geneid | 7181 |
---|---|
ensemblid | ENSG00000120798.17 |
hgncid | 7971 |
symbol | NR2C1 |
name | nuclear receptor subfamily 2 group C member 1 |
refseq_nuc | NM_003297.4 |
refseq_prot | NP_003288.2 |
ensembl_nuc | ENST00000333003.10 |
ensembl_prot | ENSP00000333275.4 |
mane_status | MANE Select |
chr | chr12 |
start | 95020229 |
end | 95073618 |
strand | - |
ver | v1.2 |
region | chr12:95020229-95073618 |
region5000 | chr12:95015229-95078618 |
regionname0 | NR2C1_chr12_95020229_95073618 |
regionname5000 | NR2C1_chr12_95015229_95078618 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 603 | 424 | 91 | 76 | 194 | 18 | 43 | 155 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0002 | 0/0 | 603 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0003 | 0/0 | 603 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0004 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1812 | 423 | 90 | 76 | 194 | 18 | 43 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
c0002 | 0/0 | 1812 | 4 | 0 | 0 | 4 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
c0003 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
c0004 | 0/0 | 1812 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
c0005 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2247 | 283 | 53 | 49 | 145 | 7 | 28 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0002 | 0/1 | 2247 | 93 | 12 | 16 | 48 | 6 | 10 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0003 | 0/0 | 2247 | 17 | 9 | 3 | 1 | 0 | 4 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0004 | 0/0 | 2248 | 6 | 0 | 2 | 0 | 4 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0005 | 0/0 | 2248 | 5 | 0 | 4 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0006 | 0/0 | 2247 | 5 | 5 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0007 | 0/0 | 2247 | 4 | 4 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0008 | 0/0 | 2247 | 3 | 3 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0009 | 0/0 | 2247 | 2 | 0 | 0 | 0 | 1 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0010 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0011 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0012 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0013 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0014 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0015 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0016 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0017 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0018 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0019 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
t0020 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 1 | 3 | 5 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0004 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0008 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0368 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1812 | 423 | 90 | 76 | 194 | 18 | 43 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0005 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0002c0002 | 0/0 | 1812 | 4 | 0 | 0 | 4 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0003c0004 | 0/0 | 1812 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0004c0003 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4058 | 282 | 52 | 49 | 145 | 7 | 28 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0002 | 0/1 | 4058 | 87 | 11 | 16 | 44 | 6 | 9 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0003 | 0/0 | 4058 | 17 | 9 | 3 | 1 | 0 | 4 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0004 | 0/0 | 4059 | 6 | 0 | 2 | 0 | 4 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0005 | 0/0 | 4059 | 5 | 0 | 4 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0006 | 0/0 | 4058 | 5 | 5 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0007 | 0/0 | 4058 | 4 | 4 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0008 | 0/0 | 4058 | 3 | 3 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0009 | 0/0 | 4058 | 2 | 0 | 0 | 0 | 1 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0010 | 0/0 | 4058 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0011 | 0/0 | 4058 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0012 | 0/0 | 4058 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0013 | 0/0 | 4058 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0014 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0015 | 0/0 | 4058 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0016 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0017 | 0/0 | 4058 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0018 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0019 | 0/0 | 4058 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0001t0020 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0001c0005t0001 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0002c0002t0002 | 0/0 | 4058 | 4 | 0 | 0 | 4 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0003c0004t0002 | 0/0 | 4058 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
a0004c0003t0002 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | copy fasta | chr12 | 95015229 | 95078618 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 1 | 3 | 5 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0004 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0008 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0003g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0004g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0004g0368 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0004g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0004g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0004g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0004g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0006g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0006g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0006g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0006g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0006g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0007g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0007g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0007g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0007g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0008g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0008g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0008g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0009g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0009g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0010g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0010g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0011g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0012g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0013g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0014g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0015g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0016g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0017g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0018g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0019g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0001t0020g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0001c0005t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0003c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
a0004c0003t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0370 | EUR | GBR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0300 | EUR | GBR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0305 | EUR | GBR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0162 | EUR | GBR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00280 | hp1 | a0001 | c0001 | t0009 | g0084 | EUR | FIN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0071 | EUR | FIN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0386 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0064 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00733 | hp2 | a0001 | c0001 | t0011 | g0023 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0383 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01099 | hp2 | a0001 | c0001 | t0019 | g0034 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0372 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0356 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0390 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0381 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0062 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0063 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0065 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0367 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0369 | EUR | IBS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0072 | EUR | IBS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0141 | EUR | IBS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0142 | EUR | IBS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0371 | EUR | IBS | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0389 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02040 | hp1 | a0001 | c0001 | t0013 | g0032 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02055 | hp2 | a0001 | c0001 | t0018 | g0163 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CDX | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CDX | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CDX | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | CDX | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02258 | hp2 | a0001 | c0005 | t0001 | g0311 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0391 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0392 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02572 | hp1 | a0004 | c0003 | t0002 | g0170 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02622 | hp1 | a0001 | c0001 | t0020 | g0373 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0365 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0360 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0378 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0376 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02735 | hp1 | a0003 | c0004 | t0002 | g0073 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0374 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0375 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02895 | hp1 | a0001 | c0001 | t0016 | g0361 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0318 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02976 | hp1 | a0001 | c0001 | t0010 | g0267 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0384 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03130 | hp2 | a0001 | c0001 | t0014 | g0238 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0366 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0296 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0393 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0379 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0387 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0385 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03516 | hp2 | a0001 | c0001 | t0010 | g0354 | AFR | ESN | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0364 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0377 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | STU | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | STU | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03927 | hp2 | a0001 | c0001 | t0009 | g0088 | SAS | BEB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | BEB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | STU | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG04184 | hp2 | a0001 | c0001 | t0005 | g0164 | SAS | BEB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | STU | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | STU | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | STU | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | YRI | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | YRI | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | LWK | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0362 | AFR | LWK | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0380 | AFR | LWK | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0394 | AFR | LWK | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19056 | hp1 | a0001 | c0001 | t0015 | g0326 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19063 | hp2 | a0001 | c0001 | t0017 | g0315 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19082 | hp2 | a0001 | c0001 | t0012 | g0089 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | YRI | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | YRI | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ASW | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0298 | AFR | ASW | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | TSI | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0029 | EUR | TSI | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0368 | EUR | TSI | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | GIH | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0363 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | MSL | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | USA | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0382 | AFR | USA | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | USA | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0388 | AFR | LWK | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | LWK | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0008 | REF | REF | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0004 | REF | REF | NR2C1_chr12_95015229_95078618 | NR2C1 | chr12 | 95015229 | 95078618 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:95022329
|
T | C | 1 | a0004 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1712A>G | p.Lys571Arg | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 1958/4058 | 1712/1812 | 571/603 | chr12 | 95022329 | ||
chr12:95031406
|
T | G | 1 | a0003 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1336A>C | p.Asn446His | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/14 | 1582/4058 | 1336/1812 | 446/603 | chr12 | 95031406 | ||
chr12:95062591
|
T | C | 1 | a0002 | 4 | HG00408.hp1 NA18952.hp1 NA18990.hp2 others(1): Show |
missense_variant | MODERATE | c.202A>G | p.Lys68Glu | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/14 | 448/4058 | 202/1812 | 68/603 | chr12 | 95062591 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:95059925
|
T | C | 1 | a0001c0005 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.345A>G | p.Val115Val | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/14 | 591/4058 | 345/1812 | 115/603 | chr12 | 95059925 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:95020326
|
A | C | 1 | a0001c0001t0008 | 3 | HG02965.hp2 HG03209.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1903T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 1903 | chr12 | 95020326 | |||||
chr12:95020378
|
T | C | 1 | a0001c0001t0007 | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1851A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 1851 | chr12 | 95020378 | |||||
chr12:95020671
|
C | T | 1 | a0001c0001t0015 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1558G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 1558 | chr12 | 95020671 | |||||
chr12:95020686
|
G | T | 1 | a0001c0001t0014 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1543C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 1543 | chr12 | 95020686 | |||||
chr12:95020814
|
G | T | 1 | a0001c0001t0013 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1415C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 1415 | chr12 | 95020814 | |||||
chr12:95020934
|
T | A | 1 | a0001c0001t0009 | 2 | HG00280.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1295A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 1295 | chr12 | 95020934 | |||||
chr12:95020947
|
A | G | 3 | a0001c0001t0006a0001c0001t0010a0001c0001t0016 | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1282T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 1282 | chr12 | 95020947 | |||||
chr12:95020985
|
T | G | 1 | a0001c0001t0016 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1244A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 1244 | chr12 | 95020985 | |||||
chr12:95021040
|
T | C | 1 | a0001c0001t0012 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1189A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 1189 | chr12 | 95021040 | |||||
chr12:95021062
|
C | G | 1 | a0001c0001t0006 | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1167G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 1167 | chr12 | 95021062 | |||||
chr12:95021426
|
A | C | 8 | a0001c0001t0002a0001c0001t0009a0001c0001t0011others(5): Show | 98 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*803T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 803 | chr12 | 95021426 | |||||
chr12:95021568
|
T | C | 1 | a0001c0001t0017 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*661A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 661 | chr12 | 95021568 | |||||
chr12:95021593
|
T | C | 1 | a0001c0001t0018 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*636A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 636 | chr12 | 95021593 | |||||
chr12:95021639
|
T | C | 1 | a0001c0001t0019 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 590 | chr12 | 95021639 | |||||
chr12:95021651
|
G | GT | 2 | a0001c0001t0004a0001c0001t0005 | 11 | HG00099.hp1 HG00733.hp1 HG01106.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*577_*578insA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 14/14 | 577 | chr12 | 95021651 | |||||
chr12:95073439
|
G | A | 1 | a0001c0001t0004 | 6 | HG00099.hp1 HG01106.hp1 HG01496.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-67C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/14 | 6055 | chr12 | 95073439 | |||||
chr12:95073482
|
A | C | 1 | a0001c0001t0011 | 1 | HG00733.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-110T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/14 | chr12 | 95073482 | ||||||
chr12:95073547
|
G | C | 1 | a0001c0001t0020 | 1 | HG02622.hp1 | 5_prime_UTR_variant | MODIFIER | c.-175C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/14 | 6163 | chr12 | 95073547 | |||||
chr12:95073548
|
G | A | 1 | a0001c0001t0007 | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-176C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/14 | 6164 | chr12 | 95073548 | |||||
chr12:95073578
|
T | C | 1 | a0001c0001t0003 | 17 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-206A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/14 | 6194 | chr12 | 95073578 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:95022464
|
G | T | 1 | a0001c0001t0001g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1638-61C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95022464 | ||||||
chr12:95022700
|
A | AT | 37 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0130others(34): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1638-298dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95022700 | ||||||
chr12:95022700
|
A | ATT | 10 | a0001c0001t0001g0217a0001c0001t0001g0291a0001c0001t0001g0294others(7): Show | 10 | HG01884.hp1 HG02015.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1638-299_1638-298d others(4): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95022700 | ||||||
chr12:95022700
|
A | ATTT | 64 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0022others(61): Show | 68 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1638-300_1638-298d others(5): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95022700 | ||||||
chr12:95022700
|
A | ATTTT | 7 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(4): Show | 7 | HG02559.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1638-301_1638-298d others(6): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95022700 | ||||||
chr12:95022870
|
GT | G | 64 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0022others(61): Show | 68 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1638-468delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95022870 | ||||||
chr12:95022871
|
T | G | 1 | a0001c0001t0003g0390 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1638-468A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95022871 | ||||||
chr12:95022872
|
T | G | 10 | a0001c0001t0003g0378a0001c0001t0003g0381a0001c0001t0003g0382others(7): Show | 10 | HG00609.hp2 HG00738.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1638-469A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95022872 | ||||||
chr12:95022998
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638-595C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95022998 | ||||||
chr12:95023024
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1638-621G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95023024 | ||||||
chr12:95023359
|
G | A | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1638-956C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95023359 | ||||||
chr12:95023407
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1638-1004T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95023407 | ||||||
chr12:95023451
|
C | G | 1 | a0001c0001t0001g0335 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1638-1048G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95023451 | ||||||
chr12:95023485
|
A | G | 2 | a0001c0001t0003g0385a0001c0001t0003g0387 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1638-1082T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95023485 | ||||||
chr12:95023586
|
TTA | T | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1638-1185_1638-118 others(6): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95023586 | ||||||
chr12:95023728
|
G | C | 3 | a0001c0001t0008g0296a0001c0001t0008g0298a0001c0001t0008g0318 | 3 | HG02965.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1638-1325C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95023728 | ||||||
chr12:95023844
|
G | A | 1 | a0001c0001t0018g0163 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1637+1306C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95023844 | ||||||
chr12:95024026
|
A | T | 4 | a0001c0001t0003g0380a0001c0001t0003g0389a0001c0001t0003g0392others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637+1124T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95024026 | ||||||
chr12:95024133
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0287 | 2 | NA19063.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1637+1017T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95024133 | ||||||
chr12:95024221
|
TTTTA | T | 18 | a0001c0001t0001g0247a0001c0001t0003g0378a0001c0001t0003g0379others(15): Show | 18 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1637+925_1637+928d others(6): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95024221 | ||||||
chr12:95024361
|
T | A | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1637+789A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95024361 | ||||||
chr12:95024478
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1637+672C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95024478 | ||||||
chr12:95025001
|
A | G | 2 | a0001c0001t0002g0008a0003c0004t0002g0073 | 3 | HG01433.hp2 HG02735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1637+149T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 13/13 | chr12 | 95025001 | ||||||
chr12:95025310
|
G | C | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1532-55C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025310 | ||||||
chr12:95025323
|
A | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(12): Show | 16 | HG00741.hp2 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1532-68T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025323 | ||||||
chr12:95025433
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1532-178A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025433 | ||||||
chr12:95025519
|
A | G | 1 | a0001c0001t0001g0351 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1532-264T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025519 | ||||||
chr12:95025540
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0245others(1): Show | 6 | NA18947.hp2 NA18998.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.1532-285G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025540 | ||||||
chr12:95025556
|
A | G | 79 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(76): Show | 84 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1532-301T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025556 | ||||||
chr12:95025615
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1532-360C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025615 | ||||||
chr12:95025658
|
T | TA | 25 | a0001c0001t0001g0031a0001c0001t0001g0178a0001c0001t0001g0212others(22): Show | 25 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.1532-404dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025658 | ||||||
chr12:95025658
|
T | TAA | 53 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(50): Show | 58 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1532-405_1532-404d others(4): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025658 | ||||||
chr12:95025658
|
T | TAAA | 7 | a0001c0001t0001g0037a0001c0001t0001g0138a0001c0001t0001g0324others(4): Show | 7 | HG01175.hp2 HG01358.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.1532-406_1532-404d others(5): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025658 | ||||||
chr12:95025658
|
TA | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(73): Show | 87 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1532-404delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025658 | ||||||
chr12:95025659
|
A | T | 1 | a0001c0001t0001g0242 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1532-404T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025659 | ||||||
chr12:95025699
|
CCA | C | 3 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0165 | 3 | HG02818.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1532-446_1532-445d others(4): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025699 | ||||||
chr12:95025753
|
T | C | 1 | a0001c0001t0001g0259 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1532-498A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025753 | ||||||
chr12:95025858
|
T | G | 79 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(76): Show | 84 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1532-603A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025858 | ||||||
chr12:95025978
|
G | T | 1 | a0001c0001t0003g0383 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1532-723C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95025978 | ||||||
chr12:95026014
|
T | C | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1532-759A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026014 | ||||||
chr12:95026097
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1532-842G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026097 | ||||||
chr12:95026190
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1532-935C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026190 | ||||||
chr12:95026193
|
T | C | 79 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(76): Show | 84 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1532-938A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026193 | ||||||
chr12:95026202
|
G | A | 4 | a0001c0001t0003g0380a0001c0001t0003g0389a0001c0001t0003g0392others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1532-947C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026202 | ||||||
chr12:95026207
|
C | CA | 14 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0055others(11): Show | 14 | HG00621.hp1 HG02027.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1532-953dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026207 | ||||||
chr12:95026209
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1532-954T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026209 | ||||||
chr12:95026223
|
G | T | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1532-968C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026223 | ||||||
chr12:95026241
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1532-986T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026241 | ||||||
chr12:95026281
|
A | G | 1 | a0001c0001t0008g0318 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1532-1026T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026281 | ||||||
chr12:95026751
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(149): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.1532-1496T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026751 | ||||||
chr12:95026811
|
A | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0188a0001c0001t0001g0191others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1532-1556T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026811 | ||||||
chr12:95026855
|
G | C | 1 | a0001c0001t0001g0206 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1531+1532C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026855 | ||||||
chr12:95026871
|
G | A | 1 | a0001c0001t0001g0340 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1531+1516C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026871 | ||||||
chr12:95026917
|
A | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0188a0001c0001t0001g0191others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1531+1470T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026917 | ||||||
chr12:95026951
|
CA | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(267): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1531+1435delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95026951 | ||||||
chr12:95027081
|
G | T | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1531+1306C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95027081 | ||||||
chr12:95027352
|
G | C | 1 | a0001c0001t0001g0122 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1531+1035C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95027352 | ||||||
chr12:95027360
|
C | A | 1 | a0001c0001t0003g0379 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1531+1027G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95027360 | ||||||
chr12:95027497
|
G | A | 10 | a0001c0001t0003g0378a0001c0001t0003g0381a0001c0001t0003g0382others(7): Show | 10 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1531+890C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95027497 | ||||||
chr12:95027608
|
T | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1531+779A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95027608 | ||||||
chr12:95027700
|
C | T | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1531+687G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95027700 | ||||||
chr12:95027715
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1531+672C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95027715 | ||||||
chr12:95027722
|
T | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1531+665A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95027722 | ||||||
chr12:95027766
|
TA | T | 40 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0268others(37): Show | 41 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1531+620delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95027766 | ||||||
chr12:95027920
|
T | C | 3 | a0001c0001t0010g0267a0001c0001t0010g0354a0001c0001t0016g0361 | 3 | HG02895.hp1 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1531+467A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95027920 | ||||||
chr12:95027940
|
G | A | 9 | a0001c0001t0001g0028a0001c0001t0001g0189a0001c0001t0001g0277others(6): Show | 9 | HG03831.hp1 NA18942.hp2 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.1531+447C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95027940 | ||||||
chr12:95028073
|
A | G | 4 | a0001c0001t0007g0374a0001c0001t0007g0375a0001c0001t0007g0376others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1531+314T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95028073 | ||||||
chr12:95028128
|
T | C | 1 | a0001c0001t0003g0394 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1531+259A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95028128 | ||||||
chr12:95028332
|
A | G | 49 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(46): Show | 54 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1531+55T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95028332 | ||||||
chr12:95028345
|
G | A | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1531+42C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 12/13 | chr12 | 95028345 | ||||||
chr12:95028606
|
A | C | 11 | a0001c0001t0003g0378a0001c0001t0003g0381a0001c0001t0003g0382others(8): Show | 11 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1394-82T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95028606 | ||||||
chr12:95028617
|
A | T | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0137 | 3 | HG01074.hp2 HG01516.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1394-93T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95028617 | ||||||
chr12:95028619
|
T | G | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1394-95A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95028619 | ||||||
chr12:95028690
|
G | A | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394-166C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95028690 | ||||||
chr12:95028785
|
G | A | 3 | a0001c0001t0001g0324a0001c0001t0007g0374a0001c0001t0007g0375 | 3 | HG02809.hp2 HG02818.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1394-261C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95028785 | ||||||
chr12:95028966
|
C | G | 352 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(349): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.1394-442G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95028966 | ||||||
chr12:95029010
|
C | G | 4 | a0001c0001t0007g0374a0001c0001t0007g0375a0001c0001t0007g0376others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1394-486G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029010 | ||||||
chr12:95029108
|
G | T | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1394-584C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029108 | ||||||
chr12:95029396
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1394-872C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029396 | ||||||
chr12:95029514
|
ACAAAC | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394-995_1394-991d others(7): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029514 | ||||||
chr12:95029559
|
C | CT | 182 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0019others(179): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1394-1036dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029559 | ||||||
chr12:95029603
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(51): Show | 63 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1394-1079C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029603 | ||||||
chr12:95029627
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0355 | 2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1394-1103C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029627 | ||||||
chr12:95029695
|
T | G | 1 | a0001c0001t0001g0330 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1394-1171A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029695 | ||||||
chr12:95029713
|
C | G | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1394-1189G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029713 | ||||||
chr12:95029719
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1394-1195C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029719 | ||||||
chr12:95029747
|
C | T | 1 | a0004c0003t0002g0170 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1394-1223G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029747 | ||||||
chr12:95029784
|
C | T | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394-1260G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029784 | ||||||
chr12:95029824
|
T | C | 17 | a0001c0001t0003g0378a0001c0001t0003g0379a0001c0001t0003g0380others(14): Show | 17 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1394-1300A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029824 | ||||||
chr12:95029847
|
G | A | 1 | a0001c0001t0002g0155 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1394-1323C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029847 | ||||||
chr12:95029859
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1394-1335G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95029859 | ||||||
chr12:95030096
|
G | A | 1 | a0001c0001t0007g0376 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1393+1253C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95030096 | ||||||
chr12:95030137
|
G | T | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1393+1212C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95030137 | ||||||
chr12:95030239
|
G | A | 4 | a0001c0001t0007g0374a0001c0001t0007g0375a0001c0001t0007g0376others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1393+1110C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95030239 | ||||||
chr12:95030551
|
T | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0188a0001c0001t0001g0191others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1393+798A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95030551 | ||||||
chr12:95030732
|
T | C | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1393+617A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95030732 | ||||||
chr12:95030867
|
T | C | 1 | a0001c0001t0011g0023 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1393+482A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95030867 | ||||||
chr12:95030989
|
G | C | 1 | a0001c0001t0001g0116 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1393+360C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95030989 | ||||||
chr12:95031082
|
A | G | 1 | a0001c0001t0002g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1393+267T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95031082 | ||||||
chr12:95031152
|
T | C | 7 | a0001c0001t0001g0019a0001c0001t0001g0308a0001c0001t0001g0309others(4): Show | 8 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1393+197A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95031152 | ||||||
chr12:95031187
|
T | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1393+162A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95031187 | ||||||
chr12:95031189
|
AG | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1393+159delC | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95031189 | ||||||
chr12:95031257
|
ATAAT | A | 48 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 53 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1393+88_1393+91del others(4): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 11/13 | chr12 | 95031257 | ||||||
chr12:95031566
|
C | G | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1254-78G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95031566 | ||||||
chr12:95031716
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1254-228A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95031716 | ||||||
chr12:95031718
|
G | A | 1 | a0001c0001t0002g0095 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1254-230C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95031718 | ||||||
chr12:95031917
|
G | A | 1 | a0001c0001t0003g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254-429C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95031917 | ||||||
chr12:95031928
|
C | T | 1 | a0001c0001t0004g0370 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1254-440G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95031928 | ||||||
chr12:95032085
|
C | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0147 | 3 | HG00597.hp2 HG02015.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1254-597G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032085 | ||||||
chr12:95032098
|
C | T | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1254-610G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032098 | ||||||
chr12:95032119
|
T | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0036 | 3 | HG00323.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1254-631A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032119 | ||||||
chr12:95032192
|
A | C | 1 | a0001c0001t0018g0163 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1254-704T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032192 | ||||||
chr12:95032218
|
T | A | 86 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(83): Show | 94 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1254-730A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032218 | ||||||
chr12:95032389
|
C | A | 1 | a0001c0001t0003g0394 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1254-901G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032389 | ||||||
chr12:95032455
|
C | T | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1254-967G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032455 | ||||||
chr12:95032457
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1254-980_1254-970d others(13): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032457 | ||||||
chr12:95032457
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0006g0363a0001c0001t0006g0364a0001c0001t0006g0366 | 3 | HG02559.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1254-970_1254-969i others(15): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032457 | ||||||
chr12:95032457
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0006g0362a0001c0001t0006g0365a0001c0001t0010g0267others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254-970_1254-969i others(16): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032457 | ||||||
chr12:95032467
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1254-979T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032467 | ||||||
chr12:95032527
|
G | A | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1254-1039C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032527 | ||||||
chr12:95032554
|
A | C | 1 | a0001c0001t0001g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1254-1066T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032554 | ||||||
chr12:95032618
|
T | C | 1 | a0001c0001t0002g0345 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1254-1130A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032618 | ||||||
chr12:95032693
|
C | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(269): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1254-1205G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032693 | ||||||
chr12:95032783
|
C | T | 18 | a0001c0001t0001g0358a0001c0001t0003g0378a0001c0001t0003g0379others(15): Show | 18 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1254-1295G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032783 | ||||||
chr12:95032794
|
T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(270): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1254-1306A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032794 | ||||||
chr12:95032878
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1254-1390C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032878 | ||||||
chr12:95032879
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1254-1391T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95032879 | ||||||
chr12:95033043
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(51): Show | 63 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1254-1555C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95033043 | ||||||
chr12:95033148
|
C | CA | 20 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0060others(17): Show | 22 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1254-1661dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95033148 | ||||||
chr12:95033148
|
CA | C | 7 | a0001c0001t0001g0031a0001c0001t0001g0070a0001c0001t0001g0134others(4): Show | 7 | HG00323.hp1 HG01993.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254-1661delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95033148 | ||||||
chr12:95033172
|
A | G | 3 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0276 | 3 | HG00423.hp2 NA18947.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1254-1684T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95033172 | ||||||
chr12:95033196
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1254-1708A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95033196 | ||||||
chr12:95033475
|
C | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0263a0001c0001t0001g0264 | 3 | HG03831.hp2 HG04204.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1254-1987G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95033475 | ||||||
chr12:95033549
|
ATTG | A | 5 | a0001c0001t0001g0198a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | HG02165.hp1 NA18955.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254-2064_1254-206 others(7): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95033549 | ||||||
chr12:95033613
|
CCTGG | C | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1254-2129_1254-212 others(8): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95033613 | ||||||
chr12:95033644
|
T | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1254-2156A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95033644 | ||||||
chr12:95033680
|
C | T | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1254-2192G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95033680 | ||||||
chr12:95033758
|
T | C | 5 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254-2270A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95033758 | ||||||
chr12:95033935
|
C | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(269): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1254-2447G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95033935 | ||||||
chr12:95034481
|
G | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1254-2993C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95034481 | ||||||
chr12:95034542
|
G | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1254-3054C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95034542 | ||||||
chr12:95034693
|
T | TTC | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254-3207_1254-320 others(6): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95034693 | ||||||
chr12:95034700
|
T | C | 11 | a0001c0001t0004g0367a0001c0001t0004g0368a0001c0001t0004g0369others(8): Show | 11 | HG00099.hp1 HG00733.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1254-3212A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95034700 | ||||||
chr12:95034872
|
A | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1254-3384T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95034872 | ||||||
chr12:95035002
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1254-3514A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95035002 | ||||||
chr12:95035259
|
G | C | 1 | a0001c0001t0001g0194 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1254-3771C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95035259 | ||||||
chr12:95035262
|
G | A | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1254-3774C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95035262 | ||||||
chr12:95035495
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1254-4007G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95035495 | ||||||
chr12:95035603
|
C | A | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(268): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1254-4115G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95035603 | ||||||
chr12:95035656
|
G | A | 87 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(84): Show | 95 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1254-4168C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95035656 | ||||||
chr12:95035712
|
C | T | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254-4224G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95035712 | ||||||
chr12:95036050
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1253+4426C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036050 | ||||||
chr12:95036166
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1253+4310T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036166 | ||||||
chr12:95036270
|
A | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1253+4206T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036270 | ||||||
chr12:95036272
|
T | TA | 169 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(166): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1253+4203dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036272 | ||||||
chr12:95036272
|
T | TAA | 113 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(110): Show | 120 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.1253+4202_1253+420 others(6): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036272 | ||||||
chr12:95036272
|
T | TAAA | 7 | a0001c0001t0001g0302a0001c0001t0006g0362a0001c0001t0006g0363others(4): Show | 7 | HG02155.hp2 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1253+4201_1253+420 others(7): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036272 | ||||||
chr12:95036291
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1253+4185C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036291 | ||||||
chr12:95036356
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1253+4120A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036356 | ||||||
chr12:95036373
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1253+4103C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036373 | ||||||
chr12:95036435
|
AT | A | 114 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(111): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1253+4040delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036435 | ||||||
chr12:95036476
|
A | T | 1 | a0001c0001t0007g0376 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1253+4000T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036476 | ||||||
chr12:95036512
|
C | CT | 8 | a0001c0001t0001g0030a0001c0001t0001g0049a0001c0001t0001g0051others(5): Show | 8 | HG00597.hp1 HG00673.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1253+3963dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036512 | ||||||
chr12:95036512
|
CT | C | 7 | a0001c0001t0001g0066a0001c0001t0001g0221a0001c0001t0001g0240others(4): Show | 7 | HG01099.hp1 HG02523.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1253+3963delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036512 | ||||||
chr12:95036528
|
TG | T | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168 | 3 | HG02630.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1253+3947delC | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036528 | ||||||
chr12:95036530
|
A | T | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168 | 3 | HG02630.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1253+3946T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036530 | ||||||
chr12:95036531
|
A | T | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168 | 3 | HG02630.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1253+3945T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036531 | ||||||
chr12:95036543
|
C | G | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1253+3933G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036543 | ||||||
chr12:95036596
|
C | T | 1 | a0001c0001t0002g0274 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1253+3880G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036596 | ||||||
chr12:95036597
|
G | A | 17 | a0001c0001t0003g0378a0001c0001t0003g0379a0001c0001t0003g0380others(14): Show | 17 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1253+3879C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036597 | ||||||
chr12:95036646
|
G | T | 4 | a0001c0001t0007g0374a0001c0001t0007g0375a0001c0001t0007g0376others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1253+3830C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036646 | ||||||
chr12:95036656
|
A | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1253+3820T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036656 | ||||||
chr12:95036802
|
G | C | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1253+3674C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036802 | ||||||
chr12:95036891
|
A | G | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1253+3585T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95036891 | ||||||
chr12:95037247
|
A | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1253+3229T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037247 | ||||||
chr12:95037259
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1253+3217G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037259 | ||||||
chr12:95037290
|
C | T | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1253+3186G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037290 | ||||||
chr12:95037316
|
C | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1253+3160G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037316 | ||||||
chr12:95037319
|
C | T | 48 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 53 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1253+3157G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037319 | ||||||
chr12:95037398
|
A | C | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1253+3078T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037398 | ||||||
chr12:95037539
|
T | C | 2 | a0001c0001t0001g0197a0001c0001t0001g0207 | 2 | NA18946.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1253+2937A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037539 | ||||||
chr12:95037712
|
G | A | 6 | a0001c0001t0001g0259a0001c0001t0001g0262a0001c0001t0001g0268others(3): Show | 6 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1253+2764C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037712 | ||||||
chr12:95037798
|
G | C | 27 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0090others(24): Show | 31 | HG00423.hp2 HG00544.hp2 HG02165.hp2 others(28): Show |
intron_variant | MODIFIER | c.1253+2678C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037798 | ||||||
chr12:95037819
|
C | T | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1253+2657G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037819 | ||||||
chr12:95037820
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0257a0001c0001t0001g0258 | 3 | HG03540.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1253+2656C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037820 | ||||||
chr12:95037882
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1253+2594C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037882 | ||||||
chr12:95037882
|
G | C | 2 | a0001c0001t0001g0325a0001c0001t0001g0327 | 2 | NA18954.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1253+2594C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037882 | ||||||
chr12:95037894
|
C | CA | 37 | a0001c0001t0001g0042a0001c0001t0001g0118a0001c0001t0001g0127others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1253+2581dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037894 | ||||||
chr12:95037894
|
CA | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(49): Show | 57 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1253+2581delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037894 | ||||||
chr12:95037963
|
T | C | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1253+2513A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95037963 | ||||||
chr12:95038132
|
T | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0188a0001c0001t0001g0191others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1253+2344A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95038132 | ||||||
chr12:95038134
|
G | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1253+2342C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95038134 | ||||||
chr12:95038181
|
A | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(35): Show | 43 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1253+2295T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95038181 | ||||||
chr12:95038469
|
A | T | 2 | a0001c0001t0002g0008a0003c0004t0002g0073 | 3 | HG01433.hp2 HG02735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1253+2007T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95038469 | ||||||
chr12:95038573
|
C | T | 18 | a0001c0001t0001g0358a0001c0001t0003g0378a0001c0001t0003g0379others(15): Show | 18 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1253+1903G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95038573 | ||||||
chr12:95038663
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1253+1813G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95038663 | ||||||
chr12:95038715
|
G | A | 3 | a0001c0001t0005g0164a0002c0002t0002g0013a0002c0002t0002g0157 | 4 | HG04184.hp2 NA18952.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1253+1761C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95038715 | ||||||
chr12:95038758
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1253+1718G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95038758 | ||||||
chr12:95038799
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1253+1677C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95038799 | ||||||
chr12:95038820
|
G | C | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1253+1656C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95038820 | ||||||
chr12:95038927
|
A | C | 2 | a0001c0001t0006g0362a0001c0001t0006g0365 | 2 | HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1253+1549T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95038927 | ||||||
chr12:95038932
|
T | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1253+1544A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95038932 | ||||||
chr12:95039001
|
A | C | 10 | a0001c0001t0003g0378a0001c0001t0003g0381a0001c0001t0003g0382others(7): Show | 10 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1253+1475T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039001 | ||||||
chr12:95039032
|
C | T | 1 | a0001c0001t0001g0338 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1253+1444G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039032 | ||||||
chr12:95039065
|
C | T | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1253+1411G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039065 | ||||||
chr12:95039081
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0150 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1253+1395T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039081 | ||||||
chr12:95039082
|
C | A | 18 | a0001c0001t0001g0358a0001c0001t0003g0378a0001c0001t0003g0379others(15): Show | 18 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1253+1394G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039082 | ||||||
chr12:95039083
|
C | A | 15 | a0001c0001t0003g0378a0001c0001t0003g0380a0001c0001t0003g0381others(12): Show | 15 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1253+1393G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039083 | ||||||
chr12:95039201
|
G | C | 1 | a0001c0001t0002g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1253+1275C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039201 | ||||||
chr12:95039265
|
A | C | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1253+1211T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039265 | ||||||
chr12:95039584
|
T | C | 7 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1253+892A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039584 | ||||||
chr12:95039617
|
C | T | 7 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1253+859G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039617 | ||||||
chr12:95039635
|
T | C | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1253+841A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039635 | ||||||
chr12:95039679
|
G | A | 6 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0119others(3): Show | 6 | HG00438.hp2 HG02129.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1253+797C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039679 | ||||||
chr12:95039947
|
T | G | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1253+529A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039947 | ||||||
chr12:95039981
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1253+495A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95039981 | ||||||
chr12:95040011
|
C | CT | 6 | a0001c0001t0001g0185a0001c0001t0002g0166a0001c0001t0002g0167others(3): Show | 6 | HG02572.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1253+464dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95040011 | ||||||
chr12:95040011
|
CT | C | 9 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0316others(6): Show | 9 | HG01257.hp1 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1253+464delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95040011 | ||||||
chr12:95040040
|
A | G | 15 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(12): Show | 18 | HG01243.hp1 HG02132.hp1 HG03139.hp1 others(15): Show |
intron_variant | MODIFIER | c.1253+436T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95040040 | ||||||
chr12:95040071
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1253+405G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95040071 | ||||||
chr12:95040111
|
G | A | 1 | a0001c0001t0020g0373 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1253+365C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95040111 | ||||||
chr12:95040119
|
A | C | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1253+357T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95040119 | ||||||
chr12:95040165
|
GTCTC | G | 88 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(85): Show | 96 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1253+307_1253+310d others(6): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95040165 | ||||||
chr12:95040208
|
A | ATGCTAGC others(1228): Show |
1 | a0001c0001t0001g0335 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1253+267_1253+268i others(1237): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95040208 | ||||||
chr12:95040291
|
T | G | 11 | a0001c0001t0003g0378a0001c0001t0003g0381a0001c0001t0003g0382others(8): Show | 11 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1253+185A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95040291 | ||||||
chr12:95040340
|
T | A | 115 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(112): Show | 121 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1253+136A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 10/13 | chr12 | 95040340 | ||||||
chr12:95040672
|
T | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0129a0001c0001t0001g0132 | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1132-75A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95040672 | ||||||
chr12:95040676
|
C | T | 32 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0061others(29): Show | 35 | HG00140.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1132-79G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95040676 | ||||||
chr12:95040677
|
G | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1132-80C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95040677 | ||||||
chr12:95040739
|
C | T | 2 | a0001c0001t0002g0093a0001c0001t0002g0096 | 2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1132-142G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95040739 | ||||||
chr12:95040799
|
C | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1132-202G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95040799 | ||||||
chr12:95041174
|
G | A | 3 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0276 | 3 | HG00423.hp2 NA18947.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1132-577C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95041174 | ||||||
chr12:95041294
|
C | T | 78 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 83 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1132-697G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95041294 | ||||||
chr12:95041312
|
C | T | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1132-715G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95041312 | ||||||
chr12:95041762
|
A | C | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1132-1165T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95041762 | ||||||
chr12:95041771
|
A | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1132-1174T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95041771 | ||||||
chr12:95041938
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1132-1341A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95041938 | ||||||
chr12:95042113
|
G | A | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1132-1516C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042113 | ||||||
chr12:95042219
|
C | CT | 31 | a0001c0001t0001g0018a0001c0001t0001g0054a0001c0001t0001g0055others(28): Show | 32 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.1132-1623dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042219 | ||||||
chr12:95042219
|
CT | C | 60 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(57): Show | 65 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1132-1623delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042219 | ||||||
chr12:95042371
|
C | T | 1 | a0001c0001t0002g0169 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1132-1774G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042371 | ||||||
chr12:95042427
|
C | G | 48 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 53 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1132-1830G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042427 | ||||||
chr12:95042456
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1132-1859C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042456 | ||||||
chr12:95042457
|
C | A | 1 | a0001c0001t0001g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1132-1860G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042457 | ||||||
chr12:95042545
|
C | G | 48 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 53 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1132-1948G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042545 | ||||||
chr12:95042560
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1132-1963C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042560 | ||||||
chr12:95042571
|
C | T | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1132-1974G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042571 | ||||||
chr12:95042776
|
C | T | 4 | a0001c0001t0007g0374a0001c0001t0007g0375a0001c0001t0007g0376others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1132-2179G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042776 | ||||||
chr12:95042901
|
G | A | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1132-2304C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042901 | ||||||
chr12:95042932
|
C | CA | 83 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(80): Show | 88 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1132-2336dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042932 | ||||||
chr12:95042932
|
C | CAA | 24 | a0001c0001t0001g0030a0001c0001t0001g0328a0001c0001t0001g0358others(21): Show | 25 | HG01070.hp1 HG01071.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.1132-2337_1132-233 others(6): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042932 | ||||||
chr12:95042975
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0150 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1132-2378T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95042975 | ||||||
chr12:95043034
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1132-2437C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043034 | ||||||
chr12:95043068
|
A | C | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132-2471T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043068 | ||||||
chr12:95043187
|
G | A | 87 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(84): Show | 95 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1132-2590C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043187 | ||||||
chr12:95043389
|
C | CA | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1132-2793dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043389 | ||||||
chr12:95043396
|
G | A | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132-2799C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043396 | ||||||
chr12:95043412
|
G | A | 3 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | NA18951.hp1 NA18985.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1132-2815C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043412 | ||||||
chr12:95043476
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1132-2879C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043476 | ||||||
chr12:95043555
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0207 | 2 | NA18946.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1132-2958C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043555 | ||||||
chr12:95043600
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1132-3003C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043600 | ||||||
chr12:95043603
|
C | T | 78 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 83 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1132-3006G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043603 | ||||||
chr12:95043617
|
C | G | 78 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 83 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1132-3020G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043617 | ||||||
chr12:95043654
|
T | C | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1132-3057A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043654 | ||||||
chr12:95043689
|
C | CA | 9 | a0001c0001t0001g0052a0001c0001t0001g0112a0001c0001t0001g0123others(6): Show | 9 | HG00741.hp2 HG01109.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.1132-3093dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAA | 8 | a0001c0001t0003g0381a0001c0001t0003g0382a0001c0001t0003g0383others(5): Show | 8 | HG00609.hp2 HG00738.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1132-3095_1132-309 others(7): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0007g0375 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1132-3102_1132-309 others(14): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0313 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1132-3104_1132-309 others(16): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(6): Show |
11 | a0001c0001t0001g0291a0001c0001t0001g0293a0001c0001t0001g0295others(8): Show | 11 | HG00639.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1132-3105_1132-309 others(17): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(7): Show |
13 | a0001c0001t0001g0019a0001c0001t0001g0292a0001c0001t0001g0299others(10): Show | 14 | HG01109.hp1 HG01169.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1132-3106_1132-309 others(18): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0316a0001c0001t0001g0319 | 2 | HG01257.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1132-3093_1132-309 others(19): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(9): Show |
5 | a0001c0001t0001g0294a0001c0001t0001g0300a0001c0001t0001g0301others(2): Show | 5 | HG00099.hp2 HG01258.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132-3093_1132-309 others(20): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(10): Show |
3 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0001g0360 | 3 | HG00140.hp1 HG02683.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1132-3093_1132-309 others(21): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0020a0001c0001t0001g0349 | 3 | HG02132.hp2 NA18959.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1132-3093_1132-309 others(22): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(12): Show |
18 | a0001c0001t0001g0006a0001c0001t0001g0271a0001c0001t0001g0321others(15): Show | 20 | HG00558.hp2 HG00621.hp1 NA18942.hp1 others(17): Show |
intron_variant | MODIFIER | c.1132-3093_1132-309 others(23): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(13): Show |
16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0217others(13): Show | 18 | HG00609.hp1 HG00673.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.1132-3093_1132-309 others(24): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(14): Show |
3 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0003g0391 | 3 | HG02015.hp2 HG02074.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1132-3093_1132-309 others(25): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(19): Show |
4 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1132-3093_1132-309 others(30): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(20): Show |
6 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0039others(3): Show | 6 | HG00323.hp1 HG01081.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.1132-3093_1132-309 others(31): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(21): Show |
2 | a0001c0001t0003g0380a0001c0001t0003g0393 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1132-3093_1132-309 others(32): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1132-3093_1132-309 others(33): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0038 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1132-3093_1132-309 others(36): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CCAAAAAA others(6): Show |
2 | a0001c0001t0006g0363a0001c0001t0016g0361 | 2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1132-3093_1132-309 others(17): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CCAAAAAA others(7): Show |
4 | a0001c0001t0006g0362a0001c0001t0006g0364a0001c0001t0006g0365others(1): Show | 4 | HG02630.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1132-3093_1132-309 others(18): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CCAAAAAA others(8): Show |
1 | a0001c0001t0010g0267 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1132-3093_1132-309 others(19): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
C | CCAAAAAA others(9): Show |
1 | a0001c0001t0010g0354 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1132-3093_1132-309 others(20): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043689
|
CA | C | 12 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0239others(9): Show | 12 | HG00099.hp1 HG01515.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1132-3093delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043689 | ||||||
chr12:95043711
|
C | G | 18 | a0001c0001t0001g0358a0001c0001t0003g0378a0001c0001t0003g0379others(15): Show | 18 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1132-3114G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043711 | ||||||
chr12:95043874
|
G | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1132-3277C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043874 | ||||||
chr12:95043948
|
A | G | 18 | a0001c0001t0001g0358a0001c0001t0003g0378a0001c0001t0003g0379others(15): Show | 18 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1132-3351T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043948 | ||||||
chr12:95043949
|
TA | T | 10 | a0001c0001t0004g0367a0001c0001t0004g0368a0001c0001t0004g0369others(7): Show | 10 | HG00099.hp1 HG00733.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1132-3353delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95043949 | ||||||
chr12:95044079
|
T | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1132-3482A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044079 | ||||||
chr12:95044162
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1132-3565A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044162 | ||||||
chr12:95044221
|
T | C | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1132-3624A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044221 | ||||||
chr12:95044226
|
C | T | 5 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132-3629G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044226 | ||||||
chr12:95044251
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1132-3654T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044251 | ||||||
chr12:95044263
|
G | A | 2 | a0001c0001t0002g0169a0004c0003t0002g0170 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1132-3666C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044263 | ||||||
chr12:95044434
|
A | AT | 9 | a0001c0001t0001g0132a0001c0001t0001g0220a0001c0001t0001g0294others(6): Show | 9 | HG01433.hp1 HG01884.hp1 HG04115.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132-3838dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044434 | ||||||
chr12:95044434
|
A | ATT | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1132-3839_1132-383 others(6): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044434 | ||||||
chr12:95044476
|
C | T | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1132-3879G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044476 | ||||||
chr12:95044504
|
C | G | 90 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(87): Show | 98 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1132-3907G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044504 | ||||||
chr12:95044615
|
T | C | 1 | a0001c0001t0002g0105 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1132-4018A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044615 | ||||||
chr12:95044650
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0207 | 2 | NA18946.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1132-4053G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044650 | ||||||
chr12:95044696
|
T | C | 3 | a0001c0001t0001g0320a0001c0001t0001g0322a0001c0001t0001g0323 | 3 | HG01169.hp1 HG01192.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1132-4099A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044696 | ||||||
chr12:95044932
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1131+4136C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044932 | ||||||
chr12:95044954
|
CT | C | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1131+4113delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95044954 | ||||||
chr12:95045002
|
G | C | 7 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0001g0124others(4): Show | 7 | HG01074.hp2 HG01168.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1131+4066C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95045002 | ||||||
chr12:95045009
|
G | C | 8 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0078others(5): Show | 8 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.1131+4059C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95045009 | ||||||
chr12:95045091
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1131+3977G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95045091 | ||||||
chr12:95045191
|
T | C | 2 | a0001c0001t0003g0382a0001c0001t0003g0390 | 2 | HG01175.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1131+3877A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95045191 | ||||||
chr12:95045275
|
A | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1131+3793T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95045275 | ||||||
chr12:95045302
|
C | G | 1 | a0001c0001t0003g0392 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1131+3766G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95045302 | ||||||
chr12:95045326
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1131+3742C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95045326 | ||||||
chr12:95045327
|
G | T | 1 | a0001c0001t0001g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1131+3741C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95045327 | ||||||
chr12:95045438
|
AAAAG | A | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131+3626_1131+362 others(8): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95045438 | ||||||
chr12:95045601
|
C | T | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1131+3467G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95045601 | ||||||
chr12:95045607
|
C | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1131+3461G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95045607 | ||||||
chr12:95045932
|
C | T | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1131+3136G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95045932 | ||||||
chr12:95046088
|
C | T | 7 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0080others(4): Show | 7 | HG00733.hp2 HG01192.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1131+2980G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046088 | ||||||
chr12:95046089
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0188a0001c0001t0001g0191others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1131+2979C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046089 | ||||||
chr12:95046165
|
G | T | 1 | a0001c0001t0001g0243 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1131+2903C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046165 | ||||||
chr12:95046166
|
C | G | 1 | a0001c0001t0001g0243 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1131+2902G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046166 | ||||||
chr12:95046169
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1131+2899A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046169 | ||||||
chr12:95046249
|
A | G | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1131+2819T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046249 | ||||||
chr12:95046437
|
A | C | 1 | a0001c0001t0005g0164 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1131+2631T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046437 | ||||||
chr12:95046463
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1131+2605G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046463 | ||||||
chr12:95046676
|
A | G | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1131+2392T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046676 | ||||||
chr12:95046859
|
T | G | 1 | a0001c0001t0001g0243 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1131+2209A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046859 | ||||||
chr12:95046860
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1131+2208C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046860 | ||||||
chr12:95046861
|
A | C | 1 | a0001c0001t0001g0243 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1131+2207T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046861 | ||||||
chr12:95046993
|
A | C | 7 | a0001c0001t0002g0011a0001c0001t0002g0069a0001c0001t0002g0144others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1131+2075T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95046993 | ||||||
chr12:95047014
|
A | C | 1 | a0001c0001t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1131+2054T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95047014 | ||||||
chr12:95047081
|
A | T | 1 | a0001c0001t0001g0243 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1131+1987T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95047081 | ||||||
chr12:95047366
|
G | C | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1131+1702C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95047366 | ||||||
chr12:95047385
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0188a0001c0001t0001g0191others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1131+1683T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95047385 | ||||||
chr12:95047482
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1131+1586G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95047482 | ||||||
chr12:95047554
|
C | T | 26 | a0001c0001t0001g0358a0001c0001t0003g0378a0001c0001t0003g0379others(23): Show | 26 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.1131+1514G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95047554 | ||||||
chr12:95047593
|
T | G | 1 | a0001c0005t0001g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1131+1475A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95047593 | ||||||
chr12:95047647
|
C | T | 9 | a0001c0001t0003g0378a0001c0001t0003g0381a0001c0001t0003g0382others(6): Show | 9 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1131+1421G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95047647 | ||||||
chr12:95047758
|
A | G | 26 | a0001c0001t0001g0358a0001c0001t0003g0378a0001c0001t0003g0379others(23): Show | 26 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.1131+1310T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95047758 | ||||||
chr12:95047842
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048 | 3 | NA19070.hp2 NA19077.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1131+1226A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95047842 | ||||||
chr12:95047923
|
G | C | 1 | a0001c0001t0002g0169 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1131+1145C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95047923 | ||||||
chr12:95048192
|
C | T | 17 | a0001c0001t0003g0378a0001c0001t0003g0379a0001c0001t0003g0380others(14): Show | 17 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1131+876G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048192 | ||||||
chr12:95048342
|
T | C | 11 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0001g0124others(8): Show | 11 | HG01074.hp2 HG01168.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1131+726A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048342 | ||||||
chr12:95048419
|
T | C | 10 | a0001c0001t0003g0378a0001c0001t0003g0381a0001c0001t0003g0382others(7): Show | 10 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1131+649A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048419 | ||||||
chr12:95048454
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1131+614T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048454 | ||||||
chr12:95048466
|
A | G | 56 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(53): Show | 61 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1131+602T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048466 | ||||||
chr12:95048494
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0002g0104a0001c0001t0002g0105others(1): Show | 4 | HG00423.hp2 HG04228.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.1131+574G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048494 | ||||||
chr12:95048507
|
T | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0236 | 2 | NA18966.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1131+561A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048507 | ||||||
chr12:95048557
|
T | C | 49 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(46): Show | 54 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1131+511A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048557 | ||||||
chr12:95048622
|
G | GC | 35 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(32): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1131+445_1131+446i others(3): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048622 | ||||||
chr12:95048622
|
G | GT | 79 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(76): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1131+445dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048622 | ||||||
chr12:95048622
|
G | GTT | 6 | a0001c0001t0001g0119a0001c0001t0001g0129a0001c0001t0007g0374others(3): Show | 6 | HG02129.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1131+444_1131+445d others(4): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048622 | ||||||
chr12:95048622
|
GT | G | 12 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0197others(9): Show | 12 | HG01074.hp2 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1131+445delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048622 | ||||||
chr12:95048623
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1131+445A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048623 | ||||||
chr12:95048627
|
T | G | 1 | a0001c0001t0002g0099 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1131+441A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048627 | ||||||
chr12:95048631
|
T | G | 1 | a0001c0001t0002g0274 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1131+437A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048631 | ||||||
chr12:95048669
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(52): Show | 64 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1131+399C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048669 | ||||||
chr12:95048772
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0188a0001c0001t0001g0191others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1131+296C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048772 | ||||||
chr12:95048859
|
G | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1131+209C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048859 | ||||||
chr12:95048948
|
C | T | 294 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(291): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1131+120G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95048948 | ||||||
chr12:95049003
|
T | A | 1 | a0001c0001t0001g0243 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1131+65A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95049003 | ||||||
chr12:95049039
|
T | G | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131+29A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 9/13 | chr12 | 95049039 | ||||||
chr12:95049258
|
G | C | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(7): Show | 10 | HG00323.hp1 HG01081.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.966-25C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95049258 | ||||||
chr12:95049399
|
T | C | 26 | a0001c0001t0001g0358a0001c0001t0003g0378a0001c0001t0003g0379others(23): Show | 26 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.966-166A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95049399 | ||||||
chr12:95049458
|
A | G | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.966-225T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95049458 | ||||||
chr12:95049646
|
G | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.966-413C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95049646 | ||||||
chr12:95049650
|
G | GAT | 4 | a0001c0001t0001g0196a0001c0001t0010g0267a0001c0001t0010g0354others(1): Show | 4 | HG02895.hp1 HG02976.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.966-419_966-418dup others(2): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95049650 | ||||||
chr12:95049650
|
G | GATAT | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.966-421_966-418dup others(4): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95049650 | ||||||
chr12:95049654
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.966-421A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95049654 | ||||||
chr12:95049713
|
A | G | 89 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(86): Show | 97 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.966-480T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95049713 | ||||||
chr12:95049756
|
C | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(52): Show | 64 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.966-523G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95049756 | ||||||
chr12:95049935
|
G | T | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.966-702C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95049935 | ||||||
chr12:95049942
|
T | C | 1 | a0001c0001t0003g0386 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.966-709A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95049942 | ||||||
chr12:95049947
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(52): Show | 64 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.966-714C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95049947 | ||||||
chr12:95050097
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.966-864C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95050097 | ||||||
chr12:95050311
|
T | C | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.966-1078A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95050311 | ||||||
chr12:95050312
|
G | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.966-1079C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95050312 | ||||||
chr12:95050317
|
G | A | 4 | a0001c0001t0007g0374a0001c0001t0007g0375a0001c0001t0007g0376others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.966-1084C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95050317 | ||||||
chr12:95050411
|
C | T | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.966-1178G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95050411 | ||||||
chr12:95050561
|
G | A | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.965+1201C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95050561 | ||||||
chr12:95050765
|
G | A | 4 | a0001c0001t0003g0380a0001c0001t0003g0389a0001c0001t0003g0392others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.965+997C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95050765 | ||||||
chr12:95050785
|
C | T | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.965+977G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95050785 | ||||||
chr12:95050868
|
G | A | 1 | a0001c0001t0003g0394 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.965+894C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95050868 | ||||||
chr12:95051130
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(52): Show | 64 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.965+632A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95051130 | ||||||
chr12:95051243
|
G | A | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.965+519C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95051243 | ||||||
chr12:95051272
|
T | A | 26 | a0001c0001t0001g0358a0001c0001t0003g0378a0001c0001t0003g0379others(23): Show | 26 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.965+490A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95051272 | ||||||
chr12:95051357
|
C | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | NA18979.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.965+405G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95051357 | ||||||
chr12:95051446
|
G | A | 26 | a0001c0001t0001g0358a0001c0001t0003g0378a0001c0001t0003g0379others(23): Show | 26 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.965+316C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95051446 | ||||||
chr12:95051635
|
G | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.965+127C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 8/13 | chr12 | 95051635 | ||||||
chr12:95051995
|
C | T | 1 | a0001c0001t0007g0376 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.784-52G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95051995 | ||||||
chr12:95052094
|
C | T | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-151G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052094 | ||||||
chr12:95052158
|
G | GT | 56 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(53): Show | 61 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.784-216dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052158 | ||||||
chr12:95052161
|
T | G | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.784-218A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052161 | ||||||
chr12:95052198
|
T | C | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-255A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052198 | ||||||
chr12:95052297
|
A | G | 1 | a0001c0001t0013g0032 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.784-354T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052297 | ||||||
chr12:95052353
|
AC | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-411delG | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052353 | ||||||
chr12:95052388
|
T | G | 6 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(3): Show | 6 | HG02257.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.784-445A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052388 | ||||||
chr12:95052433
|
C | T | 39 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(36): Show | 44 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.784-490G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052433 | ||||||
chr12:95052475
|
G | C | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.784-532C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052475 | ||||||
chr12:95052512
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(53): Show | 65 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.784-569T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052512 | ||||||
chr12:95052848
|
T | C | 79 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(76): Show | 84 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.784-905A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052848 | ||||||
chr12:95052929
|
C | A | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.784-986G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052929 | ||||||
chr12:95052985
|
T | C | 86 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(83): Show | 94 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.784-1042A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052985 | ||||||
chr12:95052990
|
CT | C | 12 | a0001c0001t0001g0349a0001c0001t0003g0378a0001c0001t0003g0381others(9): Show | 12 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.784-1048delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95052990 | ||||||
chr12:95053039
|
A | G | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.784-1096T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053039 | ||||||
chr12:95053107
|
C | A | 1 | a0001c0001t0002g0075 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.784-1164G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053107 | ||||||
chr12:95053119
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0134 | 2 | NA18961.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.784-1176C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053119 | ||||||
chr12:95053132
|
T | C | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-1189A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053132 | ||||||
chr12:95053212
|
G | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(36): Show | 44 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.784-1269C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053212 | ||||||
chr12:95053257
|
A | G | 1 | a0001c0001t0005g0062 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.784-1314T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053257 | ||||||
chr12:95053490
|
A | G | 2 | a0001c0001t0002g0074a0001c0001t0002g0075 | 2 | NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.784-1547T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053490 | ||||||
chr12:95053598
|
A | T | 1 | a0001c0001t0001g0287 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.784-1655T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053598 | ||||||
chr12:95053639
|
A | G | 1 | a0001c0001t0003g0389 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.784-1696T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053639 | ||||||
chr12:95053681
|
G | GT | 63 | a0001c0001t0001g0016a0001c0001t0001g0045a0001c0001t0001g0049others(60): Show | 64 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.784-1739dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053681 | ||||||
chr12:95053681
|
G | GTT | 6 | a0001c0001t0001g0341a0001c0001t0002g0029a0001c0001t0003g0391others(3): Show | 6 | HG02280.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.784-1740_784-1739d others(4): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053681 | ||||||
chr12:95053681
|
G | GTTT | 40 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(37): Show | 45 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.784-1741_784-1739d others(5): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053681 | ||||||
chr12:95053681
|
G | GTTTT | 9 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(6): Show | 9 | HG00609.hp1 HG02027.hp2 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.784-1742_784-1739d others(6): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053681 | ||||||
chr12:95053681
|
G | GTTTTTTT others(4): Show |
3 | a0001c0001t0006g0363a0001c0001t0006g0364a0001c0001t0006g0366 | 3 | HG02559.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.784-1749_784-1739d others(13): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053681 | ||||||
chr12:95053681
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0006g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.784-1750_784-1739d others(14): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053681 | ||||||
chr12:95053681
|
G | GTTTTTTT others(6): Show |
1 | a0001c0001t0006g0365 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.784-1751_784-1739d others(15): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053681 | ||||||
chr12:95053681
|
GT | G | 40 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0138others(37): Show | 41 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.784-1739delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053681 | ||||||
chr12:95053681
|
GTTTTTTT others(3): Show |
G | 3 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0019g0034 | 3 | HG01081.hp1 HG01099.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.784-1748_784-1739d others(12): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053681 | ||||||
chr12:95053714
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.784-1771A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053714 | ||||||
chr12:95053723
|
C | T | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-1780G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053723 | ||||||
chr12:95053752
|
C | T | 17 | a0001c0001t0003g0378a0001c0001t0003g0379a0001c0001t0003g0380others(14): Show | 17 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.784-1809G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053752 | ||||||
chr12:95053753
|
G | A | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-1810C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053753 | ||||||
chr12:95053772
|
C | T | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-1829G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053772 | ||||||
chr12:95053884
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.784-1941A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053884 | ||||||
chr12:95053898
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.784-1955G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053898 | ||||||
chr12:95053899
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.784-1956T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95053899 | ||||||
chr12:95054147
|
C | T | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.784-2204G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054147 | ||||||
chr12:95054300
|
C | CT | 38 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0060others(35): Show | 39 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.784-2358dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054300 | ||||||
chr12:95054300
|
CT | C | 6 | a0001c0001t0001g0067a0001c0001t0001g0199a0001c0001t0007g0374others(3): Show | 6 | HG01256.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.784-2358delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054300 | ||||||
chr12:95054453
|
T | G | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.784-2510A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054453 | ||||||
chr12:95054501
|
G | A | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.784-2558C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054501 | ||||||
chr12:95054613
|
T | C | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.784-2670A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054613 | ||||||
chr12:95054650
|
A | G | 1 | a0001c0001t0005g0164 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.784-2707T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054650 | ||||||
chr12:95054662
|
T | C | 1 | a0001c0001t0014g0238 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.784-2719A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054662 | ||||||
chr12:95054778
|
G | C | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.783+2775C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054778 | ||||||
chr12:95054848
|
GCAGATAA others(9): Show |
G | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.783+2689_783+2704d others(18): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054848 | ||||||
chr12:95054871
|
T | C | 2 | a0001c0001t0001g0304a0001c0001t0001g0306 | 2 | HG02258.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.783+2682A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054871 | ||||||
chr12:95054897
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0207 | 2 | NA18946.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.783+2656G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054897 | ||||||
chr12:95054901
|
A | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+2652T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054901 | ||||||
chr12:95054929
|
T | A | 1 | a0001c0001t0001g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.783+2624A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054929 | ||||||
chr12:95054943
|
G | A | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.783+2610C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054943 | ||||||
chr12:95054962
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.783+2591G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054962 | ||||||
chr12:95054974
|
C | T | 2 | a0001c0001t0003g0382a0001c0001t0003g0390 | 2 | HG01175.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.783+2579G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95054974 | ||||||
chr12:95055011
|
C | T | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+2542G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055011 | ||||||
chr12:95055027
|
C | A | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.783+2526G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055027 | ||||||
chr12:95055034
|
T | A | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 5 | HG00280.hp2 HG00639.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.783+2519A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055034 | ||||||
chr12:95055082
|
C | T | 3 | a0001c0001t0003g0379a0001c0001t0010g0267a0001c0001t0010g0354 | 3 | HG02976.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.783+2471G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055082 | ||||||
chr12:95055233
|
T | C | 1 | a0001c0001t0002g0160 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.783+2320A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055233 | ||||||
chr12:95055454
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.783+2099G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055454 | ||||||
chr12:95055458
|
A | AAGAT | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+2091_783+2094d others(6): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055458 | ||||||
chr12:95055501
|
C | G | 3 | a0001c0001t0005g0063a0001c0001t0005g0064a0001c0001t0005g0065 | 3 | HG00733.hp1 HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.783+2052G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055501 | ||||||
chr12:95055568
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.783+1985C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055568 | ||||||
chr12:95055675
|
C | T | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(7): Show | 10 | HG00323.hp1 HG01081.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.783+1878G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055675 | ||||||
chr12:95055729
|
G | A | 1 | a0001c0001t0003g0379 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.783+1824C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055729 | ||||||
chr12:95055746
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.783+1807C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055746 | ||||||
chr12:95055794
|
A | C | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(7): Show | 10 | HG00323.hp1 HG01081.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.783+1759T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055794 | ||||||
chr12:95055884
|
C | T | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.783+1669G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055884 | ||||||
chr12:95055902
|
G | A | 1 | a0001c0001t0014g0238 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.783+1651C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055902 | ||||||
chr12:95055952
|
C | CA | 84 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(81): Show | 95 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.783+1600dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055952 | ||||||
chr12:95055952
|
C | CAA | 84 | a0001c0001t0001g0044a0001c0001t0001g0113a0001c0001t0001g0114others(81): Show | 91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.783+1599_783+1600d others(4): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055952 | ||||||
chr12:95055952
|
C | CAAA | 22 | a0001c0001t0002g0009a0001c0001t0002g0069a0001c0001t0002g0080others(19): Show | 23 | HG00597.hp2 HG01192.hp2 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.783+1598_783+1600d others(5): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055952 | ||||||
chr12:95055952
|
CA | C | 43 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(40): Show | 48 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.783+1600delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95055952 | ||||||
chr12:95056256
|
G | A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+1297C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056256 | ||||||
chr12:95056308
|
T | G | 1 | a0001c0001t0002g0345 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.783+1245A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056308 | ||||||
chr12:95056686
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.783+867A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056686 | ||||||
chr12:95056688
|
C | G | 1 | a0001c0001t0001g0213 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.783+865G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056688 | ||||||
chr12:95056717
|
G | C | 1 | a0001c0005t0001g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.783+836C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056717 | ||||||
chr12:95056769
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.783+784A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056769 | ||||||
chr12:95056774
|
A | T | 1 | a0001c0001t0001g0351 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.783+779T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056774 | ||||||
chr12:95056875
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.783+678G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056875 | ||||||
chr12:95056934
|
C | T | 1 | a0002c0002t0002g0157 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.783+619G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056934 | ||||||
chr12:95056935
|
G | A | 4 | a0001c0001t0003g0380a0001c0001t0003g0389a0001c0001t0003g0392others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+618C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056935 | ||||||
chr12:95056958
|
C | CA | 21 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0053others(18): Show | 21 | HG00099.hp1 HG00733.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.783+594dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056958 | ||||||
chr12:95056958
|
CA | C | 46 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(43): Show | 51 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.783+594delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056958 | ||||||
chr12:95056974
|
A | AC | 5 | a0001c0001t0002g0086a0001c0001t0002g0143a0001c0001t0002g0160others(2): Show | 5 | HG01928.hp1 HG03516.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+578_783+579ins others(1): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056974 | ||||||
chr12:95056974
|
A | C | 84 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(81): Show | 92 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.783+579T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95056974 | ||||||
chr12:95057098
|
A | AT | 44 | a0001c0001t0001g0044a0001c0001t0001g0112a0001c0001t0001g0113others(41): Show | 44 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.783+454dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95057098 | ||||||
chr12:95057098
|
AT | A | 18 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0140others(15): Show | 18 | HG01175.hp2 HG01192.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.783+454delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95057098 | ||||||
chr12:95057098
|
ATT | A | 24 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0035others(21): Show | 24 | HG00323.hp1 HG00609.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.783+453_783+454del others(2): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95057098 | ||||||
chr12:95057098
|
ATTT | A | 37 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(34): Show | 42 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.783+452_783+454del others(3): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95057098 | ||||||
chr12:95057154
|
G | GA | 7 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+398dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95057154 | ||||||
chr12:95057208
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0240others(3): Show | 8 | NA18945.hp2 NA18956.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.783+345C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95057208 | ||||||
chr12:95057266
|
A | G | 4 | a0001c0001t0007g0374a0001c0001t0007g0375a0001c0001t0007g0376others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+287T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95057266 | ||||||
chr12:95057294
|
G | C | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.783+259C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95057294 | ||||||
chr12:95057356
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.783+197G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 7/13 | chr12 | 95057356 | ||||||
chr12:95057701
|
A | C | 1 | a0001c0001t0001g0332 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.692+30T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 6/13 | chr12 | 95057701 | ||||||
chr12:95058105
|
C | T | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.544+205G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 5/13 | chr12 | 95058105 | ||||||
chr12:95058112
|
G | A | 2 | a0001c0001t0007g0374a0001c0001t0007g0375 | 2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.544+198C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 5/13 | chr12 | 95058112 | ||||||
chr12:95058529
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.365-40T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95058529 | ||||||
chr12:95058535
|
G | C | 2 | a0001c0001t0002g0029a0001c0001t0002g0082 | 2 | HG02004.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.365-46C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95058535 | ||||||
chr12:95058567
|
T | G | 1 | a0001c0001t0001g0346 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.365-78A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95058567 | ||||||
chr12:95058722
|
C | T | 1 | a0001c0001t0003g0394 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.365-233G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95058722 | ||||||
chr12:95058752
|
C | G | 114 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(111): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.365-263G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95058752 | ||||||
chr12:95058773
|
C | T | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.365-284G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95058773 | ||||||
chr12:95059078
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(52): Show | 64 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.365-589C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059078 | ||||||
chr12:95059176
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.365-687G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059176 | ||||||
chr12:95059202
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0207 | 2 | NA18946.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.364+704G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059202 | ||||||
chr12:95059301
|
C | CA | 140 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(137): Show | 153 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.364+604dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059301 | ||||||
chr12:95059315
|
AT | A | 7 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.364+590delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059315 | ||||||
chr12:95059316
|
T | A | 1 | a0001c0001t0002g0101 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.364+590A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059316 | ||||||
chr12:95059330
|
G | C | 1 | a0001c0001t0001g0281 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.364+576C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059330 | ||||||
chr12:95059334
|
A | T | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.364+572T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059334 | ||||||
chr12:95059395
|
T | C | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG00597.hp1 HG00673.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.364+511A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059395 | ||||||
chr12:95059471
|
C | T | 17 | a0001c0001t0003g0378a0001c0001t0003g0379a0001c0001t0003g0380others(14): Show | 17 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.364+435G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059471 | ||||||
chr12:95059475
|
G | A | 15 | a0001c0001t0003g0378a0001c0001t0003g0380a0001c0001t0003g0381others(12): Show | 15 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.364+431C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059475 | ||||||
chr12:95059503
|
C | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(269): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.364+403G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059503 | ||||||
chr12:95059573
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0129a0001c0001t0001g0132 | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.364+333C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059573 | ||||||
chr12:95059588
|
T | A | 1 | a0001c0001t0001g0133 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.364+318A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059588 | ||||||
chr12:95059684
|
C | T | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.364+222G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059684 | ||||||
chr12:95059726
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.364+180C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059726 | ||||||
chr12:95059784
|
CTTT | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(35): Show | 43 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.364+119_364+121del others(3): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 4/13 | chr12 | 95059784 | ||||||
chr12:95059986
|
T | TA | 20 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0028others(17): Show | 22 | HG02300.hp2 HG02647.hp2 HG02895.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.286-3dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95059986 | ||||||
chr12:95059986
|
TA | T | 35 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0057others(32): Show | 35 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(32): Show |
splice_region_variant&intron_variant | LOW | c.286-3delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95059986 | ||||||
chr12:95059986
|
TAA | T | 45 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(42): Show | 50 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(47): Show |
splice_region_variant&intron_variant | LOW | c.286-4_286-3delTT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95059986 | ||||||
chr12:95060004
|
A | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0188a0001c0001t0001g0191others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.286-20T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95060004 | ||||||
chr12:95060010
|
A | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.286-26T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95060010 | ||||||
chr12:95060096
|
T | C | 1 | a0001c0001t0001g0350 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.286-112A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95060096 | ||||||
chr12:95060126
|
G | C | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.286-142C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95060126 | ||||||
chr12:95060275
|
C | T | 78 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 83 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.286-291G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95060275 | ||||||
chr12:95060345
|
T | C | 5 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-361A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95060345 | ||||||
chr12:95060474
|
T | C | 4 | a0001c0001t0001g0248a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02965.hp1 HG03540.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-490A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95060474 | ||||||
chr12:95060526
|
G | C | 18 | a0001c0001t0001g0358a0001c0001t0003g0378a0001c0001t0003g0379others(15): Show | 18 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.286-542C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95060526 | ||||||
chr12:95060886
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.286-902A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95060886 | ||||||
chr12:95060888
|
T | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0188a0001c0001t0001g0191others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.286-904A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95060888 | ||||||
chr12:95060952
|
T | A | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.286-968A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95060952 | ||||||
chr12:95061136
|
G | A | 1 | a0001c0001t0003g0388 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.286-1152C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061136 | ||||||
chr12:95061213
|
A | G | 10 | a0001c0001t0004g0367a0001c0001t0004g0368a0001c0001t0004g0369others(7): Show | 10 | HG00099.hp1 HG00733.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.286-1229T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061213 | ||||||
chr12:95061276
|
A | C | 1 | a0001c0001t0001g0206 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.285+1232T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061276 | ||||||
chr12:95061295
|
A | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048 | 3 | NA19070.hp2 NA19077.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.285+1213T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061295 | ||||||
chr12:95061383
|
C | T | 2 | a0001c0001t0003g0379a0001c0001t0003g0391 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.285+1125G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061383 | ||||||
chr12:95061385
|
G | C | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.285+1123C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061385 | ||||||
chr12:95061588
|
T | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0024others(22): Show | 27 | HG00741.hp2 HG01168.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.285+920A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061588 | ||||||
chr12:95061620
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG00639.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.285+888C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061620 | ||||||
chr12:95061648
|
T | A | 1 | a0001c0001t0001g0320 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.285+860A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061648 | ||||||
chr12:95061648
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.285+860A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061648 | ||||||
chr12:95061711
|
A | G | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+797T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061711 | ||||||
chr12:95061716
|
C | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(49): Show | 57 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.285+792G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061716 | ||||||
chr12:95061747
|
TC | T | 4 | a0001c0001t0003g0380a0001c0001t0003g0389a0001c0001t0003g0392others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+760delG | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061747 | ||||||
chr12:95061997
|
G | C | 2 | a0001c0001t0003g0379a0001c0001t0003g0391 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.285+511C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95061997 | ||||||
chr12:95062026
|
C | A | 2 | a0001c0001t0002g0102a0001c0001t0002g0108 | 2 | NA18962.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.285+482G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95062026 | ||||||
chr12:95062178
|
G | C | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.285+330C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95062178 | ||||||
chr12:95062210
|
C | T | 7 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(4): Show | 7 | HG00741.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+298G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95062210 | ||||||
chr12:95062240
|
G | A | 78 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 83 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.285+268C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95062240 | ||||||
chr12:95062413
|
A | C | 1 | a0001c0001t0003g0391 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.285+95T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95062413 | ||||||
chr12:95062458
|
A | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.285+50T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95062458 | ||||||
chr12:95062471
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.285+37T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 3/13 | chr12 | 95062471 | ||||||
chr12:95062771
|
T | G | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.55-33A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95062771 | ||||||
chr12:95062932
|
A | ACATT | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.55-198_55-195dupAA others(2): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95062932 | ||||||
chr12:95062971
|
C | T | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.55-233G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95062971 | ||||||
chr12:95062996
|
CAT | C | 10 | a0001c0001t0003g0378a0001c0001t0003g0381a0001c0001t0003g0382others(7): Show | 10 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-260_55-259delAT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95062996 | ||||||
chr12:95063072
|
T | A | 1 | a0001c0001t0003g0392 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.55-334A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95063072 | ||||||
chr12:95063516
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(151): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.55-778A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95063516 | ||||||
chr12:95063582
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.55-844A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95063582 | ||||||
chr12:95063639
|
G | A | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-901C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95063639 | ||||||
chr12:95063674
|
C | CA | 99 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(96): Show | 105 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.55-937dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95063674 | ||||||
chr12:95063674
|
C | CAA | 13 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(10): Show | 13 | HG00323.hp1 HG01081.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.55-938_55-937dupTT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95063674 | ||||||
chr12:95063758
|
A | G | 33 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0061others(30): Show | 36 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-1020T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95063758 | ||||||
chr12:95063848
|
G | A | 1 | a0001c0001t0007g0376 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.55-1110C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95063848 | ||||||
chr12:95063855
|
C | T | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-1117G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95063855 | ||||||
chr12:95063871
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.55-1133T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95063871 | ||||||
chr12:95063897
|
C | T | 6 | a0001c0001t0004g0367a0001c0001t0004g0368a0001c0001t0004g0369others(3): Show | 6 | HG00099.hp1 HG01106.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-1159G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95063897 | ||||||
chr12:95063955
|
G | A | 88 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(85): Show | 96 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.55-1217C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95063955 | ||||||
chr12:95064007
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.55-1269G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064007 | ||||||
chr12:95064025
|
C | CA | 103 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(100): Show | 111 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.55-1288dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064025 | ||||||
chr12:95064025
|
C | CAA | 10 | a0001c0001t0001g0266a0001c0001t0002g0083a0001c0001t0002g0085others(7): Show | 10 | HG00280.hp1 HG01175.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-1289_55-1288dup others(2): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064025 | ||||||
chr12:95064025
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0007g0374a0001c0001t0007g0375a0001c0001t0007g0376others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-1297_55-1288del others(10): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064025 | ||||||
chr12:95064143
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.55-1405G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064143 | ||||||
chr12:95064328
|
CA | C | 91 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0199others(88): Show | 99 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.55-1591delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064328 | ||||||
chr12:95064328
|
CAA | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(160): Show | 178 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.55-1592_55-1591del others(2): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064328 | ||||||
chr12:95064328
|
CAAA | C | 11 | a0001c0001t0001g0325a0001c0001t0004g0367a0001c0001t0004g0368others(8): Show | 11 | HG00099.hp1 HG00733.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.55-1593_55-1591del others(3): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064328 | ||||||
chr12:95064386
|
T | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(35): Show | 43 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.55-1648A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064386 | ||||||
chr12:95064652
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.55-1914C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064652 | ||||||
chr12:95064819
|
C | T | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-2081G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064819 | ||||||
chr12:95064940
|
G | A | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-2202C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064940 | ||||||
chr12:95064946
|
A | G | 17 | a0001c0001t0003g0378a0001c0001t0003g0379a0001c0001t0003g0380others(14): Show | 17 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.55-2208T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95064946 | ||||||
chr12:95065065
|
T | C | 3 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0276 | 3 | HG00423.hp2 NA18947.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.54+2266A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95065065 | ||||||
chr12:95065458
|
A | G | 1 | a0001c0001t0003g0379 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.54+1873T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95065458 | ||||||
chr12:95065610
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.54+1721G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95065610 | ||||||
chr12:95065726
|
C | T | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+1605G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95065726 | ||||||
chr12:95065818
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.54+1513G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95065818 | ||||||
chr12:95065871
|
A | T | 1 | a0001c0001t0001g0183 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.54+1460T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95065871 | ||||||
chr12:95065894
|
G | A | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+1437C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95065894 | ||||||
chr12:95065949
|
C | CA | 58 | a0001c0001t0001g0045a0001c0001t0001g0257a0001c0001t0001g0258others(55): Show | 62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.54+1381dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95065949 | ||||||
chr12:95065949
|
CA | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(60): Show | 73 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.54+1381delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95065949 | ||||||
chr12:95065980
|
T | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0262 | 2 | NA18978.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.54+1351A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95065980 | ||||||
chr12:95066032
|
T | G | 1 | a0001c0001t0011g0023 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.54+1299A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066032 | ||||||
chr12:95066141
|
A | G | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+1190T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066141 | ||||||
chr12:95066149
|
T | C | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+1182A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066149 | ||||||
chr12:95066181
|
T | C | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+1150A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066181 | ||||||
chr12:95066195
|
G | A | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | HG00140.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.54+1136C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066195 | ||||||
chr12:95066248
|
T | C | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+1083A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066248 | ||||||
chr12:95066364
|
A | G | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.54+967T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066364 | ||||||
chr12:95066399
|
G | A | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+932C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066399 | ||||||
chr12:95066442
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.54+889T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066442 | ||||||
chr12:95066538
|
C | G | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.54+793G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066538 | ||||||
chr12:95066748
|
A | C | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+583T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066748 | ||||||
chr12:95066748
|
A | G | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+583T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066748 | ||||||
chr12:95066822
|
A | G | 9 | a0001c0001t0003g0378a0001c0001t0003g0381a0001c0001t0003g0382others(6): Show | 9 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.54+509T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95066822 | ||||||
chr12:95067004
|
A | G | 76 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(73): Show | 81 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.54+327T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95067004 | ||||||
chr12:95067006
|
G | C | 76 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(73): Show | 81 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.54+325C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95067006 | ||||||
chr12:95067076
|
T | TTTCC | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+251_54+254dupGG others(2): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95067076 | ||||||
chr12:95067173
|
T | C | 1 | a0001c0001t0003g0381 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.54+158A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 2/13 | chr12 | 95067173 | ||||||
chr12:95067444
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-7-53T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067444 | ||||||
chr12:95067466
|
TATG | T | 3 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | NA18951.hp1 NA18985.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-7-78_-7-76delCAT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067466 | ||||||
chr12:95067557
|
T | C | 2 | a0001c0001t0003g0379a0001c0001t0003g0391 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-7-166A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067557 | ||||||
chr12:95067575
|
A | AT | 8 | a0001c0001t0001g0191a0001c0001t0004g0367a0001c0001t0004g0368others(5): Show | 8 | HG00099.hp1 HG01106.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-185dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067575 | ||||||
chr12:95067575
|
AT | A | 8 | a0001c0001t0001g0060a0001c0001t0001g0136a0001c0001t0001g0137others(5): Show | 8 | HG00140.hp2 HG01069.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-185delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067575 | ||||||
chr12:95067580
|
T | A | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-189A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067580 | ||||||
chr12:95067581
|
T | A | 89 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(86): Show | 95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-7-190A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067581 | ||||||
chr12:95067582
|
T | A | 10 | a0001c0001t0001g0289a0001c0001t0002g0176a0001c0001t0003g0379others(7): Show | 10 | HG02280.hp2 HG02293.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-191A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067582 | ||||||
chr12:95067589
|
T | A | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-198A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067589 | ||||||
chr12:95067878
|
C | CT | 59 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(56): Show | 68 | HG00438.hp2 HG00735.hp2 HG01074.hp2 others(65): Show |
intron_variant | MODIFIER | c.-7-488dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067878 | ||||||
chr12:95067878
|
CT | C | 99 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(96): Show | 107 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-7-488delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067878 | ||||||
chr12:95067981
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-7-590A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067981 | ||||||
chr12:95067983
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-7-592G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067983 | ||||||
chr12:95067996
|
T | C | 4 | a0001c0001t0007g0374a0001c0001t0007g0375a0001c0001t0007g0376others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-605A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95067996 | ||||||
chr12:95068434
|
C | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-7-1043G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95068434 | ||||||
chr12:95068547
|
C | T | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-1156G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95068547 | ||||||
chr12:95068742
|
C | T | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-1351G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95068742 | ||||||
chr12:95068794
|
C | T | 55 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(52): Show | 60 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.-7-1403G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95068794 | ||||||
chr12:95068796
|
TA | T | 14 | a0001c0001t0001g0028a0001c0001t0001g0054a0001c0001t0001g0055others(11): Show | 14 | HG02257.hp1 HG02647.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-1406delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95068796 | ||||||
chr12:95068832
|
G | A | 2 | a0001c0001t0003g0382a0001c0001t0003g0390 | 2 | HG01175.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-7-1441C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95068832 | ||||||
chr12:95068850
|
C | T | 2 | a0001c0001t0006g0362a0001c0001t0006g0365 | 2 | HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-7-1459G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95068850 | ||||||
chr12:95068877
|
C | A | 1 | a0001c0001t0001g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-7-1486G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95068877 | ||||||
chr12:95068917
|
C | T | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-7-1526G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95068917 | ||||||
chr12:95069217
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-7-1826G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95069217 | ||||||
chr12:95069341
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-7-1950T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95069341 | ||||||
chr12:95069365
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-7-1974C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95069365 | ||||||
chr12:95069762
|
C | CCATCCAT others(25): Show |
1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-7-2403_-7-2372dup others(32): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95069762 | ||||||
chr12:95069804
|
A | G | 4 | a0001c0001t0003g0378a0001c0001t0003g0381a0001c0001t0003g0382others(1): Show | 4 | HG01175.hp2 HG01255.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-2413T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95069804 | ||||||
chr12:95069852
|
T | A | 10 | a0001c0001t0004g0367a0001c0001t0004g0368a0001c0001t0004g0369others(7): Show | 10 | HG00099.hp1 HG00733.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-2461A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95069852 | ||||||
chr12:95069852
|
T | TA | 15 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(12): Show | 15 | HG00323.hp1 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7-2462dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95069852 | ||||||
chr12:95069937
|
T | C | 4 | a0001c0001t0007g0374a0001c0001t0007g0375a0001c0001t0007g0376others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-2546A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95069937 | ||||||
chr12:95069963
|
T | C | 17 | a0001c0001t0003g0378a0001c0001t0003g0379a0001c0001t0003g0380others(14): Show | 17 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.-7-2572A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95069963 | ||||||
chr12:95070013
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-7-2622G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070013 | ||||||
chr12:95070121
|
TTTTTTTG | T | 26 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(23): Show | 26 | HG00323.hp1 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-7-2737_-7-2731del others(7): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070121 | ||||||
chr12:95070182
|
AGTGCAGT others(1): Show |
A | 17 | a0001c0001t0003g0378a0001c0001t0003g0379a0001c0001t0003g0380others(14): Show | 17 | HG00609.hp2 HG00738.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.-7-2799_-7-2792del others(8): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070182 | ||||||
chr12:95070206
|
A | T | 2 | a0001c0001t0003g0379a0001c0001t0003g0391 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-7-2815T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070206 | ||||||
chr12:95070257
|
G | A | 1 | a0001c0001t0005g0164 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-7-2866C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070257 | ||||||
chr12:95070259
|
G | C | 1 | a0001c0001t0001g0352 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-7-2868C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070259 | ||||||
chr12:95070294
|
G | A | 1 | a0001c0001t0003g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-7-2903C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070294 | ||||||
chr12:95070346
|
G | A | 3 | a0001c0001t0005g0063a0001c0001t0005g0064a0001c0001t0005g0065 | 3 | HG00733.hp1 HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-7-2955C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070346 | ||||||
chr12:95070368
|
G | A | 1 | a0001c0001t0003g0388 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-7-2977C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070368 | ||||||
chr12:95070534
|
T | C | 7 | a0001c0001t0001g0019a0001c0001t0001g0308a0001c0001t0001g0309others(4): Show | 8 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+2846A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070534 | ||||||
chr12:95070660
|
G | T | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+2720C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070660 | ||||||
chr12:95070793
|
T | G | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+2587A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070793 | ||||||
chr12:95070841
|
C | T | 3 | a0001c0001t0001g0325a0001c0001t0001g0327a0001c0001t0015g0326 | 3 | NA18954.hp2 NA19056.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-8+2539G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070841 | ||||||
chr12:95070879
|
C | T | 1 | a0001c0001t0003g0394 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-8+2501G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070879 | ||||||
chr12:95070927
|
C | T | 36 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-8+2453G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070927 | ||||||
chr12:95070930
|
T | C | 4 | a0001c0001t0003g0380a0001c0001t0003g0389a0001c0001t0003g0392others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+2450A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070930 | ||||||
chr12:95070937
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+2443G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070937 | ||||||
chr12:95070970
|
C | G | 4 | a0001c0001t0007g0374a0001c0001t0007g0375a0001c0001t0007g0376others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+2410G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95070970 | ||||||
chr12:95071201
|
C | CA | 18 | a0001c0001t0001g0052a0001c0001t0001g0172a0001c0001t0001g0173others(15): Show | 18 | HG02293.hp1 HG02572.hp1 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8+2178dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95071201 | ||||||
chr12:95071201
|
CA | C | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0183others(18): Show | 21 | HG00609.hp2 HG00738.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8+2178delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95071201 | ||||||
chr12:95071201
|
CAA | C | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+2177_-8+2178del others(2): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95071201 | ||||||
chr12:95071219
|
A | T | 10 | a0001c0001t0004g0367a0001c0001t0004g0368a0001c0001t0004g0369others(7): Show | 10 | HG00099.hp1 HG00733.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+2161T>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95071219 | ||||||
chr12:95071397
|
G | A | 2 | a0001c0001t0010g0267a0001c0001t0010g0354 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-8+1983C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95071397 | ||||||
chr12:95071476
|
C | T | 10 | a0001c0001t0004g0367a0001c0001t0004g0368a0001c0001t0004g0369others(7): Show | 10 | HG00099.hp1 HG00733.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+1904G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95071476 | ||||||
chr12:95071562
|
G | A | 1 | a0001c0001t0002g0285 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8+1818C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95071562 | ||||||
chr12:95071691
|
T | A | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+1689A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95071691 | ||||||
chr12:95071749
|
C | CT | 10 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(7): Show | 10 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+1630dupA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95071749 | ||||||
chr12:95071818
|
A | G | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-8+1562T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95071818 | ||||||
chr12:95071920
|
G | T | 1 | a0001c0001t0001g0286 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-8+1460C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95071920 | ||||||
chr12:95071976
|
G | C | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+1404C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95071976 | ||||||
chr12:95072139
|
C | G | 1 | a0001c0001t0002g0061 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8+1241G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072139 | ||||||
chr12:95072229
|
C | T | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 5 | HG00280.hp2 HG00639.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+1151G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072229 | ||||||
chr12:95072234
|
C | A | 2 | a0001c0001t0001g0269a0001c0001t0001g0290 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-8+1146G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072234 | ||||||
chr12:95072279
|
C | A | 1 | a0001c0001t0016g0361 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-8+1101G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072279 | ||||||
chr12:95072285
|
C | A | 2 | a0001c0001t0003g0379a0001c0001t0003g0391 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-8+1095G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072285 | ||||||
chr12:95072291
|
C | A | 2 | a0001c0001t0003g0379a0001c0001t0003g0391 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-8+1089G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072291 | ||||||
chr12:95072294
|
A | AC | 3 | a0001c0001t0007g0374a0001c0001t0007g0375a0001c0001t0007g0376 | 3 | HG02717.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-8+1085_-8+1086ins others(1): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072294 | ||||||
chr12:95072295
|
A | AC | 48 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 53 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.-8+1084_-8+1085ins others(1): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072295 | ||||||
chr12:95072296
|
AC | A | 38 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0291others(35): Show | 39 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-8+1083delG | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072296 | ||||||
chr12:95072297
|
C | A | 73 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(70): Show | 78 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.-8+1083G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072297 | ||||||
chr12:95072416
|
G | A | 1 | a0001c0001t0002g0177 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-8+964C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072416 | ||||||
chr12:95072434
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(151): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-8+946T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072434 | ||||||
chr12:95072435
|
G | A | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-8+945C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072435 | ||||||
chr12:95072455
|
C | CA | 66 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0024others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-8+924dupT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072455 | ||||||
chr12:95072455
|
C | CAA | 12 | a0001c0001t0001g0026a0001c0001t0001g0316a0001c0001t0001g0317others(9): Show | 12 | HG01169.hp1 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8+923_-8+924dupTT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072455 | ||||||
chr12:95072455
|
C | CAAA | 13 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(10): Show | 13 | HG00323.hp1 HG00558.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+922_-8+924dupTT others(1): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072455 | ||||||
chr12:95072455
|
C | CAAAA | 34 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(31): Show | 39 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.-8+921_-8+924dupTT others(2): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072455 | ||||||
chr12:95072455
|
CA | C | 8 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(5): Show | 8 | HG02647.hp2 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8+924delT | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072455 | ||||||
chr12:95072469
|
A | G | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG00597.hp1 HG00673.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+911T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072469 | ||||||
chr12:95072470
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-8+910T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072470 | ||||||
chr12:95072471
|
A | AG | 3 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364 | 3 | HG02559.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-8+908_-8+909insC | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072471 | ||||||
chr12:95072471
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG00438.hp1 NA18960.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+909T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072471 | ||||||
chr12:95072475
|
G | A | 2 | a0001c0001t0001g0358a0001c0001t0010g0354 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-8+905C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072475 | ||||||
chr12:95072597
|
G | C | 1 | a0001c0001t0001g0355 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-8+783C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072597 | ||||||
chr12:95072644
|
G | C | 1 | a0001c0001t0001g0356 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-8+736C>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072644 | ||||||
chr12:95072646
|
T | C | 1 | a0001c0001t0001g0357 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-8+734A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072646 | ||||||
chr12:95072647
|
T | C | 1 | a0001c0001t0003g0392 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-8+733A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072647 | ||||||
chr12:95072757
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-8+623C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072757 | ||||||
chr12:95072802
|
G | GCCCAGCC others(46): Show |
1 | a0001c0001t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8+577_-8+578insTG others(51): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072802 | ||||||
chr12:95072804
|
C | G | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8+576G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072804 | ||||||
chr12:95072824
|
T | C | 1 | a0001c0001t0001g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+556A>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072824 | ||||||
chr12:95072841
|
A | C | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8+539T>G | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072841 | ||||||
chr12:95072871
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8+509A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072871 | ||||||
chr12:95072882
|
T | G | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8+498A>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072882 | ||||||
chr12:95072885
|
AAGCACGG others(7): Show |
A | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8+481_-8+494delCT others(12): Show |
NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072885 | ||||||
chr12:95072911
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A | G | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8+469T>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072911 | ||||||
chr12:95072934
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C | G | 1 | a0001c0001t0003g0393 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-8+446G>C | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072934 | ||||||
chr12:95072972
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G | A | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+408C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072972 | ||||||
chr12:95072996
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C | A | 1 | a0001c0001t0003g0393 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-8+384G>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95072996 | ||||||
chr12:95073023
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G | A | 1 | a0001c0001t0003g0394 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-8+357C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95073023 | ||||||
chr12:95073081
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G | A | 1 | a0001c0001t0001g0359 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-8+299C>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95073081 | ||||||
chr12:95073122
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C | T | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(8): Show | 11 | HG00323.hp1 HG01081.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+258G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95073122 | ||||||
chr12:95073126
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G | T | 1 | a0001c0001t0001g0028 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-8+254C>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95073126 | ||||||
chr12:95073139
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T | A | 1 | a0001c0001t0001g0360 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-8+241A>T | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95073139 | ||||||
chr12:95073160
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C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+220G>A | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95073160 | ||||||
chr12:95073328
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CT | C | 6 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+51delA | NR2C1 | ENSG00000120798.17 | transcript | ENST00000333003.10 | protein_coding | 1/13 | chr12 | 95073328 |