geneid | 9971 |
---|---|
ensemblid | ENSG00000012504.15 |
hgncid | 7967 |
symbol | NR1H4 |
name | nuclear receptor subfamily 1 group H member 4 |
refseq_nuc | NM_001206979.2 |
refseq_prot | NP_001193908.1 |
ensembl_nuc | ENST00000392986.8 |
ensembl_prot | ENSP00000376712.3 |
mane_status | MANE Select |
chr | chr12 |
start | 100473866 |
end | 100564414 |
strand | + |
ver | v1.2 |
region | chr12:100473866-100564414 |
region5000 | chr12:100468866-100569414 |
regionname0 | NR1H4_chr12_100473866_100564414 |
regionname5000 | NR1H4_chr12_100468866_100569414 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 476 | 300 | 74 | 42 | 138 | 11 | 33 | 104 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0002 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0003 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0004 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0005 | 0/0 | 476 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0006 | 0/0 | 476 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0007 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0008 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1431 | 298 | 74 | 42 | 136 | 11 | 33 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
c0002 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
c0003 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
c0004 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
c0005 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
c0006 | 0/0 | 1431 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
c0007 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
c0008 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
c0009 | 0/0 | 1431 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
c0010 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1309 | 250 | 72 | 38 | 98 | 11 | 29 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
t0002 | 0/0 | 1309 | 47 | 2 | 0 | 41 | 0 | 4 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
t0003 | 0/0 | 1309 | 6 | 0 | 4 | 0 | 1 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
t0004 | 0/0 | 1309 | 3 | 3 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
t0005 | 0/0 | 1309 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
t0006 | 0/0 | 1309 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1431 | 298 | 74 | 42 | 136 | 11 | 33 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0001c0008 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0001c0010 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0002c0002 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0003c0005 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0004c0007 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0005c0009 | 0/0 | 1431 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0006c0006 | 0/0 | 1431 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0007c0004 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0008c0003 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2739 | 241 | 68 | 38 | 95 | 10 | 28 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0001c0001t0002 | 0/0 | 2739 | 47 | 2 | 0 | 41 | 0 | 4 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0001c0001t0003 | 0/0 | 2739 | 6 | 0 | 4 | 0 | 1 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0001c0001t0004 | 0/0 | 2739 | 3 | 3 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0001c0001t0006 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0001c0008t0005 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0001c0010t0001 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0002c0002t0001 | 0/0 | 2739 | 2 | 2 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0003c0005t0001 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0004c0007t0001 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0005c0009t0001 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0006c0006t0001 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0007c0004t0001 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
a0008c0003t0001 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | copy fasta | chr12 | 100468866 | 100569414 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0008t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0001c0010t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0002c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0002c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0003c0005t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0004c0007t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0005c0009t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0006c0006t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0007c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
a0008c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00099 | hp2 | a0006 | c0006 | t0001 | g0292 | EUR | GBR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | FIN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | FIN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | FIN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00673 | hp1 | a0001 | c0008 | t0005 | g0281 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | IBS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0271 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CDX | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CDX | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02615 | hp1 | a0003 | c0005 | t0001 | g0260 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03453 | hp2 | a0007 | c0004 | t0001 | g0166 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0258 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03688 | hp2 | a0005 | c0009 | t0001 | g0255 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | BEB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | YRI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18979 | hp1 | a0004 | c0007 | t0001 | g0197 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18990 | hp1 | a0001 | c0010 | t0001 | g0191 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19081 | hp2 | a0008 | c0003 | t0001 | g0215 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ASW | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ASW | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0219 | EUR | TSI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | GIH | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | GIH | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0177 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | USA | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | USA | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | USA | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | USA | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0116 | REF | REF | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0168 | REF | REF | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:100510780
|
G | A | 1 | a0002 | 2 | HG02257.hp2 HG02965.hp2 |
missense_variant&splice_region_variant | MODERATE | c.82G>A | p.Val28Ile | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/11 | 465/2739 | 82/1431 | 28/476 | chr12 | 100510780 | ||
chr12:100510798
|
G | C | 1 | a0008 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.100G>C | p.Ala34Pro | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/11 | 483/2739 | 100/1431 | 34/476 | chr12 | 100510798 | ||
chr12:100510799
|
C | G | 1 | a0008 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.101C>G | p.Ala34Gly | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/11 | 484/2739 | 101/1431 | 34/476 | chr12 | 100510799 | ||
chr12:100511044
|
G | A | 1 | a0007 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.346G>A | p.Ala116Thr | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/11 | 729/2739 | 346/1431 | 116/476 | chr12 | 100511044 | ||
chr12:100511090
|
G | A | 1 | a0003 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.392G>A | p.Gly131Glu | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/11 | 775/2739 | 392/1431 | 131/476 | chr12 | 100511090 | ||
chr12:100532530
|
T | C | 1 | a0006 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.518T>C | p.Met173Thr | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/11 | 901/2739 | 518/1431 | 173/476 | chr12 | 100532530 | ||
chr12:100532591
|
G | C | 1 | a0004 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.579G>C | p.Leu193Phe | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/11 | 962/2739 | 579/1431 | 193/476 | chr12 | 100532591 | ||
chr12:100561906
|
C | T | 1 | a0005 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.1100C>T | p.Thr367Ile | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 10/11 | 1483/2739 | 1100/1431 | 367/476 | chr12 | 100561906 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:100536574
|
C | T | 1 | a0001c0010 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.795C>T | p.Asn265Asn | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 7/11 | 1178/2739 | 795/1431 | 265/476 | chr12 | 100536574 | ||
chr12:100540781
|
G | A | 1 | a0001c0008 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.1041G>A | p.Gly347Gly | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/11 | 1424/2739 | 1041/1431 | 347/476 | chr12 | 100540781 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:100473878
|
G | A | 1 | a0001c0001t0004 | 3 | HG02257.hp1 HG02559.hp2 NA20300.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-371G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/11 | chr12 | 100473878 | ||||||
chr12:100473949
|
G | A | 1 | a0001c0008t0005 | 1 | HG00673.hp1 | 5_prime_UTR_variant | MODIFIER | c.-300G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/11 | 19375 | chr12 | 100473949 | |||||
chr12:100473966
|
A | C | 1 | a0001c0001t0006 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-283A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/11 | 19358 | chr12 | 100473966 | |||||
chr12:100493323
|
G | T | 1 | a0001c0001t0002 | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-1G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/11 | 1 | chr12 | 100493323 | |||||
chr12:100563670
|
A | G | 1 | a0001c0001t0003 | 6 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*181A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 11/11 | 181 | chr12 | 100563670 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:100474117
|
T | C | 2 | a0002c0002t0001g0006a0002c0002t0001g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-190+58T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474117 | ||||||
chr12:100474151
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | HG00621.hp2 NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-190+92T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474151 | ||||||
chr12:100474404
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-190+345T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474404 | ||||||
chr12:100474431
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-190+372G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474431 | ||||||
chr12:100474657
|
G | A | 2 | a0002c0002t0001g0006a0002c0002t0001g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-190+598G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474657 | ||||||
chr12:100474730
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(84): Show | 91 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-190+671G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474730 | ||||||
chr12:100474905
|
T | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(84): Show | 91 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-190+846T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474905 | ||||||
chr12:100474906
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-190+847C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474906 | ||||||
chr12:100474918
|
AT | A | 16 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(13): Show | 17 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-190+861delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100474918 | |||||
chr12:100474954
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-190+895T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474954 | ||||||
chr12:100474986
|
T | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG01261.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-190+927T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474986 | ||||||
chr12:100475121
|
T | TTACCTAT others(9): Show |
2 | a0001c0001t0001g0075a0001c0001t0002g0074 | 2 | HG02559.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-190+1065_-190+108 others(20): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475121 | |||||
chr12:100475124
|
C | CCTAT | 21 | a0001c0001t0001g0094a0001c0001t0001g0228a0001c0001t0001g0229others(18): Show | 21 | HG00597.hp1 HG00609.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.-190+1097_-190+110 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | |||||
chr12:100475124
|
C | CCTATCTA others(1): Show |
33 | a0001c0001t0001g0005a0001c0001t0001g0083a0001c0001t0001g0084others(30): Show | 34 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.-190+1093_-190+110 others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | |||||
chr12:100475124
|
C | CCTATCTA others(5): Show |
26 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0001g0092others(23): Show | 26 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-190+1089_-190+110 others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | |||||
chr12:100475124
|
C | CCTATCTA others(13): Show |
4 | a0001c0001t0001g0027a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02622.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190+1080_-190+108 others(24): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | |||||
chr12:100475124
|
C | CCTATCTA others(17): Show |
3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0079 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-190+1080_-190+108 others(28): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | |||||
chr12:100475124
|
C | CCTATCTA others(9): Show |
1 | a0001c0001t0001g0300 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-190+1085_-190+110 others(20): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | |||||
chr12:100475124
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-190+1065C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475124 | ||||||
chr12:100475124
|
CCTAT | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02886.hp1 HG02922.hp1 NA19090.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190+1097_-190+110 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | |||||
chr12:100475128
|
T | TCTATCTA others(5): Show |
43 | a0001c0001t0001g0032a0001c0001t0001g0062a0001c0001t0001g0063others(40): Show | 46 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-190+1080_-190+108 others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475128 | |||||
chr12:100475132
|
T | TCTATCTA others(1): Show |
17 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(14): Show | 18 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-190+1080_-190+108 others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475132 | |||||
chr12:100475140
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-190+1081T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475140 | ||||||
chr12:100475158
|
T | TATCTATC others(6): Show |
4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | HG02145.hp1 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190+1100_-190+110 others(17): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475158 | |||||
chr12:100475158
|
T | TATCTATC others(10): Show |
1 | a0001c0001t0001g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-190+1100_-190+110 others(21): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475158 | |||||
chr12:100475159
|
A | ATCTATCT others(4): Show |
1 | a0001c0001t0001g0299 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-190+1100_-190+110 others(15): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475159 | ||||||
chr12:100475161
|
A | AT | 79 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(76): Show | 83 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-190+1111dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475161 | |||||
chr12:100475161
|
A | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0082a0001c0001t0001g0087others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-190+1102A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475161 | ||||||
chr12:100475328
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-190+1269G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475328 | ||||||
chr12:100475473
|
C | A | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190+1414C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475473 | ||||||
chr12:100475665
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0092 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-190+1606C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475665 | ||||||
chr12:100475712
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-190+1653C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475712 | ||||||
chr12:100475767
|
G | A | 14 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(11): Show | 14 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.-190+1708G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475767 | ||||||
chr12:100475796
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190+1737C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475796 | ||||||
chr12:100475805
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0095others(72): Show | 77 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.-190+1746G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475805 | ||||||
chr12:100476069
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 5 | HG01099.hp1 HG01257.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190+2010A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476069 | ||||||
chr12:100476198
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 5 | HG00140.hp1 HG00280.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190+2139C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476198 | ||||||
chr12:100476498
|
T | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0092 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-190+2439T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476498 | ||||||
chr12:100476532
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-190+2473A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476532 | ||||||
chr12:100476629
|
A | C | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190+2570A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476629 | ||||||
chr12:100476783
|
C | T | 14 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(11): Show | 14 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.-190+2724C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476783 | ||||||
chr12:100476841
|
A | G | 13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(10): Show | 13 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.-190+2782A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476841 | ||||||
chr12:100476898
|
T | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0249 | 2 | HG03139.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-190+2839T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476898 | ||||||
chr12:100476961
|
A | C | 1 | a0001c0001t0001g0272 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-190+2902A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476961 | ||||||
chr12:100476964
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-190+2905A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476964 | ||||||
chr12:100477115
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-190+3056G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100477115 | ||||||
chr12:100477496
|
T | A | 13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(10): Show | 13 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.-190+3437T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100477496 | ||||||
chr12:100478224
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190+4165A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100478224 | ||||||
chr12:100478448
|
G | T | 4 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(1): Show | 4 | NA18961.hp2 NA18979.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190+4389G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100478448 | ||||||
chr12:100478689
|
T | C | 14 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(11): Show | 14 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.-190+4630T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100478689 | ||||||
chr12:100478825
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-190+4766G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100478825 | ||||||
chr12:100479192
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-190+5133G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479192 | ||||||
chr12:100479198
|
C | A | 16 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(13): Show | 17 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-190+5139C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479198 | ||||||
chr12:100479222
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-190+5163A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479222 | ||||||
chr12:100479223
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-190+5164C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479223 | ||||||
chr12:100479273
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-190+5214T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479273 | ||||||
chr12:100479345
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-190+5286C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479345 | ||||||
chr12:100479596
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-190+5537G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479596 | ||||||
chr12:100479719
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-190+5660G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479719 | ||||||
chr12:100479746
|
C | T | 2 | a0002c0002t0001g0006a0002c0002t0001g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-190+5687C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479746 | ||||||
chr12:100479751
|
T | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(13): Show | 17 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-190+5692T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479751 | ||||||
chr12:100479791
|
A | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(84): Show | 91 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-190+5732A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479791 | ||||||
chr12:100479912
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-190+5853C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479912 | ||||||
chr12:100480214
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190+6155C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100480214 | ||||||
chr12:100480286
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-190+6227C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100480286 | ||||||
chr12:100480292
|
T | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(81): Show | 88 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-190+6233T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100480292 | ||||||
chr12:100480520
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-190+6461C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100480520 | ||||||
chr12:100480943
|
G | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-190+6884G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100480943 | ||||||
chr12:100481015
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-190+6956C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481015 | ||||||
chr12:100481079
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-190+7020G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481079 | ||||||
chr12:100481123
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0161others(29): Show | 33 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(30): Show |
intron_variant | MODIFIER | c.-190+7064C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481123 | ||||||
chr12:100481292
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190+7233C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481292 | ||||||
chr12:100481491
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-190+7432C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481491 | ||||||
chr12:100481596
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-190+7537A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481596 | ||||||
chr12:100481711
|
G | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0228 | 2 | HG01074.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-190+7652G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481711 | ||||||
chr12:100482045
|
C | T | 2 | a0001c0001t0001g0297a0003c0005t0001g0260 | 2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-190+7986C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482045 | ||||||
chr12:100482285
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(85): Show | 92 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-190+8226A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482285 | ||||||
chr12:100482299
|
CA | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(2): Show | 5 | HG02109.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190+8250delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100482299 | |||||
chr12:100482448
|
T | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-190+8389T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482448 | ||||||
chr12:100482670
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-190+8611C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482670 | ||||||
chr12:100482733
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0092 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-190+8674G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482733 | ||||||
chr12:100482845
|
G | T | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG01346.hp1 HG01358.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.-190+8786G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482845 | ||||||
chr12:100482854
|
G | A | 52 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(49): Show | 55 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-190+8795G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482854 | ||||||
chr12:100482934
|
T | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0287a0001c0001t0001g0300 | 3 | HG02602.hp2 HG03017.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-190+8875T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482934 | ||||||
chr12:100483091
|
A | G | 2 | a0001c0001t0001g0287a0001c0001t0001g0300 | 2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-190+9032A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483091 | ||||||
chr12:100483204
|
G | T | 1 | a0001c0001t0001g0143 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-190+9145G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483204 | ||||||
chr12:100483289
|
T | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(85): Show | 92 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-189-9214T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483289 | ||||||
chr12:100483523
|
A | G | 1 | a0001c0001t0002g0069 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-189-8980A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483523 | ||||||
chr12:100483572
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-189-8931C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483572 | ||||||
chr12:100483684
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | HG02055.hp2 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-189-8819C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483684 | ||||||
chr12:100483721
|
C | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG02647.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189-8782C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483721 | ||||||
chr12:100483724
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0006g0271 | 2 | HG00099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.-189-8779C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483724 | ||||||
chr12:100483963
|
A | G | 2 | a0002c0002t0001g0006a0002c0002t0001g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-189-8540A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483963 | ||||||
chr12:100483976
|
T | C | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 3 | HG02698.hp1 HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-189-8527T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483976 | ||||||
chr12:100483985
|
G | GA | 73 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(70): Show | 77 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.-189-8498dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100483985 | |||||
chr12:100483985
|
GAA | G | 8 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0087others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-189-8499_-189-849 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100483985 | |||||
chr12:100484009
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-189-8494T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484009 | ||||||
chr12:100484091
|
T | C | 5 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02559.hp1 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189-8412T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484091 | ||||||
chr12:100484112
|
A | G | 8 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-189-8391A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484112 | ||||||
chr12:100484354
|
G | A | 2 | a0002c0002t0001g0006a0002c0002t0001g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-189-8149G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484354 | ||||||
chr12:100484389
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-189-8114A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484389 | ||||||
chr12:100484609
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-189-7894G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484609 | ||||||
chr12:100484827
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-189-7676C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484827 | ||||||
chr12:100484832
|
G | A | 2 | a0001c0001t0001g0297a0003c0005t0001g0260 | 2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-189-7671G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484832 | ||||||
chr12:100484836
|
G | T | 1 | a0001c0001t0001g0286 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-189-7667G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484836 | ||||||
chr12:100484842
|
C | T | 3 | a0001c0001t0001g0086a0002c0002t0001g0006a0002c0002t0001g0007 | 3 | HG02257.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-189-7661C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484842 | ||||||
chr12:100484893
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-189-7610T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484893 | ||||||
chr12:100485184
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-189-7319G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485184 | ||||||
chr12:100485335
|
C | A | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG00323.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-189-7168C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485335 | ||||||
chr12:100485595
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-189-6908C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485595 | ||||||
chr12:100485727
|
T | G | 1 | a0001c0001t0001g0274 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-189-6776T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485727 | ||||||
chr12:100485753
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-189-6750C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485753 | ||||||
chr12:100485782
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-189-6721C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485782 | ||||||
chr12:100485824
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-189-6679A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485824 | ||||||
chr12:100485835
|
CTAGTTCA others(18): Show |
C | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-189-6660_-189-663 others(29): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100485835 | |||||
chr12:100486081
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-189-6422C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100486081 | ||||||
chr12:100486113
|
G | A | 9 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0087others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-189-6390G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100486113 | ||||||
chr12:100486169
|
C | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG02647.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189-6334C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100486169 | ||||||
chr12:100486313
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0300 | 2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-189-6190T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100486313 | ||||||
chr12:100486326
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-189-6177G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100486326 | ||||||
chr12:100486578
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-189-5925C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100486578 | ||||||
chr12:100487068
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-189-5435T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487068 | ||||||
chr12:100487070
|
T | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(73): Show | 80 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-189-5433T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487070 | ||||||
chr12:100487230
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(73): Show | 80 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-189-5273T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487230 | ||||||
chr12:100487326
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-189-5177C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487326 | ||||||
chr12:100487395
|
G | A | 14 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 14 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189-5108G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487395 | ||||||
chr12:100487451
|
G | C | 1 | a0001c0001t0001g0290 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-189-5052G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487451 | ||||||
chr12:100487595
|
C | CT | 80 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.-189-4889dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100487595 | |||||
chr12:100487595
|
CT | C | 21 | a0001c0001t0001g0028a0001c0001t0001g0087a0001c0001t0001g0088others(18): Show | 21 | HG00597.hp2 HG00673.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.-189-4889delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100487595 | |||||
chr12:100487854
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0296 | 2 | HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.-189-4649C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487854 | ||||||
chr12:100487888
|
A | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(73): Show | 80 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-189-4615A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487888 | ||||||
chr12:100487946
|
A | G | 1 | a0001c0001t0002g0064 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-189-4557A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487946 | ||||||
chr12:100488001
|
CCTTT | C | 3 | a0001c0001t0001g0086a0002c0002t0001g0006a0002c0002t0001g0007 | 3 | HG02257.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-189-4493_-189-449 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100488001 | |||||
chr12:100488052
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0092 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-189-4451G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100488052 | ||||||
chr12:100488819
|
A | G | 140 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(137): Show | 143 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.-189-3684A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100488819 | ||||||
chr12:100488834
|
A | T | 10 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-189-3669A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100488834 | ||||||
chr12:100488952
|
G | A | 55 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(52): Show | 58 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-189-3551G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100488952 | ||||||
chr12:100489094
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-189-3409G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489094 | ||||||
chr12:100489157
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-189-3346A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489157 | ||||||
chr12:100489225
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-189-3278C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489225 | ||||||
chr12:100489283
|
A | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0079 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-189-3220A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489283 | ||||||
chr12:100489304
|
C | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(8): Show | 11 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-189-3199C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489304 | ||||||
chr12:100489336
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-189-3167G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489336 | ||||||
chr12:100489461
|
A | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 79 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-189-3042A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489461 | ||||||
chr12:100489565
|
A | C | 1 | a0001c0001t0002g0061 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-189-2938A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489565 | ||||||
chr12:100489607
|
C | T | 1 | a0002c0002t0001g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-189-2896C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489607 | ||||||
chr12:100489720
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-189-2783G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489720 | ||||||
chr12:100489858
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0079 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-189-2645C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489858 | ||||||
chr12:100490337
|
T | A | 44 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(41): Show | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-189-2166T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100490337 | ||||||
chr12:100490338
|
C | T | 44 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(41): Show | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-189-2165C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100490338 | ||||||
chr12:100490611
|
A | G | 66 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(63): Show | 69 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.-189-1892A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100490611 | ||||||
chr12:100490620
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-189-1883C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100490620 | ||||||
chr12:100490667
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-189-1836T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100490667 | ||||||
chr12:100491074
|
C | A | 2 | a0002c0002t0001g0006a0002c0002t0001g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-189-1429C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491074 | ||||||
chr12:100491084
|
T | C | 14 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 14 | HG02109.hp1 HG02451.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.-189-1419T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491084 | ||||||
chr12:100491329
|
G | A | 231 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(228): Show | 236 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.-189-1174G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491329 | ||||||
chr12:100491371
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG02451.hp2 HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-189-1132G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491371 | ||||||
chr12:100491487
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-189-1016G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491487 | ||||||
chr12:100491732
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-189-771C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491732 | ||||||
chr12:100491738
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-189-765A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491738 | ||||||
chr12:100491801
|
G | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-189-702G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491801 | ||||||
chr12:100491841
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG00609.hp1 HG02040.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-189-662C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491841 | ||||||
chr12:100491887
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.-189-616C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491887 | ||||||
chr12:100492062
|
G | A | 57 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(54): Show | 57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.-189-441G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100492062 | ||||||
chr12:100492839
|
T | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02486.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-55+202T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100492839 | ||||||
chr12:100493032
|
T | G | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-54-238T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100493032 | ||||||
chr12:100493065
|
G | A | 67 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(64): Show | 67 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-54-205G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100493065 | ||||||
chr12:100493068
|
C | T | 13 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-54-202C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100493068 | ||||||
chr12:100493069
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(3): Show | 6 | HG02109.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54-201G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100493069 | ||||||
chr12:100493193
|
C | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0082a0001c0001t0001g0094others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-77C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100493193 | ||||||
chr12:100493232
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-54-38G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100493232 | ||||||
chr12:100493518
|
C | G | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79+116C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100493518 | ||||||
chr12:100493523
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.79+121T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100493523 | ||||||
chr12:100493826
|
C | T | 44 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(41): Show | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+424C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100493826 | ||||||
chr12:100493883
|
A | G | 18 | a0001c0001t0001g0214a0001c0001t0001g0237a0001c0001t0001g0250others(15): Show | 18 | HG00597.hp2 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+481A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100493883 | ||||||
chr12:100494037
|
T | C | 3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG02257.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.79+635T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494037 | ||||||
chr12:100494106
|
G | A | 56 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(53): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.79+704G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494106 | ||||||
chr12:100494130
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0139 | 3 | HG01258.hp1 HG01358.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.79+728G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494130 | ||||||
chr12:100494374
|
G | C | 7 | a0001c0001t0001g0110a0001c0001t0001g0144a0001c0001t0001g0249others(4): Show | 7 | NA18948.hp1 NA18977.hp1 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+972G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494374 | ||||||
chr12:100494578
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.79+1176C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494578 | ||||||
chr12:100494638
|
C | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0091 | 3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.79+1236C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494638 | ||||||
chr12:100494680
|
C | A | 44 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(41): Show | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+1278C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494680 | ||||||
chr12:100494886
|
G | T | 1 | a0001c0001t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.79+1484G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494886 | ||||||
chr12:100495126
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.79+1724G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495126 | ||||||
chr12:100495204
|
A | G | 6 | a0001c0001t0001g0175a0001c0001t0001g0257a0001c0001t0003g0174others(3): Show | 6 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1802A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495204 | ||||||
chr12:100495546
|
CATGGTTA | C | 18 | a0001c0001t0001g0214a0001c0001t0001g0237a0001c0001t0001g0250others(15): Show | 18 | HG00597.hp2 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+2146_79+2152del others(7): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100495546 | |||||
chr12:100495583
|
T | C | 9 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(6): Show | 9 | NA18966.hp2 NA18968.hp2 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+2181T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495583 | ||||||
chr12:100495659
|
G | GAGT | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(282): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.79+2257_79+2258ins others(3): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495659 | ||||||
chr12:100495740
|
C | CA | 13 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+2348dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100495740 | |||||
chr12:100495744
|
A | C | 1 | a0001c0001t0001g0150 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.79+2342A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495744 | ||||||
chr12:100495822
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.79+2420C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495822 | ||||||
chr12:100495956
|
C | T | 2 | a0002c0002t0001g0006a0002c0002t0001g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.79+2554C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495956 | ||||||
chr12:100496051
|
G | C | 3 | a0001c0001t0001g0082a0002c0002t0001g0006a0002c0002t0001g0007 | 3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.79+2649G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496051 | ||||||
chr12:100496138
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79+2736C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496138 | ||||||
chr12:100496221
|
AAT | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.79+2821_79+2822del others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100496221 | |||||
chr12:100496449
|
C | T | 56 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(53): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.79+3047C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496449 | ||||||
chr12:100496483
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+3081T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496483 | ||||||
chr12:100496540
|
G | A | 54 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(51): Show | 54 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.79+3138G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496540 | ||||||
chr12:100496677
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.79+3275T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496677 | ||||||
chr12:100496689
|
G | T | 1 | a0001c0001t0001g0282 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.79+3287G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496689 | ||||||
chr12:100496967
|
A | G | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.79+3565A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496967 | ||||||
chr12:100497021
|
T | G | 5 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(2): Show | 5 | NA18951.hp2 NA18962.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+3619T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497021 | ||||||
chr12:100497073
|
C | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 146 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.79+3671C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497073 | ||||||
chr12:100497202
|
C | T | 2 | a0002c0002t0001g0006a0002c0002t0001g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.79+3800C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497202 | ||||||
chr12:100497318
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.79+3916G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497318 | ||||||
chr12:100497729
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.79+4327G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497729 | ||||||
chr12:100497758
|
A | T | 44 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(41): Show | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+4356A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497758 | ||||||
chr12:100497804
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.79+4402T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497804 | ||||||
chr12:100498349
|
G | A | 18 | a0001c0001t0001g0214a0001c0001t0001g0237a0001c0001t0001g0250others(15): Show | 18 | HG00597.hp2 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+4947G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498349 | ||||||
chr12:100498365
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.79+4963G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498365 | ||||||
chr12:100498454
|
C | T | 44 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(41): Show | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+5052C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498454 | ||||||
chr12:100498467
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.79+5065C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498467 | ||||||
chr12:100498498
|
C | T | 44 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(41): Show | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+5096C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498498 | ||||||
chr12:100498752
|
T | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 146 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.79+5350T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498752 | ||||||
chr12:100498780
|
G | A | 44 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(41): Show | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+5378G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498780 | ||||||
chr12:100498798
|
A | C | 17 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 17 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.79+5396A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498798 | ||||||
chr12:100498800
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.79+5398G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498800 | ||||||
chr12:100499303
|
C | T | 67 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(64): Show | 67 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.79+5901C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499303 | ||||||
chr12:100499565
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0091 | 3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.79+6163T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499565 | ||||||
chr12:100499570
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+6168C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499570 | ||||||
chr12:100499625
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+6223G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499625 | ||||||
chr12:100499631
|
C | T | 16 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(13): Show | 16 | HG02109.hp1 HG02257.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.79+6229C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499631 | ||||||
chr12:100499792
|
G | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+6390G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499792 | ||||||
chr12:100499858
|
C | T | 67 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(64): Show | 67 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.79+6456C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499858 | ||||||
chr12:100500058
|
G | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+6656G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500058 | ||||||
chr12:100500059
|
A | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+6657A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500059 | ||||||
chr12:100500188
|
A | G | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220 | 3 | HG03831.hp2 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.79+6786A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500188 | ||||||
chr12:100500250
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+6848A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500250 | ||||||
chr12:100500313
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.79+6911C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500313 | ||||||
chr12:100500353
|
A | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.79+6951A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500353 | ||||||
chr12:100500422
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.79+7020C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500422 | ||||||
chr12:100500858
|
C | T | 44 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(41): Show | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+7456C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500858 | ||||||
chr12:100500864
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.79+7462T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500864 | ||||||
chr12:100500878
|
C | T | 1 | a0007c0004t0001g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.79+7476C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500878 | ||||||
chr12:100501035
|
T | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.79+7633T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501035 | ||||||
chr12:100501121
|
C | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0221 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.79+7719C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501121 | ||||||
chr12:100501142
|
A | G | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220 | 3 | HG03831.hp2 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.79+7740A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501142 | ||||||
chr12:100501236
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.79+7834G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501236 | ||||||
chr12:100501248
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0091 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.79+7846A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501248 | ||||||
chr12:100501368
|
A | AC | 61 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(58): Show | 64 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.79+7970dupC | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100501368 | |||||
chr12:100501372
|
C | CT | 76 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 77 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.79+7970_79+7971ins others(1): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501372 | ||||||
chr12:100501454
|
G | T | 1 | a0001c0001t0002g0058 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.79+8052G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501454 | ||||||
chr12:100501649
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.79+8247C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501649 | ||||||
chr12:100501757
|
A | G | 2 | a0001c0001t0001g0275a0001c0001t0001g0298 | 2 | HG01346.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.79+8355A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501757 | ||||||
chr12:100502220
|
T | C | 5 | a0001c0001t0001g0075a0001c0001t0001g0082a0001c0001t0001g0094others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-8558T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502220 | ||||||
chr12:100502294
|
T | C | 3 | a0001c0001t0001g0082a0002c0002t0001g0006a0002c0002t0001g0007 | 3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.80-8484T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502294 | ||||||
chr12:100502445
|
C | T | 5 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-8333C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502445 | ||||||
chr12:100502446
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.80-8332G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502446 | ||||||
chr12:100502489
|
C | A | 61 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(58): Show | 64 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.80-8289C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502489 | ||||||
chr12:100502540
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.80-8238A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502540 | ||||||
chr12:100502574
|
C | T | 1 | a0001c0001t0002g0058 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.80-8204C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502574 | ||||||
chr12:100502972
|
G | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0221 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.80-7806G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502972 | ||||||
chr12:100503023
|
C | A | 3 | a0001c0001t0001g0082a0002c0002t0001g0006a0002c0002t0001g0007 | 3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.80-7755C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503023 | ||||||
chr12:100503042
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80-7736C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503042 | ||||||
chr12:100503062
|
C | A | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG01346.hp1 HG01358.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-7716C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503062 | ||||||
chr12:100503225
|
A | T | 1 | a0001c0001t0001g0210 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.80-7553A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503225 | ||||||
chr12:100503438
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-7340C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503438 | ||||||
chr12:100503453
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-7325G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503453 | ||||||
chr12:100503473
|
T | G | 2 | a0002c0002t0001g0006a0002c0002t0001g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.80-7305T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503473 | ||||||
chr12:100503631
|
A | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.80-7147A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503631 | ||||||
chr12:100503670
|
A | G | 17 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 17 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.80-7108A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503670 | ||||||
chr12:100503755
|
T | G | 7 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | HG00735.hp1 HG01069.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-7023T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503755 | ||||||
chr12:100503898
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG00735.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.80-6880G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503898 | ||||||
chr12:100503943
|
T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 146 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.80-6835T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503943 | ||||||
chr12:100503980
|
T | C | 61 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(58): Show | 64 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.80-6798T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503980 | ||||||
chr12:100504003
|
T | C | 2 | a0001c0001t0002g0047a0001c0001t0002g0067 | 2 | NA18985.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.80-6775T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504003 | ||||||
chr12:100504302
|
C | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01884.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-6476C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504302 | ||||||
chr12:100504393
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG00140.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.80-6385G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504393 | ||||||
chr12:100504439
|
A | G | 3 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0248 | 3 | HG01069.hp1 HG01255.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.80-6339A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504439 | ||||||
chr12:100504448
|
T | C | 72 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(69): Show | 72 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.80-6330T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504448 | ||||||
chr12:100504557
|
G | A | 2 | a0001c0001t0001g0264a0006c0006t0001g0292 | 2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.80-6221G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504557 | ||||||
chr12:100504635
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-6143T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504635 | ||||||
chr12:100504675
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.80-6103C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504675 | ||||||
chr12:100504783
|
G | A | 3 | a0001c0001t0001g0082a0002c0002t0001g0006a0002c0002t0001g0007 | 3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.80-5995G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504783 | ||||||
chr12:100504869
|
G | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 82 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.80-5909G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504869 | ||||||
chr12:100504918
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.80-5860T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504918 | ||||||
chr12:100505029
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80-5749G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505029 | ||||||
chr12:100505101
|
CA | C | 59 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(56): Show | 62 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.80-5666delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100505101 | |||||
chr12:100505112
|
A | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-5666A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505112 | ||||||
chr12:100505156
|
A | G | 3 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0248 | 3 | HG01069.hp1 HG01255.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.80-5622A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505156 | ||||||
chr12:100505290
|
G | C | 1 | a0001c0001t0002g0103 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.80-5488G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505290 | ||||||
chr12:100505649
|
C | T | 57 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(54): Show | 60 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.80-5129C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505649 | ||||||
chr12:100505712
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.80-5066A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505712 | ||||||
chr12:100505812
|
C | T | 59 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(56): Show | 59 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.80-4966C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505812 | ||||||
chr12:100505882
|
C | G | 56 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(53): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.80-4896C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505882 | ||||||
chr12:100506002
|
A | AAC | 80 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022others(77): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.80-4736_80-4735dup others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506002 | |||||
chr12:100506002
|
A | AACAC | 13 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 13 | HG00621.hp2 HG02071.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-4738_80-4735dup others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506002 | |||||
chr12:100506002
|
A | AACACAC | 7 | a0001c0001t0001g0086a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG00408.hp1 HG02129.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-4740_80-4735dup others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506002 | |||||
chr12:100506002
|
A | AACACACA others(3): Show |
1 | a0002c0002t0001g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.80-4744_80-4735dup others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506002 | |||||
chr12:100506002
|
AAC | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0133others(15): Show | 19 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.80-4736_80-4735del others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506002 | |||||
chr12:100506002
|
AACAC | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 5 | HG03139.hp2 NA18944.hp2 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-4738_80-4735del others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506002 | |||||
chr12:100506030
|
CACACACA others(9): Show |
C | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-4746_80-4731del others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506030 | |||||
chr12:100506032
|
CACACACA others(7): Show |
C | 3 | a0001c0001t0001g0078a0001c0001t0001g0092a0001c0001t0002g0068 | 3 | HG02109.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.80-4744_80-4731del others(14): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506032 | |||||
chr12:100506034
|
CACACACA others(5): Show |
C | 41 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(38): Show | 44 | HG00408.hp2 HG00558.hp1 HG02083.hp2 others(41): Show |
intron_variant | MODIFIER | c.80-4742_80-4731del others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506034 | |||||
chr12:100506036
|
CACACACA others(3): Show |
C | 2 | a0001c0001t0002g0048a0001c0001t0002g0058 | 2 | HG00423.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.80-4740_80-4731del others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506036 | |||||
chr12:100506040
|
C | G | 2 | a0001c0001t0001g0098a0008c0003t0001g0215 | 2 | HG02886.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.80-4738C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506040 | ||||||
chr12:100506042
|
C | CACACACA others(5): Show |
1 | a0001c0001t0001g0016 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.80-4735_80-4734ins others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506042 | |||||
chr12:100506042
|
C | CACACACA others(3): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.80-4735_80-4734ins others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506042 | |||||
chr12:100506042
|
C | CACACACA others(1): Show |
7 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 8 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-4735_80-4734ins others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506042 | |||||
chr12:100506042
|
C | CACACAG | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02647.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-4735_80-4734ins others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506042 | |||||
chr12:100506042
|
C | G | 8 | a0001c0001t0001g0098a0001c0001t0001g0110a0001c0001t0001g0144others(5): Show | 8 | HG02886.hp1 NA18948.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-4736C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506042 | ||||||
chr12:100506044
|
G | C | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0276 | 3 | HG02622.hp2 HG03516.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.80-4734G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506044 | ||||||
chr12:100506232
|
G | A | 13 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-4546G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506232 | ||||||
chr12:100506252
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.80-4526G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506252 | ||||||
chr12:100506517
|
G | T | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.80-4261G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506517 | ||||||
chr12:100506518
|
T | G | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.80-4260T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506518 | ||||||
chr12:100506665
|
G | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(55): Show | 58 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.80-4113G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506665 | ||||||
chr12:100506671
|
C | A | 2 | a0001c0001t0001g0152a0001c0001t0006g0271 | 2 | HG00099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.80-4107C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506671 | ||||||
chr12:100506729
|
AACTCCTT others(3): Show |
A | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG02132.hp2 NA18968.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-4048_80-4039del others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506729 | ||||||
chr12:100506740
|
T | C | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG02132.hp2 NA18968.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-4038T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506740 | ||||||
chr12:100506902
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.80-3876A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506902 | ||||||
chr12:100507118
|
G | T | 1 | a0001c0001t0001g0186 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.80-3660G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507118 | ||||||
chr12:100507456
|
GTTTTGT | G | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(55): Show | 58 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.80-3305_80-3300del others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100507456 | |||||
chr12:100507473
|
G | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA19055.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.80-3305G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507473 | ||||||
chr12:100507475
|
T | G | 61 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(58): Show | 64 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.80-3303T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507475 | ||||||
chr12:100507616
|
C | A | 1 | a0001c0001t0001g0210 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.80-3162C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507616 | ||||||
chr12:100507618
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.80-3160A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507618 | ||||||
chr12:100507698
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.80-3080T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507698 | ||||||
chr12:100507699
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.80-3079G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507699 | ||||||
chr12:100507743
|
G | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(8): Show | 11 | HG02109.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-3035G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507743 | ||||||
chr12:100507993
|
T | C | 4 | a0001c0001t0001g0237a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | HG02055.hp1 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-2785T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507993 | ||||||
chr12:100508040
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.80-2738G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508040 | ||||||
chr12:100508079
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0275a0001c0001t0001g0298 | 4 | HG00140.hp1 HG01346.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-2699G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508079 | ||||||
chr12:100508103
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-2675G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508103 | ||||||
chr12:100508263
|
C | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.80-2515C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508263 | ||||||
chr12:100508506
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.80-2272C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508506 | ||||||
chr12:100508512
|
C | CTTTGAGA others(10): Show |
1 | a0001c0001t0001g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.80-2265_80-2249dup others(17): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100508512 | |||||
chr12:100508566
|
A | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 82 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.80-2212A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508566 | ||||||
chr12:100508642
|
T | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(55): Show | 58 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.80-2136T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508642 | ||||||
chr12:100508747
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.80-2031C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508747 | ||||||
chr12:100508910
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.80-1868C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508910 | ||||||
chr12:100508913
|
T | C | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.80-1865T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508913 | ||||||
chr12:100508925
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.80-1853C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508925 | ||||||
chr12:100508999
|
T | G | 1 | a0001c0001t0001g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.80-1779T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508999 | ||||||
chr12:100509204
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80-1574G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509204 | ||||||
chr12:100509264
|
C | G | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.80-1514C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509264 | ||||||
chr12:100509554
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-1224A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509554 | ||||||
chr12:100509574
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0263 | 2 | HG00597.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.80-1204A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509574 | ||||||
chr12:100509596
|
C | G | 2 | a0002c0002t0001g0006a0002c0002t0001g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.80-1182C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509596 | ||||||
chr12:100509616
|
T | A | 2 | a0001c0001t0001g0165a0007c0004t0001g0166 | 2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.80-1162T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509616 | ||||||
chr12:100509908
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.80-870C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509908 | ||||||
chr12:100509910
|
TGC | T | 10 | a0001c0001t0001g0076a0001c0001t0001g0085a0001c0001t0001g0087others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-863_80-862delGC | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100509910 | |||||
chr12:100509913
|
GCGCA | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(61): Show | 64 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-863_80-860delGC others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100509913 | |||||
chr12:100509913
|
GCGCACA | G | 3 | a0001c0001t0001g0075a0002c0002t0001g0006a0002c0002t0001g0007 | 3 | HG02257.hp2 HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.80-863_80-858delGC others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100509913 | |||||
chr12:100509915
|
G | A | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0071others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-863G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509915 | ||||||
chr12:100509915
|
G | GCA | 42 | a0001c0001t0001g0111a0001c0001t0002g0001a0001c0001t0002g0033others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.80-838_80-837dupCA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100509915 | |||||
chr12:100509915
|
GCACA | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(7): Show | 11 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-840_80-837delCA others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100509915 | |||||
chr12:100509917
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0277 | 2 | HG02071.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.80-861A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509917 | ||||||
chr12:100509921
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-857A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509921 | ||||||
chr12:100509960
|
G | A | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.80-818G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509960 | ||||||
chr12:100510203
|
A | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-575A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510203 | ||||||
chr12:100510354
|
C | T | 1 | a0001c0001t0002g0103 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.80-424C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510354 | ||||||
chr12:100510399
|
A | T | 1 | a0001c0001t0001g0082 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.80-379A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510399 | ||||||
chr12:100510445
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.80-333C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510445 | ||||||
chr12:100510573
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80-205A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510573 | ||||||
chr12:100510607
|
T | A | 1 | a0001c0010t0001g0191 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.80-171T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510607 | ||||||
chr12:100510607
|
T | TA | 3 | a0001c0001t0001g0112a0001c0001t0001g0228a0001c0001t0001g0234 | 3 | HG00323.hp1 HG01169.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.80-171_80-170insA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510607 | ||||||
chr12:100510607
|
T | TATATATA others(8): Show |
1 | a0001c0001t0001g0246 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.80-171_80-170insAT others(13): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510607 | ||||||
chr12:100510607
|
T | TTA | 22 | a0001c0001t0001g0062a0001c0001t0001g0096a0001c0001t0001g0098others(19): Show | 22 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.80-144_80-143dupTA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
T | TTATA | 7 | a0001c0001t0001g0153a0001c0001t0001g0167a0001c0001t0001g0169others(4): Show | 7 | HG00621.hp1 HG01516.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-146_80-143dupTA others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
T | TTATATA | 3 | a0001c0001t0001g0087a0001c0001t0001g0093a0001c0001t0001g0216 | 3 | HG02922.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.80-148_80-143dupTA others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0089a0001c0001t0001g0090others(1): Show | 4 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-150_80-143dupTA others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
T | TTATATAT others(3): Show |
19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(16): Show | 19 | HG00609.hp2 HG00673.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.80-152_80-143dupTA others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
T | TTATATAT others(5): Show |
18 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(15): Show | 18 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-154_80-143dupTA others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
T | TTATATAT others(7): Show |
14 | a0001c0001t0001g0011a0001c0001t0001g0163a0001c0001t0001g0182others(11): Show | 14 | HG00735.hp1 HG01069.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-156_80-143dupTA others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
T | TTATATAT others(9): Show |
7 | a0001c0001t0001g0081a0001c0001t0001g0100a0001c0001t0001g0202others(4): Show | 7 | HG02132.hp2 HG02922.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-158_80-143dupTA others(14): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
T | TTATATAT others(11): Show |
5 | a0001c0001t0001g0002a0001c0001t0001g0203a0001c0001t0001g0204others(2): Show | 6 | HG01257.hp2 HG01258.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-160_80-143dupTA others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
T | TTATATAT others(15): Show |
2 | a0001c0001t0001g0020a0001c0001t0001g0082 | 2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.80-164_80-143dupTA others(20): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
T | TTATATAT others(17): Show |
1 | a0001c0001t0001g0210 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.80-166_80-143dupTA others(22): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
TTA | T | 14 | a0001c0001t0001g0118a0001c0001t0001g0237a0001c0001t0001g0239others(11): Show | 14 | HG00673.hp1 HG02055.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.80-144_80-143delTA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
TTATA | T | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(48): Show | 54 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.80-146_80-143delTA others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510607
|
TTATATA | T | 11 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(8): Show | 11 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-148_80-143delTA others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | |||||
chr12:100510647
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-131T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510647 | ||||||
chr12:100510669
|
AT | A | 59 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(56): Show | 59 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.80-108delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510669 | ||||||
chr12:100510711
|
G | A | 13 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-67G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510711 | ||||||
chr12:100511365
|
T | G | 56 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(53): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.445+222T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511365 | ||||||
chr12:100511438
|
T | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(83): Show | 90 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.445+295T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511438 | ||||||
chr12:100511519
|
C | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 82 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.445+376C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511519 | ||||||
chr12:100511633
|
AT | A | 12 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(9): Show | 12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.445+491delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511633 | ||||||
chr12:100511637
|
T | A | 1 | a0008c0003t0001g0215 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.445+494T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511637 | ||||||
chr12:100511750
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.445+607C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511750 | ||||||
chr12:100511751
|
G | A | 72 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(69): Show | 72 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.445+608G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511751 | ||||||
chr12:100511778
|
T | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(158): Show | 165 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.445+635T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511778 | ||||||
chr12:100511931
|
AT | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 13 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.445+802delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100511931 | |||||
chr12:100512012
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.445+869C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512012 | ||||||
chr12:100512013
|
G | A | 12 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(9): Show | 12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.445+870G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512013 | ||||||
chr12:100512030
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.445+887C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512030 | ||||||
chr12:100512158
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.445+1015G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512158 | ||||||
chr12:100512199
|
C | T | 13 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.445+1056C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512199 | ||||||
chr12:100512364
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG03704.hp2 HG04115.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.445+1221G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512364 | ||||||
chr12:100512489
|
A | C | 9 | a0001c0001t0001g0214a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 9 | HG00597.hp2 HG02015.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+1346A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512489 | ||||||
chr12:100512558
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.445+1415G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512558 | ||||||
chr12:100512606
|
A | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0299 | 2 | HG02083.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.445+1463A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512606 | ||||||
chr12:100512641
|
C | CA | 79 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 83 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.445+1511dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100512641 | |||||
chr12:100512666
|
A | G | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.445+1523A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512666 | ||||||
chr12:100512716
|
T | C | 1 | a0001c0001t0001g0259 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.445+1573T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512716 | ||||||
chr12:100512821
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445+1678G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512821 | ||||||
chr12:100512898
|
C | T | 14 | a0001c0001t0001g0214a0001c0001t0001g0250a0001c0001t0001g0251others(11): Show | 14 | HG00597.hp2 HG00673.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.445+1755C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512898 | ||||||
chr12:100512987
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.445+1844T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512987 | ||||||
chr12:100513431
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.445+2288G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513431 | ||||||
chr12:100513582
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.445+2439G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513582 | ||||||
chr12:100513589
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.445+2446G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513589 | ||||||
chr12:100513798
|
CAGAAAGG others(9): Show |
C | 1 | a0001c0001t0001g0149 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.445+2658_445+2673d others(18): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513798 | |||||
chr12:100513798
|
CAGAAAGG others(12): Show |
C | 1 | a0001c0001t0001g0115 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.445+2657_445+2675d others(21): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513798 | |||||
chr12:100513801
|
A | AAAGG | 5 | a0001c0001t0001g0078a0001c0001t0001g0088a0001c0001t0001g0226others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+2725_445+2728d others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
A | AAAGGAAG others(1): Show |
3 | a0001c0001t0001g0018a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG02486.hp2 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.445+2721_445+2728d others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
A | AAAGGAAG others(5): Show |
1 | a0001c0001t0001g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445+2717_445+2728d others(14): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
A | AAAGGAAG others(9): Show |
2 | a0001c0001t0001g0031a0001c0001t0001g0072 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.445+2713_445+2728d others(18): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
AAAGG | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(20): Show | 25 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(22): Show |
intron_variant | MODIFIER | c.445+2725_445+2728d others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
AAAGGAAG others(1): Show |
A | 33 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0022others(30): Show | 34 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.445+2721_445+2728d others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
AAAGGAAG others(5): Show |
A | 38 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0087others(35): Show | 38 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.445+2717_445+2728d others(14): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
AAAGGAAG others(9): Show |
A | 68 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0029others(65): Show | 69 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.445+2713_445+2728d others(18): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
AAAGGAAG others(13): Show |
A | 55 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(52): Show | 55 | HG00140.hp2 HG00609.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.445+2709_445+2728d others(22): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
AAAGGAAG others(17): Show |
A | 10 | a0001c0001t0001g0011a0001c0001t0001g0083a0001c0001t0001g0092others(7): Show | 10 | HG02451.hp1 HG02647.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.445+2705_445+2728d others(26): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
AAAGGAAG others(21): Show |
A | 3 | a0001c0001t0001g0203a0001c0001t0001g0243a0001c0001t0001g0247 | 3 | NA18944.hp2 NA18946.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.445+2701_445+2728d others(30): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
AAAGGAAG others(25): Show |
A | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.445+2697_445+2728d others(34): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
AAAGGAAG others(29): Show |
A | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.445+2693_445+2728d others(38): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513801
|
AAAGGAAG others(33): Show |
A | 40 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(37): Show | 43 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.445+2689_445+2728d others(42): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | |||||
chr12:100513847
|
A | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0093 | 3 | HG02145.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.445+2704A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513847 | ||||||
chr12:100513852
|
GGAAGGAA others(12): Show |
G | 1 | a0001c0001t0001g0160 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.445+2710_445+2728d others(21): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513852 | ||||||
chr12:100513853
|
GAAGGAAG others(10): Show |
G | 1 | a0001c0001t0001g0139 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.445+2713_445+2729d others(19): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513853 | |||||
chr12:100513882
|
A | G | 59 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(56): Show | 59 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.445+2739A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513882 | ||||||
chr12:100513937
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.445+2794T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513937 | ||||||
chr12:100513995
|
A | G | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220 | 3 | HG03831.hp2 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.445+2852A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513995 | ||||||
chr12:100514001
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445+2858G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100514001 | ||||||
chr12:100514803
|
CTATAT | C | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.445+3670_445+3674d others(7): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100514803 | |||||
chr12:100515021
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.445+3878A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515021 | ||||||
chr12:100515111
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.445+3968C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515111 | ||||||
chr12:100515144
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.445+4001G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515144 | ||||||
chr12:100515165
|
C | CT | 35 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(32): Show | 35 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.445+4045dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100515165 | |||||
chr12:100515165
|
CT | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(60): Show | 67 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.445+4045delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100515165 | |||||
chr12:100515228
|
T | C | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(55): Show | 58 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.445+4085T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515228 | ||||||
chr12:100515699
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.445+4556C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515699 | ||||||
chr12:100515739
|
A | G | 8 | a0001c0001t0001g0106a0001c0001t0001g0113a0001c0001t0001g0117others(5): Show | 8 | HG00558.hp2 HG00621.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.445+4596A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515739 | ||||||
chr12:100515741
|
C | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0091 | 3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.445+4598C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515741 | ||||||
chr12:100516139
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.445+4996T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516139 | ||||||
chr12:100516160
|
T | C | 3 | a0001c0001t0001g0082a0002c0002t0001g0006a0002c0002t0001g0007 | 3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.445+5017T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516160 | ||||||
chr12:100516341
|
C | A | 1 | a0001c0008t0005g0281 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.445+5198C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516341 | ||||||
chr12:100516515
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.445+5372T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516515 | ||||||
chr12:100516527
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0079 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.445+5384C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516527 | ||||||
chr12:100516618
|
G | T | 8 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0087others(5): Show | 8 | HG02145.hp1 HG02647.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.445+5475G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516618 | ||||||
chr12:100516686
|
G | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0193a0001c0001t0001g0199others(4): Show | 7 | HG02074.hp1 NA18961.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.445+5543G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516686 | ||||||
chr12:100517053
|
CTT | C | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.445+5911_445+5912d others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100517053 | ||||||
chr12:100517160
|
G | A | 54 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(51): Show | 57 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.445+6017G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100517160 | ||||||
chr12:100517281
|
T | C | 9 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(6): Show | 9 | NA18966.hp2 NA18968.hp2 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+6138T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100517281 | ||||||
chr12:100517334
|
C | T | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 3 | HG02698.hp1 HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.445+6191C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100517334 | ||||||
chr12:100517426
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.445+6283C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100517426 | ||||||
chr12:100517432
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.445+6289T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100517432 | ||||||
chr12:100518038
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.445+6895G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518038 | ||||||
chr12:100518118
|
G | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0079 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.445+6975G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518118 | ||||||
chr12:100518258
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0079 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.445+7115G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518258 | ||||||
chr12:100518364
|
G | A | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(17): Show | 20 | HG00609.hp2 HG00621.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.445+7221G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518364 | ||||||
chr12:100518451
|
A | C | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.445+7308A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518451 | ||||||
chr12:100518478
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.445+7335C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518478 | ||||||
chr12:100518535
|
A | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 144 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.445+7392A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518535 | ||||||
chr12:100518597
|
A | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0091 | 3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.445+7454A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518597 | ||||||
chr12:100518788
|
C | CT | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(72): Show | 80 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.445+7667dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100518788 | |||||
chr12:100518788
|
CT | C | 12 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00099.hp1 HG02559.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.445+7667delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100518788 | |||||
chr12:100518823
|
C | T | 1 | a0006c0006t0001g0292 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.445+7680C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518823 | ||||||
chr12:100518928
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.445+7785C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518928 | ||||||
chr12:100518953
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.445+7810A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518953 | ||||||
chr12:100519034
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+7891C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100519034 | ||||||
chr12:100519295
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.445+8152T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100519295 | ||||||
chr12:100519684
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.445+8541G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100519684 | ||||||
chr12:100519698
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445+8555C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100519698 | ||||||
chr12:100519965
|
G | T | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.445+8822G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100519965 | ||||||
chr12:100520092
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.445+8949G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520092 | ||||||
chr12:100520109
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.445+8966T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520109 | ||||||
chr12:100520129
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.445+8986G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520129 | ||||||
chr12:100520452
|
G | A | 12 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(9): Show | 12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.445+9309G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520452 | ||||||
chr12:100520708
|
C | T | 4 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0002g0069others(1): Show | 4 | HG00558.hp1 NA18944.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+9565C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520708 | ||||||
chr12:100520722
|
A | C | 6 | a0001c0001t0001g0175a0001c0001t0001g0257a0001c0001t0003g0174others(3): Show | 6 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.445+9579A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520722 | ||||||
chr12:100520747
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445+9604C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520747 | ||||||
chr12:100520803
|
A | G | 3 | a0001c0001t0001g0082a0002c0002t0001g0006a0002c0002t0001g0007 | 3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.445+9660A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520803 | ||||||
chr12:100520934
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.445+9791T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520934 | ||||||
chr12:100520967
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.445+9824G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520967 | ||||||
chr12:100521091
|
A | T | 2 | a0002c0002t0001g0006a0002c0002t0001g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.445+9948A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521091 | ||||||
chr12:100521105
|
C | G | 4 | a0001c0001t0001g0082a0001c0001t0001g0094a0002c0002t0001g0006others(1): Show | 4 | HG02257.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.445+9962C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521105 | ||||||
chr12:100521127
|
A | T | 2 | a0001c0001t0001g0297a0003c0005t0001g0260 | 2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.445+9984A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521127 | ||||||
chr12:100521183
|
A | T | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.445+10040A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521183 | ||||||
chr12:100521217
|
T | G | 3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG02257.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.445+10074T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521217 | ||||||
chr12:100521278
|
T | A | 1 | a0001c0001t0001g0296 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.445+10135T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521278 | ||||||
chr12:100521329
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.445+10186A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521329 | ||||||
chr12:100521548
|
G | T | 1 | a0001c0001t0001g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.445+10405G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521548 | ||||||
chr12:100521631
|
A | AT | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.445+10493dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100521631 | |||||
chr12:100521734
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.445+10591T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521734 | ||||||
chr12:100521808
|
C | G | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-10650C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521808 | ||||||
chr12:100521891
|
T | A | 14 | a0001c0001t0001g0214a0001c0001t0001g0250a0001c0001t0001g0251others(11): Show | 14 | HG00597.hp2 HG00673.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.446-10567T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521891 | ||||||
chr12:100521904
|
G | C | 5 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-10554G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521904 | ||||||
chr12:100522096
|
A | AT | 81 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 82 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.446-10362_446-1036 others(5): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522096 | ||||||
chr12:100522138
|
AATGGTG | A | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG01346.hp1 HG01358.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.446-10301_446-1029 others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100522138 | |||||
chr12:100522281
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.446-10177T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522281 | ||||||
chr12:100522484
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.446-9974A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522484 | ||||||
chr12:100522496
|
T | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.446-9962T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522496 | ||||||
chr12:100522544
|
GT | G | 8 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 8 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-9901delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100522544 | |||||
chr12:100522553
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.446-9905T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522553 | ||||||
chr12:100522871
|
G | A | 13 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.446-9587G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522871 | ||||||
chr12:100522948
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.446-9510C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522948 | ||||||
chr12:100522989
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.446-9469C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522989 | ||||||
chr12:100523142
|
T | C | 1 | a0001c0001t0002g0080 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.446-9316T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523142 | ||||||
chr12:100523194
|
C | G | 1 | a0001c0001t0001g0277 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.446-9264C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523194 | ||||||
chr12:100523277
|
A | C | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(55): Show | 58 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.446-9181A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523277 | ||||||
chr12:100523346
|
A | G | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(55): Show | 58 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.446-9112A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523346 | ||||||
chr12:100523365
|
G | A | 13 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.446-9093G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523365 | ||||||
chr12:100523499
|
G | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.446-8959G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523499 | ||||||
chr12:100523547
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.446-8911C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523547 | ||||||
chr12:100523811
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0223 | 2 | NA19043.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.446-8647G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523811 | ||||||
chr12:100523883
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0160 | 3 | HG01258.hp1 HG01358.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.446-8575T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523883 | ||||||
chr12:100523944
|
C | G | 1 | a0001c0001t0001g0220 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.446-8514C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523944 | ||||||
chr12:100524077
|
G | C | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-8381G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524077 | ||||||
chr12:100524169
|
T | C | 2 | a0002c0002t0001g0006a0002c0002t0001g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.446-8289T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524169 | ||||||
chr12:100524179
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0296 | 2 | HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.446-8279C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524179 | ||||||
chr12:100524221
|
T | A | 1 | a0001c0001t0001g0287 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.446-8237T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524221 | ||||||
chr12:100524240
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.446-8218G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524240 | ||||||
chr12:100524288
|
A | C | 1 | a0001c0001t0001g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.446-8170A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524288 | ||||||
chr12:100524474
|
A | G | 59 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(56): Show | 59 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.446-7984A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524474 | ||||||
chr12:100524702
|
T | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 144 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.446-7756T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524702 | ||||||
chr12:100524826
|
T | C | 12 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(9): Show | 12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.446-7632T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524826 | ||||||
chr12:100524836
|
C | T | 3 | a0001c0001t0001g0082a0002c0002t0001g0006a0002c0002t0001g0007 | 3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.446-7622C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524836 | ||||||
chr12:100524868
|
G | T | 54 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(51): Show | 57 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.446-7590G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524868 | ||||||
chr12:100524917
|
G | A | 2 | a0001c0001t0001g0256a0001c0001t0002g0033 | 2 | HG02698.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.446-7541G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524917 | ||||||
chr12:100524971
|
C | A | 12 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(9): Show | 12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.446-7487C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524971 | ||||||
chr12:100525073
|
T | G | 13 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.446-7385T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100525073 | ||||||
chr12:100525222
|
T | G | 14 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 14 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.446-7236T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100525222 | ||||||
chr12:100525484
|
A | G | 80 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 84 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.446-6974A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100525484 | ||||||
chr12:100525588
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.446-6870A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100525588 | ||||||
chr12:100525827
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.446-6631T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100525827 | ||||||
chr12:100525894
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 9 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.446-6564G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100525894 | ||||||
chr12:100526028
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.446-6430G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526028 | ||||||
chr12:100526162
|
A | G | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG02132.hp2 NA18968.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.446-6296A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526162 | ||||||
chr12:100526193
|
A | AT | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.446-6253dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100526193 | |||||
chr12:100526193
|
A | ATT | 64 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0028others(61): Show | 67 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.446-6254_446-6253d others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100526193 | |||||
chr12:100526193
|
A | ATTT | 15 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(12): Show | 16 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.446-6255_446-6253d others(5): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100526193 | |||||
chr12:100526329
|
G | T | 1 | a0001c0001t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.446-6129G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526329 | ||||||
chr12:100526448
|
C | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0086 | 2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.446-6010C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526448 | ||||||
chr12:100526456
|
A | G | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-6002A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526456 | ||||||
chr12:100526526
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0086 | 2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.446-5932G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526526 | ||||||
chr12:100526552
|
T | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(19): Show | 23 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.446-5906T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526552 | ||||||
chr12:100526555
|
T | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(19): Show | 23 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.446-5903T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526555 | ||||||
chr12:100526566
|
C | T | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-5892C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526566 | ||||||
chr12:100526657
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.446-5801G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526657 | ||||||
chr12:100526703
|
C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | NA18959.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.446-5755C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526703 | ||||||
chr12:100526743
|
T | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0230a0001c0001t0001g0231others(1): Show | 4 | HG00735.hp2 HG01169.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-5715T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526743 | ||||||
chr12:100526788
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.446-5670C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526788 | ||||||
chr12:100526905
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0026 | 3 | HG02055.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.446-5553G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526905 | ||||||
chr12:100527109
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | HG00621.hp2 NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.446-5349G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527109 | ||||||
chr12:100527136
|
C | T | 4 | a0001c0001t0001g0076a0001c0001t0001g0082a0002c0002t0001g0006others(1): Show | 4 | HG02257.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-5322C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527136 | ||||||
chr12:100527334
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.446-5124C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527334 | ||||||
chr12:100527766
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(22): Show | 26 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.446-4692G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527766 | ||||||
chr12:100527779
|
G | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0086 | 2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.446-4679G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527779 | ||||||
chr12:100527879
|
A | T | 1 | a0001c0001t0001g0259 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.446-4579A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527879 | ||||||
chr12:100527964
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.446-4494T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527964 | ||||||
chr12:100528136
|
C | T | 2 | a0001c0001t0001g0297a0003c0005t0001g0260 | 2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.446-4322C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528136 | ||||||
chr12:100528220
|
T | G | 9 | a0001c0001t0001g0214a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 9 | HG00597.hp2 HG02015.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.446-4238T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528220 | ||||||
chr12:100528264
|
T | A | 5 | a0001c0001t0001g0257a0001c0001t0003g0174a0001c0001t0003g0240others(2): Show | 5 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-4194T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528264 | ||||||
chr12:100528372
|
G | GA | 11 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.446-4074dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100528372 | |||||
chr12:100528401
|
G | A | 57 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(54): Show | 57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.446-4057G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528401 | ||||||
chr12:100528403
|
G | A | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-4055G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528403 | ||||||
chr12:100528650
|
A | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0216 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.446-3808A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528650 | ||||||
chr12:100528875
|
T | C | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-3583T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528875 | ||||||
chr12:100528894
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.446-3564G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528894 | ||||||
chr12:100528906
|
A | G | 7 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0083others(4): Show | 7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.446-3552A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528906 | ||||||
chr12:100528940
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0140a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG00280.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.446-3518G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528940 | ||||||
chr12:100528953
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.446-3505T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528953 | ||||||
chr12:100529184
|
C | A | 7 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0083others(4): Show | 7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.446-3274C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100529184 | ||||||
chr12:100529358
|
T | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0070others(2): Show | 5 | HG02109.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-3100T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100529358 | ||||||
chr12:100529569
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.446-2889C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100529569 | ||||||
chr12:100530089
|
A | C | 7 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0083others(4): Show | 7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.446-2369A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530089 | ||||||
chr12:100530097
|
T | C | 1 | a0005c0009t0001g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.446-2361T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530097 | ||||||
chr12:100530129
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.446-2329A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530129 | ||||||
chr12:100530316
|
T | C | 4 | a0001c0001t0001g0076a0001c0001t0001g0082a0002c0002t0001g0006others(1): Show | 4 | HG02257.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-2142T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530316 | ||||||
chr12:100530380
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.446-2078A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530380 | ||||||
chr12:100530586
|
A | G | 1 | a0001c0010t0001g0191 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.446-1872A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530586 | ||||||
chr12:100530623
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.446-1835T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530623 | ||||||
chr12:100530788
|
C | T | 4 | a0001c0001t0001g0076a0001c0001t0001g0082a0002c0002t0001g0006others(1): Show | 4 | HG02257.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-1670C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530788 | ||||||
chr12:100531014
|
C | A | 1 | a0001c0001t0001g0270 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.446-1444C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531014 | ||||||
chr12:100531226
|
C | T | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-1232C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531226 | ||||||
chr12:100531235
|
C | G | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | NA18968.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.446-1223C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531235 | ||||||
chr12:100531317
|
G | A | 57 | a0001c0001t0001g0004a0001c0001t0001g0102a0001c0001t0001g0105others(54): Show | 58 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.446-1141G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531317 | ||||||
chr12:100531492
|
G | A | 1 | a0007c0004t0001g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.446-966G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531492 | ||||||
chr12:100531524
|
A | C | 1 | a0001c0001t0001g0232 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.446-934A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531524 | ||||||
chr12:100531540
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.446-918C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531540 | ||||||
chr12:100531808
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.446-650G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531808 | ||||||
chr12:100532216
|
C | A | 1 | a0001c0001t0001g0298 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.446-242C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100532216 | ||||||
chr12:100532306
|
C | T | 9 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(6): Show | 9 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.446-152C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100532306 | ||||||
chr12:100532427
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.446-31C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100532427 | ||||||
chr12:100532796
|
G | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.598+186G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100532796 | ||||||
chr12:100532941
|
A | C | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.598+331A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100532941 | ||||||
chr12:100533303
|
T | C | 57 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(54): Show | 57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.598+693T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533303 | ||||||
chr12:100533324
|
T | C | 2 | a0001c0001t0001g0297a0003c0005t0001g0260 | 2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.598+714T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533324 | ||||||
chr12:100533409
|
A | G | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 3 | HG02698.hp1 HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.598+799A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533409 | ||||||
chr12:100533636
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.598+1026A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533636 | ||||||
chr12:100533668
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.598+1058G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533668 | ||||||
chr12:100533752
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.599-1138C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533752 | ||||||
chr12:100533890
|
C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0083others(6): Show | 9 | HG02257.hp2 HG02647.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.599-994_599-986dup others(9): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 100533890 | |||||
chr12:100533902
|
T | G | 1 | a0001c0001t0001g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.599-988T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533902 | ||||||
chr12:100533924
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.599-966C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533924 | ||||||
chr12:100533938
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(22): Show | 26 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.599-952G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533938 | ||||||
chr12:100533944
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0093 | 3 | HG02145.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.599-946C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533944 | ||||||
chr12:100534131
|
C | CATG | 13 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(10): Show | 13 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.599-757_599-756ins others(3): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 100534131 | |||||
chr12:100534149
|
T | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(64): Show | 71 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.599-741T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100534149 | ||||||
chr12:100534337
|
T | C | 1 | a0005c0009t0001g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.599-553T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100534337 | ||||||
chr12:100534737
|
G | A | 1 | a0001c0001t0002g0057 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.599-153G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100534737 | ||||||
chr12:100535226
|
T | G | 7 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0083others(4): Show | 7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+203T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100535226 | ||||||
chr12:100535430
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+407C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100535430 | ||||||
chr12:100536327
|
A | T | 3 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0091 | 3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.733-185A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100536327 | ||||||
chr12:100536388
|
T | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0213 | 2 | NA18961.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.733-124T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100536388 | ||||||
chr12:100536402
|
C | CT | 11 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 12 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.733-99dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 100536402 | |||||
chr12:100536402
|
CT | C | 9 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(6): Show | 9 | HG02257.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.733-99delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 100536402 | |||||
chr12:100536435
|
C | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0102a0001c0001t0001g0105others(54): Show | 58 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.733-77C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100536435 | ||||||
chr12:100536440
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.733-72G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100536440 | ||||||
chr12:100536486
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(25): Show | 29 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.733-26C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100536486 | ||||||
chr12:100536816
|
C | A | 1 | a0001c0001t0001g0207 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.832-132C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 7/10 | chr12 | 100536816 | ||||||
chr12:100536816
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.832-132C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 7/10 | chr12 | 100536816 | ||||||
chr12:100536917
|
T | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.832-31T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 7/10 | chr12 | 100536917 | ||||||
chr12:100536932
|
T | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(35): Show | 39 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(36): Show |
intron_variant | MODIFIER | c.832-16T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 7/10 | chr12 | 100536932 | ||||||
chr12:100537066
|
A | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0171 | 2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.931+19A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537066 | ||||||
chr12:100537204
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.931+157A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537204 | ||||||
chr12:100537328
|
A | T | 3 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0091 | 3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.931+281A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537328 | ||||||
chr12:100537387
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.931+340T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537387 | ||||||
chr12:100537518
|
G | A | 10 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0081others(7): Show | 10 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.931+471G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537518 | ||||||
chr12:100537592
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.931+545G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537592 | ||||||
chr12:100537597
|
G | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0093 | 3 | HG02145.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.931+550G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537597 | ||||||
chr12:100537706
|
T | G | 5 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0001g0119others(2): Show | 5 | HG00423.hp1 NA18747.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+659T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537706 | ||||||
chr12:100537775
|
A | G | 100 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(97): Show | 103 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.931+728A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537775 | ||||||
chr12:100538184
|
A | G | 57 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(54): Show | 57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.931+1137A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538184 | ||||||
chr12:100538373
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.931+1326G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538373 | ||||||
chr12:100538490
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(28): Show | 32 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.931+1443G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538490 | ||||||
chr12:100538597
|
T | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0095others(12): Show | 16 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.931+1550T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538597 | ||||||
chr12:100538632
|
CT | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0020 | 3 | HG01109.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.931+1586delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538632 | ||||||
chr12:100538944
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 25 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.932-1728A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538944 | ||||||
chr12:100538970
|
A | C | 1 | a0001c0001t0001g0218 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.932-1702A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538970 | ||||||
chr12:100539011
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.932-1661A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100539011 | ||||||
chr12:100539366
|
A | G | 7 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0083others(4): Show | 7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-1306A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100539366 | ||||||
chr12:100539535
|
C | T | 14 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0077others(11): Show | 14 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.932-1137C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100539535 | ||||||
chr12:100539681
|
G | A | 7 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0083others(4): Show | 7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-991G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100539681 | ||||||
chr12:100539703
|
G | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 146 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.932-969G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100539703 | ||||||
chr12:100540053
|
C | T | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.932-619C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100540053 | ||||||
chr12:100540114
|
T | G | 1 | a0001c0001t0001g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.932-558T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100540114 | ||||||
chr12:100540468
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.932-204C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100540468 | ||||||
chr12:100540469
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.932-203C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100540469 | ||||||
chr12:100540600
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.932-72A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100540600 | ||||||
chr12:100540635
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.932-37A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100540635 | ||||||
chr12:100540884
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0090others(1): Show | 4 | HG02922.hp2 HG03098.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078+66G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100540884 | ||||||
chr12:100541013
|
A | G | 80 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 84 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1078+195A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541013 | ||||||
chr12:100541067
|
C | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 25 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.1078+249C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541067 | ||||||
chr12:100541139
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1078+321A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541139 | ||||||
chr12:100541173
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1078+355C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541173 | ||||||
chr12:100541274
|
C | CT | 80 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 84 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1078+462dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100541274 | |||||
chr12:100541289
|
CT | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0070a0001c0001t0001g0071others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078+483delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100541289 | |||||
chr12:100541351
|
G | C | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1078+533G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541351 | ||||||
chr12:100541453
|
G | T | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1078+635G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541453 | ||||||
chr12:100541519
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1078+701C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541519 | ||||||
chr12:100541571
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1078+753C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541571 | ||||||
chr12:100541605
|
CT | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 83 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.1078+800delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100541605 | |||||
chr12:100541611
|
T | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(26): Show | 30 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1078+793T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541611 | ||||||
chr12:100541808
|
G | A | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1078+990G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541808 | ||||||
chr12:100541906
|
C | G | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078+1088C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541906 | ||||||
chr12:100542102
|
T | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 16 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1078+1284T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542102 | ||||||
chr12:100542116
|
G | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0082others(2): Show | 5 | HG02257.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078+1298G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542116 | ||||||
chr12:100542302
|
G | A | 42 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1078+1484G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542302 | ||||||
chr12:100542346
|
G | GAA | 7 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0083others(4): Show | 7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078+1536_1078+153 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100542346 | |||||
chr12:100542367
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1078+1549T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542367 | ||||||
chr12:100542510
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02486.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1078+1692C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542510 | ||||||
chr12:100542549
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1078+1731C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542549 | ||||||
chr12:100542824
|
GGTAGATT others(7880): Show |
G | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1078+2008_1078+989 others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100542824 | |||||
chr12:100542884
|
A | G | 7 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0083others(4): Show | 7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078+2066A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542884 | ||||||
chr12:100542923
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1078+2105G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542923 | ||||||
chr12:100543040
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1078+2222C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100543040 | ||||||
chr12:100543058
|
G | A | 43 | a0001c0001t0001g0217a0001c0001t0002g0001a0001c0001t0002g0033others(40): Show | 46 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1078+2240G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100543058 | ||||||
chr12:100543538
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1078+2720T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100543538 | ||||||
chr12:100543559
|
T | TTG | 54 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0031others(51): Show | 58 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1078+2769_1078+277 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100543559 | |||||
chr12:100543559
|
T | TTGTG | 3 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0091 | 3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1078+2767_1078+277 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100543559 | |||||
chr12:100543663
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1078+2845C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100543663 | ||||||
chr12:100543975
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1078+3157G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100543975 | ||||||
chr12:100544106
|
G | A | 3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG02257.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1078+3288G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100544106 | ||||||
chr12:100544208
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1078+3390C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100544208 | ||||||
chr12:100544253
|
C | CA | 122 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 126 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.1078+3456dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100544253 | |||||
chr12:100544253
|
C | CAA | 19 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(16): Show | 19 | HG00423.hp2 HG00673.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.1078+3455_1078+345 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100544253 | |||||
chr12:100544253
|
CA | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0076others(5): Show | 9 | HG00140.hp1 HG02257.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1078+3456delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100544253 | |||||
chr12:100544452
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1078+3634C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100544452 | ||||||
chr12:100545006
|
G | A | 57 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(54): Show | 57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1078+4188G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545006 | ||||||
chr12:100545011
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1078+4193A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545011 | ||||||
chr12:100545048
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1078+4230G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545048 | ||||||
chr12:100545070
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1078+4252G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545070 | ||||||
chr12:100545093
|
C | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0086 | 2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1078+4275C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545093 | ||||||
chr12:100545201
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1078+4383G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545201 | ||||||
chr12:100545242
|
CTGAGG | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0275a0001c0001t0001g0298 | 4 | HG00140.hp1 HG01346.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078+4427_1078+443 others(9): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545242 | |||||
chr12:100545286
|
G | C | 1 | a0001c0001t0002g0103 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1078+4468G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545286 | ||||||
chr12:100545616
|
T | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(24): Show | 28 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1078+4798T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545616 | ||||||
chr12:100545641
|
C | CA | 62 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0022others(59): Show | 65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1078+4851dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545641 | |||||
chr12:100545641
|
C | CAA | 12 | a0001c0001t0001g0107a0001c0001t0001g0122a0001c0001t0001g0238others(9): Show | 12 | HG02083.hp2 HG02615.hp2 HG03669.hp1 others(9): Show |
intron_variant | MODIFIER | c.1078+4850_1078+485 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545641 | |||||
chr12:100545641
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0216 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1078+4841_1078+485 others(15): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545641 | |||||
chr12:100545641
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1078+4840_1078+485 others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545641 | |||||
chr12:100545641
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0083a0001c0001t0001g0085 | 2 | HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1078+4839_1078+485 others(17): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545641 | |||||
chr12:100545660
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1078+4842A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545660 | ||||||
chr12:100545664
|
A | AAAC | 13 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(10): Show | 13 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078+4848_1078+484 others(7): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545664 | |||||
chr12:100545664
|
A | AAC | 8 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 9 | HG01257.hp2 HG01258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078+4847_1078+484 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545664 | |||||
chr12:100545669
|
AC | A | 46 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(43): Show | 47 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.1078+4853delC | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545669 | |||||
chr12:100545670
|
C | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1078+4852C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545670 | ||||||
chr12:100545671
|
C | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(22): Show | 26 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1078+4853C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545671 | ||||||
chr12:100545875
|
C | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02486.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1078+5057C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545875 | ||||||
chr12:100545899
|
A | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG02451.hp2 HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1078+5081A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545899 | ||||||
chr12:100545929
|
T | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(36): Show | 40 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(37): Show |
intron_variant | MODIFIER | c.1078+5111T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545929 | ||||||
chr12:100546127
|
T | TGGAGGCT others(7): Show |
1 | a0001c0001t0001g0128 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1078+5310_1078+532 others(18): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100546127 | |||||
chr12:100546438
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1078+5620G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100546438 | ||||||
chr12:100546450
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1078+5632C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100546450 | ||||||
chr12:100546481
|
G | T | 57 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(54): Show | 57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1078+5663G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100546481 | ||||||
chr12:100546651
|
T | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 84 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1078+5833T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100546651 | ||||||
chr12:100546709
|
C | A | 1 | a0001c0001t0001g0239 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1078+5891C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100546709 | ||||||
chr12:100546754
|
C | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0090others(1): Show | 4 | HG02922.hp2 HG03098.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078+5936C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100546754 | ||||||
chr12:100547028
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1078+6210A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547028 | ||||||
chr12:100547597
|
AGGCAGTT others(9): Show |
A | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078+6783_1078+679 others(20): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100547597 | |||||
chr12:100547705
|
T | TTTTA | 47 | a0001c0001t0001g0011a0001c0001t0001g0252a0001c0001t0001g0268others(44): Show | 50 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1078+6915_1078+691 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100547705 | |||||
chr12:100547705
|
TTTTA | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(28): Show | 32 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.1078+6915_1078+691 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100547705 | |||||
chr12:100547705
|
TTTTATTT others(1): Show |
T | 36 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0023others(33): Show | 36 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1078+6911_1078+691 others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100547705 | |||||
chr12:100547705
|
TTTTATTT others(5): Show |
T | 1 | a0001c0001t0001g0184 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1078+6907_1078+691 others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100547705 | |||||
chr12:100547824
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1078+7006G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547824 | ||||||
chr12:100547910
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1078+7092C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547910 | ||||||
chr12:100547918
|
T | C | 5 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0082others(2): Show | 5 | HG02257.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078+7100T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547918 | ||||||
chr12:100547942
|
G | C | 1 | a0001c0001t0001g0022 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1078+7124G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547942 | ||||||
chr12:100547956
|
A | G | 1 | a0001c0001t0002g0067 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1078+7138A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547956 | ||||||
chr12:100547961
|
T | C | 1 | a0001c0001t0002g0067 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1078+7143T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547961 | ||||||
chr12:100547963
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1078+7145G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547963 | ||||||
chr12:100547971
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1078+7153T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547971 | ||||||
chr12:100547979
|
C | G | 4 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02647.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078+7161C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547979 | ||||||
chr12:100548000
|
T | G | 44 | a0001c0001t0001g0011a0001c0001t0001g0183a0001c0001t0001g0184others(41): Show | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1078+7182T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548000 | ||||||
chr12:100548093
|
T | C | 113 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(110): Show | 116 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1078+7275T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548093 | ||||||
chr12:100548095
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1078+7277C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548095 | ||||||
chr12:100548195
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1078+7377G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548195 | ||||||
chr12:100548223
|
C | T | 42 | a0001c0001t0001g0277a0001c0001t0002g0001a0001c0001t0002g0033others(39): Show | 45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1078+7405C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548223 | ||||||
chr12:100548238
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1078+7420G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548238 | ||||||
chr12:100548299
|
G | A | 55 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(52): Show | 55 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1078+7481G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548299 | ||||||
chr12:100548315
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1078+7497C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548315 | ||||||
chr12:100548370
|
TA | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(89): Show | 93 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1078+7568delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100548370 | |||||
chr12:100548370
|
TAA | T | 55 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(52): Show | 58 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1078+7567_1078+756 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100548370 | |||||
chr12:100548594
|
A | C | 1 | a0001c0001t0001g0205 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1078+7776A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548594 | ||||||
chr12:100548705
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG00323.hp1 HG03942.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1078+7887C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548705 | ||||||
chr12:100549430
|
T | C | 54 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(51): Show | 54 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.1078+8612T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100549430 | ||||||
chr12:100549500
|
C | A | 1 | a0001c0001t0001g0297 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1078+8682C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100549500 | ||||||
chr12:100550076
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1078+9258T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550076 | ||||||
chr12:100550170
|
G | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 141 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1078+9352G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550170 | ||||||
chr12:100550181
|
A | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG01361.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1078+9363A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550181 | ||||||
chr12:100550310
|
A | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG01361.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1078+9492A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550310 | ||||||
chr12:100550526
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0160 | 3 | HG01258.hp1 HG01358.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1078+9708G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550526 | ||||||
chr12:100550712
|
G | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1078+9894G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550712 | ||||||
chr12:100550939
|
A | G | 55 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(52): Show | 55 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1078+10121A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550939 | ||||||
chr12:100551093
|
T | G | 1 | a0001c0001t0001g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1078+10275T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100551093 | ||||||
chr12:100551302
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1078+10484T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100551302 | ||||||
chr12:100551385
|
GT | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0070a0001c0001t0001g0072others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079-10496delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100551385 | |||||
chr12:100551474
|
A | G | 82 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(79): Show | 83 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1079-10411A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100551474 | ||||||
chr12:100551491
|
A | T | 1 | a0001c0001t0001g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1079-10394A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100551491 | ||||||
chr12:100551914
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1079-9971G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100551914 | ||||||
chr12:100552029
|
G | GATCAAAC others(1): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0216 | 3 | HG02922.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1079-9856_1079-985 others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100552029 | ||||||
chr12:100552030
|
T | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0216 | 3 | HG02922.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1079-9855T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100552030 | ||||||
chr12:100552251
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1079-9634G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100552251 | ||||||
chr12:100552500
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1079-9385C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100552500 | ||||||
chr12:100552720
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1079-9165C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100552720 | ||||||
chr12:100552919
|
A | AT | 76 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(73): Show | 76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1079-8965dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100552919 | |||||
chr12:100552920
|
T | TA | 9 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG01069.hp1 HG02015.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1079-8952dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100552920 | |||||
chr12:100552921
|
A | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0148 | 2 | HG01358.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1079-8964A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100552921 | ||||||
chr12:100553022
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0082 | 2 | HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1079-8863G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553022 | ||||||
chr12:100553047
|
A | G | 232 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(229): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1079-8838A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553047 | ||||||
chr12:100553072
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1079-8813C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553072 | ||||||
chr12:100553213
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0279 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1079-8672T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553213 | ||||||
chr12:100553323
|
T | C | 3 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0223 | 3 | NA19063.hp2 NA19074.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1079-8562T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553323 | ||||||
chr12:100553376
|
T | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-8509T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553376 | ||||||
chr12:100553471
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1079-8414A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553471 | ||||||
chr12:100553524
|
G | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0165a0007c0004t0001g0166 | 3 | HG02895.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1079-8361G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553524 | ||||||
chr12:100553568
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1079-8317C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553568 | ||||||
chr12:100553735
|
T | G | 14 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0072others(11): Show | 14 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1079-8150T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553735 | ||||||
chr12:100553747
|
G | A | 186 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(183): Show | 190 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1079-8138G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553747 | ||||||
chr12:100553749
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1079-8136C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553749 | ||||||
chr12:100553916
|
A | T | 12 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0091others(9): Show | 12 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1079-7969A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553916 | ||||||
chr12:100554133
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1079-7752T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554133 | ||||||
chr12:100554179
|
G | A | 15 | a0001c0001t0001g0031a0001c0001t0001g0082a0001c0001t0001g0083others(12): Show | 15 | HG02145.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1079-7706G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554179 | ||||||
chr12:100554336
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1079-7549T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554336 | ||||||
chr12:100554341
|
G | T | 3 | a0001c0001t0001g0094a0002c0002t0001g0006a0002c0002t0001g0007 | 3 | HG02257.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1079-7544G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554341 | ||||||
chr12:100554392
|
A | AAC | 25 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0016others(22): Show | 26 | HG00323.hp1 HG01099.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1079-7462_1079-746 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | |||||
chr12:100554392
|
A | AACAC | 44 | a0001c0001t0001g0091a0001c0001t0001g0134a0001c0001t0001g0193others(41): Show | 47 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1079-7464_1079-746 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | |||||
chr12:100554392
|
A | AACACAC | 12 | a0001c0001t0001g0032a0001c0001t0001g0083a0001c0001t0001g0085others(9): Show | 12 | HG01361.hp1 HG02615.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1079-7466_1079-746 others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | |||||
chr12:100554392
|
A | AACACACA others(1): Show |
58 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0010others(55): Show | 59 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1079-7468_1079-746 others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | |||||
chr12:100554392
|
A | AACACACA others(3): Show |
10 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079-7470_1079-746 others(14): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | |||||
chr12:100554392
|
A | AACACACA others(5): Show |
5 | a0001c0001t0001g0153a0001c0001t0001g0214a0001c0001t0001g0254others(2): Show | 5 | HG00597.hp2 HG00621.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-7472_1079-746 others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | |||||
chr12:100554392
|
AAC | A | 4 | a0001c0001t0001g0031a0001c0001t0001g0081a0001c0001t0001g0082others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1079-7462_1079-746 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | |||||
chr12:100554392
|
AACACACA others(3): Show |
A | 64 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0070others(61): Show | 64 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.1079-7470_1079-746 others(14): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | |||||
chr12:100554621
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1079-7264G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554621 | ||||||
chr12:100554697
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1079-7188C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554697 | ||||||
chr12:100554737
|
C | T | 36 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0078others(33): Show | 37 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1079-7148C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554737 | ||||||
chr12:100554744
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1079-7141G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554744 | ||||||
chr12:100554938
|
T | G | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1079-6947T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554938 | ||||||
chr12:100554986
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1079-6899T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554986 | ||||||
chr12:100555529
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1079-6356C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100555529 | ||||||
chr12:100555818
|
T | C | 51 | a0001c0001t0001g0032a0001c0001t0001g0134a0001c0001t0001g0193others(48): Show | 54 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1079-6067T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100555818 | ||||||
chr12:100555840
|
G | A | 96 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0021others(93): Show | 97 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1079-6045G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100555840 | ||||||
chr12:100555916
|
T | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0299a0001c0001t0002g0052 | 3 | NA18969.hp2 NA18983.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1079-5969T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100555916 | ||||||
chr12:100555976
|
T | TTGCTCAA others(18): Show |
1 | a0001c0001t0001g0120 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1079-5907_1079-588 others(29): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100555976 | |||||
chr12:100556104
|
T | G | 4 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079-5781T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556104 | ||||||
chr12:100556257
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0238 | 2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1079-5628C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556257 | ||||||
chr12:100556292
|
A | G | 3 | a0001c0001t0001g0093a0001c0001t0001g0165a0007c0004t0001g0166 | 3 | HG02895.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1079-5593A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556292 | ||||||
chr12:100556422
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079-5463G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556422 | ||||||
chr12:100556467
|
C | CA | 14 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0094others(11): Show | 14 | HG02145.hp2 HG02257.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1079-5415dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100556467 | |||||
chr12:100556471
|
G | A | 109 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0016others(106): Show | 110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1079-5414G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556471 | ||||||
chr12:100556482
|
C | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0078others(33): Show | 37 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1079-5403C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556482 | ||||||
chr12:100556527
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1079-5358C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556527 | ||||||
chr12:100556593
|
G | T | 110 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0016others(107): Show | 111 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1079-5292G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556593 | ||||||
chr12:100556981
|
T | C | 5 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-4904T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556981 | ||||||
chr12:100557084
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1079-4801G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557084 | ||||||
chr12:100557198
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1079-4687G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557198 | ||||||
chr12:100557240
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1079-4645G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557240 | ||||||
chr12:100557245
|
G | A | 108 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0016others(105): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1079-4640G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557245 | ||||||
chr12:100557269
|
AT | A | 108 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0016others(105): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1079-4615delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557269 | ||||||
chr12:100557404
|
CA | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0165a0007c0004t0001g0166 | 3 | HG02895.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1079-4478delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100557404 | |||||
chr12:100557492
|
C | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0095others(31): Show | 35 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.1079-4393C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557492 | ||||||
chr12:100557536
|
G | A | 5 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-4349G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557536 | ||||||
chr12:100557609
|
T | C | 168 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0016others(165): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1079-4276T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557609 | ||||||
chr12:100557903
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1079-3982C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557903 | ||||||
chr12:100557948
|
G | T | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(244): Show | 252 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.1079-3937G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557948 | ||||||
chr12:100557988
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1079-3897A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557988 | ||||||
chr12:100558032
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1079-3853A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558032 | ||||||
chr12:100558119
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1079-3766G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558119 | ||||||
chr12:100558127
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079-3758G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558127 | ||||||
chr12:100558144
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1079-3741A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558144 | ||||||
chr12:100558157
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1079-3728G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558157 | ||||||
chr12:100558204
|
C | CA | 57 | a0001c0001t0001g0086a0001c0001t0001g0093a0001c0001t0001g0094others(54): Show | 60 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1079-3662dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558204 | |||||
chr12:100558204
|
C | CAA | 14 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(11): Show | 14 | HG00558.hp1 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1079-3663_1079-366 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558204 | |||||
chr12:100558204
|
CA | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(57): Show | 62 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.1079-3662delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558204 | |||||
chr12:100558281
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1079-3604G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558281 | ||||||
chr12:100558306
|
G | A | 5 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-3579G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558306 | ||||||
chr12:100558330
|
C | T | 54 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(51): Show | 57 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1079-3555C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558330 | ||||||
chr12:100558349
|
C | CA | 23 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(20): Show | 23 | HG00621.hp1 HG01433.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.1079-3509dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558349 | |||||
chr12:100558349
|
CA | C | 12 | a0001c0001t0001g0075a0001c0001t0001g0081a0001c0001t0001g0083others(9): Show | 12 | HG02451.hp2 HG02559.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1079-3509delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558349 | |||||
chr12:100558349
|
CAAAAAAA | C | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG01884.hp2 HG02809.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1079-3515_1079-350 others(11): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558349 | |||||
chr12:100558349
|
CAAAAAAA others(1): Show |
C | 89 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0021others(86): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1079-3516_1079-350 others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558349 | |||||
chr12:100558356
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1079-3529A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558356 | ||||||
chr12:100558369
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0237 | 2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1079-3516A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558369 | ||||||
chr12:100558481
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1079-3404C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558481 | ||||||
chr12:100558724
|
G | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0058 | 2 | HG00408.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1079-3161G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558724 | ||||||
chr12:100558759
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1079-3126T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558759 | ||||||
chr12:100558817
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1079-3068G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558817 | ||||||
chr12:100558832
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1079-3053G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558832 | ||||||
chr12:100558943
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1079-2942C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558943 | ||||||
chr12:100559022
|
A | G | 54 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(51): Show | 57 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1079-2863A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559022 | ||||||
chr12:100559161
|
TATGTG | T | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1079-2716_1079-271 others(9): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100559161 | |||||
chr12:100559176
|
G | C | 1 | a0001c0001t0001g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1079-2709G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559176 | ||||||
chr12:100559189
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1079-2696G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559189 | ||||||
chr12:100559438
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG00735.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1079-2447C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559438 | ||||||
chr12:100559499
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1079-2386C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559499 | ||||||
chr12:100559517
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1079-2368G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559517 | ||||||
chr12:100559582
|
C | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0163others(2): Show | 5 | HG02040.hp1 NA18967.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-2303C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559582 | ||||||
chr12:100559737
|
C | T | 105 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0016others(102): Show | 106 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1079-2148C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559737 | ||||||
chr12:100559768
|
C | T | 95 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0021others(92): Show | 96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1079-2117C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559768 | ||||||
chr12:100559789
|
A | G | 169 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0016others(166): Show | 173 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1079-2096A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559789 | ||||||
chr12:100560227
|
A | C | 101 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0021others(98): Show | 102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1079-1658A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560227 | ||||||
chr12:100560322
|
A | G | 1 | a0001c0001t0002g0046 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1079-1563A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560322 | ||||||
chr12:100560336
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1079-1549C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560336 | ||||||
chr12:100560337
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1079-1548G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560337 | ||||||
chr12:100560344
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1079-1541G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560344 | ||||||
chr12:100560363
|
C | T | 76 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1079-1522C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560363 | ||||||
chr12:100560397
|
G | GT | 78 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(75): Show | 79 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1079-1487dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100560397 | |||||
chr12:100560450
|
G | A | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0172others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079-1435G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560450 | ||||||
chr12:100560543
|
G | A | 1 | a0001c0001t0002g0054 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1079-1342G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560543 | ||||||
chr12:100560633
|
A | C | 95 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0021others(92): Show | 96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1079-1252A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560633 | ||||||
chr12:100560687
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0072 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1079-1198C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560687 | ||||||
chr12:100560979
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1079-906G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560979 | ||||||
chr12:100561037
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1079-848G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100561037 | ||||||
chr12:100561343
|
A | G | 108 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0016others(105): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1079-542A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100561343 | ||||||
chr12:100561354
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1079-531C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100561354 | ||||||
chr12:100561401
|
AAAAAT | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079-475_1079-471d others(7): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100561401 | |||||
chr12:100561526
|
C | T | 5 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-359C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100561526 | ||||||
chr12:100561600
|
C | G | 101 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0021others(98): Show | 102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1079-285C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100561600 | ||||||
chr12:100561620
|
A | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079-265A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100561620 | ||||||
chr12:100562252
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1192+254G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 10/10 | chr12 | 100562252 | ||||||
chr12:100562385
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1192+387A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 10/10 | chr12 | 100562385 | ||||||
chr12:100562419
|
C | CAGGAGGC others(1106): Show |
1 | a0001c0001t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1192+435_1192+436i others(1115): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 100562419 | |||||
chr12:100562922
|
T | C | 4 | a0001c0001t0001g0106a0001c0001t0001g0113a0001c0001t0001g0130others(1): Show | 4 | HG02129.hp2 NA18940.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1193-329T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 10/10 | chr12 | 100562922 | ||||||
chr12:100563004
|
T | A | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1193-247T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 10/10 | chr12 | 100563004 |