||
chr11:75780259
|
C | T | 2 | a0001c0001t0002g0004a0001c0001t0002g0089 | 7 | HG01192.hp1 NA18946.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-4359C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780259 | ||||||
chr11:75780434
|
C | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0136 | 3 | HG02698.hp2 HG02738.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.122-4184C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780434 | ||||||
chr11:75780451
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0102a0001c0001t0001g0103 | 5 | HG01123.hp2 HG01192.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-4167C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780451 | ||||||
chr11:75780479
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.122-4139G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780479 | ||||||
chr11:75780732
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0095 | 4 | NA18939.hp2 NA18956.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-3886G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780732 | ||||||
chr11:75780851
|
A | G | 3 | a0001c0001t0002g0056a0001c0001t0002g0086a0001c0001t0002g0087 | 3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.122-3767A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780851 | ||||||
chr11:75780918
|
T | A | 1 | a0001c0001t0006g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.122-3700T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780918 | ||||||
chr11:75780930
|
C | T | 1 | a0001c0001t0013g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122-3688C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780930 | ||||||
chr11:75780959
|
C | T | 4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0083others(1): Show | 6 | HG02622.hp1 HG02895.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-3659C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780959 | ||||||
chr11:75781029
|
C | T | 16 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.122-3589C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75781029 | ||||||
chr11:75781045
|
G | A | 3 | a0001c0001t0002g0056a0001c0001t0002g0086a0001c0001t0002g0087 | 3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.122-3573G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75781045 | ||||||
chr11:75781158
|
T | C | 61 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(58): Show | 110 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.122-3460T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75781158 | ||||||
chr11:75781382
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.122-3236G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75781382 | ||||||
chr11:75781484
|
TG | T | 2 | a0001c0001t0002g0004a0001c0001t0002g0089 | 7 | HG01192.hp1 NA18946.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-3131delG | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 75781484 | |||||
chr11:75781759
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.122-2859G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75781759 | ||||||
chr11:75781987
|
A | C | 1 | a0002c0002t0003g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.122-2631A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75781987 | ||||||
chr11:75782024
|
C | T | 7 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-2594C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782024 | ||||||
chr11:75782089
|
A | G | 61 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(58): Show | 110 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.122-2529A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782089 | ||||||
chr11:75782133
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02055.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.122-2485G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782133 | ||||||
chr11:75782159
|
C | T | 3 | a0001c0001t0002g0056a0001c0001t0002g0086a0001c0001t0002g0087 | 3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.122-2459C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782159 | ||||||
chr11:75782164
|
A | G | 61 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(58): Show | 110 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.122-2454A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782164 | ||||||
chr11:75782295
|
C | G | 1 | a0001c0001t0002g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.122-2323C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782295 | ||||||
chr11:75782338
|
G | A | 3 | a0003c0004t0001g0104a0003c0004t0001g0111a0003c0004t0001g0139 | 3 | NA18942.hp1 NA18984.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.122-2280G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782338 | ||||||
chr11:75782691
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.122-1927A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782691 | ||||||
chr11:75782692
|
A | G | 3 | a0001c0001t0002g0044a0001c0001t0002g0046a0001c0001t0002g0047 | 3 | HG01243.hp1 HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.122-1926A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782692 | ||||||
chr11:75782820
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.122-1798G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782820 | ||||||
chr11:75782849
|
T | C | 1 | a0001c0001t0004g0112 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.122-1769T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782849 | ||||||
chr11:75782866
|
G | T | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-1752G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782866 | ||||||
chr11:75782937
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.122-1681G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782937 | ||||||
chr11:75783021
|
G | A | 16 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.122-1597G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783021 | ||||||
chr11:75783165
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.122-1453A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783165 | ||||||
chr11:75783178
|
G | A | 1 | a0001c0001t0002g0050 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.122-1440G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783178 | ||||||
chr11:75783283
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.122-1335G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783283 | ||||||
chr11:75783581
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.122-1037A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783581 | ||||||
chr11:75783582
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.122-1036G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783582 | ||||||
chr11:75783768
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.122-850C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783768 | ||||||
chr11:75783776
|
T | C | 79 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(76): Show | 135 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.122-842T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783776 | ||||||
chr11:75783968
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.122-650T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783968 | ||||||
chr11:75784181
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.122-437A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75784181 | ||||||
chr11:75784377
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.122-241C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75784377 | ||||||
chr11:75784475
|
G | A | 8 | a0001c0001t0002g0007a0001c0001t0002g0023a0001c0001t0002g0049others(5): Show | 12 | HG00438.hp1 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.122-143G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75784475 | ||||||
chr11:75784531
|
G | T | 1 | a0001c0003t0002g0012 | 3 | HG01884.hp1 HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.122-87G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75784531 | ||||||
chr11:75784857
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.250+111C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75784857 | ||||||
chr11:75785199
|
A | G | 1 | a0001c0001t0006g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.250+453A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785199 | ||||||
chr11:75785348
|
T | A | 1 | a0001c0001t0001g0034 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.250+602T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785348 | ||||||
chr11:75785410
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.250+664C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785410 | ||||||
chr11:75785424
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.250+678G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785424 | ||||||
chr11:75785649
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.250+903C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785649 | ||||||
chr11:75785783
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.250+1037G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785783 | ||||||
chr11:75785787
|
A | G | 1 | a0001c0001t0005g0133 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.250+1041A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785787 | ||||||
chr11:75785970
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.250+1224A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785970 | ||||||
chr11:75786024
|
G | A | 1 | a0004c0010t0001g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.250+1278G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75786024 | ||||||
chr11:75786186
|
TAA | T | 16 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.250+1442_250+1443d others(4): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 75786186 | |||||
chr11:75786246
|
A | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0102a0001c0001t0001g0103 | 5 | HG01123.hp2 HG01192.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+1500A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75786246 | ||||||
chr11:75786323
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.250+1577T>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75786323 | ||||||
chr11:75786398
|
A | C | 1 | a0001c0001t0001g0132 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.250+1652A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75786398 | ||||||
chr11:75786749
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.250+2003C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75786749 | ||||||
chr11:75786948
|
C | A | 1 | a0001c0003t0002g0067 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.250+2202C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75786948 | ||||||
chr11:75787076
|
GAT | G | 24 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(21): Show | 66 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.250+2333_250+2334d others(4): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 75787076 | |||||
chr11:75787189
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.250+2443A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787189 | ||||||
chr11:75787195
|
A | G | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(29): Show | 75 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.250+2449A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787195 | ||||||
chr11:75787218
|
AT | A | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.250+2473delT | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787218 | ||||||
chr11:75787386
|
C | A | 16 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.250+2640C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787386 | ||||||
chr11:75787393
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0108a0001c0001t0001g0132 | 4 | HG00597.hp2 HG00621.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+2647C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787393 | ||||||
chr11:75787486
|
A | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0094a0001c0001t0001g0161 | 6 | NA18953.hp2 NA18954.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-2702A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787486 | ||||||
chr11:75787489
|
G | A | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.251-2699G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787489 | ||||||
chr11:75787596
|
A | T | 8 | a0001c0003t0002g0011a0002c0002t0002g0066a0002c0002t0003g0025others(5): Show | 12 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.251-2592A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787596 | ||||||
chr11:75787867
|
G | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0117 | 3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.251-2321G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787867 | ||||||
chr11:75787968
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.251-2220G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787968 | ||||||
chr11:75787969
|
C | G | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.251-2219C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787969 | ||||||
chr11:75788192
|
T | C | 1 | a0001c0001t0002g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.251-1996T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75788192 | ||||||
chr11:75788332
|
G | A | 2 | a0001c0001t0001g0113a0001c0005t0001g0016 | 4 | HG00621.hp2 HG02129.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-1856G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75788332 | ||||||
chr11:75788407
|
T | C | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(29): Show | 75 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.251-1781T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75788407 | ||||||
chr11:75788626
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.251-1562A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75788626 | ||||||
chr11:75788677
|
A | C | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.251-1511A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75788677 | ||||||
chr11:75788839
|
A | G | 2 | a0001c0001t0002g0056a0001c0001t0002g0087 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.251-1349A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75788839 | ||||||
chr11:75788970
|
AAG | A | 3 | a0001c0001t0002g0056a0001c0001t0002g0086a0001c0001t0002g0087 | 3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.251-1212_251-1211d others(4): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 75788970 | |||||
chr11:75789091
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.251-1097A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789091 | ||||||
chr11:75789117
|
C | T | 1 | a0001c0001t0013g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.251-1071C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789117 | ||||||
chr11:75789148
|
G | GT | 7 | a0001c0001t0001g0037a0001c0001t0001g0103a0001c0001t0001g0126others(4): Show | 9 | HG01192.hp2 HG02132.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-1027dupT | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 75789148 | |||||
chr11:75789211
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0136 | 3 | HG02698.hp2 HG02738.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.251-977G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789211 | ||||||
chr11:75789467
|
C | G | 2 | a0001c0001t0002g0056a0001c0001t0002g0087 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.251-721C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789467 | ||||||
chr11:75789521
|
T | C | 7 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-667T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789521 | ||||||
chr11:75789568
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | NA18989.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.251-620G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789568 | ||||||
chr11:75789757
|
A | C | 1 | a0001c0001t0001g0053 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.251-431A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789757 | ||||||
chr11:75789792
|
CAG | C | 8 | a0001c0001t0002g0007a0001c0001t0002g0023a0001c0001t0002g0049others(5): Show | 12 | HG00438.hp1 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.251-393_251-392del others(2): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 75789792 | |||||
chr11:75789975
|
C | T | 7 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-213C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789975 | ||||||
chr11:75790002
|
G | T | 1 | a0001c0001t0002g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.251-186G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75790002 | ||||||
chr11:75790026
|
G | A | 1 | a0002c0002t0003g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.251-162G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75790026 | ||||||
chr11:75790034
|
A | G | 4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0083others(1): Show | 6 | HG02622.hp1 HG02895.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-154A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75790034 | ||||||
chr11:75790162
|
C | G | 61 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(58): Show | 110 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.251-26C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75790162 | ||||||
chr11:75790429
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0118 | 2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.358+134G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 3/7 | chr11 | 75790429 | ||||||
chr11:75790429
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.358+134G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 3/7 | chr11 | 75790429 | ||||||
chr11:75790807
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(180): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.429+76A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75790807 | ||||||
chr11:75790829
|
T | C | 5 | a0002c0002t0003g0025a0002c0002t0003g0026a0002c0002t0003g0062others(2): Show | 7 | HG02145.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+98T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75790829 | ||||||
chr11:75791092
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.429+361G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791092 | ||||||
chr11:75791137
|
C | G | 7 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+406C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791137 | ||||||
chr11:75791147
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.429+416C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791147 | ||||||
chr11:75791173
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.429+442G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791173 | ||||||
chr11:75791196
|
C | A | 16 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.429+465C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791196 | ||||||
chr11:75791216
|
G | A | 12 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(9): Show | 12 | HG01243.hp1 HG02257.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.429+485G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791216 | ||||||
chr11:75791414
|
G | A | 5 | a0002c0002t0003g0025a0002c0002t0003g0026a0002c0002t0003g0062others(2): Show | 7 | HG02145.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+683G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791414 | ||||||
chr11:75791487
|
G | T | 3 | a0001c0001t0002g0056a0001c0001t0002g0086a0001c0001t0002g0087 | 3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.429+756G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791487 | ||||||
chr11:75791673
|
A | G | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0067others(1): Show | 8 | HG01074.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+942A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791673 | ||||||
chr11:75792181
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429+1450C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792181 | ||||||
chr11:75792272
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.429+1541C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792272 | ||||||
chr11:75792379
|
G | A | 9 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(6): Show | 9 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+1648G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792379 | ||||||
chr11:75792468
|
A | G | 2 | a0001c0001t0002g0013a0002c0002t0003g0062 | 4 | HG02622.hp2 NA18986.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+1737A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792468 | ||||||
chr11:75792518
|
C | T | 3 | a0001c0001t0002g0056a0001c0001t0002g0086a0001c0001t0002g0087 | 3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.429+1787C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792518 | ||||||
chr11:75792544
|
C | T | 1 | a0001c0001t0006g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.429+1813C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792544 | ||||||
chr11:75792595
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.429+1864G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792595 | ||||||
chr11:75792601
|
A | G | 1 | a0001c0001t0002g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.429+1870A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792601 | ||||||
chr11:75792710
|
G | A | 6 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+1979G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792710 | ||||||
chr11:75792711
|
C | G | 1 | a0001c0001t0001g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.429+1980C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792711 | ||||||
chr11:75792765
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.429+2034A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792765 | ||||||
chr11:75792915
|
C | A | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.429+2184C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792915 | ||||||
chr11:75792922
|
T | C | 1 | a0001c0001t0013g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429+2191T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792922 | ||||||
chr11:75793047
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.429+2316C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75793047 | ||||||
chr11:75793124
|
G | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0055 | 3 | HG02280.hp2 HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.429+2393G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75793124 | ||||||
chr11:75793136
|
C | T | 9 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(6): Show | 9 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+2405C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75793136 | ||||||
chr11:75793265
|
G | C | 6 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+2534G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75793265 | ||||||
chr11:75793614
|
C | T | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.430-2714C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75793614 | ||||||
chr11:75793724
|
A | C | 1 | a0001c0001t0013g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.430-2604A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75793724 | ||||||
chr11:75793919
|
TA | T | 58 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(55): Show | 107 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.430-2407delA | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 75793919 | |||||
chr11:75794166
|
G | A | 16 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.430-2162G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794166 | ||||||
chr11:75794239
|
C | G | 4 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-2089C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794239 | ||||||
chr11:75794782
|
T | C | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 84 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.430-1546T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794782 | ||||||
chr11:75794905
|
C | T | 16 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.430-1423C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794905 | ||||||
chr11:75794938
|
TCCCC | T | 5 | a0001c0001t0002g0056a0001c0001t0002g0061a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02257.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-1388_430-1385d others(6): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 75794938 | |||||
chr11:75794942
|
C | CT | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(167): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.430-1386_430-1385i others(3): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794942 | ||||||
chr11:75794942
|
C | CTCCCCT | 9 | a0001c0001t0002g0005a0001c0001t0002g0043a0001c0001t0002g0044others(6): Show | 13 | HG01243.hp1 HG02071.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.430-1386_430-1385i others(8): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794942 | ||||||
chr11:75794942
|
C | CTCTCCTC others(14): Show |
1 | a0001c0001t0001g0121 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.430-1386_430-1385i others(23): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794942 | ||||||
chr11:75794944
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.430-1384T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794944 | ||||||
chr11:75794949
|
C | T | 1 | a0001c0001t0013g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.430-1379C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794949 | ||||||
chr11:75794966
|
C | T | 7 | a0002c0002t0002g0066a0002c0002t0003g0025a0002c0002t0003g0026others(4): Show | 9 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.430-1362C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794966 | ||||||
chr11:75794969
|
C | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(35): Show | 68 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.430-1359C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794969 | ||||||
chr11:75794978
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.430-1350G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794978 | ||||||
chr11:75795130
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.430-1198T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795130 | ||||||
chr11:75795342
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.430-986A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795342 | ||||||
chr11:75795390
|
C | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 6 | NA18943.hp1 NA18951.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-938C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795390 | ||||||
chr11:75795419
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.430-909C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795419 | ||||||
chr11:75795476
|
A | G | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.430-852A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795476 | ||||||
chr11:75795540
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.430-788A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795540 | ||||||
chr11:75795692
|
A | G | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.430-636A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795692 | ||||||
chr11:75795704
|
G | A | 3 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0164 | 3 | HG01074.hp2 HG01256.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.430-624G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795704 | ||||||
chr11:75795940
|
C | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0117 | 3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.430-388C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795940 | ||||||
chr11:75796044
|
A | C | 1 | a0001c0003t0002g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.430-284A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75796044 | ||||||
chr11:75796078
|
A | G | 4 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-250A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75796078 | ||||||
chr11:75796189
|
A | C | 61 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(58): Show | 110 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.430-139A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75796189 | ||||||
chr11:75796251
|
A | G | 1 | a0001c0001t0001g0035 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.430-77A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75796251 | ||||||
chr11:75796712
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 6 | NA18943.hp1 NA18951.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+180T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 5/7 | chr11 | 75796712 | ||||||
chr11:75796807
|
T | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0083a0001c0001t0001g0084 | 4 | HG02895.hp2 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+275T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 5/7 | chr11 | 75796807 | ||||||
chr11:75797112
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T | C | 1 | a0001c0001t0001g0155 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.635-46T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 5/7 | chr11 | 75797112 | ||||||
chr11:75797692
|
C | G | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02055.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.809+360C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75797692 | ||||||
chr11:75797737
|
C | G | 1 | a0001c0001t0001g0161 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.809+405C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75797737 | ||||||
chr11:75797743
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G | A | 1 | a0001c0001t0001g0158 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.809+411G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75797743 | ||||||
chr11:75797848
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.810-379C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75797848 | ||||||
chr11:75797941
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G | C | 12 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(9): Show | 12 | HG01243.hp1 HG02257.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.810-286G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75797941 | ||||||
chr11:75798102
|
C | A | 1 | a0001c0001t0001g0143 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.810-125C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75798102 | ||||||
chr11:75798172
|
A | G | 4 | a0002c0002t0003g0025a0002c0002t0003g0062a0002c0002t0003g0064others(1): Show | 5 | HG02145.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.810-55A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75798172 | ||||||
chr11:75798173
|
T | G | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.810-54T>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75798173 | ||||||
chr11:75798451
|
C | T | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1012+22C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75798451 | ||||||
chr11:75798591
|
GGTA | G | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(29): Show | 75 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1012+170_1012+172d others(5): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 75798591 | |||||
chr11:75798750
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1012+321A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75798750 | ||||||
chr11:75798768
|
T | C | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060 | 3 | HG02055.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1012+339T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75798768 | ||||||
chr11:75798805
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0148a0001c0001t0001g0159others(2): Show | 8 | HG01169.hp2 HG01243.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012+376A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75798805 | ||||||
chr11:75798935
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G | A | 1 | a0001c0001t0001g0168 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1012+506G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75798935 | ||||||
chr11:75799170
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T | C | 1 | a0001c0001t0001g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1012+741T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799170 | ||||||
chr11:75799436
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A | G | 1 | a0001c0008t0010g0147 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1013-918A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799436 | ||||||
chr11:75799540
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G | A | 4 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-814G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799540 | ||||||
chr11:75799585
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1013-769C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799585 | ||||||
chr11:75799611
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A | T | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0067others(1): Show | 8 | HG01074.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1013-743A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799611 | ||||||
chr11:75799616
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T | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0100others(6): Show | 11 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1013-738T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799616 | ||||||
chr11:75799617
|
T | A | 3 | a0001c0001t0002g0056a0001c0001t0002g0086a0001c0001t0002g0087 | 3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1013-737T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799617 | ||||||
chr11:75799626
|
A | T | 2 | a0001c0003t0002g0011a0001c0003t0002g0012 | 6 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1013-728A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799626 | ||||||
chr11:75799717
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1013-637G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799717 | ||||||
chr11:75799758
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1013-596C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799758 | ||||||
chr11:75799994
|
A | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0149a0001c0001t0001g0152others(2): Show | 7 | HG00544.hp2 NA18962.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.1013-360A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799994 | ||||||
chr11:75800276
|
G | A | 2 | a0001c0001t0002g0056a0001c0001t0002g0087 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1013-78G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75800276 | ||||||
chr11:75800291
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0163 | 2 | HG01169.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1013-63A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75800291 |