geneid | 2908 |
---|---|
ensemblid | ENSG00000113580.15 |
hgncid | 7978 |
symbol | NR3C1 |
name | nuclear receptor subfamily 3 group C member 1 |
refseq_nuc | NM_000176.3 |
refseq_prot | NP_000167.1 |
ensembl_nuc | ENST00000394464.7 |
ensembl_prot | ENSP00000377977.2 |
mane_status | MANE Select |
chr | chr5 |
start | 143277934 |
end | 143403686 |
strand | - |
ver | v1.2 |
region | chr5:143277934-143403686 |
region5000 | chr5:143272934-143408686 |
regionname0 | NR3C1_chr5_143277934_143403686 |
regionname5000 | NR3C1_chr5_143272934_143408686 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 777 | 261 | 83 | 44 | 94 | 15 | 23 | 68 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0002 | 0/0 | 777 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0003 | 0/0 | 777 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0004 | 0/0 | 777 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2334 | 207 | 60 | 38 | 71 | 13 | 23 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
c0002 | 0/0 | 2334 | 16 | 0 | 0 | 16 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
c0003 | 0/0 | 2334 | 13 | 13 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
c0004 | 0/0 | 2334 | 12 | 4 | 6 | 0 | 2 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
c0005 | 0/0 | 2334 | 7 | 0 | 0 | 7 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
c0006 | 0/0 | 2334 | 6 | 6 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
c0007 | 0/0 | 2334 | 3 | 3 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
c0008 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
c0009 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4446 | 107 | 35 | 17 | 41 | 5 | 9 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0002 | 0/1 | 4447 | 41 | 1 | 7 | 23 | 4 | 5 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0003 | 0/0 | 4449 | 19 | 2 | 9 | 0 | 3 | 5 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0004 | 0/0 | 4446 | 14 | 4 | 5 | 4 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0005 | 0/0 | 4448 | 13 | 10 | 2 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0006 | 0/0 | 4447 | 12 | 3 | 0 | 9 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0007 | 0/0 | 4447 | 11 | 11 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0008 | 0/0 | 4447 | 9 | 9 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0009 | 0/0 | 4451 | 7 | 0 | 0 | 7 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0010 | 0/0 | 4447 | 5 | 0 | 2 | 1 | 0 | 2 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0011 | 0/0 | 4446 | 2 | 2 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0012 | 0/0 | 4446 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0013 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0014 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0015 | 1/0 | 4445 | 1 | 0 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0016 | 0/0 | 4448 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0017 | 0/0 | 4447 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0018 | 0/0 | 4447 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0019 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0020 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0021 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0022 | 0/0 | 4449 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0023 | 0/0 | 4448 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0024 | 0/0 | 4447 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0025 | 0/0 | 4447 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0026 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0027 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0028 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0029 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0030 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0031 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0032 | 0/0 | 4445 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0033 | 0/0 | 4445 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0034 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0035 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0036 | 0/0 | 4447 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
t0037 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0002 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0016 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2334 | 207 | 60 | 38 | 71 | 13 | 23 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0002 | 0/0 | 2334 | 16 | 0 | 0 | 16 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0003 | 0/0 | 2334 | 13 | 13 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0004 | 0/0 | 2334 | 12 | 4 | 6 | 0 | 2 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0005 | 0/0 | 2334 | 7 | 0 | 0 | 7 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0006 | 0/0 | 2334 | 6 | 6 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0002c0007 | 0/0 | 2334 | 3 | 3 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0003c0008 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0004c0009 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6779 | 99 | 29 | 17 | 41 | 4 | 8 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0002 | 0/1 | 6780 | 41 | 1 | 7 | 23 | 4 | 5 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0003 | 0/0 | 6782 | 18 | 2 | 9 | 0 | 2 | 5 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0004 | 0/0 | 6779 | 2 | 1 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0005 | 0/0 | 6781 | 12 | 9 | 2 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0007 | 0/0 | 6780 | 11 | 11 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0010 | 0/0 | 6780 | 5 | 0 | 2 | 1 | 0 | 2 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0012 | 0/0 | 6779 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0013 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0014 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0015 | 1/0 | 6778 | 1 | 0 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0020 | 0/0 | 6779 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0021 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0022 | 0/0 | 6782 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0023 | 0/0 | 6781 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0024 | 0/0 | 6780 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0025 | 0/0 | 6780 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0026 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0028 | 0/0 | 6779 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0029 | 0/0 | 6779 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0030 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0031 | 0/0 | 6779 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0032 | 0/0 | 6778 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0035 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0036 | 0/0 | 6780 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0001t0037 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0002t0004 | 0/0 | 6779 | 3 | 0 | 0 | 3 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0002t0006 | 0/0 | 6780 | 9 | 0 | 0 | 9 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0002t0016 | 0/0 | 6781 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0002t0017 | 0/0 | 6780 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0002t0018 | 0/0 | 6780 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0002t0019 | 0/0 | 6779 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0003t0004 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0003t0006 | 0/0 | 6780 | 3 | 3 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0003t0008 | 0/0 | 6780 | 9 | 9 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0004t0001 | 0/0 | 6779 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0004t0004 | 0/0 | 6779 | 8 | 2 | 5 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0004t0005 | 0/0 | 6781 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0004t0027 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0004t0033 | 0/0 | 6778 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0005t0009 | 0/0 | 6784 | 7 | 0 | 0 | 7 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0001c0006t0001 | 0/0 | 6779 | 6 | 6 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0002c0007t0011 | 0/0 | 6779 | 2 | 2 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0002c0007t0034 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0003c0008t0003 | 0/0 | 6782 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
a0004c0009t0001 | 0/0 | 6779 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | copy fasta | chr5 | 143272934 | 143408686 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0007g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0010g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0010g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0010g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0010g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0010g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0012g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0014g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0015g0016 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0020g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0021g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0022g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0023g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0024g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0025g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0026g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0028g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0029g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0030g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0031g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0032g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0035g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0036g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0001t0037g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0016g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0017g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0018g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0002t0019g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0003t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0004t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0004t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0004t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0004t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0004t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0004t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0004t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0004t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0004t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0004t0027g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0004t0033g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0005t0009g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0005t0009g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0005t0009g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0005t0009g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0005t0009g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0005t0009g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0006t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0006t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0006t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0006t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0001c0006t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0002c0007t0011g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0002c0007t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0002c0007t0034g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0003c0008t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
a0004c0009t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0022 | g0186 | EUR | GBR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | GBR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0187 | EUR | GBR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00280 | hp1 | a0001 | c0004 | t0004 | g0052 | EUR | FIN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00323 | hp1 | a0001 | c0001 | t0005 | g0063 | EUR | FIN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00323 | hp2 | a0003 | c0008 | t0003 | g0179 | EUR | FIN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00408 | hp1 | a0001 | c0001 | t0031 | g0128 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00438 | hp1 | a0001 | c0002 | t0006 | g0037 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00544 | hp2 | a0001 | c0001 | t0029 | g0124 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00639 | hp1 | a0001 | c0001 | t0010 | g0095 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00733 | hp2 | a0001 | c0004 | t0004 | g0057 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00738 | hp1 | a0001 | c0004 | t0004 | g0053 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01070 | hp2 | a0001 | c0004 | t0004 | g0056 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0222 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01256 | hp2 | a0001 | c0004 | t0033 | g0051 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01346 | hp2 | a0001 | c0001 | t0010 | g0061 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0201 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01515 | hp2 | a0001 | c0001 | t0023 | g0208 | EUR | IBS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0219 | EUR | IBS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01516 | hp2 | a0001 | c0004 | t0001 | g0137 | EUR | IBS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0217 | EUR | IBS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01884 | hp1 | a0002 | c0007 | t0011 | g0255 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01884 | hp2 | a0001 | c0004 | t0004 | g0059 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01934 | hp1 | a0001 | c0001 | t0024 | g0206 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG01978 | hp2 | a0001 | c0004 | t0004 | g0050 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02027 | hp1 | a0001 | c0005 | t0009 | g0251 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02055 | hp1 | a0001 | c0003 | t0008 | g0043 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02074 | hp2 | a0001 | c0005 | t0009 | g0249 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02132 | hp2 | a0001 | c0002 | t0006 | g0036 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02135 | hp1 | a0001 | c0005 | t0009 | g0250 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02148 | hp2 | a0001 | c0004 | t0004 | g0055 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02165 | hp1 | a0001 | c0002 | t0004 | g0167 | EAS | CDX | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02258 | hp2 | a0001 | c0003 | t0006 | g0023 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02572 | hp2 | a0001 | c0006 | t0001 | g0102 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02647 | hp2 | a0001 | c0006 | t0001 | g0103 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0253 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02698 | hp2 | a0001 | c0001 | t0010 | g0070 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02717 | hp1 | a0001 | c0006 | t0001 | g0099 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0198 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0211 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02809 | hp1 | a0002 | c0007 | t0034 | g0256 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02886 | hp1 | a0001 | c0003 | t0008 | g0026 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02886 | hp2 | a0001 | c0001 | t0026 | g0115 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02895 | hp2 | a0001 | c0003 | t0008 | g0025 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02896 | hp1 | a0001 | c0003 | t0008 | g0045 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02922 | hp1 | a0001 | c0001 | t0035 | g0117 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0010 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02965 | hp1 | a0001 | c0006 | t0001 | g0101 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02970 | hp2 | a0001 | c0003 | t0008 | g0027 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03139 | hp1 | a0001 | c0003 | t0008 | g0044 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03209 | hp2 | a0001 | c0001 | t0014 | g0019 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03453 | hp1 | a0002 | c0007 | t0011 | g0254 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03453 | hp2 | a0001 | c0006 | t0001 | g0098 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03540 | hp2 | a0001 | c0006 | t0001 | g0100 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03579 | hp2 | a0001 | c0003 | t0008 | g0035 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03688 | hp1 | a0001 | c0001 | t0010 | g0064 | SAS | STU | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0185 | SAS | STU | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03704 | hp2 | a0001 | c0001 | t0036 | g0214 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03710 | hp2 | a0001 | c0001 | t0012 | g0009 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | BEB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0189 | SAS | STU | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG04204 | hp1 | a0001 | c0001 | t0032 | g0065 | SAS | STU | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | STU | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | YRI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | CHB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18906 | hp1 | a0001 | c0001 | t0037 | g0258 | AFR | YRI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | YRI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18940 | hp1 | a0001 | c0002 | t0004 | g0168 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18942 | hp1 | a0001 | c0001 | t0020 | g0047 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18942 | hp2 | a0001 | c0002 | t0006 | g0033 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18946 | hp2 | a0001 | c0002 | t0006 | g0032 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18959 | hp2 | a0001 | c0001 | t0010 | g0088 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18969 | hp2 | a0001 | c0002 | t0018 | g0040 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18972 | hp1 | a0001 | c0002 | t0019 | g0039 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18974 | hp1 | a0001 | c0002 | t0006 | g0028 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18982 | hp2 | a0001 | c0005 | t0009 | g0252 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18985 | hp2 | a0001 | c0002 | t0016 | g0029 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18988 | hp1 | a0001 | c0002 | t0017 | g0034 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18995 | hp1 | a0001 | c0002 | t0006 | g0031 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19001 | hp2 | a0001 | c0005 | t0009 | g0257 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19003 | hp2 | a0001 | c0002 | t0004 | g0060 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19004 | hp1 | a0001 | c0001 | t0025 | g0224 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19007 | hp1 | a0001 | c0002 | t0006 | g0041 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19057 | hp2 | a0001 | c0005 | t0009 | g0008 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19063 | hp1 | a0001 | c0002 | t0006 | g0030 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19064 | hp1 | a0001 | c0002 | t0006 | g0038 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19070 | hp1 | a0001 | c0005 | t0009 | g0008 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19082 | hp2 | a0001 | c0001 | t0028 | g0160 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0204 | AFR | YRI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA20129 | hp1 | a0001 | c0004 | t0027 | g0058 | AFR | ASW | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA20129 | hp2 | a0001 | c0003 | t0006 | g0046 | AFR | ASW | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0190 | EUR | TSI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | GIH | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA20905 | hp2 | a0004 | c0009 | t0001 | g0075 | SAS | GIH | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02109 | hp1 | a0001 | c0003 | t0004 | g0054 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02109 | hp2 | a0001 | c0004 | t0004 | g0049 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02486 | hp2 | a0001 | c0003 | t0008 | g0042 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03471 | hp1 | a0001 | c0003 | t0006 | g0022 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG03471 | hp2 | a0001 | c0004 | t0005 | g0048 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG06807 | hp1 | a0001 | c0001 | t0030 | g0194 | AFR | USA | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
HG06807 | hp2 | a0001 | c0001 | t0021 | g0082 | AFR | USA | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA20300 | hp1 | a0001 | c0003 | t0008 | g0024 | AFR | USA | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | USA | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0245 | REF | REF | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0015 | g0016 | REF | REF | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:143300662
|
T | C | 1 | a0004 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1570A>G | p.Thr524Ala | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/9 | 2059/6778 | 1570/2334 | 524/777 | chr5 | 143300662 | ||
chr5:143400647
|
A | C | 1 | a0002 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.193T>G | p.Phe65Val | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/9 | 682/6778 | 193/2334 | 65/777 | chr5 | 143400647 | ||
chr5:143400772
|
C | T | 1 | a0003 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.68G>A | p.Arg23Lys | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/9 | 557/6778 | 68/2334 | 23/777 | chr5 | 143400772 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:143281925
|
A | G | 3 | a0001c0002a0001c0003a0001c0004 | 41 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(38): Show |
synonymous_variant | LOW | c.2298T>C | p.Asn766Asn | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2787/6778 | 2298/2334 | 766/777 | chr5 | 143281925 | ||
chr5:143281973
|
G | A | 1 | a0001c0005 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
synonymous_variant | LOW | c.2250C>T | p.Pro750Pro | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2739/6778 | 2250/2334 | 750/777 | chr5 | 143281973 | ||
chr5:143282715
|
G | A | 2 | a0001c0002a0001c0003 | 29 | HG00438.hp1 HG02055.hp1 HG02109.hp1 others(26): Show |
synonymous_variant | LOW | c.2034C>T | p.Asp678Asp | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/9 | 2523/6778 | 2034/2334 | 678/777 | chr5 | 143282715 | ||
chr5:143298796
|
G | A | 1 | a0001c0002 | 16 | HG00438.hp1 HG02132.hp2 HG02165.hp1 others(13): Show |
synonymous_variant | LOW | c.1764C>T | p.His588His | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/9 | 2253/6778 | 1764/2334 | 588/777 | chr5 | 143298796 | ||
chr5:143314111
|
T | C | 1 | a0001c0005 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
synonymous_variant | LOW | c.1242A>G | p.Thr414Thr | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/9 | 1731/6778 | 1242/2334 | 414/777 | chr5 | 143314111 | ||
chr5:143399943
|
T | C | 1 | a0001c0005 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
synonymous_variant | LOW | c.897A>G | p.Thr299Thr | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/9 | 1386/6778 | 897/2334 | 299/777 | chr5 | 143399943 | ||
chr5:143399961
|
C | T | 1 | a0001c0006 | 6 | HG02572.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
synonymous_variant | LOW | c.879G>A | p.Lys293Lys | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/9 | 1368/6778 | 879/2334 | 293/777 | chr5 | 143399961 | ||
chr5:143400774
|
C | T | 1 | a0003c0008 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.66G>A | p.Glu22Glu | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/9 | 555/6778 | 66/2334 | 22/777 | chr5 | 143400774 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:143278056
|
T | C | 5 | a0001c0001t0003a0001c0001t0022a0001c0001t0023others(2): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3833A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3833 | chr5 | 143278056 | |||||
chr5:143278113
|
C | T | 1 | a0001c0001t0028 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3776G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3776 | chr5 | 143278113 | |||||
chr5:143278138
|
T | A | 1 | a0001c0001t0029 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3751A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3751 | chr5 | 143278138 | |||||
chr5:143278172
|
C | T | 1 | a0001c0002t0017 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3717G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3717 | chr5 | 143278172 | |||||
chr5:143278589
|
C | A | 1 | a0001c0001t0025 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3300G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3300 | chr5 | 143278589 | |||||
chr5:143278591
|
C | A | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(27): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*3298G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3298 | chr5 | 143278591 | |||||
chr5:143278736
|
G | A | 1 | a0001c0005t0009 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3153C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3153 | chr5 | 143278736 | |||||
chr5:143278813
|
G | A | 1 | a0001c0005t0009 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3076C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3076 | chr5 | 143278813 | |||||
chr5:143278927
|
T | C | 1 | a0001c0001t0031 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2962A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2962 | chr5 | 143278927 | |||||
chr5:143279050
|
A | G | 1 | a0001c0001t0022 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2839T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2839 | chr5 | 143279050 | |||||
chr5:143279450
|
T | A | 1 | a0001c0001t0014 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2439A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2439 | chr5 | 143279450 | |||||
chr5:143279522
|
G | A | 1 | a0001c0002t0018 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2367C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2367 | chr5 | 143279522 | |||||
chr5:143279543
|
T | C | 1 | a0001c0001t0014 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2346A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2346 | chr5 | 143279543 | |||||
chr5:143279701
|
T | C | 1 | a0001c0003t0008 | 9 | HG02055.hp1 HG02486.hp2 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2188A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2188 | chr5 | 143279701 | |||||
chr5:143279845
|
C | G | 1 | a0001c0004t0027 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2044G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2044 | chr5 | 143279845 | |||||
chr5:143279847
|
G | A | 1 | a0001c0005t0009 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2042C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2042 | chr5 | 143279847 | |||||
chr5:143280009
|
T | C | 1 | a0002c0007t0011 | 2 | HG01884.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1880A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 1880 | chr5 | 143280009 | |||||
chr5:143280663
|
A | AATCAGT | 1 | a0001c0005t0009 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1220_*1225dupACTG others(2): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 1225 | chr5 | 143280663 | |||||
chr5:143280820
|
C | G | 1 | a0001c0001t0026 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1069G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 1069 | chr5 | 143280820 | |||||
chr5:143280952
|
G | T | 1 | a0002c0007t0034 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*937C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 937 | chr5 | 143280952 | |||||
chr5:143281053
|
G | T | 1 | a0001c0001t0024 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 836 | chr5 | 143281053 | |||||
chr5:143281119
|
C | CT | 8 | a0001c0001t0002a0001c0001t0010a0001c0001t0013others(5): Show | 52 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*769dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 769 | chr5 | 143281119 | |||||
chr5:143281119
|
C | CTT | 4 | a0001c0001t0005a0001c0001t0007a0001c0001t0023others(1): Show | 25 | HG00323.hp1 HG01074.hp1 HG01496.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*768_*769dupAA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 769 | chr5 | 143281119 | |||||
chr5:143281119
|
C | CTTT | 3 | a0001c0001t0003a0001c0001t0022a0003c0008t0003 | 20 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*767_*769dupAAA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 769 | chr5 | 143281119 | |||||
chr5:143281119
|
CT | C | 4 | a0001c0001t0032a0001c0002t0019a0001c0004t0033others(1): Show | 10 | HG01256.hp2 HG02027.hp1 HG02074.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*769delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 769 | chr5 | 143281119 | |||||
chr5:143281237
|
T | A | 1 | a0002c0007t0034 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*652A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 652 | chr5 | 143281237 | |||||
chr5:143281446
|
A | G | 1 | a0001c0001t0021 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*443T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 443 | chr5 | 143281446 | |||||
chr5:143281599
|
T | G | 1 | a0001c0005t0009 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*290A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 290 | chr5 | 143281599 | |||||
chr5:143281630
|
G | A | 1 | a0001c0001t0035 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*259C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 259 | chr5 | 143281630 | |||||
chr5:143281874
|
T | C | 1 | a0001c0001t0036 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 15 | chr5 | 143281874 | |||||
chr5:143403227
|
G | T | 1 | a0001c0001t0020 | 1 | NA18942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2388 | chr5 | 143403227 | |||||
chr5:143403255
|
C | A | 1 | a0001c0001t0037 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2416 | chr5 | 143403255 | |||||
chr5:143403312
|
A | AT | 7 | a0001c0002t0006a0001c0002t0016a0001c0002t0017others(4): Show | 25 | HG00438.hp1 HG02055.hp1 HG02132.hp2 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-116dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2474 | chr5 | 143403312 | |||||
chr5:143403334
|
A | T | 1 | a0001c0001t0013 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2495 | chr5 | 143403334 | |||||
chr5:143403448
|
A | G | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
5_prime_UTR_variant | MODIFIER | c.-251T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2609 | chr5 | 143403448 | |||||
chr5:143403450
|
G | GC | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
5_prime_UTR_variant | MODIFIER | c.-254_-253insG | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2612 | chr5 | 143403450 | |||||
chr5:143403522
|
A | C | 1 | a0001c0001t0012 | 1 | HG03710.hp2 | 5_prime_UTR_variant | MODIFIER | c.-325T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2683 | chr5 | 143403522 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:143282050
|
G | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2182-9C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282050 | ||||||
chr5:143282187
|
C | T | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2182-146G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282187 | ||||||
chr5:143282199
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2182-158T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282199 | ||||||
chr5:143282222
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2182-181C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282222 | ||||||
chr5:143282277
|
G | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2182-236C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282277 | ||||||
chr5:143282324
|
A | G | 79 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.2181+244T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282324 | ||||||
chr5:143282365
|
T | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2181+203A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282365 | ||||||
chr5:143282487
|
C | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2181+81G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282487 | ||||||
chr5:143282772
|
CTTTTCT | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-53_2024-48del others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143282772 | ||||||
chr5:143282777
|
C | CT | 9 | a0001c0001t0007g0001a0001c0001t0007g0011a0001c0001t0007g0012others(6): Show | 10 | HG00099.hp1 HG01884.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2024-53dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143282777 | ||||||
chr5:143282834
|
CAGTGGCA others(100): Show |
C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-216_2024-110d others(2): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143282834 | ||||||
chr5:143283048
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-323A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283048 | ||||||
chr5:143283321
|
G | A | 2 | a0001c0002t0006g0028a0001c0002t0006g0031 | 2 | NA18974.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2024-596C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283321 | ||||||
chr5:143283358
|
A | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2024-633T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283358 | ||||||
chr5:143283590
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2024-865G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283590 | ||||||
chr5:143283593
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-868A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283593 | ||||||
chr5:143283851
|
A | G | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2024-1126T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283851 | ||||||
chr5:143283975
|
G | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-1250C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283975 | ||||||
chr5:143284236
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2024-1511G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284236 | ||||||
chr5:143284329
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-1604C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284329 | ||||||
chr5:143284374
|
T | G | 29 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(26): Show | 29 | HG00438.hp1 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2024-1649A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284374 | ||||||
chr5:143284470
|
C | CATTACTA others(16): Show |
28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.2024-1768_2024-174 others(27): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284470 | ||||||
chr5:143284524
|
TTATAGTT others(13): Show |
T | 7 | a0001c0001t0012g0009a0001c0005t0009g0008a0001c0005t0009g0249others(4): Show | 8 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.2024-1819_2024-180 others(24): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284524 | ||||||
chr5:143284564
|
G | A | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2024-1839C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284564 | ||||||
chr5:143284777
|
A | G | 12 | a0001c0001t0007g0001a0001c0001t0007g0011a0001c0001t0007g0012others(9): Show | 13 | HG02572.hp1 HG02615.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.2024-2052T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284777 | ||||||
chr5:143284883
|
C | T | 2 | a0001c0001t0005g0210a0001c0001t0005g0211 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2024-2158G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284883 | ||||||
chr5:143284951
|
T | TAATTTAT others(58): Show |
1 | a0001c0001t0001g0148 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2024-2291_2024-222 others(69): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284951 | ||||||
chr5:143284951
|
T | TAATTTAT others(123): Show |
1 | a0001c0001t0001g0106 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2024-2356_2024-222 others(134): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284951 | ||||||
chr5:143284951
|
TAATTTAT others(58): Show |
T | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0067others(216): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2024-2291_2024-222 others(69): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284951 | ||||||
chr5:143284951
|
TAATTTAT others(123): Show |
T | 8 | a0001c0001t0001g0066a0001c0001t0001g0119a0001c0001t0001g0120others(5): Show | 8 | HG00741.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2024-2356_2024-222 others(4): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284951 | ||||||
chr5:143285042
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2024-2317G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285042 | ||||||
chr5:143285389
|
A | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-2664T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285389 | ||||||
chr5:143285456
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2024-2731C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285456 | ||||||
chr5:143285461
|
A | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-2736T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285461 | ||||||
chr5:143285965
|
CTGAT | C | 27 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.2024-3244_2024-324 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285965 | ||||||
chr5:143285970
|
T | A | 1 | a0001c0001t0003g0253 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2024-3245A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285970 | ||||||
chr5:143285970
|
TA | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0069others(20): Show | 25 | HG00423.hp2 HG01070.hp1 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.2024-3246delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285970 | ||||||
chr5:143286247
|
C | G | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.2024-3522G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286247 | ||||||
chr5:143286467
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2024-3742T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286467 | ||||||
chr5:143286512
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-3787T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286512 | ||||||
chr5:143286540
|
A | G | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2024-3815T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286540 | ||||||
chr5:143286641
|
G | A | 2 | a0001c0001t0003g0180a0001c0001t0003g0181 | 2 | HG01256.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2024-3916C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286641 | ||||||
chr5:143286642
|
A | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2024-3917T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286642 | ||||||
chr5:143286789
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2024-4064A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286789 | ||||||
chr5:143286930
|
G | C | 1 | a0001c0001t0002g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2024-4205C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286930 | ||||||
chr5:143287364
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2024-4639A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143287364 | ||||||
chr5:143287365
|
C | A | 1 | a0001c0004t0033g0051 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2024-4640G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143287365 | ||||||
chr5:143287691
|
T | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-4966A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143287691 | ||||||
chr5:143287806
|
T | G | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2024-5081A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143287806 | ||||||
chr5:143287990
|
C | G | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2024-5265G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143287990 | ||||||
chr5:143288118
|
A | AT | 12 | a0001c0001t0001g0086a0001c0001t0001g0157a0001c0001t0010g0088others(9): Show | 13 | HG00099.hp2 HG01884.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.2024-5394dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288118 | ||||||
chr5:143288222
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-5497C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288222 | ||||||
chr5:143288276
|
G | A | 2 | a0001c0001t0003g0185a0003c0008t0003g0179 | 2 | HG00323.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2024-5551C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288276 | ||||||
chr5:143288411
|
G | A | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2024-5686C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288411 | ||||||
chr5:143288419
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-5694T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288419 | ||||||
chr5:143288606
|
G | A | 2 | a0001c0001t0005g0210a0001c0001t0005g0211 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2024-5881C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288606 | ||||||
chr5:143288662
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-5937T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288662 | ||||||
chr5:143288698
|
C | G | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2024-5973G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288698 | ||||||
chr5:143288899
|
G | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2024-6174C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288899 | ||||||
chr5:143288933
|
C | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-6208G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288933 | ||||||
chr5:143289072
|
C | CA | 56 | a0001c0001t0001g0094a0001c0001t0001g0107a0001c0001t0002g0004others(53): Show | 61 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.2024-6348dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289072 | ||||||
chr5:143289072
|
CA | C | 12 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(9): Show | 13 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.2024-6348delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289072 | ||||||
chr5:143289306
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+6154T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289306 | ||||||
chr5:143289366
|
G | A | 1 | a0001c0003t0004g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2023+6094C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289366 | ||||||
chr5:143289385
|
T | C | 1 | a0001c0006t0001g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2023+6075A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289385 | ||||||
chr5:143289420
|
C | T | 8 | a0001c0001t0001g0114a0001c0001t0001g0139a0001c0001t0001g0140others(5): Show | 8 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2023+6040G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289420 | ||||||
chr5:143289471
|
G | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2023+5989C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289471 | ||||||
chr5:143289583
|
T | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+5877A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289583 | ||||||
chr5:143289601
|
G | A | 1 | a0001c0002t0018g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2023+5859C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289601 | ||||||
chr5:143289658
|
A | G | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.2023+5802T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289658 | ||||||
chr5:143289886
|
A | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2023+5574T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289886 | ||||||
chr5:143289922
|
C | T | 1 | a0003c0008t0003g0179 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2023+5538G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289922 | ||||||
chr5:143290504
|
A | T | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2023+4956T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290504 | ||||||
chr5:143290686
|
G | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+4774C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290686 | ||||||
chr5:143290743
|
T | G | 68 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.2023+4717A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290743 | ||||||
chr5:143290753
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2023+4707G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290753 | ||||||
chr5:143290762
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+4698C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290762 | ||||||
chr5:143290813
|
CAGCCTCC others(24): Show |
C | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2023+4616_2023+464 others(35): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290813 | ||||||
chr5:143290983
|
A | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2023+4477T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290983 | ||||||
chr5:143291174
|
T | C | 1 | a0001c0001t0013g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2023+4286A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291174 | ||||||
chr5:143291273
|
T | G | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2023+4187A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291273 | ||||||
chr5:143291504
|
G | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2023+3956C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291504 | ||||||
chr5:143291527
|
A | ATTACTTT others(13): Show |
118 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.2023+3932_2023+393 others(24): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291527 | ||||||
chr5:143291566
|
A | C | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2023+3894T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291566 | ||||||
chr5:143291644
|
T | C | 3 | a0001c0001t0001g0116a0001c0001t0026g0115a0001c0001t0035g0117 | 3 | HG02559.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2023+3816A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291644 | ||||||
chr5:143291692
|
G | A | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2023+3768C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291692 | ||||||
chr5:143291835
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2023+3625C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291835 | ||||||
chr5:143291954
|
T | G | 1 | a0001c0001t0005g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2023+3506A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291954 | ||||||
chr5:143292093
|
A | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+3367T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292093 | ||||||
chr5:143292096
|
C | G | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.2023+3364G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292096 | ||||||
chr5:143292217
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+3243C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292217 | ||||||
chr5:143292220
|
C | T | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2023+3240G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292220 | ||||||
chr5:143292316
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+3144C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292316 | ||||||
chr5:143292323
|
A | G | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2023+3137T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292323 | ||||||
chr5:143292348
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0126a0001c0001t0001g0131 | 3 | HG01169.hp1 HG01934.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2023+3112T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292348 | ||||||
chr5:143292468
|
G | A | 12 | a0001c0001t0007g0001a0001c0001t0007g0011a0001c0001t0007g0012others(9): Show | 13 | HG02572.hp1 HG02615.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.2023+2992C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292468 | ||||||
chr5:143292470
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2023+2990A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292470 | ||||||
chr5:143292520
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2023+2940G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292520 | ||||||
chr5:143292589
|
C | T | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2023+2871G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292589 | ||||||
chr5:143292751
|
G | A | 38 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(35): Show | 38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.2023+2709C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292751 | ||||||
chr5:143293143
|
C | G | 1 | a0001c0002t0006g0028 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2023+2317G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293143 | ||||||
chr5:143293178
|
C | A | 1 | a0001c0003t0004g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2023+2282G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293178 | ||||||
chr5:143293297
|
A | C | 6 | a0001c0006t0001g0098a0001c0006t0001g0099a0001c0006t0001g0100others(3): Show | 6 | HG02572.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2023+2163T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293297 | ||||||
chr5:143293397
|
G | GAAAGACT others(43): Show |
1 | a0001c0001t0001g0177 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2023+2013_2023+206 others(54): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293397 | ||||||
chr5:143293524
|
C | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0126a0001c0001t0001g0131 | 3 | HG01169.hp1 HG01934.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2023+1936G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293524 | ||||||
chr5:143293613
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2023+1847A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293613 | ||||||
chr5:143293832
|
A | G | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.2023+1628T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293832 | ||||||
chr5:143293864
|
CT | C | 9 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0003g0197others(6): Show | 9 | HG00323.hp2 HG01257.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2023+1595delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293864 | ||||||
chr5:143293864
|
CTT | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+1594_2023+159 others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293864 | ||||||
chr5:143293868
|
T | C | 2 | a0001c0001t0005g0210a0001c0001t0005g0211 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2023+1592A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293868 | ||||||
chr5:143293992
|
C | T | 1 | a0001c0001t0004g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2023+1468G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293992 | ||||||
chr5:143294002
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+1458T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294002 | ||||||
chr5:143294322
|
A | G | 3 | a0001c0001t0007g0013a0001c0001t0007g0017a0001c0001t0007g0018 | 3 | HG03098.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2023+1138T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294322 | ||||||
chr5:143294355
|
A | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2023+1105T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294355 | ||||||
chr5:143294374
|
AT | A | 41 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(38): Show | 45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.2023+1085delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294374 | ||||||
chr5:143294377
|
C | G | 41 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(38): Show | 45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.2023+1083G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294377 | ||||||
chr5:143294391
|
G | A | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2023+1069C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294391 | ||||||
chr5:143294394
|
C | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+1066G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294394 | ||||||
chr5:143294580
|
T | C | 1 | a0001c0001t0002g0004 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2023+880A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294580 | ||||||
chr5:143294582
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+878C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294582 | ||||||
chr5:143294791
|
C | T | 2 | a0001c0001t0005g0210a0001c0001t0005g0211 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2023+669G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294791 | ||||||
chr5:143294876
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2023+584G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294876 | ||||||
chr5:143295011
|
C | A | 1 | a0001c0001t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2023+449G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143295011 | ||||||
chr5:143295113
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+347A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143295113 | ||||||
chr5:143295125
|
G | A | 78 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2023+335C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143295125 | ||||||
chr5:143295747
|
G | A | 1 | a0001c0001t0002g0245 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1893-157C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143295747 | ||||||
chr5:143296201
|
A | C | 3 | a0001c0002t0006g0028a0001c0002t0006g0031a0001c0002t0017g0034 | 3 | NA18974.hp1 NA18988.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1893-611T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296201 | ||||||
chr5:143296258
|
C | T | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1893-668G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296258 | ||||||
chr5:143296276
|
A | AT | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1893-687dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296276 | ||||||
chr5:143296276
|
AT | A | 11 | a0001c0001t0020g0047a0001c0005t0009g0008a0001c0005t0009g0249others(8): Show | 12 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1893-687delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296276 | ||||||
chr5:143296369
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1893-779G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296369 | ||||||
chr5:143296381
|
ATAAAT | A | 9 | a0001c0004t0004g0049a0001c0004t0004g0050a0001c0004t0004g0052others(6): Show | 9 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1893-796_1893-792d others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296381 | ||||||
chr5:143296616
|
AAAC | A | 39 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(36): Show | 39 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1893-1029_1893-102 others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296616 | ||||||
chr5:143296627
|
AT | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1893-1038delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296627 | ||||||
chr5:143296763
|
G | A | 1 | a0001c0001t0028g0160 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1893-1173C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296763 | ||||||
chr5:143296839
|
G | T | 67 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(64): Show | 67 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.1893-1249C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296839 | ||||||
chr5:143296905
|
C | T | 12 | a0001c0001t0007g0001a0001c0001t0007g0011a0001c0001t0007g0012others(9): Show | 13 | HG02572.hp1 HG02615.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1893-1315G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296905 | ||||||
chr5:143296906
|
G | A | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1893-1316C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296906 | ||||||
chr5:143297075
|
C | CA | 50 | a0001c0001t0001g0105a0001c0001t0001g0171a0001c0001t0001g0174others(47): Show | 52 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1893-1486dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143297075 | ||||||
chr5:143297075
|
CA | C | 18 | a0001c0001t0001g0069a0001c0001t0001g0123a0001c0001t0001g0135others(15): Show | 19 | HG01099.hp1 HG01109.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1893-1486delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143297075 | ||||||
chr5:143297443
|
T | A | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG02055.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1892+1225A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143297443 | ||||||
chr5:143297639
|
C | G | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1892+1029G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143297639 | ||||||
chr5:143297656
|
C | T | 1 | a0001c0003t0008g0045 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1892+1012G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143297656 | ||||||
chr5:143297780
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1892+888A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143297780 | ||||||
chr5:143298102
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1892+566G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298102 | ||||||
chr5:143298137
|
T | C | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1892+531A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298137 | ||||||
chr5:143298170
|
TCTC | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1892+495_1892+497d others(5): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298170 | ||||||
chr5:143298175
|
C | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1892+493G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298175 | ||||||
chr5:143298215
|
C | T | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1892+453G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298215 | ||||||
chr5:143298299
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1892+369G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298299 | ||||||
chr5:143298338
|
C | T | 2 | a0001c0001t0001g0074a0004c0009t0001g0075 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1892+330G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298338 | ||||||
chr5:143298405
|
C | T | 1 | a0004c0009t0001g0075 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1892+263G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298405 | ||||||
chr5:143298539
|
T | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0169 | 2 | NA19081.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1892+129A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298539 | ||||||
chr5:143299001
|
T | G | 1 | a0001c0001t0002g0246 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1748-189A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299001 | ||||||
chr5:143299005
|
G | GT | 83 | a0001c0001t0001g0113a0001c0001t0001g0126a0001c0001t0001g0134others(80): Show | 87 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1748-194dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299005 | ||||||
chr5:143299005
|
G | GTT | 32 | a0001c0001t0002g0213a0001c0001t0002g0221a0001c0001t0002g0229others(29): Show | 32 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.1748-195_1748-194d others(4): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299005 | ||||||
chr5:143299005
|
G | GTTTT | 5 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(2): Show | 6 | HG02074.hp2 HG02135.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1748-197_1748-194d others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299005 | ||||||
chr5:143299010
|
T | G | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1748-198A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299010 | ||||||
chr5:143299084
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1748-272C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299084 | ||||||
chr5:143299343
|
T | TA | 6 | a0001c0001t0001g0123a0001c0001t0001g0146a0001c0001t0001g0171others(3): Show | 6 | HG01175.hp1 HG02027.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1748-532dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299343 | ||||||
chr5:143299343
|
T | TAA | 6 | a0001c0001t0002g0223a0001c0001t0010g0061a0001c0001t0024g0206others(3): Show | 6 | HG01346.hp2 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1748-533_1748-532d others(4): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299343 | ||||||
chr5:143299343
|
TAAAA | T | 37 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(34): Show | 37 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1748-535_1748-532d others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299343 | ||||||
chr5:143299434
|
C | T | 3 | a0001c0001t0007g0014a0001c0001t0007g0015a0001c0001t0013g0010 | 3 | HG02572.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1748-622G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299434 | ||||||
chr5:143299490
|
C | T | 1 | a0001c0001t0007g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1748-678G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299490 | ||||||
chr5:143299587
|
G | C | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1748-775C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299587 | ||||||
chr5:143299642
|
C | T | 1 | a0001c0006t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1748-830G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299642 | ||||||
chr5:143299670
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1747+815C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299670 | ||||||
chr5:143299783
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1747+702C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299783 | ||||||
chr5:143299832
|
C | T | 69 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(66): Show | 73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.1747+653G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299832 | ||||||
chr5:143299850
|
C | G | 1 | a0001c0006t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1747+635G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299850 | ||||||
chr5:143299858
|
A | C | 4 | a0001c0001t0003g0183a0001c0001t0003g0187a0001c0001t0003g0207others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747+627T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299858 | ||||||
chr5:143299997
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1747+488A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299997 | ||||||
chr5:143300067
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1747+418A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143300067 | ||||||
chr5:143300394
|
C | G | 2 | a0001c0006t0001g0098a0001c0006t0001g0100 | 2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1747+91G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143300394 | ||||||
chr5:143300779
|
C | A | 78 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1469-16G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143300779 | ||||||
chr5:143300892
|
T | C | 1 | a0001c0005t0009g0257 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1469-129A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143300892 | ||||||
chr5:143301033
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469-270C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301033 | ||||||
chr5:143301037
|
T | C | 1 | a0001c0006t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1469-274A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301037 | ||||||
chr5:143301402
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469-639A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301402 | ||||||
chr5:143301441
|
A | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0248a0001c0001t0026g0115others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-678T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301441 | ||||||
chr5:143301522
|
A | ATAAAT | 32 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0108others(29): Show | 32 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1469-764_1469-760d others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301522 | ||||||
chr5:143301594
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469-831A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301594 | ||||||
chr5:143301715
|
C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1469-952G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301715 | ||||||
chr5:143301946
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1469-1183C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301946 | ||||||
chr5:143302204
|
T | A | 1 | a0001c0006t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1469-1441A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143302204 | ||||||
chr5:143302211
|
T | C | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1469-1448A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143302211 | ||||||
chr5:143303008
|
A | G | 2 | a0001c0001t0005g0210a0001c0001t0005g0211 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1469-2245T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303008 | ||||||
chr5:143303046
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1469-2283T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303046 | ||||||
chr5:143303133
|
CT | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469-2371delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303133 | ||||||
chr5:143303247
|
G | A | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1469-2484C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303247 | ||||||
chr5:143303272
|
A | G | 1 | a0001c0001t0030g0194 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1469-2509T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303272 | ||||||
chr5:143303809
|
A | G | 1 | a0001c0003t0004g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1469-3046T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303809 | ||||||
chr5:143303856
|
G | A | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1469-3093C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303856 | ||||||
chr5:143303904
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469-3141T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303904 | ||||||
chr5:143304158
|
A | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1469-3395T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143304158 | ||||||
chr5:143304176
|
T | C | 79 | a0001c0001t0001g0146a0001c0001t0003g0180a0001c0001t0003g0181others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1469-3413A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143304176 | ||||||
chr5:143304215
|
G | A | 1 | a0001c0004t0004g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1469-3452C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143304215 | ||||||
chr5:143304375
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1469-3612C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143304375 | ||||||
chr5:143304491
|
A | T | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1469-3728T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143304491 | ||||||
chr5:143304829
|
G | A | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1469-4066C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143304829 | ||||||
chr5:143305117
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1469-4354T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305117 | ||||||
chr5:143305345
|
A | G | 2 | a0001c0003t0006g0023a0001c0003t0006g0046 | 2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1469-4582T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305345 | ||||||
chr5:143305349
|
AATTAAGA others(8): Show |
A | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1469-4601_1469-458 others(19): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305349 | ||||||
chr5:143305367
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1469-4604G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305367 | ||||||
chr5:143305547
|
T | A | 1 | a0001c0002t0018g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1468+4550A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305547 | ||||||
chr5:143305592
|
A | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0069others(6): Show | 10 | HG02451.hp2 HG02615.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1468+4505T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305592 | ||||||
chr5:143305695
|
T | C | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1468+4402A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305695 | ||||||
chr5:143305873
|
T | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1468+4224A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305873 | ||||||
chr5:143305916
|
A | G | 2 | a0001c0001t0003g0184a0001c0001t0003g0188 | 2 | HG01175.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1468+4181T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305916 | ||||||
chr5:143305980
|
C | T | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1468+4117G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305980 | ||||||
chr5:143305990
|
C | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+4107G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305990 | ||||||
chr5:143306040
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0010g0064 | 2 | HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1468+4057G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306040 | ||||||
chr5:143306104
|
T | TA | 7 | a0001c0001t0001g0093a0001c0005t0009g0008a0001c0005t0009g0249others(4): Show | 8 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1468+3992dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306104 | ||||||
chr5:143306105
|
A | T | 8 | a0001c0004t0004g0049a0001c0004t0004g0050a0001c0004t0004g0052others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1468+3992T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306105 | ||||||
chr5:143306138
|
T | C | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1468+3959A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306138 | ||||||
chr5:143306161
|
C | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+3936G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306161 | ||||||
chr5:143306314
|
C | T | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1468+3783G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306314 | ||||||
chr5:143306361
|
T | TA | 53 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0069others(50): Show | 58 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1468+3735dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306361 | ||||||
chr5:143306646
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1468+3451T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306646 | ||||||
chr5:143306746
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0151 | 2 | HG00544.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1468+3351G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306746 | ||||||
chr5:143306793
|
G | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+3304C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306793 | ||||||
chr5:143306874
|
A | ATTT | 5 | a0001c0001t0002g0238a0001c0001t0007g0001a0001c0001t0007g0011others(2): Show | 6 | HG02258.hp2 HG02683.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1468+3220_1468+322 others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0007g0013a0001c0001t0007g0017 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1468+3212_1468+322 others(15): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
A | ATTTTTTT others(9): Show |
1 | a0001c0001t0007g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1468+3207_1468+322 others(20): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
AT | A | 11 | a0001c0001t0005g0063a0001c0001t0005g0211a0001c0002t0006g0028others(8): Show | 11 | HG00323.hp1 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1468+3222delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATT | A | 11 | a0001c0001t0002g0243a0001c0001t0005g0222a0001c0002t0004g0168others(8): Show | 11 | HG00438.hp1 HG01074.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1468+3221_1468+322 others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTT | A | 12 | a0001c0001t0002g0006a0001c0001t0002g0062a0001c0001t0002g0242others(9): Show | 13 | HG00597.hp2 HG01934.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1468+3220_1468+322 others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTTT | A | 20 | a0001c0001t0002g0007a0001c0001t0002g0212a0001c0001t0002g0215others(17): Show | 21 | HG01109.hp1 HG01891.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1468+3219_1468+322 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTTTT | A | 31 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0213others(28): Show | 33 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(30): Show |
intron_variant | MODIFIER | c.1468+3218_1468+322 others(9): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0005t0009g0252 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1468+3213_1468+322 others(14): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0003t0008g0045 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1468+3212_1468+322 others(15): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0003g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1468+3211_1468+322 others(16): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTTTTTT others(6): Show |
A | 10 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0003g0190others(7): Show | 10 | HG01099.hp1 HG01169.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1468+3210_1468+322 others(17): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0004t0004g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1468+3209_1468+322 others(18): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTTTTTT others(8): Show |
A | 7 | a0001c0004t0004g0049a0001c0004t0004g0050a0001c0004t0004g0052others(4): Show | 7 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468+3208_1468+322 others(19): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTTTTTT others(9): Show |
A | 13 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0134others(10): Show | 13 | HG00544.hp2 HG00733.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1468+3207_1468+322 others(20): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTTTTTT others(10): Show |
A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(103): Show | 108 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1468+3206_1468+322 others(21): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTTTTTT others(11): Show |
A | 3 | a0001c0001t0001g0073a0001c0001t0001g0113a0001c0001t0001g0164 | 3 | HG03041.hp2 NA18950.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1468+3205_1468+322 others(22): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306874
|
ATTTTTTT others(16): Show |
A | 1 | a0001c0001t0002g0221 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1468+3200_1468+322 others(27): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | ||||||
chr5:143306927
|
C | T | 7 | a0001c0001t0032g0065a0001c0005t0009g0008a0001c0005t0009g0249others(4): Show | 8 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1468+3170G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306927 | ||||||
chr5:143307045
|
C | T | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1468+3052G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307045 | ||||||
chr5:143307118
|
G | A | 1 | a0001c0001t0032g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1468+2979C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307118 | ||||||
chr5:143307216
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+2881A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307216 | ||||||
chr5:143307239
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1468+2858T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307239 | ||||||
chr5:143307371
|
G | A | 26 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0062others(23): Show | 28 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1468+2726C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307371 | ||||||
chr5:143307426
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1468+2671A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307426 | ||||||
chr5:143307710
|
A | T | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1468+2387T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307710 | ||||||
chr5:143307916
|
T | G | 4 | a0001c0002t0006g0030a0001c0002t0006g0033a0001c0002t0006g0041others(1): Show | 4 | NA18942.hp2 NA18985.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+2181A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307916 | ||||||
chr5:143307929
|
A | G | 78 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1468+2168T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307929 | ||||||
chr5:143308134
|
T | C | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1468+1963A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143308134 | ||||||
chr5:143308177
|
T | C | 9 | a0001c0004t0004g0049a0001c0004t0004g0050a0001c0004t0004g0052others(6): Show | 9 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1468+1920A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143308177 | ||||||
chr5:143308505
|
T | C | 3 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0247 | 3 | HG02148.hp1 HG02273.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1468+1592A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143308505 | ||||||
chr5:143308664
|
T | G | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1468+1433A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143308664 | ||||||
chr5:143308758
|
T | C | 68 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1468+1339A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143308758 | ||||||
chr5:143308914
|
G | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+1183C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143308914 | ||||||
chr5:143309073
|
C | CT | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0067others(83): Show | 88 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1468+1023dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309073 | ||||||
chr5:143309127
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+970T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309127 | ||||||
chr5:143309234
|
C | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+863G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309234 | ||||||
chr5:143309306
|
C | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(17): Show | 21 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1468+791G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309306 | ||||||
chr5:143309313
|
C | T | 1 | a0001c0002t0006g0033 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1468+784G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309313 | ||||||
chr5:143309372
|
C | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+725G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309372 | ||||||
chr5:143309469
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1468+628G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309469 | ||||||
chr5:143309486
|
T | C | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1468+611A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309486 | ||||||
chr5:143309540
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1468+557G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309540 | ||||||
chr5:143309629
|
GT | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+467delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309629 | ||||||
chr5:143309652
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1468+445G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309652 | ||||||
chr5:143309678
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+419C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309678 | ||||||
chr5:143310270
|
A | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1352-57T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310270 | ||||||
chr5:143310420
|
A | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1352-207T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310420 | ||||||
chr5:143310466
|
A | G | 3 | a0001c0001t0007g0013a0001c0001t0007g0017a0001c0001t0007g0018 | 3 | HG03098.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1352-253T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310466 | ||||||
chr5:143310830
|
A | C | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1352-617T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310830 | ||||||
chr5:143310877
|
C | T | 4 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG02080.hp1 HG02129.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1352-664G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310877 | ||||||
chr5:143310934
|
G | A | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1352-721C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310934 | ||||||
chr5:143310958
|
T | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1352-745A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310958 | ||||||
chr5:143311031
|
T | C | 40 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1352-818A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311031 | ||||||
chr5:143311162
|
G | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1352-949C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311162 | ||||||
chr5:143311407
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1352-1194A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311407 | ||||||
chr5:143311783
|
A | G | 6 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1352-1570T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311783 | ||||||
chr5:143311788
|
G | GT | 38 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0069others(35): Show | 39 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1352-1576dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311788 | ||||||
chr5:143311788
|
GT | G | 61 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.1352-1576delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311788 | ||||||
chr5:143311788
|
GTT | G | 6 | a0001c0001t0001g0094a0001c0005t0009g0008a0001c0005t0009g0249others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1352-1577_1352-157 others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311788 | ||||||
chr5:143311808
|
T | C | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1352-1595A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311808 | ||||||
chr5:143311828
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1352-1615C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311828 | ||||||
chr5:143311925
|
ACAGCCCA others(21): Show |
A | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1352-1740_1352-171 others(32): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311925 | ||||||
chr5:143312188
|
C | A | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1351+1814G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143312188 | ||||||
chr5:143312249
|
C | T | 7 | a0001c0001t0012g0009a0001c0005t0009g0008a0001c0005t0009g0249others(4): Show | 8 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1351+1753G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143312249 | ||||||
chr5:143312722
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1351+1280G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143312722 | ||||||
chr5:143312824
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1351+1178C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143312824 | ||||||
chr5:143312845
|
G | A | 1 | a0001c0001t0005g0203 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1351+1157C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143312845 | ||||||
chr5:143312968
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(32): Show | 37 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.1351+1034C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143312968 | ||||||
chr5:143313467
|
T | G | 5 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0083others(2): Show | 5 | HG01255.hp1 HG06807.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.1351+535A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143313467 | ||||||
chr5:143313833
|
T | C | 68 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1351+169A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143313833 | ||||||
chr5:143313922
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0156 | 2 | NA19000.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1351+80T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143313922 | ||||||
chr5:143314260
|
TCA | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-94_1185-93del others(2): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314260 | ||||||
chr5:143314281
|
A | G | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1185-113T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314281 | ||||||
chr5:143314386
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-218T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314386 | ||||||
chr5:143314421
|
CT | C | 9 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0108others(6): Show | 9 | HG00597.hp1 HG01256.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1185-254delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314421 | ||||||
chr5:143314421
|
CTT | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-255_1185-254d others(4): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314421 | ||||||
chr5:143314424
|
T | C | 3 | a0001c0001t0001g0139a0001c0003t0008g0024a0001c0003t0008g0025 | 3 | HG02647.hp1 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1185-256A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314424 | ||||||
chr5:143314736
|
A | G | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-568T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314736 | ||||||
chr5:143315000
|
C | T | 2 | a0001c0001t0003g0185a0001c0001t0003g0253 | 2 | HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1185-832G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143315000 | ||||||
chr5:143315248
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-1080C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143315248 | ||||||
chr5:143315677
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1185-1509A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143315677 | ||||||
chr5:143315736
|
T | C | 2 | a0001c0001t0003g0180a0001c0001t0003g0181 | 2 | HG01256.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1185-1568A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143315736 | ||||||
chr5:143315765
|
T | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-1597A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143315765 | ||||||
chr5:143315877
|
C | T | 1 | a0001c0003t0008g0045 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1185-1709G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143315877 | ||||||
chr5:143316030
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1185-1862G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143316030 | ||||||
chr5:143316471
|
G | A | 38 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0006g0028others(35): Show | 38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1185-2303C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143316471 | ||||||
chr5:143316541
|
C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-2373G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143316541 | ||||||
chr5:143316882
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-2714C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143316882 | ||||||
chr5:143316941
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1185-2773C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143316941 | ||||||
chr5:143316947
|
G | C | 6 | a0001c0006t0001g0098a0001c0006t0001g0099a0001c0006t0001g0100others(3): Show | 6 | HG02572.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-2779C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143316947 | ||||||
chr5:143317004
|
G | C | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1185-2836C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143317004 | ||||||
chr5:143317093
|
G | A | 1 | a0001c0001t0002g0220 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1185-2925C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143317093 | ||||||
chr5:143317484
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1185-3316A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143317484 | ||||||
chr5:143317709
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1185-3541A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143317709 | ||||||
chr5:143317730
|
A | T | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1185-3562T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143317730 | ||||||
chr5:143317994
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-3826T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143317994 | ||||||
chr5:143318065
|
G | A | 1 | a0001c0001t0005g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1185-3897C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318065 | ||||||
chr5:143318209
|
A | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-4041T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318209 | ||||||
chr5:143318364
|
A | G | 2 | a0001c0001t0001g0086a0001c0001t0004g0087 | 2 | HG00099.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1185-4196T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318364 | ||||||
chr5:143318435
|
T | G | 2 | a0001c0001t0003g0184a0001c0001t0003g0188 | 2 | HG01175.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1185-4267A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318435 | ||||||
chr5:143318660
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1185-4492A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318660 | ||||||
chr5:143318675
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1185-4507C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318675 | ||||||
chr5:143318791
|
A | G | 1 | a0001c0001t0010g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1185-4623T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318791 | ||||||
chr5:143319029
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1185-4861G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319029 | ||||||
chr5:143319180
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-5012A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319180 | ||||||
chr5:143319342
|
A | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-5174T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319342 | ||||||
chr5:143319347
|
T | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-5179A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319347 | ||||||
chr5:143319378
|
A | C | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-5210T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319378 | ||||||
chr5:143319448
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-5280A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319448 | ||||||
chr5:143319479
|
A | G | 1 | a0001c0001t0029g0124 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1185-5311T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319479 | ||||||
chr5:143319632
|
G | A | 3 | a0001c0001t0003g0185a0001c0001t0003g0253a0003c0008t0003g0179 | 3 | HG00323.hp2 HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1185-5464C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319632 | ||||||
chr5:143319634
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-5466A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319634 | ||||||
chr5:143319943
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1185-5775A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319943 | ||||||
chr5:143320023
|
G | A | 6 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | NA18946.hp1 NA18974.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-5855C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320023 | ||||||
chr5:143320154
|
A | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(251): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1185-5986T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320154 | ||||||
chr5:143320203
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1185-6035A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320203 | ||||||
chr5:143320206
|
A | G | 1 | a0001c0004t0004g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1185-6038T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320206 | ||||||
chr5:143320236
|
A | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-6068T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320236 | ||||||
chr5:143320237
|
T | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-6069A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320237 | ||||||
chr5:143320239
|
T | TTTAGCAG others(3): Show |
1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-6072_1185-607 others(14): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320239 | ||||||
chr5:143320472
|
T | C | 3 | a0001c0001t0005g0199a0001c0001t0005g0200a0001c0001t0005g0201 | 3 | HG01496.hp1 HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1185-6304A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320472 | ||||||
chr5:143320934
|
C | T | 38 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(35): Show | 38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1185-6766G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320934 | ||||||
chr5:143321028
|
G | A | 2 | a0001c0001t0005g0210a0001c0001t0005g0211 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1185-6860C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321028 | ||||||
chr5:143321106
|
T | C | 1 | a0001c0002t0017g0034 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1185-6938A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321106 | ||||||
chr5:143321238
|
A | G | 2 | a0001c0001t0002g0212a0001c0001t0002g0227 | 2 | NA19009.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1185-7070T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321238 | ||||||
chr5:143321291
|
G | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1185-7123C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321291 | ||||||
chr5:143321438
|
A | G | 1 | a0001c0006t0001g0098 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1185-7270T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321438 | ||||||
chr5:143321457
|
C | T | 1 | a0001c0001t0026g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1185-7289G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321457 | ||||||
chr5:143321985
|
T | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-7817A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321985 | ||||||
chr5:143322010
|
T | G | 1 | a0001c0001t0001g0110 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1185-7842A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143322010 | ||||||
chr5:143322115
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1185-7947T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143322115 | ||||||
chr5:143322315
|
A | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-8147T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143322315 | ||||||
chr5:143322336
|
T | C | 1 | a0001c0005t0009g0257 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1185-8168A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143322336 | ||||||
chr5:143322402
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-8234C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143322402 | ||||||
chr5:143322496
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-8328C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143322496 | ||||||
chr5:143323374
|
T | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-9206A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323374 | ||||||
chr5:143323405
|
C | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-9237G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323405 | ||||||
chr5:143323424
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1185-9256G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323424 | ||||||
chr5:143323437
|
C | T | 1 | a0001c0001t0014g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1185-9269G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323437 | ||||||
chr5:143323757
|
C | T | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-9589G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323757 | ||||||
chr5:143323769
|
G | A | 1 | a0001c0006t0001g0103 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1185-9601C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323769 | ||||||
chr5:143323875
|
T | C | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1185-9707A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323875 | ||||||
chr5:143324008
|
G | GCAGGGTA | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-9841_1185-984 others(11): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143324008 | ||||||
chr5:143324082
|
G | A | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-9914C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143324082 | ||||||
chr5:143324441
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1185-10273C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143324441 | ||||||
chr5:143324485
|
C | T | 1 | a0001c0002t0016g0029 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1185-10317G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143324485 | ||||||
chr5:143325168
|
A | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-11000T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325168 | ||||||
chr5:143325247
|
C | T | 1 | a0001c0001t0014g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1185-11079G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325247 | ||||||
chr5:143325297
|
A | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-11129T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325297 | ||||||
chr5:143325463
|
C | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-11295G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325463 | ||||||
chr5:143325484
|
C | T | 2 | a0001c0001t0001g0074a0004c0009t0001g0075 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1185-11316G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325484 | ||||||
chr5:143325559
|
T | C | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-11391A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325559 | ||||||
chr5:143325769
|
C | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00597.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1185-11601G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325769 | ||||||
chr5:143325856
|
G | A | 67 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(64): Show | 67 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.1185-11688C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325856 | ||||||
chr5:143326034
|
C | A | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-11866G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143326034 | ||||||
chr5:143326330
|
T | G | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1185-12162A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143326330 | ||||||
chr5:143326580
|
C | T | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1185-12412G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143326580 | ||||||
chr5:143326833
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1185-12665C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143326833 | ||||||
chr5:143327047
|
T | C | 1 | a0001c0001t0003g0191 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1185-12879A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327047 | ||||||
chr5:143327361
|
C | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-13193G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327361 | ||||||
chr5:143327584
|
A | T | 7 | a0001c0004t0004g0049a0001c0004t0004g0050a0001c0004t0004g0052others(4): Show | 7 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-13416T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327584 | ||||||
chr5:143327658
|
C | T | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-13490G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327658 | ||||||
chr5:143327768
|
C | T | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-13600G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327768 | ||||||
chr5:143327829
|
G | A | 1 | a0001c0001t0032g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1185-13661C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327829 | ||||||
chr5:143327910
|
G | C | 1 | a0001c0001t0002g0231 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1185-13742C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327910 | ||||||
chr5:143328087
|
T | A | 1 | a0001c0004t0004g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1185-13919A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328087 | ||||||
chr5:143328136
|
C | T | 6 | a0001c0003t0008g0024a0001c0003t0008g0025a0001c0003t0008g0026others(3): Show | 6 | HG00738.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-13968G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328136 | ||||||
chr5:143328137
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-13969C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328137 | ||||||
chr5:143328169
|
C | T | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1185-14001G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328169 | ||||||
chr5:143328416
|
T | C | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-14248A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328416 | ||||||
chr5:143328765
|
C | T | 4 | a0001c0002t0006g0030a0001c0002t0006g0033a0001c0002t0006g0041others(1): Show | 4 | NA18942.hp2 NA18985.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1185-14597G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328765 | ||||||
chr5:143328780
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1185-14612A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328780 | ||||||
chr5:143328815
|
T | C | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1185-14647A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328815 | ||||||
chr5:143328841
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1185-14673G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328841 | ||||||
chr5:143328862
|
A | G | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-14694T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328862 | ||||||
chr5:143328904
|
G | C | 68 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1185-14736C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328904 | ||||||
chr5:143328994
|
T | G | 2 | a0001c0001t0005g0210a0001c0001t0005g0211 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1185-14826A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328994 | ||||||
chr5:143329169
|
T | C | 40 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1185-15001A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329169 | ||||||
chr5:143329287
|
G | A | 40 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1185-15119C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329287 | ||||||
chr5:143329310
|
T | C | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-15142A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329310 | ||||||
chr5:143329404
|
A | G | 1 | a0001c0001t0003g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1185-15236T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329404 | ||||||
chr5:143329422
|
A | G | 2 | a0001c0003t0008g0024a0001c0003t0008g0025 | 2 | HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1185-15254T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329422 | ||||||
chr5:143329547
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-15379T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329547 | ||||||
chr5:143329823
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1185-15655A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329823 | ||||||
chr5:143329889
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-15721T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329889 | ||||||
chr5:143330158
|
T | C | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1185-15990A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330158 | ||||||
chr5:143330344
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-16176T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330344 | ||||||
chr5:143330421
|
C | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1185-16253G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330421 | ||||||
chr5:143330745
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1185-16577G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330745 | ||||||
chr5:143330766
|
C | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-16598G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330766 | ||||||
chr5:143330775
|
C | G | 2 | a0001c0001t0002g0217a0001c0001t0002g0219 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1185-16607G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330775 | ||||||
chr5:143330892
|
C | T | 6 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0200others(3): Show | 6 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-16724G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330892 | ||||||
chr5:143330976
|
A | C | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG02055.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-16808T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330976 | ||||||
chr5:143331046
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1185-16878G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331046 | ||||||
chr5:143331079
|
C | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-16911G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331079 | ||||||
chr5:143331131
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1185-16963G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331131 | ||||||
chr5:143331324
|
A | C | 1 | a0001c0001t0037g0258 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1185-17156T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331324 | ||||||
chr5:143331446
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1185-17278C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331446 | ||||||
chr5:143331475
|
A | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-17307T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331475 | ||||||
chr5:143331480
|
T | C | 1 | a0001c0001t0004g0239 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1185-17312A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331480 | ||||||
chr5:143331523
|
G | A | 2 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1185-17355C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331523 | ||||||
chr5:143331863
|
C | G | 6 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-17695G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331863 | ||||||
chr5:143331866
|
C | G | 2 | a0001c0001t0005g0063a0001c0001t0005g0222 | 2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1185-17698G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331866 | ||||||
chr5:143331938
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-17770A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331938 | ||||||
chr5:143332312
|
G | GTT | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-18146_1185-18 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332312 | ||||||
chr5:143332393
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-18225C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332393 | ||||||
chr5:143332406
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1185-18238C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332406 | ||||||
chr5:143332413
|
G | C | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG02080.hp1 HG02129.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1185-18245C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332413 | ||||||
chr5:143332471
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1185-18303C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332471 | ||||||
chr5:143332499
|
G | A | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1185-18331C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332499 | ||||||
chr5:143332526
|
C | A | 38 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(35): Show | 38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1185-18358G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332526 | ||||||
chr5:143332610
|
GT | G | 78 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1185-18443delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332610 | ||||||
chr5:143332767
|
T | C | 1 | a0001c0005t0009g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-18599A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332767 | ||||||
chr5:143332793
|
G | A | 1 | a0001c0001t0002g0235 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1185-18625C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332793 | ||||||
chr5:143333032
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1185-18864C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333032 | ||||||
chr5:143333158
|
T | TA | 68 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1185-18991dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333158 | ||||||
chr5:143333314
|
C | A | 3 | a0001c0001t0003g0185a0001c0001t0003g0253a0003c0008t0003g0179 | 3 | HG00323.hp2 HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1185-19146G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333314 | ||||||
chr5:143333745
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1185-19577G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333745 | ||||||
chr5:143333760
|
C | G | 6 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0200others(3): Show | 6 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-19592G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333760 | ||||||
chr5:143333767
|
A | G | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-19599T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333767 | ||||||
chr5:143333769
|
A | AAAAC | 3 | a0001c0001t0001g0081a0001c0003t0008g0042a0001c0003t0008g0043 | 3 | HG02055.hp1 HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1185-19605_1185-19 others(10): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333769 | ||||||
chr5:143333769
|
AAAAC | A | 15 | a0001c0001t0001g0106a0001c0003t0008g0024a0001c0003t0008g0025others(12): Show | 16 | HG00408.hp2 HG01884.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.1185-19605_1185-19 others(10): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333769 | ||||||
chr5:143333807
|
T | C | 1 | a0001c0003t0006g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1185-19639A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333807 | ||||||
chr5:143333963
|
C | T | 5 | a0001c0001t0002g0216a0001c0001t0002g0233a0001c0001t0002g0234others(2): Show | 5 | HG00438.hp2 NA18747.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-19795G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333963 | ||||||
chr5:143334001
|
T | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-19833A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334001 | ||||||
chr5:143334008
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1185-19840A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334008 | ||||||
chr5:143334107
|
C | T | 1 | a0001c0001t0013g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1185-19939G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334107 | ||||||
chr5:143334215
|
C | G | 1 | a0001c0004t0033g0051 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1185-20047G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334215 | ||||||
chr5:143334413
|
T | C | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1185-20245A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334413 | ||||||
chr5:143334521
|
G | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-20353C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334521 | ||||||
chr5:143334600
|
A | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-20432T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334600 | ||||||
chr5:143334725
|
G | GA | 43 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(40): Show | 47 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1185-20558dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334725 | ||||||
chr5:143334725
|
G | GAA | 6 | a0001c0001t0002g0237a0001c0005t0009g0008a0001c0005t0009g0249others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-20559_1185-20 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334725 | ||||||
chr5:143334924
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-20756T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334924 | ||||||
chr5:143334972
|
T | G | 1 | a0001c0004t0004g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1185-20804A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334972 | ||||||
chr5:143335046
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1185-20878C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335046 | ||||||
chr5:143335077
|
C | A | 8 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0127others(5): Show | 8 | HG00408.hp1 HG02165.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.1185-20909G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335077 | ||||||
chr5:143335193
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1185-21025C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335193 | ||||||
chr5:143335624
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 7 | HG02451.hp2 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185-21456T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335624 | ||||||
chr5:143335694
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1185-21526T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335694 | ||||||
chr5:143335879
|
G | A | 1 | a0001c0002t0016g0029 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1185-21711C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335879 | ||||||
chr5:143335918
|
T | C | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-21750A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335918 | ||||||
chr5:143336121
|
G | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-21953C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336121 | ||||||
chr5:143336214
|
A | G | 2 | a0001c0006t0001g0098a0001c0006t0001g0100 | 2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1185-22046T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336214 | ||||||
chr5:143336232
|
T | C | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1185-22064A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336232 | ||||||
chr5:143336714
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1185-22546C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336714 | ||||||
chr5:143336737
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22569A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336737 | ||||||
chr5:143336738
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22570T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336738 | ||||||
chr5:143336740
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22572T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336740 | ||||||
chr5:143336743
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22575T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336743 | ||||||
chr5:143336747
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22579T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336747 | ||||||
chr5:143336753
|
CTTGACGT others(3): Show |
C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22595_1185-22 others(16): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336753 | ||||||
chr5:143336774
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22606C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336774 | ||||||
chr5:143336780
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22612A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336780 | ||||||
chr5:143336783
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22615T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336783 | ||||||
chr5:143336786
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22618A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336786 | ||||||
chr5:143336790
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22622C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336790 | ||||||
chr5:143336792
|
C | T | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1185-22624G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336792 | ||||||
chr5:143336793
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22625A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336793 | ||||||
chr5:143336795
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22627A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336795 | ||||||
chr5:143336799
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22631G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336799 | ||||||
chr5:143336801
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22633A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336801 | ||||||
chr5:143336804
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22636G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336804 | ||||||
chr5:143336812
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22644A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336812 | ||||||
chr5:143336815
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22647A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336815 | ||||||
chr5:143336820
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22652A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336820 | ||||||
chr5:143336841
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22673A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336841 | ||||||
chr5:143336842
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22674T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336842 | ||||||
chr5:143336844
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22676C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336844 | ||||||
chr5:143336850
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22682T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336850 | ||||||
chr5:143336851
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22683A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336851 | ||||||
chr5:143336852
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22684T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336852 | ||||||
chr5:143336859
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22691T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336859 | ||||||
chr5:143336863
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22695A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336863 | ||||||
chr5:143336871
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22703G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336871 | ||||||
chr5:143336875
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22707A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336875 | ||||||
chr5:143336876
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22708A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336876 | ||||||
chr5:143336883
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22715T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336883 | ||||||
chr5:143336891
|
A | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22723T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336891 | ||||||
chr5:143336892
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22724T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336892 | ||||||
chr5:143336895
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22727A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336895 | ||||||
chr5:143336903
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22735T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336903 | ||||||
chr5:143336909
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22741A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336909 | ||||||
chr5:143336914
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22746C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336914 | ||||||
chr5:143336915
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22747G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336915 | ||||||
chr5:143336927
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22759T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336927 | ||||||
chr5:143336931
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22763G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336931 | ||||||
chr5:143336932
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22764A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336932 | ||||||
chr5:143336933
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22765C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336933 | ||||||
chr5:143336934
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22766A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336934 | ||||||
chr5:143336937
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1185-22769G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336937 | ||||||
chr5:143336938
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22770C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336938 | ||||||
chr5:143336956
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22788A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336956 | ||||||
chr5:143336964
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22796A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336964 | ||||||
chr5:143336970
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22802G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336970 | ||||||
chr5:143336972
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22804A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336972 | ||||||
chr5:143336982
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22815_1185-22 others(36): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336982 | ||||||
chr5:143337036
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22868G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337036 | ||||||
chr5:143337237
|
G | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-23069C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337237 | ||||||
chr5:143337463
|
T | C | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-23295A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337463 | ||||||
chr5:143337671
|
C | T | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-23503G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337671 | ||||||
chr5:143337691
|
C | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-23523G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337691 | ||||||
chr5:143337718
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-23550A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337718 | ||||||
chr5:143337759
|
T | C | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-23591A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337759 | ||||||
chr5:143337804
|
T | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-23636A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337804 | ||||||
chr5:143337856
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-23688G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337856 | ||||||
chr5:143337966
|
A | G | 1 | a0001c0001t0025g0224 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1185-23798T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337966 | ||||||
chr5:143338160
|
C | A | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-23992G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338160 | ||||||
chr5:143338161
|
A | C | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-23993T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338161 | ||||||
chr5:143338162
|
T | A | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-23994A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338162 | ||||||
chr5:143338234
|
CA | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-24067delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338234 | ||||||
chr5:143338344
|
C | CT | 39 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(36): Show | 39 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1185-24177dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338344 | ||||||
chr5:143338467
|
C | T | 1 | a0001c0002t0019g0039 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1185-24299G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338467 | ||||||
chr5:143338488
|
T | C | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-24320A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338488 | ||||||
chr5:143338696
|
A | G | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-24528T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338696 | ||||||
chr5:143338725
|
G | C | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1185-24557C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338725 | ||||||
chr5:143338985
|
G | A | 2 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1185-24817C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338985 | ||||||
chr5:143339068
|
C | T | 1 | a0001c0001t0004g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1185-24900G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339068 | ||||||
chr5:143339240
|
TA | T | 38 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(35): Show | 38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1185-25073delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339240 | ||||||
chr5:143339373
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-25205G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339373 | ||||||
chr5:143339549
|
T | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-25381A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339549 | ||||||
chr5:143339551
|
A | C | 1 | a0001c0001t0036g0214 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1185-25383T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339551 | ||||||
chr5:143339654
|
T | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | NA18974.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1185-25486A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339654 | ||||||
chr5:143339853
|
G | A | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-25685C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339853 | ||||||
chr5:143339940
|
A | AG | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-25773dupC | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339940 | ||||||
chr5:143340135
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-25967A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340135 | ||||||
chr5:143340277
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1185-26109T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340277 | ||||||
chr5:143340349
|
C | CT | 41 | a0001c0001t0002g0237a0001c0002t0004g0060a0001c0002t0004g0167others(38): Show | 41 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1185-26182dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340349 | ||||||
chr5:143340364
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1185-26196A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340364 | ||||||
chr5:143340411
|
A | T | 3 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0252 | 4 | HG02074.hp2 NA18982.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-26243T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340411 | ||||||
chr5:143340476
|
A | AT | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(97): Show | 103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1185-26309dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340476 | ||||||
chr5:143340476
|
A | ATT | 43 | a0001c0001t0001g0071a0001c0001t0001g0077a0001c0001t0001g0078others(40): Show | 44 | HG00408.hp2 HG00423.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1185-26310_1185-26 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340476 | ||||||
chr5:143340476
|
A | ATTT | 7 | a0001c0001t0002g0007a0001c0001t0002g0223a0001c0001t0002g0227others(4): Show | 8 | HG02027.hp1 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-26311_1185-26 others(9): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340476 | ||||||
chr5:143340476
|
AT | A | 37 | a0001c0001t0002g0237a0001c0001t0003g0181a0001c0001t0005g0204others(34): Show | 37 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1185-26309delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340476 | ||||||
chr5:143340513
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1185-26345G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340513 | ||||||
chr5:143340556
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1185-26388G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340556 | ||||||
chr5:143340628
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1185-26460C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340628 | ||||||
chr5:143340631
|
C | T | 7 | a0001c0004t0004g0053a0001c0005t0009g0008a0001c0005t0009g0249others(4): Show | 8 | HG00738.hp1 HG02027.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1185-26463G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340631 | ||||||
chr5:143340717
|
G | A | 1 | a0001c0001t0002g0226 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1185-26549C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340717 | ||||||
chr5:143340786
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-26618C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340786 | ||||||
chr5:143341025
|
C | A | 3 | a0001c0001t0007g0001a0001c0001t0007g0020a0001c0001t0007g0021 | 4 | HG02896.hp2 HG02897.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-26857G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341025 | ||||||
chr5:143341028
|
A | G | 1 | a0001c0004t0004g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1185-26860T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341028 | ||||||
chr5:143341056
|
G | T | 1 | a0001c0001t0002g0237 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1185-26888C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341056 | ||||||
chr5:143341059
|
C | G | 1 | a0001c0001t0002g0237 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1185-26891G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341059 | ||||||
chr5:143341060
|
A | C | 1 | a0001c0001t0002g0237 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1185-26892T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341060 | ||||||
chr5:143341161
|
T | C | 56 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(53): Show | 58 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1185-26993A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341161 | ||||||
chr5:143341185
|
G | T | 1 | a0001c0001t0002g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1185-27017C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341185 | ||||||
chr5:143341375
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1185-27207G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341375 | ||||||
chr5:143341500
|
T | A | 5 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0129others(2): Show | 5 | HG00408.hp1 NA18747.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-27332A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341500 | ||||||
chr5:143341526
|
T | C | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-27358A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341526 | ||||||
chr5:143341965
|
C | A | 1 | a0001c0001t0002g0238 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1185-27797G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341965 | ||||||
chr5:143342015
|
G | A | 1 | a0001c0001t0002g0243 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1185-27847C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143342015 | ||||||
chr5:143342192
|
C | T | 2 | a0001c0001t0005g0210a0001c0001t0005g0211 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1185-28024G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143342192 | ||||||
chr5:143342193
|
G | A | 6 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0200others(3): Show | 6 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-28025C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143342193 | ||||||
chr5:143342788
|
T | C | 40 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1185-28620A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143342788 | ||||||
chr5:143342828
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-28660G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143342828 | ||||||
chr5:143343095
|
G | C | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1185-28927C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343095 | ||||||
chr5:143343146
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1185-28978G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343146 | ||||||
chr5:143343297
|
C | T | 11 | a0001c0001t0003g0184a0001c0001t0003g0188a0001c0001t0003g0189others(8): Show | 11 | HG01099.hp1 HG01169.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1185-29129G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343297 | ||||||
chr5:143343316
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1185-29148A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343316 | ||||||
chr5:143343351
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1185-29183A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343351 | ||||||
chr5:143343450
|
T | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 6 | HG02451.hp2 HG03098.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-29282A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343450 | ||||||
chr5:143343657
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0031g0128 | 2 | HG00408.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1185-29489G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343657 | ||||||
chr5:143343719
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1185-29551C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343719 | ||||||
chr5:143343772
|
T | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 7 | HG02451.hp2 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185-29604A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343772 | ||||||
chr5:143343808
|
G | C | 40 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1185-29640C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343808 | ||||||
chr5:143343851
|
T | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-29683A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343851 | ||||||
chr5:143343868
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-29700G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343868 | ||||||
chr5:143344030
|
T | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-29862A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344030 | ||||||
chr5:143344067
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1185-29899T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344067 | ||||||
chr5:143344156
|
T | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-29988A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344156 | ||||||
chr5:143344372
|
T | G | 34 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0108others(31): Show | 34 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.1185-30204A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344372 | ||||||
chr5:143344599
|
G | A | 1 | a0001c0001t0003g0191 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1185-30431C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344599 | ||||||
chr5:143344643
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-30475G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344643 | ||||||
chr5:143344865
|
G | A | 39 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(36): Show | 39 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1185-30697C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344865 | ||||||
chr5:143344892
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1185-30724G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344892 | ||||||
chr5:143345025
|
TGTGTGTG others(31): Show |
T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30895_1185-30 others(44): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345025 | ||||||
chr5:143345090
|
G | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30922C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345090 | ||||||
chr5:143345102
|
G | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30934C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345102 | ||||||
chr5:143345146
|
T | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30978A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345146 | ||||||
chr5:143345148
|
T | A | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30980A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345148 | ||||||
chr5:143345149
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30981T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345149 | ||||||
chr5:143345151
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30983C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345151 | ||||||
chr5:143345186
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31018T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345186 | ||||||
chr5:143345227
|
T | TGTGGGGG others(3): Show |
1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31060_1185-31 others(16): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345227 | ||||||
chr5:143345228
|
T | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31060A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345228 | ||||||
chr5:143345230
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31062T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345230 | ||||||
chr5:143345241
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31073T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345241 | ||||||
chr5:143345242
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31074C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345242 | ||||||
chr5:143345256
|
C | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31088G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345256 | ||||||
chr5:143345258
|
G | C | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31090C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345258 | ||||||
chr5:143345267
|
G | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31099C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345267 | ||||||
chr5:143345272
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31104G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345272 | ||||||
chr5:143345273
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31105T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345273 | ||||||
chr5:143345314
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31146T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345314 | ||||||
chr5:143345519
|
A | T | 78 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1185-31351T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345519 | ||||||
chr5:143345748
|
A | G | 2 | a0001c0001t0002g0006a0001c0001t0002g0241 | 3 | HG00597.hp2 NA19007.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1185-31580T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345748 | ||||||
chr5:143345907
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0138 | 3 | NA18747.hp2 NA18940.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1185-31739A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345907 | ||||||
chr5:143345995
|
T | C | 1 | a0001c0001t0025g0224 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1185-31827A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345995 | ||||||
chr5:143346270
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-32102C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143346270 | ||||||
chr5:143346300
|
C | A | 1 | a0001c0001t0010g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-32132G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143346300 | ||||||
chr5:143346605
|
C | T | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1185-32437G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143346605 | ||||||
chr5:143346630
|
C | A | 1 | a0001c0001t0002g0226 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1185-32462G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143346630 | ||||||
chr5:143346960
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-32792C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143346960 | ||||||
chr5:143347329
|
C | CACACACA others(1): Show |
6 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-33169_1185-33 others(14): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143347329 | ||||||
chr5:143347564
|
C | T | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-33396G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143347564 | ||||||
chr5:143347628
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(117): Show | 122 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1185-33460C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143347628 | ||||||
chr5:143347680
|
A | G | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-33512T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143347680 | ||||||
chr5:143347845
|
A | C | 1 | a0001c0001t0002g0213 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1185-33677T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143347845 | ||||||
chr5:143347977
|
GT | G | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-33810delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143347977 | ||||||
chr5:143348165
|
C | T | 2 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1185-33997G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348165 | ||||||
chr5:143348197
|
T | C | 1 | a0001c0001t0032g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1185-34029A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348197 | ||||||
chr5:143348381
|
C | T | 1 | a0001c0001t0002g0226 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1185-34213G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348381 | ||||||
chr5:143348466
|
T | C | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-34298A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348466 | ||||||
chr5:143348494
|
C | T | 1 | a0001c0001t0035g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1185-34326G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348494 | ||||||
chr5:143348764
|
A | G | 4 | a0001c0001t0005g0204a0001c0001t0005g0205a0001c0001t0005g0210others(1): Show | 4 | HG02723.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1185-34596T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348764 | ||||||
chr5:143348781
|
A | G | 22 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.1185-34613T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348781 | ||||||
chr5:143348854
|
A | G | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1185-34686T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348854 | ||||||
chr5:143348859
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-34691C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348859 | ||||||
chr5:143348900
|
T | C | 2 | a0001c0001t0001g0074a0004c0009t0001g0075 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1185-34732A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348900 | ||||||
chr5:143349121
|
T | C | 1 | a0001c0004t0004g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1185-34953A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349121 | ||||||
chr5:143349141
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1185-34973C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349141 | ||||||
chr5:143349143
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-34975A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349143 | ||||||
chr5:143349194
|
T | C | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-35026A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349194 | ||||||
chr5:143349539
|
G | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-35371C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349539 | ||||||
chr5:143349638
|
T | G | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1185-35470A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349638 | ||||||
chr5:143349874
|
G | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-35706C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349874 | ||||||
chr5:143350251
|
G | A | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1185-36083C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350251 | ||||||
chr5:143350358
|
A | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-36190T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350358 | ||||||
chr5:143350640
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-36472A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350640 | ||||||
chr5:143350811
|
G | C | 34 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0108others(31): Show | 34 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.1185-36643C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350811 | ||||||
chr5:143350867
|
G | T | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1185-36699C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350867 | ||||||
chr5:143350904
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-36736C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350904 | ||||||
chr5:143350915
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1185-36747T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350915 | ||||||
chr5:143351120
|
C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-36952G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143351120 | ||||||
chr5:143351291
|
G | A | 1 | a0001c0001t0003g0192 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1185-37123C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143351291 | ||||||
chr5:143351392
|
TA | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-37225delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143351392 | ||||||
chr5:143351444
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1185-37276A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143351444 | ||||||
chr5:143352016
|
A | C | 1 | a0001c0001t0001g0127 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1185-37848T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143352016 | ||||||
chr5:143352821
|
A | G | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-38653T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143352821 | ||||||
chr5:143352941
|
A | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-38773T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143352941 | ||||||
chr5:143353042
|
C | T | 29 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(26): Show | 29 | HG00438.hp1 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1185-38874G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353042 | ||||||
chr5:143353356
|
G | A | 1 | a0001c0002t0017g0034 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1185-39188C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353356 | ||||||
chr5:143353498
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1185-39330G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353498 | ||||||
chr5:143353502
|
C | T | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-39334G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353502 | ||||||
chr5:143353522
|
G | C | 1 | a0001c0001t0003g0187 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1185-39354C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353522 | ||||||
chr5:143353576
|
T | G | 1 | a0001c0006t0001g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1185-39408A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353576 | ||||||
chr5:143353608
|
A | G | 6 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-39440T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353608 | ||||||
chr5:143353626
|
G | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0248a0001c0001t0026g0115others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1185-39458C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353626 | ||||||
chr5:143353636
|
A | T | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1185-39468T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353636 | ||||||
chr5:143353724
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-39556G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353724 | ||||||
chr5:143353814
|
G | A | 1 | a0001c0001t0003g0207 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1185-39646C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353814 | ||||||
chr5:143354043
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1185-39875A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354043 | ||||||
chr5:143354054
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1185-39886G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354054 | ||||||
chr5:143354220
|
T | C | 1 | a0001c0004t0004g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1185-40052A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354220 | ||||||
chr5:143354510
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-40342A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354510 | ||||||
chr5:143354537
|
G | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-40369C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354537 | ||||||
chr5:143354576
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-40408C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354576 | ||||||
chr5:143354586
|
T | C | 40 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1185-40418A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354586 | ||||||
chr5:143354674
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1185-40506C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354674 | ||||||
chr5:143354675
|
C | A | 1 | a0001c0001t0001g0175 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1185-40507G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354675 | ||||||
chr5:143354768
|
C | T | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-40600G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354768 | ||||||
chr5:143354827
|
G | A | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1185-40659C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354827 | ||||||
chr5:143354940
|
G | A | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-40772C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354940 | ||||||
chr5:143354970
|
G | A | 10 | a0001c0001t0003g0184a0001c0001t0003g0188a0001c0001t0003g0189others(7): Show | 10 | HG01175.hp2 HG01192.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-40802C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354970 | ||||||
chr5:143355141
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-40973G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143355141 | ||||||
chr5:143355177
|
T | C | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(251): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1185-41009A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143355177 | ||||||
chr5:143355482
|
A | AATAATAA others(6): Show |
6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-41315_1185-41 others(19): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143355482 | ||||||
chr5:143355483
|
T | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-41315A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143355483 | ||||||
chr5:143355483
|
T | TAATAAAT others(5): Show |
3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-41327_1185-41 others(18): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143355483 | ||||||
chr5:143355974
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1185-41806G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143355974 | ||||||
chr5:143356000
|
CAT | C | 5 | a0001c0003t0008g0024a0001c0003t0008g0025a0001c0003t0008g0026others(2): Show | 5 | HG02886.hp1 HG02895.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-41834_1185-41 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356000 | ||||||
chr5:143356002
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0097 | 3 | HG02451.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1185-41834A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356002 | ||||||
chr5:143356273
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-42105C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356273 | ||||||
chr5:143356417
|
G | A | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-42249C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356417 | ||||||
chr5:143356423
|
T | C | 1 | a0001c0001t0003g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1185-42255A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356423 | ||||||
chr5:143356445
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-42277A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356445 | ||||||
chr5:143356688
|
C | CA | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(117): Show | 122 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1185-42521dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356688 | ||||||
chr5:143356688
|
CA | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-42521delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356688 | ||||||
chr5:143356699
|
A | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-42531T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356699 | ||||||
chr5:143356822
|
A | C | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-42654T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356822 | ||||||
chr5:143357059
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1184+42597C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357059 | ||||||
chr5:143357084
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1184+42572A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357084 | ||||||
chr5:143357217
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+42439C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357217 | ||||||
chr5:143357253
|
A | AT | 29 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(26): Show | 29 | HG00438.hp1 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1184+42402dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357253 | ||||||
chr5:143357275
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+42381C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357275 | ||||||
chr5:143357317
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+42339A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357317 | ||||||
chr5:143357347
|
G | A | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+42309C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357347 | ||||||
chr5:143357401
|
T | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG02055.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+42255A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357401 | ||||||
chr5:143357499
|
T | C | 1 | a0001c0002t0018g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1184+42157A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357499 | ||||||
chr5:143357549
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+42107T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357549 | ||||||
chr5:143357651
|
T | G | 1 | a0001c0003t0006g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1184+42005A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357651 | ||||||
chr5:143357700
|
T | C | 1 | a0001c0001t0007g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1184+41956A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357700 | ||||||
chr5:143358006
|
A | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+41650T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358006 | ||||||
chr5:143358163
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1184+41493C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358163 | ||||||
chr5:143358194
|
A | G | 2 | a0001c0001t0003g0195a0001c0001t0003g0196 | 2 | HG01099.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1184+41462T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358194 | ||||||
chr5:143358215
|
A | C | 5 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0083others(2): Show | 5 | HG01255.hp1 HG06807.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+41441T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358215 | ||||||
chr5:143358231
|
T | A | 1 | a0001c0001t0001g0173 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1184+41425A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358231 | ||||||
chr5:143358624
|
G | A | 1 | a0001c0001t0002g0237 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1184+41032C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358624 | ||||||
chr5:143358699
|
C | T | 8 | a0001c0001t0001g0114a0001c0001t0001g0139a0001c0001t0001g0140others(5): Show | 8 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+40957G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358699 | ||||||
chr5:143358768
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1184+40888G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358768 | ||||||
chr5:143358800
|
T | C | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1184+40856A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358800 | ||||||
chr5:143358894
|
C | T | 2 | a0001c0001t0007g0014a0001c0001t0013g0010 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1184+40762G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358894 | ||||||
chr5:143358898
|
T | C | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+40758A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358898 | ||||||
chr5:143358900
|
CA | C | 9 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0127others(6): Show | 9 | HG00408.hp1 HG02165.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.1184+40755delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358900 | ||||||
chr5:143359062
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1184+40594A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359062 | ||||||
chr5:143359124
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1184+40532T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359124 | ||||||
chr5:143359181
|
G | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+40475C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359181 | ||||||
chr5:143359215
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1184+40441G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359215 | ||||||
chr5:143359424
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1184+40232C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359424 | ||||||
chr5:143359606
|
C | T | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+40050G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359606 | ||||||
chr5:143359681
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+39975C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359681 | ||||||
chr5:143360167
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1184+39489G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143360167 | ||||||
chr5:143360327
|
T | C | 1 | a0001c0001t0007g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1184+39329A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143360327 | ||||||
chr5:143360601
|
G | A | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+39055C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143360601 | ||||||
chr5:143360950
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1184+38706T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143360950 | ||||||
chr5:143361005
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1184+38651G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361005 | ||||||
chr5:143361175
|
T | C | 1 | a0001c0001t0002g0238 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1184+38481A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361175 | ||||||
chr5:143361181
|
G | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+38475C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361181 | ||||||
chr5:143361190
|
G | T | 1 | a0001c0001t0007g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1184+38466C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361190 | ||||||
chr5:143361228
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+38428C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361228 | ||||||
chr5:143361381
|
T | C | 1 | a0001c0001t0002g0220 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1184+38275A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361381 | ||||||
chr5:143361390
|
T | C | 3 | a0001c0001t0007g0013a0001c0001t0007g0017a0001c0001t0007g0018 | 3 | HG03098.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1184+38266A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361390 | ||||||
chr5:143361462
|
C | T | 78 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1184+38194G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361462 | ||||||
chr5:143361464
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1184+38192A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361464 | ||||||
chr5:143361680
|
G | A | 3 | a0001c0001t0007g0001a0001c0001t0007g0020a0001c0001t0007g0021 | 4 | HG02896.hp2 HG02897.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+37976C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361680 | ||||||
chr5:143361874
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+37782T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361874 | ||||||
chr5:143362176
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+37480G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362176 | ||||||
chr5:143362341
|
A | C | 1 | a0001c0001t0001g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1184+37315T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362341 | ||||||
chr5:143362360
|
G | GT | 19 | a0001c0001t0001g0066a0001c0001t0001g0089a0001c0001t0001g0114others(16): Show | 19 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184+37295dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362360 | ||||||
chr5:143362453
|
T | C | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+37203A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362453 | ||||||
chr5:143362508
|
C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+37148G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362508 | ||||||
chr5:143362525
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+37131A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362525 | ||||||
chr5:143362552
|
A | G | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+37104T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362552 | ||||||
chr5:143362583
|
AATCTCCT others(9): Show |
A | 1 | a0001c0001t0001g0138 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1184+37057_1184+37 others(22): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362583 | ||||||
chr5:143362629
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+37027C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362629 | ||||||
chr5:143362878
|
A | G | 1 | a0001c0001t0014g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1184+36778T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362878 | ||||||
chr5:143362926
|
C | T | 78 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1184+36730G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362926 | ||||||
chr5:143362972
|
T | C | 40 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1184+36684A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362972 | ||||||
chr5:143362995
|
T | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+36661A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362995 | ||||||
chr5:143363040
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+36616C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363040 | ||||||
chr5:143363134
|
A | G | 4 | a0001c0001t0005g0204a0001c0001t0005g0205a0001c0001t0005g0210others(1): Show | 4 | HG02723.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+36522T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363134 | ||||||
chr5:143363397
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1184+36259G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363397 | ||||||
chr5:143363490
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1184+36166C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363490 | ||||||
chr5:143363503
|
G | T | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+36153C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363503 | ||||||
chr5:143363538
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+36118T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363538 | ||||||
chr5:143363581
|
TA | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1184+36074delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363581 | ||||||
chr5:143363760
|
C | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+35896G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363760 | ||||||
chr5:143363905
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+35751A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363905 | ||||||
chr5:143364028
|
A | G | 1 | a0001c0002t0004g0060 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1184+35628T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364028 | ||||||
chr5:143364054
|
A | G | 1 | a0001c0001t0007g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+35602T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364054 | ||||||
chr5:143364292
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1184+35364G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364292 | ||||||
chr5:143364295
|
T | C | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+35361A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364295 | ||||||
chr5:143364527
|
G | C | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+35129C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364527 | ||||||
chr5:143364614
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1184+35042T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364614 | ||||||
chr5:143364712
|
T | C | 6 | a0001c0006t0001g0098a0001c0006t0001g0099a0001c0006t0001g0100others(3): Show | 6 | HG02572.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+34944A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364712 | ||||||
chr5:143364732
|
G | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1184+34924C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364732 | ||||||
chr5:143365249
|
C | A | 1 | a0001c0001t0036g0214 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1184+34407G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365249 | ||||||
chr5:143365284
|
G | T | 1 | a0001c0001t0025g0224 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1184+34372C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365284 | ||||||
chr5:143365398
|
A | C | 40 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1184+34258T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365398 | ||||||
chr5:143365420
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+34236C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365420 | ||||||
chr5:143365480
|
A | G | 1 | a0001c0001t0014g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1184+34176T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365480 | ||||||
chr5:143365495
|
C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+34161G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365495 | ||||||
chr5:143365610
|
C | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+34046G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365610 | ||||||
chr5:143365750
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1184+33906A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365750 | ||||||
chr5:143365809
|
C | T | 1 | a0001c0005t0009g0257 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1184+33847G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365809 | ||||||
chr5:143365902
|
C | T | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1184+33754G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365902 | ||||||
chr5:143365937
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1184+33719C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365937 | ||||||
chr5:143366390
|
A | G | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1184+33266T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366390 | ||||||
chr5:143366458
|
C | T | 38 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1184+33198G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366458 | ||||||
chr5:143366463
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+33193A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366463 | ||||||
chr5:143366477
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1184+33179A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366477 | ||||||
chr5:143366510
|
CA | C | 46 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(43): Show | 47 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.1184+33145delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366510 | ||||||
chr5:143366528
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1184+33128A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366528 | ||||||
chr5:143366614
|
G | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+33042C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366614 | ||||||
chr5:143366798
|
A | C | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1184+32858T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366798 | ||||||
chr5:143367036
|
C | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+32620G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367036 | ||||||
chr5:143367070
|
C | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+32586G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367070 | ||||||
chr5:143367088
|
A | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+32568T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367088 | ||||||
chr5:143367282
|
G | A | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1184+32374C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367282 | ||||||
chr5:143367700
|
A | G | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+31956T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367700 | ||||||
chr5:143367723
|
A | G | 1 | a0001c0001t0030g0194 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1184+31933T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367723 | ||||||
chr5:143367755
|
A | G | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+31901T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367755 | ||||||
chr5:143368168
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1184+31488C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368168 | ||||||
chr5:143368534
|
T | TAC | 46 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(43): Show | 47 | HG00438.hp2 HG00639.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1184+31120_1184+31 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368534 | ||||||
chr5:143368534
|
T | TACAC | 5 | a0001c0001t0003g0193a0001c0001t0003g0197a0001c0001t0004g0239others(2): Show | 5 | HG01243.hp2 HG01257.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+31118_1184+31 others(10): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368534 | ||||||
chr5:143368534
|
TAC | T | 35 | a0001c0001t0001g0086a0001c0001t0004g0087a0001c0002t0004g0060others(32): Show | 36 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.1184+31120_1184+31 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368534 | ||||||
chr5:143368534
|
TACAC | T | 4 | a0001c0001t0024g0206a0002c0007t0011g0254a0002c0007t0011g0255others(1): Show | 4 | HG01884.hp1 HG01934.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+31118_1184+31 others(10): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368534 | ||||||
chr5:143368534
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0002g0004 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1184+31108_1184+31 others(20): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368534 | ||||||
chr5:143368686
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+30970C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368686 | ||||||
chr5:143368700
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1184+30956T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368700 | ||||||
chr5:143368786
|
A | G | 1 | a0001c0001t0002g0223 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1184+30870T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368786 | ||||||
chr5:143369009
|
T | C | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1184+30647A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369009 | ||||||
chr5:143369114
|
T | C | 1 | a0001c0003t0006g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1184+30542A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369114 | ||||||
chr5:143369391
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+30265A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369391 | ||||||
chr5:143369489
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1184+30167T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369489 | ||||||
chr5:143369743
|
A | G | 1 | a0001c0001t0029g0124 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1184+29913T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369743 | ||||||
chr5:143369784
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+29872G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369784 | ||||||
chr5:143369847
|
T | C | 2 | a0001c0001t0003g0182a0001c0001t0030g0194 | 2 | HG02602.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1184+29809A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369847 | ||||||
chr5:143370222
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1184+29434A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370222 | ||||||
chr5:143370302
|
G | A | 1 | a0001c0006t0001g0098 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1184+29354C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370302 | ||||||
chr5:143370639
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1184+29017G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370639 | ||||||
chr5:143370657
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG01496.hp2 NA18971.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+28999C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370657 | ||||||
chr5:143370736
|
A | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(213): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.1184+28920T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370736 | ||||||
chr5:143370881
|
C | T | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+28775G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370881 | ||||||
chr5:143370884
|
A | G | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1184+28772T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370884 | ||||||
chr5:143370968
|
T | G | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+28688A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370968 | ||||||
chr5:143371147
|
T | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+28509A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143371147 | ||||||
chr5:143371178
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1184+28478A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143371178 | ||||||
chr5:143371257
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+28399A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143371257 | ||||||
chr5:143371605
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+28051C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143371605 | ||||||
chr5:143371654
|
G | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+28002C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143371654 | ||||||
chr5:143371863
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+27793G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143371863 | ||||||
chr5:143372259
|
C | T | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+27397G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372259 | ||||||
chr5:143372425
|
T | C | 9 | a0001c0004t0004g0049a0001c0004t0004g0050a0001c0004t0004g0052others(6): Show | 9 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+27231A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372425 | ||||||
chr5:143372534
|
C | T | 2 | a0001c0001t0005g0063a0001c0001t0005g0222 | 2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1184+27122G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372534 | ||||||
chr5:143372617
|
C | T | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1184+27039G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372617 | ||||||
chr5:143372627
|
G | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+27029C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372627 | ||||||
chr5:143372754
|
A | G | 1 | a0001c0001t0010g0088 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1184+26902T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372754 | ||||||
chr5:143372762
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1184+26894G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372762 | ||||||
chr5:143372801
|
C | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+26855G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372801 | ||||||
chr5:143372915
|
C | T | 8 | a0001c0004t0004g0049a0001c0004t0004g0050a0001c0004t0004g0052others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+26741G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372915 | ||||||
chr5:143372990
|
A | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+26666T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372990 | ||||||
chr5:143373300
|
G | C | 1 | a0001c0001t0007g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1184+26356C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373300 | ||||||
chr5:143373466
|
G | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+26190C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373466 | ||||||
chr5:143373606
|
T | C | 1 | a0001c0004t0001g0137 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1184+26050A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373606 | ||||||
chr5:143373688
|
TAG | T | 9 | a0001c0003t0008g0024a0001c0003t0008g0025a0001c0003t0008g0026others(6): Show | 9 | HG02055.hp1 HG02486.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+25966_1184+25 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373688 | ||||||
chr5:143373691
|
G | C | 9 | a0001c0003t0008g0024a0001c0003t0008g0025a0001c0003t0008g0026others(6): Show | 9 | HG02055.hp1 HG02486.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+25965C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373691 | ||||||
chr5:143373739
|
A | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+25917T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373739 | ||||||
chr5:143373774
|
G | A | 1 | a0001c0001t0030g0194 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1184+25882C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373774 | ||||||
chr5:143373900
|
T | C | 1 | a0001c0006t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1184+25756A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373900 | ||||||
chr5:143373908
|
TG | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+25747delC | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373908 | ||||||
chr5:143373971
|
G | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+25685C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373971 | ||||||
chr5:143374054
|
C | T | 7 | a0001c0001t0001g0123a0001c0005t0009g0008a0001c0005t0009g0249others(4): Show | 8 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+25602G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374054 | ||||||
chr5:143374104
|
C | A | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+25552G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374104 | ||||||
chr5:143374148
|
G | C | 1 | a0001c0001t0012g0009 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1184+25508C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374148 | ||||||
chr5:143374218
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+25438A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374218 | ||||||
chr5:143374220
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+25436A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374220 | ||||||
chr5:143374221
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+25435C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374221 | ||||||
chr5:143374231
|
G | A | 37 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(34): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1184+25425C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374231 | ||||||
chr5:143374258
|
C | T | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+25398G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374258 | ||||||
chr5:143374264
|
G | T | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1184+25392C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374264 | ||||||
chr5:143374306
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1184+25350G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374306 | ||||||
chr5:143374308
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1184+25348G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374308 | ||||||
chr5:143374342
|
A | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+25314T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374342 | ||||||
chr5:143374422
|
C | T | 1 | a0001c0006t0001g0098 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1184+25234G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374422 | ||||||
chr5:143374423
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1184+25233C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374423 | ||||||
chr5:143374490
|
C | CA | 36 | a0001c0001t0002g0240a0001c0001t0003g0180a0001c0001t0003g0181others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.1184+25165dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374490 | ||||||
chr5:143374490
|
CA | C | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+25165delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374490 | ||||||
chr5:143374699
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1184+24957G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374699 | ||||||
chr5:143374705
|
G | A | 1 | a0001c0003t0008g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1184+24951C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374705 | ||||||
chr5:143374943
|
G | A | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1184+24713C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374943 | ||||||
chr5:143375125
|
T | C | 42 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1184+24531A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375125 | ||||||
chr5:143375238
|
C | T | 1 | a0001c0001t0004g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1184+24418G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375238 | ||||||
chr5:143375268
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 6 | HG02451.hp2 HG02615.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+24388C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375268 | ||||||
chr5:143375339
|
T | C | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+24317A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375339 | ||||||
chr5:143375432
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+24224C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375432 | ||||||
chr5:143375566
|
T | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+24090A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375566 | ||||||
chr5:143375889
|
A | G | 1 | a0001c0002t0006g0036 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1184+23767T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375889 | ||||||
chr5:143375978
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+23678G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375978 | ||||||
chr5:143376008
|
G | T | 1 | a0001c0001t0001g0169 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1184+23648C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376008 | ||||||
chr5:143376069
|
GA | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+23586delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376069 | ||||||
chr5:143376129
|
GA | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+23526delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376129 | ||||||
chr5:143376182
|
T | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+23474A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376182 | ||||||
chr5:143376397
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1184+23259A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376397 | ||||||
chr5:143376439
|
A | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(64): Show | 69 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1184+23217T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376439 | ||||||
chr5:143376640
|
T | G | 1 | a0001c0003t0006g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1184+23016A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376640 | ||||||
chr5:143376701
|
G | C | 39 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(36): Show | 39 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1184+22955C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376701 | ||||||
chr5:143376875
|
A | G | 1 | a0001c0004t0004g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1184+22781T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376875 | ||||||
chr5:143377446
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1184+22210G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143377446 | ||||||
chr5:143377547
|
C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+22109G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143377547 | ||||||
chr5:143377901
|
G | A | 1 | a0001c0001t0035g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1184+21755C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143377901 | ||||||
chr5:143377923
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0139a0001c0001t0001g0140others(5): Show | 8 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+21733C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143377923 | ||||||
chr5:143377941
|
G | A | 6 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | NA18946.hp1 NA18974.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+21715C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143377941 | ||||||
chr5:143378076
|
CCT | C | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+21578_1184+21 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378076 | ||||||
chr5:143378302
|
G | A | 1 | a0001c0003t0008g0045 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1184+21354C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378302 | ||||||
chr5:143378327
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+21329G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378327 | ||||||
chr5:143378510
|
T | C | 16 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(13): Show | 16 | HG00438.hp1 HG02132.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.1184+21146A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378510 | ||||||
chr5:143378536
|
A | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0106 | 2 | HG00408.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1184+21120T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378536 | ||||||
chr5:143378623
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+21033C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378623 | ||||||
chr5:143378829
|
T | C | 9 | a0001c0004t0004g0049a0001c0004t0004g0050a0001c0004t0004g0052others(6): Show | 9 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+20827A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378829 | ||||||
chr5:143378931
|
T | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1184+20725A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378931 | ||||||
chr5:143379035
|
T | C | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+20621A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379035 | ||||||
chr5:143379036
|
A | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+20620T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379036 | ||||||
chr5:143379320
|
A | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG02055.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+20336T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379320 | ||||||
chr5:143379646
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+20010T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379646 | ||||||
chr5:143379775
|
A | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+19881T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379775 | ||||||
chr5:143379789
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184+19867G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379789 | ||||||
chr5:143379927
|
A | G | 3 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0252 | 4 | HG02074.hp2 NA18982.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+19729T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379927 | ||||||
chr5:143380073
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1184+19583A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380073 | ||||||
chr5:143380103
|
T | C | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1184+19553A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380103 | ||||||
chr5:143380118
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1184+19538T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380118 | ||||||
chr5:143380220
|
A | G | 68 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1184+19436T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380220 | ||||||
chr5:143380235
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+19421C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380235 | ||||||
chr5:143380359
|
A | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+19297T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380359 | ||||||
chr5:143380399
|
AT | A | 4 | a0001c0006t0001g0103a0002c0007t0011g0254a0002c0007t0011g0255others(1): Show | 4 | HG01884.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+19256delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380399 | ||||||
chr5:143380431
|
G | T | 1 | a0001c0001t0005g0204 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1184+19225C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380431 | ||||||
chr5:143380561
|
T | G | 1 | a0001c0005t0009g0251 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1184+19095A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380561 | ||||||
chr5:143380694
|
C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+18962G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380694 | ||||||
chr5:143380761
|
G | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+18895C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380761 | ||||||
chr5:143380769
|
A | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+18887T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380769 | ||||||
chr5:143380975
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+18681C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380975 | ||||||
chr5:143381007
|
T | A | 1 | a0001c0002t0018g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1184+18649A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381007 | ||||||
chr5:143381018
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1184+18638C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381018 | ||||||
chr5:143381186
|
T | C | 2 | a0001c0001t0003g0195a0001c0001t0003g0196 | 2 | HG01099.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1184+18470A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381186 | ||||||
chr5:143381240
|
G | GA | 7 | a0001c0001t0001g0209a0001c0001t0007g0001a0001c0001t0007g0011others(4): Show | 8 | HG02723.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+18415dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381240 | ||||||
chr5:143381474
|
C | T | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+18182G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381474 | ||||||
chr5:143381475
|
G | A | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+18181C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381475 | ||||||
chr5:143381550
|
A | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+18106T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381550 | ||||||
chr5:143381962
|
C | A | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(182): Show | 193 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1184+17694G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381962 | ||||||
chr5:143382060
|
C | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0248a0001c0001t0026g0115others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+17596G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143382060 | ||||||
chr5:143382248
|
T | C | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+17408A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143382248 | ||||||
chr5:143382302
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1184+17354A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143382302 | ||||||
chr5:143382445
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+17211T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143382445 | ||||||
chr5:143382707
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1184+16949C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143382707 | ||||||
chr5:143382769
|
G | A | 6 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0200others(3): Show | 6 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+16887C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143382769 | ||||||
chr5:143383212
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1184+16444C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383212 | ||||||
chr5:143383413
|
G | A | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+16243C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383413 | ||||||
chr5:143383465
|
TA | T | 7 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0217others(4): Show | 9 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+16190delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383465 | ||||||
chr5:143383485
|
A | C | 1 | a0001c0004t0004g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1184+16171T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383485 | ||||||
chr5:143383492
|
A | T | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1184+16164T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383492 | ||||||
chr5:143383608
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+16048T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383608 | ||||||
chr5:143383704
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+15952G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383704 | ||||||
chr5:143384241
|
C | A | 1 | a0001c0005t0009g0252 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1184+15415G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384241 | ||||||
chr5:143384315
|
G | A | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+15341C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384315 | ||||||
chr5:143384544
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+15112G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384544 | ||||||
chr5:143384552
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1184+15104T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384552 | ||||||
chr5:143384885
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1184+14771G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384885 | ||||||
chr5:143384895
|
G | A | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+14761C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384895 | ||||||
chr5:143384911
|
T | A | 1 | a0001c0001t0002g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1184+14745A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384911 | ||||||
chr5:143384938
|
T | A | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+14718A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384938 | ||||||
chr5:143385007
|
G | A | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1184+14649C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385007 | ||||||
chr5:143385124
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1184+14532A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385124 | ||||||
chr5:143385134
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+14522A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385134 | ||||||
chr5:143385176
|
T | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1184+14480A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385176 | ||||||
chr5:143385220
|
C | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+14436G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385220 | ||||||
chr5:143385247
|
C | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+14409G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385247 | ||||||
chr5:143385304
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1184+14352A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385304 | ||||||
chr5:143385343
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+14313A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385343 | ||||||
chr5:143385534
|
T | C | 8 | a0001c0004t0004g0049a0001c0004t0004g0050a0001c0004t0004g0052others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+14122A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385534 | ||||||
chr5:143385556
|
A | G | 1 | a0001c0001t0002g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1184+14100T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385556 | ||||||
chr5:143385570
|
G | A | 78 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1184+14086C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385570 | ||||||
chr5:143385571
|
A | T | 77 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(74): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1184+14085T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385571 | ||||||
chr5:143385608
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+14048C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385608 | ||||||
chr5:143385848
|
C | T | 1 | a0001c0001t0010g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+13808G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385848 | ||||||
chr5:143385854
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+13802A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385854 | ||||||
chr5:143385868
|
T | C | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+13788A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385868 | ||||||
chr5:143385874
|
C | T | 1 | a0001c0004t0004g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1184+13782G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385874 | ||||||
chr5:143385875
|
G | A | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+13781C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385875 | ||||||
chr5:143386038
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+13618A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143386038 | ||||||
chr5:143386168
|
C | T | 8 | a0001c0004t0004g0049a0001c0004t0004g0050a0001c0004t0004g0052others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+13488G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143386168 | ||||||
chr5:143386224
|
C | T | 4 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0200others(1): Show | 4 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+13432G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143386224 | ||||||
chr5:143386256
|
T | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(253): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1184+13400A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143386256 | ||||||
chr5:143386571
|
A | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+13085T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143386571 | ||||||
chr5:143386876
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0020g0047a0001c0001t0024g0206 | 3 | HG01934.hp1 HG03486.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.1184+12780A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143386876 | ||||||
chr5:143387029
|
A | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+12627T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387029 | ||||||
chr5:143387081
|
T | C | 1 | a0001c0004t0004g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1184+12575A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387081 | ||||||
chr5:143387091
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184+12565A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387091 | ||||||
chr5:143387170
|
C | T | 1 | a0001c0001t0003g0183 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1184+12486G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387170 | ||||||
chr5:143387358
|
G | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+12298C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387358 | ||||||
chr5:143387428
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184+12228A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387428 | ||||||
chr5:143387524
|
A | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+12132T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387524 | ||||||
chr5:143387536
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1184+12120G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387536 | ||||||
chr5:143387595
|
T | C | 40 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1184+12061A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387595 | ||||||
chr5:143387690
|
C | T | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+11966G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387690 | ||||||
chr5:143387722
|
G | A | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+11934C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387722 | ||||||
chr5:143387761
|
T | C | 2 | a0002c0007t0011g0254a0002c0007t0011g0255 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+11895A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387761 | ||||||
chr5:143387851
|
C | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0164 | 2 | NA18950.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1184+11805G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387851 | ||||||
chr5:143387852
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0164 | 2 | NA18950.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1184+11804G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387852 | ||||||
chr5:143388123
|
C | T | 1 | a0001c0001t0005g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1184+11533G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388123 | ||||||
chr5:143388175
|
C | A | 30 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(27): Show | 30 | HG00408.hp2 HG00544.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1184+11481G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388175 | ||||||
chr5:143388213
|
T | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(241): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1184+11443A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388213 | ||||||
chr5:143388273
|
T | C | 4 | a0001c0001t0005g0204a0001c0001t0005g0205a0001c0001t0005g0210others(1): Show | 4 | HG02723.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+11383A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388273 | ||||||
chr5:143388400
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+11256A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388400 | ||||||
chr5:143388887
|
G | C | 1 | a0001c0003t0008g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1184+10769C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388887 | ||||||
chr5:143388895
|
G | A | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG02080.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1184+10761C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388895 | ||||||
chr5:143389075
|
T | C | 1 | a0001c0001t0004g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1184+10581A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143389075 | ||||||
chr5:143389109
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184+10547G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143389109 | ||||||
chr5:143389216
|
A | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+10440T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143389216 | ||||||
chr5:143389386
|
G | A | 1 | a0001c0002t0006g0041 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1184+10270C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143389386 | ||||||
chr5:143389416
|
G | C | 3 | a0001c0005t0009g0250a0001c0005t0009g0251a0001c0005t0009g0257 | 3 | HG02027.hp1 HG02135.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1184+10240C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143389416 | ||||||
chr5:143389476
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1184+10180G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143389476 | ||||||
chr5:143390183
|
T | C | 4 | a0001c0001t0002g0244a0001c0001t0002g0245a0001c0001t0002g0246others(1): Show | 4 | HG02148.hp1 HG02273.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+9473A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143390183 | ||||||
chr5:143390570
|
T | C | 6 | a0001c0002t0004g0060a0001c0002t0006g0036a0001c0002t0006g0037others(3): Show | 6 | HG00438.hp1 HG02132.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+9086A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143390570 | ||||||
chr5:143390660
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184+8996G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143390660 | ||||||
chr5:143390967
|
G | A | 1 | a0001c0001t0003g0197 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1184+8689C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143390967 | ||||||
chr5:143391218
|
G | A | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1184+8438C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391218 | ||||||
chr5:143391283
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1184+8373A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391283 | ||||||
chr5:143391588
|
A | G | 2 | a0001c0001t0003g0180a0001c0001t0003g0181 | 2 | HG01256.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1184+8068T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391588 | ||||||
chr5:143391632
|
T | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+8024A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391632 | ||||||
chr5:143391929
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1184+7727G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391929 | ||||||
chr5:143391954
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1184+7702T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391954 | ||||||
chr5:143391964
|
C | CTTT | 5 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(2): Show | 6 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+7689_1184+769 others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391964 | ||||||
chr5:143392005
|
G | A | 1 | a0001c0001t0004g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1184+7651C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392005 | ||||||
chr5:143392034
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0012g0009 | 2 | HG03710.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1184+7622G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392034 | ||||||
chr5:143392122
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+7534A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392122 | ||||||
chr5:143392339
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1184+7317C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392339 | ||||||
chr5:143392519
|
G | GT | 7 | a0001c0001t0001g0109a0001c0005t0009g0008a0001c0005t0009g0249others(4): Show | 8 | HG01891.hp1 HG02027.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1184+7136dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392519 | ||||||
chr5:143392749
|
A | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+6907T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392749 | ||||||
chr5:143392937
|
T | C | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1184+6719A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392937 | ||||||
chr5:143392971
|
T | C | 6 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0200others(3): Show | 6 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+6685A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392971 | ||||||
chr5:143393025
|
T | C | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+6631A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393025 | ||||||
chr5:143393056
|
C | A | 1 | a0001c0003t0006g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1184+6600G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393056 | ||||||
chr5:143393087
|
G | C | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+6569C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393087 | ||||||
chr5:143393242
|
G | A | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG02080.hp1 HG02129.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+6414C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393242 | ||||||
chr5:143393351
|
C | A | 1 | a0001c0002t0006g0041 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1184+6305G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393351 | ||||||
chr5:143393376
|
A | C | 1 | a0001c0001t0001g0169 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1184+6280T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393376 | ||||||
chr5:143393791
|
T | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+5865A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393791 | ||||||
chr5:143393865
|
G | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00597.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1184+5791C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393865 | ||||||
chr5:143394186
|
C | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+5470G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143394186 | ||||||
chr5:143394761
|
A | G | 1 | a0001c0002t0004g0167 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1184+4895T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143394761 | ||||||
chr5:143394840
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1184+4816T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143394840 | ||||||
chr5:143395127
|
C | T | 40 | a0001c0002t0004g0060a0001c0002t0004g0167a0001c0002t0004g0168others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1184+4529G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143395127 | ||||||
chr5:143395352
|
C | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+4304G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143395352 | ||||||
chr5:143395392
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0097 | 3 | HG02451.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1184+4264C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143395392 | ||||||
chr5:143395535
|
T | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+4121A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143395535 | ||||||
chr5:143395771
|
C | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+3885G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143395771 | ||||||
chr5:143395969
|
A | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+3687T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143395969 | ||||||
chr5:143396132
|
T | C | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+3524A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396132 | ||||||
chr5:143396394
|
C | G | 3 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182 | 3 | HG01256.hp1 HG02602.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1184+3262G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396394 | ||||||
chr5:143396400
|
C | T | 3 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182 | 3 | HG01256.hp1 HG02602.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1184+3256G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396400 | ||||||
chr5:143396691
|
CTTAATT | C | 28 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+2959_1184+296 others(10): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396691 | ||||||
chr5:143396732
|
T | C | 4 | a0001c0003t0008g0042a0001c0003t0008g0043a0001c0003t0008g0044others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+2924A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396732 | ||||||
chr5:143396787
|
T | G | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2869A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396787 | ||||||
chr5:143396868
|
A | G | 2 | a0001c0004t0004g0049a0001c0004t0004g0050 | 2 | HG01978.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1184+2788T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396868 | ||||||
chr5:143397119
|
T | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1184+2537A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143397119 | ||||||
chr5:143397346
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1184+2310A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143397346 | ||||||
chr5:143397550
|
G | A | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2106C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143397550 | ||||||
chr5:143397883
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+1773C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143397883 | ||||||
chr5:143397885
|
T | G | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+1771A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143397885 | ||||||
chr5:143397938
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1184+1718A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143397938 | ||||||
chr5:143398355
|
G | GGT | 69 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(66): Show | 73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.1184+1299_1184+130 others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398355 | ||||||
chr5:143398356
|
G | GT | 9 | a0001c0001t0001g0066a0001c0001t0001g0104a0001c0001t0001g0105others(6): Show | 9 | HG00741.hp1 HG01192.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1184+1299dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398356 | ||||||
chr5:143398356
|
G | GTGT | 39 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0215others(36): Show | 39 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.1184+1299_1184+130 others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398356 | ||||||
chr5:143398356
|
GT | G | 14 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0096others(11): Show | 15 | HG00639.hp1 HG01070.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1184+1299delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398356 | ||||||
chr5:143398512
|
G | T | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+1144C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398512 | ||||||
chr5:143398611
|
C | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+1045G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398611 | ||||||
chr5:143398879
|
T | G | 2 | a0001c0001t0005g0210a0001c0001t0005g0211 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1184+777A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398879 | ||||||
chr5:143399010
|
G | C | 83 | a0001c0001t0001g0169a0001c0001t0002g0004a0001c0001t0002g0005others(80): Show | 87 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1184+646C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143399010 | ||||||
chr5:143399038
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1184+618A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143399038 | ||||||
chr5:143399435
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184+221A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143399435 | ||||||
chr5:143399509
|
T | C | 7 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG00423.hp1 HG01496.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+147A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143399509 | ||||||
chr5:143399587
|
T | C | 6 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(3): Show | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+69A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143399587 | ||||||
chr5:143400982
|
T | C | 1 | a0001c0003t0006g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-13-130A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143400982 | ||||||
chr5:143401092
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-13-240T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401092 | ||||||
chr5:143401130
|
C | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(119): Show | 124 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-13-278G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401130 | ||||||
chr5:143401132
|
C | T | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(119): Show | 124 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-13-280G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401132 | ||||||
chr5:143401140
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-13-288C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401140 | ||||||
chr5:143401390
|
T | G | 1 | a0001c0003t0006g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-13-538A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401390 | ||||||
chr5:143401483
|
T | A | 1 | a0001c0002t0004g0060 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-13-631A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401483 | ||||||
chr5:143401603
|
T | C | 9 | a0001c0005t0009g0008a0001c0005t0009g0249a0001c0005t0009g0250others(6): Show | 10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13-751A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401603 | ||||||
chr5:143401756
|
A | C | 1 | a0001c0001t0010g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-13-904T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401756 | ||||||
chr5:143401976
|
G | C | 1 | a0001c0001t0003g0253 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-13-1124C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401976 | ||||||
chr5:143402002
|
C | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(35): Show | 40 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.-13-1150G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402002 | ||||||
chr5:143402147
|
C | T | 1 | a0001c0001t0007g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-14+1064G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402147 | ||||||
chr5:143402285
|
G | T | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-14+926C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402285 | ||||||
chr5:143402467
|
G | A | 3 | a0002c0007t0011g0254a0002c0007t0011g0255a0002c0007t0034g0256 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-14+744C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402467 | ||||||
chr5:143402573
|
G | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14+638C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402573 | ||||||
chr5:143402635
|
A | C | 1 | a0001c0001t0005g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-14+576T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402635 | ||||||
chr5:143402746
|
C | G | 1 | a0001c0001t0002g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-14+465G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402746 | ||||||
chr5:143402749
|
C | G | 1 | a0001c0001t0010g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-14+462G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402749 | ||||||
chr5:143402790
|
G | A | 1 | a0001c0005t0009g0257 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-14+421C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402790 | ||||||
chr5:143402836
|
A | T | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-14+375T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402836 | ||||||
chr5:143402837
|
C | T | 38 | a0001c0002t0004g0060a0001c0002t0006g0028a0001c0002t0006g0030others(35): Show | 38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-14+374G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402837 | ||||||
chr5:143403006
|
T | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(242): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-14+205A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143403006 | ||||||
chr5:143403131
|
C | T | 2 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-14+80G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143403131 |