Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7182 |
|---|---|
| ensemblid | ENSG00000177463.16 |
| hgncid | 7972 |
| symbol | NR2C2 |
| name | nuclear receptor subfamily 2 group C member 2 |
| refseq_nuc | NM_001291694.2 |
| refseq_prot | NP_001278623.1 |
| ensembl_nuc | ENST00000425241.6 |
| ensembl_prot | ENSP00000388387.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 14947583 |
| end | 15049273 |
| strand | + |
| ver | v1.2 |
| region | chr3:14947583-15049273 |
| region5000 | chr3:14942583-15054273 |
| regionname0 | NR2C2_chr3_14947583_15049273 |
| regionname5000 | NR2C2_chr3_14942583_15054273 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1791 | 262 | 51 | 59 | 106 | 7 | 37 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| c0002 | 0/0 | 1791 | 16 | 13 | 3 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| c0003 | 0/0 | 1791 | 14 | 7 | 3 | 0 | 3 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| c0004 | 0/0 | 1791 | 8 | 8 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| c0005 | 0/0 | 1791 | 3 | 3 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| c0006 | 0/0 | 1791 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| c0007 | 0/0 | 1791 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| c0008 | 0/0 | 1791 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| c0009 | 0/0 | 1791 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 6629 | 132 | 13 | 26 | 68 | 2 | 21 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0002 | 0/0 | 6633 | 38 | 3 | 13 | 18 | 1 | 3 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0003 | 0/0 | 6629 | 25 | 3 | 6 | 13 | 0 | 3 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0004 | 0/0 | 6629 | 16 | 14 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0005 | 0/0 | 6633 | 14 | 12 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0006 | 0/0 | 6629 | 10 | 3 | 3 | 0 | 3 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0007 | 0/0 | 6629 | 8 | 8 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0008 | 0/0 | 6628 | 5 | 0 | 2 | 0 | 3 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0009 | 0/0 | 6629 | 5 | 0 | 3 | 1 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0010 | 0/0 | 6633 | 4 | 0 | 0 | 4 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0011 | 0/0 | 6633 | 4 | 0 | 2 | 0 | 0 | 2 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0012 | 0/0 | 6629 | 4 | 4 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0013 | 0/0 | 6629 | 4 | 4 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0014 | 0/0 | 6633 | 3 | 2 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0015 | 0/0 | 6633 | 3 | 0 | 0 | 0 | 0 | 3 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0016 | 0/0 | 6629 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0017 | 0/0 | 6629 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0018 | 0/0 | 6633 | 2 | 1 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0019 | 0/0 | 6629 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0020 | 0/0 | 6629 | 2 | 0 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0021 | 0/0 | 6629 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0022 | 0/0 | 6629 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0023 | 0/0 | 6629 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0024 | 0/0 | 6633 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0025 | 0/0 | 6633 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0026 | 0/0 | 6633 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0027 | 0/0 | 6633 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0028 | 0/0 | 6633 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0029 | 0/0 | 6629 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0030 | 0/0 | 6629 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0031 | 0/0 | 6633 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0032 | 0/0 | 6633 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0033 | 0/0 | 6629 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0034 | 0/0 | 6629 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0035 | 0/0 | 6629 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0036 | 0/0 | 6629 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0037 | 0/0 | 6629 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0038 | 0/0 | 6629 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0039 | 0/0 | 6629 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0040 | 0/0 | 6629 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0041 | 0/0 | 6629 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0042 | 0/0 | 6629 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| t0043 | 0/0 | 6629 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1791 | 262 | 51 | 59 | 106 | 7 | 37 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0002 | 0/0 | 1791 | 16 | 13 | 3 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0003 | 0/0 | 1791 | 14 | 7 | 3 | 0 | 3 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0004 | 0/0 | 1791 | 8 | 8 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0005 | 0/0 | 1791 | 3 | 3 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0006 | 0/0 | 1791 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0007 | 0/0 | 1791 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0009 | 0/0 | 1791 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0002c0008 | 0/0 | 1791 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 8419 | 128 | 12 | 25 | 66 | 2 | 21 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0002 | 0/0 | 8423 | 35 | 0 | 13 | 18 | 1 | 3 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0003 | 0/0 | 8419 | 25 | 3 | 6 | 13 | 0 | 3 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0004 | 0/0 | 8419 | 16 | 14 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0008 | 0/0 | 8418 | 5 | 0 | 2 | 0 | 3 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0009 | 0/0 | 8419 | 5 | 0 | 3 | 1 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0010 | 0/0 | 8423 | 4 | 0 | 0 | 4 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0011 | 0/0 | 8423 | 4 | 0 | 2 | 0 | 0 | 2 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0012 | 0/0 | 8419 | 4 | 4 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0015 | 0/0 | 8423 | 3 | 0 | 0 | 0 | 0 | 3 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0016 | 0/0 | 8419 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0017 | 0/0 | 8419 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0018 | 0/0 | 8423 | 2 | 1 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0019 | 0/0 | 8419 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0020 | 0/0 | 8419 | 2 | 0 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0021 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0022 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0023 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0024 | 0/0 | 8423 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0025 | 0/0 | 8423 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0026 | 0/0 | 8423 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0027 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0028 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0029 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0030 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0031 | 0/0 | 8423 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0032 | 0/0 | 8423 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0033 | 0/0 | 8419 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0034 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0035 | 0/0 | 8419 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0036 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0037 | 0/0 | 8419 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0038 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0039 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0040 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0041 | 0/0 | 8419 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0042 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0001t0043 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0002t0005 | 0/0 | 8423 | 14 | 12 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0002t0014 | 0/0 | 8423 | 2 | 1 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0003t0006 | 0/0 | 8419 | 10 | 3 | 3 | 0 | 3 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0003t0013 | 0/0 | 8419 | 4 | 4 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0004t0007 | 0/0 | 8419 | 8 | 8 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0005t0002 | 0/0 | 8423 | 3 | 3 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0006t0001 | 0/0 | 8419 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0007t0014 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0001c0009t0001 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| a0002c0008t0001 | 0/0 | 8419 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | copy fasta | chr3 | 14942583 | 15054273 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0008g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0008g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0009g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0009g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0009g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0009g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0010g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0010g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0010g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0010g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0011g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0011g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0011g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0011g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0012g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0012g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0012g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0012g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0015g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0015g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0016g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0016g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0017g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0017g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0018g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0018g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0019g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0019g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0020g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0020g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0021g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0022g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0023g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0024g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0025g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0026g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0027g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0028g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0029g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0030g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0031g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0032g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0033g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0034g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0035g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0036g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0037g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0038g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0039g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0040g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0041g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0042g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0043g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0014g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0014g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0013g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0013g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0005t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0005t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0005t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0006t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0007t0014g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0009t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0002c0008t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0006 | g0252 | EUR | GBR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0148 | EUR | FIN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00280 | hp2 | a0001 | c0001 | t0037 | g0147 | EUR | FIN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00609 | hp1 | a0001 | c0001 | t0010 | g0060 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0177 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0215 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00642 | hp2 | a0001 | c0003 | t0006 | g0005 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00733 | hp1 | a0001 | c0003 | t0006 | g0272 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00733 | hp2 | a0001 | c0001 | t0018 | g0068 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0118 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0116 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01081 | hp2 | a0001 | c0002 | t0014 | g0006 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01109 | hp1 | a0001 | c0002 | t0005 | g0020 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0120 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01168 | hp1 | a0001 | c0002 | t0005 | g0022 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01168 | hp2 | a0001 | c0001 | t0020 | g0223 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01169 | hp2 | a0001 | c0001 | t0020 | g0224 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01175 | hp1 | a0001 | c0001 | t0033 | g0151 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0235 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01192 | hp2 | a0001 | c0001 | t0025 | g0066 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0211 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0218 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01496 | hp1 | a0001 | c0001 | t0024 | g0053 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01515 | hp1 | a0001 | c0003 | t0006 | g0005 | EUR | IBS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0161 | EUR | IBS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01884 | hp1 | a0001 | c0004 | t0007 | g0281 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01891 | hp1 | a0001 | c0004 | t0007 | g0279 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0243 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0076 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02071 | hp1 | a0001 | c0001 | t0010 | g0047 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02129 | hp1 | a0001 | c0001 | t0023 | g0095 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02132 | hp2 | a0001 | c0001 | t0036 | g0174 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CDX | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CDX | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CDX | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02257 | hp1 | a0001 | c0004 | t0007 | g0277 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02258 | hp1 | a0001 | c0003 | t0013 | g0249 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02273 | hp2 | a0002 | c0008 | t0001 | g0155 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02615 | hp1 | a0001 | c0001 | t0034 | g0115 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02622 | hp1 | a0001 | c0003 | t0013 | g0248 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02622 | hp2 | a0001 | c0001 | t0039 | g0291 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02630 | hp1 | a0001 | c0002 | t0005 | g0100 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02630 | hp2 | a0001 | c0001 | t0019 | g0292 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02683 | hp2 | a0001 | c0001 | t0032 | g0056 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02717 | hp1 | a0001 | c0002 | t0005 | g0026 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0228 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02723 | hp1 | a0001 | c0003 | t0013 | g0247 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0245 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02735 | hp2 | a0001 | c0001 | t0035 | g0143 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02809 | hp1 | a0001 | c0001 | t0017 | g0295 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0300 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0230 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02886 | hp2 | a0001 | c0001 | t0019 | g0293 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0027 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02895 | hp2 | a0001 | c0001 | t0038 | g0290 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02896 | hp1 | a0001 | c0001 | t0012 | g0285 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0239 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02897 | hp1 | a0001 | c0002 | t0005 | g0029 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0284 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0242 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0021 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02970 | hp2 | a0001 | c0002 | t0014 | g0007 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03098 | hp1 | a0001 | c0004 | t0007 | g0274 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03098 | hp2 | a0001 | c0001 | t0042 | g0231 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03130 | hp1 | a0001 | c0002 | t0005 | g0019 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03130 | hp2 | a0001 | c0001 | t0040 | g0079 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03139 | hp1 | a0001 | c0002 | t0005 | g0031 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03195 | hp1 | a0001 | c0005 | t0002 | g0298 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0276 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0023 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03225 | hp1 | a0001 | c0001 | t0029 | g0299 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03486 | hp2 | a0001 | c0001 | t0043 | g0236 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03491 | hp1 | a0001 | c0001 | t0015 | g0001 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03491 | hp2 | a0001 | c0001 | t0009 | g0270 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03492 | hp2 | a0001 | c0001 | t0015 | g0001 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03516 | hp1 | a0001 | c0001 | t0016 | g0275 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03516 | hp2 | a0001 | c0005 | t0002 | g0296 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03540 | hp1 | a0001 | c0003 | t0006 | g0253 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03540 | hp2 | a0001 | c0004 | t0007 | g0278 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03579 | hp2 | a0001 | c0002 | t0005 | g0030 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03669 | hp2 | a0001 | c0001 | t0015 | g0059 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | STU | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0258 | SAS | STU | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03710 | hp1 | a0001 | c0001 | t0011 | g0217 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03710 | hp2 | a0001 | c0001 | t0041 | g0159 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03834 | hp2 | a0001 | c0001 | t0031 | g0219 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | STU | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG04184 | hp2 | a0001 | c0001 | t0011 | g0216 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | STU | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18522 | hp1 | a0001 | c0001 | t0027 | g0072 | AFR | YRI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18522 | hp2 | a0001 | c0003 | t0013 | g0246 | AFR | YRI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | YRI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18906 | hp2 | a0001 | c0005 | t0002 | g0297 | AFR | YRI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18957 | hp2 | a0001 | c0006 | t0001 | g0204 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18988 | hp1 | a0001 | c0001 | t0026 | g0034 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18994 | hp2 | a0001 | c0006 | t0001 | g0128 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18998 | hp2 | a0001 | c0001 | t0010 | g0048 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19005 | hp2 | a0001 | c0001 | t0022 | g0179 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19030 | hp1 | a0001 | c0001 | t0030 | g0077 | AFR | LWK | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19030 | hp2 | a0001 | c0004 | t0007 | g0283 | AFR | LWK | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19043 | hp1 | a0001 | c0001 | t0021 | g0286 | AFR | LWK | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19043 | hp2 | a0001 | c0009 | t0001 | g0016 | AFR | LWK | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19082 | hp2 | a0001 | c0001 | t0009 | g0197 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19085 | hp1 | a0001 | c0001 | t0010 | g0271 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19240 | hp1 | a0001 | c0004 | t0007 | g0282 | AFR | YRI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | ASW | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20129 | hp2 | a0001 | c0003 | t0006 | g0254 | AFR | ASW | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20752 | hp2 | a0001 | c0003 | t0006 | g0251 | EUR | TSI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0261 | EUR | TSI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0192 | EUR | TSI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20905 | hp1 | a0001 | c0003 | t0006 | g0255 | SAS | GIH | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | GIH | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01123 | hp2 | a0001 | c0003 | t0006 | g0256 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02109 | hp2 | a0001 | c0004 | t0007 | g0280 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02486 | hp1 | a0001 | c0001 | t0018 | g0067 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02486 | hp2 | a0001 | c0002 | t0005 | g0024 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02559 | hp1 | a0001 | c0003 | t0006 | g0250 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03471 | hp1 | a0001 | c0007 | t0014 | g0273 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03471 | hp2 | a0001 | c0001 | t0028 | g0065 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG06807 | hp1 | a0001 | c0001 | t0017 | g0294 | AFR | USA | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG06807 | hp2 | a0001 | c0002 | t0005 | g0025 | AFR | USA | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0028 | AFR | USA | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0009 | REF | REF | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0119 | REF | REF | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15016206
|
C | T | 1 | a0002 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.328C>T | p.Arg110Trp | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/14 | 691/8419 | 328/1791 | 110/596 | chr3 | 15016206 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15003971
|
A | T | 1 | a0001c0009 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.57A>T | p.Ser19Ser | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/14 | 420/8419 | 57/1791 | 19/596 | chr3 | 15003971 | ||
| chr3:15020931
|
A | G | 1 | a0001c0006 | 2 | NA18957.hp2 NA18994.hp2 |
splice_region_variant&synonymous_variant | LOW | c.555A>G | p.Glu185Glu | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/14 | 918/8419 | 555/1791 | 185/596 | chr3 | 15020931 | ||
| chr3:15023282
|
C | A | 1 | a0001c0007 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.639C>A | p.Ile213Ile | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 6/14 | 1002/8419 | 639/1791 | 213/596 | chr3 | 15023282 | ||
| chr3:15023315
|
T | A | 1 | a0001c0004 | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
synonymous_variant | LOW | c.672T>A | p.Thr224Thr | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 6/14 | 1035/8419 | 672/1791 | 224/596 | chr3 | 15023315 | ||
| chr3:15030395
|
G | A | 1 | a0001c0005 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.1053G>A | p.Ser351Ser | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/14 | 1416/8419 | 1053/1791 | 351/596 | chr3 | 15030395 | ||
| chr3:15038076
|
G | A | 2 | a0001c0002a0001c0007 | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
synonymous_variant | LOW | c.1449G>A | p.Ala483Ala | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/14 | 1812/8419 | 1449/1791 | 483/596 | chr3 | 15038076 | ||
| chr3:15039189
|
G | A | 1 | a0001c0003 | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
synonymous_variant | LOW | c.1578G>A | p.Gln526Gln | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/14 | 1941/8419 | 1578/1791 | 526/596 | chr3 | 15039189 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:14947745
|
G | A | 3 | a0001c0001t0016a0001c0001t0021a0001c0004t0007 | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-201G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/14 | 56170 | chr3 | 14947745 | |||||
| chr3:14947778
|
C | T | 3 | a0001c0001t0004a0001c0001t0042a0001c0001t0043 | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-168C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/14 | 56137 | chr3 | 14947778 | |||||
| chr3:14947803
|
C | A | 2 | a0001c0002t0014a0001c0007t0014 | 3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-143C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/14 | 56112 | chr3 | 14947803 | |||||
| chr3:15043044
|
C | T | 1 | a0001c0001t0041 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*36C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 36 | chr3 | 15043044 | |||||
| chr3:15043108
|
T | C | 1 | a0001c0001t0022 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 100 | chr3 | 15043108 | |||||
| chr3:15043169
|
G | T | 3 | a0001c0001t0038a0001c0001t0039a0001c0001t0040 | 3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*161G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 161 | chr3 | 15043169 | |||||
| chr3:15043362
|
A | G | 2 | a0001c0001t0009a0001c0001t0037 | 6 | HG00280.hp2 HG00735.hp1 HG01081.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*354A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 354 | chr3 | 15043362 | |||||
| chr3:15043373
|
T | A | 31 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(28): Show | 141 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*365T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 365 | chr3 | 15043373 | |||||
| chr3:15043450
|
A | G | 1 | a0001c0001t0032 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*442A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 442 | chr3 | 15043450 | |||||
| chr3:15043465
|
T | C | 1 | a0001c0001t0038 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*457T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 457 | chr3 | 15043465 | |||||
| chr3:15043640
|
G | A | 2 | a0001c0001t0038a0001c0001t0039 | 2 | HG02622.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*632G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 632 | chr3 | 15043640 | |||||
| chr3:15043687
|
G | A | 1 | a0001c0001t0023 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*679G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 679 | chr3 | 15043687 | |||||
| chr3:15043916
|
G | A | 1 | a0001c0003t0013 | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*908G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 908 | chr3 | 15043916 | |||||
| chr3:15044063
|
C | T | 3 | a0001c0002t0005a0001c0002t0014a0001c0007t0014 | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1055C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1055 | chr3 | 15044063 | |||||
| chr3:15044085
|
A | T | 5 | a0001c0001t0003a0001c0001t0023a0001c0001t0038others(2): Show | 29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1077A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1077 | chr3 | 15044085 | |||||
| chr3:15044093
|
G | A | 1 | a0001c0001t0017 | 2 | HG02809.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1085G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1085 | chr3 | 15044093 | |||||
| chr3:15044189
|
G | A | 1 | a0001c0001t0033 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1181 | chr3 | 15044189 | |||||
| chr3:15044242
|
T | A | 1 | a0001c0001t0024 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1234T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1234 | chr3 | 15044242 | |||||
| chr3:15044338
|
C | T | 3 | a0001c0001t0004a0001c0001t0042a0001c0001t0043 | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1330C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1330 | chr3 | 15044338 | |||||
| chr3:15044399
|
G | A | 1 | a0001c0001t0018 | 2 | HG00733.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1391G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1391 | chr3 | 15044399 | |||||
| chr3:15044618
|
G | T | 1 | a0001c0001t0021 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1610G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1610 | chr3 | 15044618 | |||||
| chr3:15044745
|
C | T | 2 | a0001c0003t0006a0001c0003t0013 | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1737C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1737 | chr3 | 15044745 | |||||
| chr3:15045549
|
CT | C | 1 | a0001c0001t0008 | 5 | HG00280.hp1 HG00639.hp2 HG01258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2544delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 2544 | INFO_REALIGN_3_PRIME | chr3 | 15045549 | ||||
| chr3:15045630
|
G | A | 1 | a0001c0001t0042 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2622G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 2622 | chr3 | 15045630 | |||||
| chr3:15045720
|
C | G | 1 | a0001c0001t0031 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2712C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 2712 | chr3 | 15045720 | |||||
| chr3:15045965
|
C | CAGAT | 16 | a0001c0001t0002a0001c0001t0010a0001c0001t0011others(13): Show | 75 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2962_*2965dupAGAT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 2966 | INFO_REALIGN_3_PRIME | chr3 | 15045965 | ||||
| chr3:15046083
|
G | C | 1 | a0001c0001t0017 | 2 | HG02809.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3075G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 3075 | chr3 | 15046083 | |||||
| chr3:15046088
|
T | C | 1 | a0001c0004t0007 | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3080T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 3080 | chr3 | 15046088 | |||||
| chr3:15046724
|
G | T | 1 | a0001c0001t0028 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3716G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 3716 | chr3 | 15046724 | |||||
| chr3:15046914
|
G | A | 1 | a0001c0001t0010 | 4 | HG00609.hp1 HG02071.hp1 NA18998.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3906G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 3906 | chr3 | 15046914 | |||||
| chr3:15046984
|
G | A | 1 | a0001c0001t0019 | 2 | HG02630.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3976G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 3976 | chr3 | 15046984 | |||||
| chr3:15047197
|
T | C | 1 | a0001c0001t0025 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4189T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4189 | chr3 | 15047197 | |||||
| chr3:15047208
|
A | G | 1 | a0001c0001t0015 | 3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4200A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4200 | chr3 | 15047208 | |||||
| chr3:15047260
|
T | C | 1 | a0001c0001t0017 | 2 | HG02809.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4252T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4252 | chr3 | 15047260 | |||||
| chr3:15047274
|
C | G | 1 | a0001c0002t0005 | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4266C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4266 | chr3 | 15047274 | |||||
| chr3:15047445
|
T | C | 1 | a0001c0001t0034 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4437T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4437 | chr3 | 15047445 | |||||
| chr3:15047515
|
A | G | 1 | a0001c0001t0017 | 2 | HG02809.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4507A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4507 | chr3 | 15047515 | |||||
| chr3:15047631
|
T | C | 1 | a0001c0001t0017 | 2 | HG02809.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4623T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4623 | chr3 | 15047631 | |||||
| chr3:15047639
|
C | T | 1 | a0001c0001t0037 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4631C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4631 | chr3 | 15047639 | |||||
| chr3:15047696
|
C | G | 2 | a0001c0001t0011a0001c0001t0031 | 5 | HG00642.hp1 HG01361.hp1 HG03710.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4688C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4688 | chr3 | 15047696 | |||||
| chr3:15047924
|
C | T | 1 | a0001c0001t0030 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4916C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4916 | chr3 | 15047924 | |||||
| chr3:15047953
|
C | T | 1 | a0001c0001t0020 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4945C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4945 | chr3 | 15047953 | |||||
| chr3:15048121
|
T | A | 1 | a0001c0001t0026 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5113T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5113 | chr3 | 15048121 | |||||
| chr3:15048155
|
G | A | 1 | a0001c0001t0035 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5147G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5147 | chr3 | 15048155 | |||||
| chr3:15048471
|
C | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5463C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5463 | chr3 | 15048471 | |||||
| chr3:15048477
|
A | G | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5469A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5469 | chr3 | 15048477 | |||||
| chr3:15048483
|
T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5475T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5475 | chr3 | 15048483 | |||||
| chr3:15048484
|
T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5476T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5476 | chr3 | 15048484 | |||||
| chr3:15048486
|
G | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5478G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5478 | chr3 | 15048486 | |||||
| chr3:15048486
|
G | T | 1 | a0001c0001t0027 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5478G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5478 | chr3 | 15048486 | |||||
| chr3:15048491
|
T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5483T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5483 | chr3 | 15048491 | |||||
| chr3:15048492
|
T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5484T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5484 | chr3 | 15048492 | |||||
| chr3:15048493
|
G | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5485G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5485 | chr3 | 15048493 | |||||
| chr3:15048495
|
T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5487T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5487 | chr3 | 15048495 | |||||
| chr3:15048500
|
A | C | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5492A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5492 | chr3 | 15048500 | |||||
| chr3:15048501
|
T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5493T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5493 | chr3 | 15048501 | |||||
| chr3:15048506
|
G | T | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5498G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5498 | chr3 | 15048506 | |||||
| chr3:15048507
|
C | T | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5499C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5499 | chr3 | 15048507 | |||||
| chr3:15048508
|
A | G | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5500A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5500 | chr3 | 15048508 | |||||
| chr3:15048510
|
A | C | 1 | a0001c0001t0029 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5502A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5502 | chr3 | 15048510 | |||||
| chr3:15048511
|
A | C | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5503A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5503 | chr3 | 15048511 | |||||
| chr3:15048513
|
A | G | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5505A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5505 | chr3 | 15048513 | |||||
| chr3:15048514
|
G | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5506G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5506 | chr3 | 15048514 | |||||
| chr3:15048519
|
A | T | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5511A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5511 | chr3 | 15048519 | |||||
| chr3:15048522
|
A | C | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5514A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5514 | chr3 | 15048522 | |||||
| chr3:15048536
|
T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5528T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5528 | chr3 | 15048536 | |||||
| chr3:15048564
|
T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5556T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5556 | chr3 | 15048564 | |||||
| chr3:15048578
|
T | C | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5570T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5570 | chr3 | 15048578 | |||||
| chr3:15048579
|
G | T | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5571G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5571 | chr3 | 15048579 | |||||
| chr3:15048583
|
G | T | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5575G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5575 | chr3 | 15048583 | |||||
| chr3:15048594
|
T | G | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5586T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5586 | chr3 | 15048594 | |||||
| chr3:15048595
|
G | C | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5587G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5587 | chr3 | 15048595 | |||||
| chr3:15048596
|
C | T | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5588C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5588 | chr3 | 15048596 | |||||
| chr3:15048611
|
T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5603T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5603 | chr3 | 15048611 | |||||
| chr3:15048637
|
T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5629T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5629 | chr3 | 15048637 | |||||
| chr3:15049109
|
G | A | 1 | a0001c0001t0043 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6101G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 6101 | chr3 | 15049109 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:14947913
|
T | C | 2 | a0001c0002t0014g0006a0001c0002t0014g0007 | 2 | HG01081.hp2 HG02970.hp2 |
splice_region_variant&intron_variant | LOW | c.-40+7T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14947913 | ||||||
| chr3:14947954
|
G | A | 1 | a0001c0001t0003g0008 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-40+48G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14947954 | ||||||
| chr3:14947983
|
C | T | 2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-40+77C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14947983 | ||||||
| chr3:14948143
|
G | T | 1 | a0001c0001t0001g0301 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-40+237G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948143 | ||||||
| chr3:14948250
|
C | T | 2 | a0001c0001t0012g0300a0001c0001t0029g0299 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+344C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948250 | ||||||
| chr3:14948257
|
C | T | 3 | a0001c0005t0002g0296a0001c0005t0002g0297a0001c0005t0002g0298 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-40+351C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948257 | ||||||
| chr3:14948329
|
C | T | 2 | a0001c0001t0012g0300a0001c0001t0029g0299 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+423C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948329 | ||||||
| chr3:14948427
|
A | G | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+521A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948427 | ||||||
| chr3:14948476
|
C | T | 2 | a0001c0001t0019g0292a0001c0001t0019g0293 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-40+570C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948476 | ||||||
| chr3:14948487
|
G | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40+581G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948487 | ||||||
| chr3:14948567
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0009t0001g0016 | 3 | HG03139.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-40+661G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948567 | ||||||
| chr3:14948647
|
T | A | 1 | a0001c0009t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-40+741T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948647 | ||||||
| chr3:14948739
|
T | C | 13 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(10): Show | 13 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-40+833T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948739 | ||||||
| chr3:14948748
|
C | T | 2 | a0001c0001t0038g0290a0001c0001t0039g0291 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-40+842C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948748 | ||||||
| chr3:14948777
|
C | G | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-40+871C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948777 | ||||||
| chr3:14948865
|
A | T | 1 | a0001c0001t0001g0287 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-40+959A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948865 | ||||||
| chr3:14948872
|
G | T | 13 | a0001c0001t0012g0284a0001c0001t0012g0285a0001c0001t0016g0275others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-40+966G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948872 | ||||||
| chr3:14948878
|
G | A | 50 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(47): Show | 51 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.-40+972G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948878 | ||||||
| chr3:14948927
|
T | G | 2 | a0001c0001t0012g0300a0001c0001t0029g0299 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+1021T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948927 | ||||||
| chr3:14949011
|
C | T | 1 | a0001c0001t0021g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-40+1105C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949011 | ||||||
| chr3:14949029
|
G | A | 1 | a0001c0002t0005g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-40+1123G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949029 | ||||||
| chr3:14949055
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-40+1149G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949055 | ||||||
| chr3:14949076
|
C | T | 2 | a0001c0001t0012g0300a0001c0001t0029g0299 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+1170C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949076 | ||||||
| chr3:14949115
|
T | C | 3 | a0001c0001t0038g0290a0001c0001t0039g0291a0001c0001t0040g0079 | 3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-40+1209T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949115 | ||||||
| chr3:14949117
|
A | G | 3 | a0001c0001t0038g0290a0001c0001t0039g0291a0001c0001t0040g0079 | 3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-40+1211A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949117 | ||||||
| chr3:14949168
|
CTAGAGTT others(17): Show |
C | 25 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(22): Show | 26 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-40+1267_-40+1290d others(26): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14949168 | |||||
| chr3:14949209
|
G | T | 3 | a0001c0002t0014g0006a0001c0002t0014g0007a0001c0007t0014g0273 | 3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-40+1303G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949209 | ||||||
| chr3:14949244
|
A | G | 1 | a0001c0003t0006g0272 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-40+1338A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949244 | ||||||
| chr3:14949248
|
C | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+1342C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949248 | ||||||
| chr3:14949298
|
C | T | 12 | a0001c0002t0005g0019a0001c0002t0005g0021a0001c0002t0005g0022others(9): Show | 12 | HG01168.hp1 HG02486.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-40+1392C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949298 | ||||||
| chr3:14949682
|
C | T | 1 | a0001c0001t0010g0271 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-40+1776C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949682 | ||||||
| chr3:14949745
|
CAT | C | 3 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG00438.hp1 HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.-40+1840_-40+1841d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949745 | ||||||
| chr3:14949756
|
G | GATTT | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40+1871_-40+1874d others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14949756 | |||||
| chr3:14949756
|
GATTT | G | 7 | a0001c0001t0009g0270a0001c0001t0012g0076a0001c0001t0012g0284others(4): Show | 7 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40+1871_-40+1874d others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14949756 | |||||
| chr3:14949833
|
C | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+1927C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949833 | ||||||
| chr3:14949862
|
C | G | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+1956C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949862 | ||||||
| chr3:14949954
|
T | C | 4 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+2048T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949954 | ||||||
| chr3:14949968
|
C | G | 1 | a0001c0001t0001g0269 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-40+2062C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949968 | ||||||
| chr3:14950065
|
G | A | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+2159G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950065 | ||||||
| chr3:14950132
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-40+2226C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950132 | ||||||
| chr3:14950136
|
G | A | 4 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(1): Show | 4 | NA18946.hp1 NA18978.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+2230G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950136 | ||||||
| chr3:14950481
|
C | G | 1 | a0001c0001t0001g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-40+2575C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950481 | ||||||
| chr3:14950493
|
C | T | 4 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG01243.hp1 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+2587C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950493 | ||||||
| chr3:14950557
|
A | G | 1 | a0001c0001t0002g0074 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-40+2651A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950557 | ||||||
| chr3:14950628
|
C | T | 54 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(51): Show | 55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40+2722C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950628 | ||||||
| chr3:14950707
|
C | T | 27 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(24): Show | 28 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-40+2801C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950707 | ||||||
| chr3:14950846
|
GA | G | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40+2941delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950846 | ||||||
| chr3:14950850
|
C | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40+2944C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950850 | ||||||
| chr3:14951122
|
G | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+3216G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951122 | ||||||
| chr3:14951498
|
T | C | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+3592T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951498 | ||||||
| chr3:14951504
|
T | C | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+3598T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951504 | ||||||
| chr3:14951543
|
A | G | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+3637A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951543 | ||||||
| chr3:14951559
|
A | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+3653A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951559 | ||||||
| chr3:14951666
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-40+3760T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951666 | ||||||
| chr3:14951697
|
T | C | 1 | a0001c0001t0029g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-40+3791T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951697 | ||||||
| chr3:14951705
|
C | T | 148 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(145): Show | 151 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-40+3799C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951705 | ||||||
| chr3:14951754
|
G | GT | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+3857dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14951754 | |||||
| chr3:14951967
|
C | G | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+4061C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951967 | ||||||
| chr3:14951988
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-40+4082C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951988 | ||||||
| chr3:14951992
|
T | C | 1 | a0001c0004t0007g0274 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-40+4086T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951992 | ||||||
| chr3:14952030
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-40+4124G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952030 | ||||||
| chr3:14952037
|
C | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+4131C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952037 | ||||||
| chr3:14952038
|
G | A | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+4132G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952038 | ||||||
| chr3:14952145
|
C | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+4239C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952145 | ||||||
| chr3:14952160
|
C | T | 2 | a0001c0001t0004g0244a0001c0001t0004g0245 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-40+4254C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952160 | ||||||
| chr3:14952270
|
G | T | 14 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(11): Show | 14 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40+4364G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952270 | ||||||
| chr3:14952325
|
T | TCTC | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+4421_-40+4422i others(5): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14952325 | |||||
| chr3:14952369
|
C | G | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-40+4463C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952369 | ||||||
| chr3:14952501
|
A | G | 1 | a0001c0001t0002g0073 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-40+4595A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952501 | ||||||
| chr3:14952847
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-40+4941G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952847 | ||||||
| chr3:14952863
|
A | G | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0301 | 3 | HG00673.hp2 NA18991.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-40+4957A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952863 | ||||||
| chr3:14952919
|
G | C | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40+5013G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952919 | ||||||
| chr3:14953027
|
C | G | 1 | a0001c0001t0004g0243 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-40+5121C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953027 | ||||||
| chr3:14953087
|
A | G | 1 | a0001c0001t0027g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-40+5181A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953087 | ||||||
| chr3:14953110
|
C | A | 2 | a0001c0001t0012g0284a0001c0001t0012g0285 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-40+5204C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953110 | ||||||
| chr3:14953155
|
TGAAAG | T | 8 | a0001c0003t0006g0005a0001c0003t0006g0251a0001c0003t0006g0252others(5): Show | 9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-40+5250_-40+5254d others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953155 | ||||||
| chr3:14953193
|
G | A | 4 | a0001c0003t0013g0246a0001c0003t0013g0247a0001c0003t0013g0248others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+5287G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953193 | ||||||
| chr3:14953245
|
G | A | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+5339G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953245 | ||||||
| chr3:14953284
|
C | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+5378C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953284 | ||||||
| chr3:14953442
|
T | G | 1 | a0001c0001t0001g0103 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-40+5536T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953442 | ||||||
| chr3:14953518
|
A | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+5612A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953518 | ||||||
| chr3:14953609
|
C | T | 18 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0230others(15): Show | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-40+5703C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953609 | ||||||
| chr3:14953610
|
G | A | 1 | a0001c0001t0027g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-40+5704G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953610 | ||||||
| chr3:14953621
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-40+5715C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953621 | ||||||
| chr3:14953622
|
G | A | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+5716G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953622 | ||||||
| chr3:14953663
|
A | G | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40+5757A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953663 | ||||||
| chr3:14953671
|
G | A | 5 | a0001c0001t0011g0215a0001c0001t0011g0216a0001c0001t0011g0217others(2): Show | 5 | HG00642.hp1 HG01361.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40+5765G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953671 | ||||||
| chr3:14953756
|
G | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+5850G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953756 | ||||||
| chr3:14953894
|
C | CA | 55 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(52): Show | 56 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.-40+6005dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14953894 | |||||
| chr3:14953912
|
C | A | 3 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082 | 3 | HG02615.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-40+6006C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953912 | ||||||
| chr3:14953977
|
C | A | 1 | a0001c0001t0029g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-40+6071C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953977 | ||||||
| chr3:14953978
|
A | G | 1 | a0001c0001t0029g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-40+6072A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953978 | ||||||
| chr3:14954203
|
C | T | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+6297C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954203 | ||||||
| chr3:14954213
|
G | C | 1 | a0001c0004t0007g0274 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-40+6307G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954213 | ||||||
| chr3:14954308
|
TAAAC | T | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+6405_-40+6408d others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14954308 | |||||
| chr3:14954326
|
G | A | 2 | a0001c0002t0014g0006a0001c0002t0014g0007 | 2 | HG01081.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-40+6420G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954326 | ||||||
| chr3:14954596
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-40+6690A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954596 | ||||||
| chr3:14954647
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-40+6741A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954647 | ||||||
| chr3:14954695
|
T | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+6789T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954695 | ||||||
| chr3:14954729
|
G | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | NA18945.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-40+6823G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954729 | ||||||
| chr3:14955070
|
G | T | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+7164G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955070 | ||||||
| chr3:14955106
|
C | T | 1 | a0001c0001t0008g0211 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-40+7200C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955106 | ||||||
| chr3:14955250
|
T | C | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+7344T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955250 | ||||||
| chr3:14955251
|
G | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+7345G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955251 | ||||||
| chr3:14955289
|
G | A | 5 | a0001c0001t0001g0078a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG01106.hp2 HG01361.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40+7383G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955289 | ||||||
| chr3:14955574
|
G | A | 4 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+7668G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955574 | ||||||
| chr3:14955583
|
C | T | 2 | a0001c0001t0002g0071a0001c0001t0002g0263 | 2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-40+7677C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955583 | ||||||
| chr3:14955705
|
A | C | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+7799A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955705 | ||||||
| chr3:14955762
|
T | C | 2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | NA18978.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-40+7856T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955762 | ||||||
| chr3:14955826
|
T | TATGTAGT others(356): Show |
1 | a0001c0001t0001g0210 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-40+7936_-40+7937i others(365): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14955826 | |||||
| chr3:14955850
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-40+7944G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955850 | ||||||
| chr3:14955879
|
C | G | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40+7973C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955879 | ||||||
| chr3:14955958
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-40+8052A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955958 | ||||||
| chr3:14956058
|
C | G | 1 | a0001c0003t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-40+8152C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956058 | ||||||
| chr3:14956178
|
T | C | 2 | a0001c0001t0001g0114a0001c0001t0034g0115 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-40+8272T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956178 | ||||||
| chr3:14956353
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-40+8447A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956353 | ||||||
| chr3:14956422
|
G | A | 1 | a0001c0001t0003g0083 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-40+8516G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956422 | ||||||
| chr3:14956567
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-40+8661G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956567 | ||||||
| chr3:14956760
|
C | T | 9 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(6): Show | 9 | HG01099.hp2 NA18957.hp2 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40+8854C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956760 | ||||||
| chr3:14956899
|
G | C | 103 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(100): Show | 105 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.-40+8993G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956899 | ||||||
| chr3:14957049
|
A | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+9143A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957049 | ||||||
| chr3:14957068
|
C | T | 3 | a0001c0001t0018g0067a0001c0001t0018g0068a0001c0001t0025g0066 | 3 | HG00733.hp2 HG01192.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-40+9162C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957068 | ||||||
| chr3:14957331
|
T | C | 1 | a0001c0001t0009g0116 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-40+9425T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957331 | ||||||
| chr3:14957477
|
G | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+9571G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957477 | ||||||
| chr3:14957488
|
T | C | 18 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0230others(15): Show | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-40+9582T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957488 | ||||||
| chr3:14957493
|
C | T | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+9587C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957493 | ||||||
| chr3:14957533
|
T | C | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+9627T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957533 | ||||||
| chr3:14957709
|
T | C | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+9803T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957709 | ||||||
| chr3:14957764
|
A | G | 1 | a0001c0002t0005g0020 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-40+9858A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957764 | ||||||
| chr3:14957805
|
AT | A | 28 | a0001c0001t0001g0117a0001c0001t0003g0002a0001c0001t0003g0008others(25): Show | 29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-40+9910delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14957805 | |||||
| chr3:14957927
|
T | TTGCC | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(294): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.-40+10022_-40+1002 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14957927 | |||||
| chr3:14957975
|
A | G | 1 | a0001c0002t0005g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-40+10069A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957975 | ||||||
| chr3:14958114
|
G | A | 54 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(51): Show | 55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40+10208G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958114 | ||||||
| chr3:14958275
|
A | G | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+10369A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958275 | ||||||
| chr3:14958336
|
A | G | 1 | a0001c0007t0014g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-40+10430A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958336 | ||||||
| chr3:14958340
|
C | CT | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+10445dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14958340 | |||||
| chr3:14958431
|
G | A | 49 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(46): Show | 50 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-40+10525G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958431 | ||||||
| chr3:14958506
|
G | A | 18 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0230others(15): Show | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-40+10600G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958506 | ||||||
| chr3:14958530
|
T | G | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+10624T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958530 | ||||||
| chr3:14958563
|
T | C | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+10657T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958563 | ||||||
| chr3:14958614
|
G | T | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+10708G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958614 | ||||||
| chr3:14958674
|
T | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+10768T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958674 | ||||||
| chr3:14958687
|
T | A | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+10781T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958687 | ||||||
| chr3:14958758
|
T | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+10852T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958758 | ||||||
| chr3:14958844
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-40+10938C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958844 | ||||||
| chr3:14958956
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-40+11050C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958956 | ||||||
| chr3:14958970
|
G | A | 7 | a0001c0001t0001g0122a0001c0001t0012g0076a0001c0001t0012g0284others(4): Show | 7 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40+11064G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958970 | ||||||
| chr3:14959137
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-40+11231T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14959137 | ||||||
| chr3:14959682
|
C | G | 3 | a0001c0002t0014g0006a0001c0002t0014g0007a0001c0007t0014g0273 | 3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-40+11776C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14959682 | ||||||
| chr3:14960334
|
G | A | 18 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0230others(15): Show | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-40+12428G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14960334 | ||||||
| chr3:14960372
|
C | A | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+12466C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14960372 | ||||||
| chr3:14960476
|
T | C | 32 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(29): Show | 33 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-40+12570T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14960476 | ||||||
| chr3:14960752
|
A | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+12846A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14960752 | ||||||
| chr3:14960952
|
TTG | T | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+13050_-40+1305 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14960952 | |||||
| chr3:14961062
|
A | G | 1 | a0001c0002t0005g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-40+13156A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961062 | ||||||
| chr3:14961157
|
A | T | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+13251A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961157 | ||||||
| chr3:14961285
|
G | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-40+13379G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961285 | ||||||
| chr3:14961384
|
G | A | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+13478G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961384 | ||||||
| chr3:14961435
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0009t0001g0016 | 3 | HG03139.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-40+13529A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961435 | ||||||
| chr3:14961501
|
T | G | 19 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(16): Show | 20 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-40+13595T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961501 | ||||||
| chr3:14961544
|
T | A | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-40+13638T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961544 | ||||||
| chr3:14961550
|
A | G | 3 | a0001c0002t0014g0006a0001c0002t0014g0007a0001c0007t0014g0273 | 3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-40+13644A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961550 | ||||||
| chr3:14961617
|
C | T | 1 | a0001c0001t0009g0120 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-40+13711C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961617 | ||||||
| chr3:14961873
|
G | A | 2 | a0001c0001t0012g0300a0001c0001t0029g0299 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+13967G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961873 | ||||||
| chr3:14961918
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-40+14012C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961918 | ||||||
| chr3:14962541
|
A | G | 19 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(16): Show | 20 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-40+14635A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14962541 | ||||||
| chr3:14962602
|
C | T | 19 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(16): Show | 20 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-40+14696C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14962602 | ||||||
| chr3:14962655
|
C | CT | 31 | a0001c0001t0001g0107a0001c0001t0001g0121a0001c0001t0001g0199others(28): Show | 31 | HG00544.hp1 HG01081.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-40+14769dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14962655 | |||||
| chr3:14962655
|
CT | C | 26 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0108others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.-40+14769delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14962655 | |||||
| chr3:14962686
|
G | T | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40+14780G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14962686 | ||||||
| chr3:14962809
|
C | T | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+14903C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14962809 | ||||||
| chr3:14962845
|
G | T | 1 | a0001c0001t0001g0226 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-40+14939G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14962845 | ||||||
| chr3:14962919
|
T | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | NA18960.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-40+15013T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14962919 | ||||||
| chr3:14963023
|
T | A | 54 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(51): Show | 55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40+15117T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963023 | ||||||
| chr3:14963024
|
C | T | 54 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(51): Show | 55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40+15118C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963024 | ||||||
| chr3:14963224
|
G | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(39): Show | 43 | HG01070.hp2 HG01071.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.-40+15318G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963224 | ||||||
| chr3:14963269
|
A | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+15363A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963269 | ||||||
| chr3:14963336
|
ATAAG | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+15434_-40+1543 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14963336 | |||||
| chr3:14963389
|
C | T | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+15483C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963389 | ||||||
| chr3:14963460
|
CATTTTTT | C | 9 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0009g0197others(6): Show | 9 | HG00438.hp2 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40+15576_-40+1558 others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14963460 | |||||
| chr3:14963618
|
G | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+15712G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963618 | ||||||
| chr3:14963671
|
T | C | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+15765T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963671 | ||||||
| chr3:14963910
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | HG01884.hp2 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-40+16004G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963910 | ||||||
| chr3:14963917
|
A | G | 1 | a0001c0001t0035g0143 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-40+16011A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963917 | ||||||
| chr3:14964161
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0196 | 2 | NA18951.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-40+16255A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964161 | ||||||
| chr3:14964255
|
A | G | 1 | a0001c0005t0002g0296 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-40+16349A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964255 | ||||||
| chr3:14964423
|
G | A | 1 | a0001c0009t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-40+16517G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964423 | ||||||
| chr3:14964496
|
TTATTTTC | T | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+16597_-40+1660 others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14964496 | |||||
| chr3:14964503
|
CTATTTTA | C | 292 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(289): Show | 297 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.-40+16604_-40+1661 others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14964503 | |||||
| chr3:14964503
|
CTATTTTA others(7): Show |
C | 1 | a0001c0001t0018g0068 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-40+16604_-40+1661 others(18): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14964503 | |||||
| chr3:14964510
|
A | T | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+16604A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964510 | ||||||
| chr3:14964577
|
C | T | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+16671C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964577 | ||||||
| chr3:14964615
|
C | T | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+16709C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964615 | ||||||
| chr3:14964660
|
G | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+16754G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964660 | ||||||
| chr3:14964676
|
G | A | 1 | a0001c0001t0040g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-40+16770G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964676 | ||||||
| chr3:14964681
|
A | AT | 20 | a0001c0001t0001g0107a0001c0001t0002g0033a0001c0002t0005g0019others(17): Show | 20 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-40+16790dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14964681 | |||||
| chr3:14964724
|
G | A | 1 | a0001c0001t0002g0040 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-40+16818G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964724 | ||||||
| chr3:14964726
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-40+16820G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964726 | ||||||
| chr3:14964765
|
G | A | 8 | a0001c0003t0006g0005a0001c0003t0006g0251a0001c0003t0006g0252others(5): Show | 9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-40+16859G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964765 | ||||||
| chr3:14964802
|
G | A | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+16896G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964802 | ||||||
| chr3:14964811
|
C | T | 11 | a0001c0001t0004g0235a0001c0001t0004g0237a0001c0001t0004g0238others(8): Show | 11 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-40+16905C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964811 | ||||||
| chr3:14965030
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-40+17124A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965030 | ||||||
| chr3:14965090
|
A | G | 18 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0230others(15): Show | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-40+17184A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965090 | ||||||
| chr3:14965140
|
A | C | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+17234A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965140 | ||||||
| chr3:14965141
|
C | CT | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+17242dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965141 | |||||
| chr3:14965273
|
C | T | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+17367C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965273 | ||||||
| chr3:14965380
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-40+17474G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965380 | ||||||
| chr3:14965451
|
G | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+17545G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965451 | ||||||
| chr3:14965522
|
C | CA | 71 | a0001c0001t0001g0078a0001c0001t0001g0117a0001c0001t0001g0149others(68): Show | 72 | HG00609.hp1 HG00642.hp1 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.-40+17640dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | |||||
| chr3:14965522
|
C | CAA | 34 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0212others(31): Show | 34 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.-40+17639_-40+1764 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | |||||
| chr3:14965522
|
CA | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0146a0001c0001t0001g0194others(3): Show | 6 | HG01169.hp2 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40+17640delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | |||||
| chr3:14965522
|
CAAA | C | 23 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(20): Show | 24 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.-40+17638_-40+1764 others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | |||||
| chr3:14965522
|
CAAAAAA | C | 7 | a0001c0001t0001g0104a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 7 | HG02723.hp2 HG02809.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40+17635_-40+1764 others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | |||||
| chr3:14965522
|
CAAAAAAA | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(39): Show | 43 | HG01070.hp2 HG01071.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.-40+17634_-40+1764 others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | |||||
| chr3:14965522
|
CAAAAAAA others(3): Show |
C | 16 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(13): Show | 16 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-40+17631_-40+1764 others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | |||||
| chr3:14965522
|
CAAAAAAA others(4): Show |
C | 12 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(9): Show | 13 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.-40+17630_-40+1764 others(15): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | |||||
| chr3:14965522
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0225 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-40+17629_-40+1764 others(16): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | |||||
| chr3:14965637
|
GCT | G | 3 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-40+17732_-40+1773 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965637 | ||||||
| chr3:14965640
|
G | GT | 113 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(110): Show | 116 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-40+17742dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965640 | |||||
| chr3:14965640
|
G | T | 3 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-40+17734G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965640 | ||||||
| chr3:14965648
|
T | G | 3 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-40+17742T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965648 | ||||||
| chr3:14965648
|
T | TG | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40+17743dupG | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965648 | |||||
| chr3:14965649
|
G | T | 1 | a0001c0003t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-40+17743G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965649 | ||||||
| chr3:14965825
|
G | A | 2 | a0001c0002t0005g0026a0001c0002t0005g0031 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-40+17919G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965825 | ||||||
| chr3:14965862
|
G | A | 6 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0049others(3): Show | 6 | NA18945.hp2 NA18972.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+17956G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965862 | ||||||
| chr3:14965910
|
C | G | 71 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(68): Show | 72 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.-40+18004C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965910 | ||||||
| chr3:14966195
|
A | G | 4 | a0001c0003t0013g0246a0001c0003t0013g0247a0001c0003t0013g0248others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+18289A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966195 | ||||||
| chr3:14966207
|
A | C | 54 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(51): Show | 55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40+18301A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966207 | ||||||
| chr3:14966227
|
A | G | 148 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(145): Show | 151 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-40+18321A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966227 | ||||||
| chr3:14966657
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-40+18751A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966657 | ||||||
| chr3:14966711
|
A | G | 1 | a0001c0002t0005g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-40+18805A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966711 | ||||||
| chr3:14966823
|
A | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+18917A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966823 | ||||||
| chr3:14966900
|
A | C | 4 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+18994A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966900 | ||||||
| chr3:14966927
|
A | G | 2 | a0001c0001t0004g0233a0001c0001t0004g0234 | 2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-40+19021A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966927 | ||||||
| chr3:14967075
|
A | T | 2 | a0001c0004t0007g0280a0001c0004t0007g0281 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-40+19169A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967075 | ||||||
| chr3:14967288
|
T | G | 1 | a0001c0001t0002g0041 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-40+19382T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967288 | ||||||
| chr3:14967361
|
T | C | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+19455T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967361 | ||||||
| chr3:14967403
|
T | A | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+19497T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967403 | ||||||
| chr3:14967558
|
T | A | 1 | a0001c0001t0029g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-40+19652T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967558 | ||||||
| chr3:14967622
|
G | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-40+19716G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967622 | ||||||
| chr3:14967747
|
G | C | 3 | a0001c0005t0002g0296a0001c0005t0002g0297a0001c0005t0002g0298 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-40+19841G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967747 | ||||||
| chr3:14967793
|
T | C | 1 | a0001c0007t0014g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-40+19887T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967793 | ||||||
| chr3:14967851
|
T | G | 1 | a0001c0001t0041g0159 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-40+19945T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967851 | ||||||
| chr3:14967981
|
A | ATCAGTTC | 3 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-40+20078_-40+2007 others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14967981 | |||||
| chr3:14967985
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-40+20079A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967985 | ||||||
| chr3:14968068
|
A | G | 3 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082 | 3 | HG02615.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-40+20162A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968068 | ||||||
| chr3:14968172
|
G | A | 1 | a0001c0001t0003g0084 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-40+20266G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968172 | ||||||
| chr3:14968209
|
A | T | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+20303A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968209 | ||||||
| chr3:14968234
|
G | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+20328G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968234 | ||||||
| chr3:14968544
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-40+20638A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968544 | ||||||
| chr3:14968568
|
A | T | 19 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(16): Show | 20 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-40+20662A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968568 | ||||||
| chr3:14968570
|
A | G | 19 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(16): Show | 20 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-40+20664A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968570 | ||||||
| chr3:14968573
|
G | A | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40+20667G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968573 | ||||||
| chr3:14968720
|
G | T | 9 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(6): Show | 9 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40+20814G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968720 | ||||||
| chr3:14968728
|
C | A | 36 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(33): Show | 37 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.-40+20822C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968728 | ||||||
| chr3:14968787
|
A | G | 1 | a0001c0001t0029g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-40+20881A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968787 | ||||||
| chr3:14968876
|
A | C | 1 | a0001c0002t0005g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-40+20970A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968876 | ||||||
| chr3:14968906
|
A | G | 1 | a0001c0003t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-40+21000A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968906 | ||||||
| chr3:14969059
|
C | G | 3 | a0001c0002t0014g0006a0001c0002t0014g0007a0001c0007t0014g0273 | 3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-40+21153C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969059 | ||||||
| chr3:14969059
|
C | T | 3 | a0001c0001t0010g0047a0001c0001t0010g0048a0001c0001t0010g0060 | 3 | HG00609.hp1 HG02071.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-40+21153C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969059 | ||||||
| chr3:14969134
|
A | T | 1 | a0001c0001t0001g0014 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-40+21228A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969134 | ||||||
| chr3:14969200
|
T | C | 54 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(51): Show | 55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40+21294T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969200 | ||||||
| chr3:14969244
|
C | CT | 28 | a0001c0001t0001g0014a0001c0001t0001g0107a0001c0001t0001g0110others(25): Show | 28 | HG01081.hp1 HG01106.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-40+21357dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14969244 | |||||
| chr3:14969244
|
CT | C | 65 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0160others(62): Show | 66 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.-40+21357delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14969244 | |||||
| chr3:14969244
|
CTT | C | 8 | a0001c0001t0002g0073a0001c0004t0007g0274a0001c0004t0007g0277others(5): Show | 8 | HG01891.hp1 HG01993.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40+21356_-40+2135 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14969244 | |||||
| chr3:14969354
|
C | T | 1 | a0001c0001t0010g0048 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-40+21448C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969354 | ||||||
| chr3:14969430
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-40+21524A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969430 | ||||||
| chr3:14969442
|
T | C | 1 | a0001c0001t0040g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-40+21536T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969442 | ||||||
| chr3:14969457
|
G | T | 3 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-40+21551G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969457 | ||||||
| chr3:14969503
|
A | G | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-40+21597A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969503 | ||||||
| chr3:14969560
|
C | T | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+21654C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969560 | ||||||
| chr3:14969719
|
C | G | 6 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0205others(3): Show | 6 | NA18960.hp1 NA18964.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+21813C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969719 | ||||||
| chr3:14970152
|
T | G | 1 | a0001c0001t0002g0071 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-40+22246T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14970152 | ||||||
| chr3:14970269
|
G | A | 1 | a0001c0001t0009g0197 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-40+22363G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14970269 | ||||||
| chr3:14970277
|
T | TG | 15 | a0001c0001t0001g0106a0001c0001t0001g0121a0001c0001t0001g0129others(12): Show | 15 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.-40+22378dupG | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14970277 | |||||
| chr3:14970327
|
G | A | 1 | a0001c0001t0019g0293 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-40+22421G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14970327 | ||||||
| chr3:14970787
|
C | T | 2 | a0001c0001t0016g0275a0001c0001t0016g0276 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-40+22881C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14970787 | ||||||
| chr3:14971005
|
G | T | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+23099G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971005 | ||||||
| chr3:14971111
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0130 | 2 | NA18954.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-40+23205T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971111 | ||||||
| chr3:14971124
|
T | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-40+23218T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971124 | ||||||
| chr3:14971156
|
CGCCCAGG others(684): Show |
C | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+23268_-40+2395 others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14971156 | |||||
| chr3:14971203
|
T | C | 142 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(139): Show | 145 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-40+23297T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971203 | ||||||
| chr3:14971308
|
G | A | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+23402G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971308 | ||||||
| chr3:14971457
|
A | G | 1 | a0001c0001t0008g0192 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-40+23551A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971457 | ||||||
| chr3:14971571
|
C | T | 1 | a0001c0001t0002g0038 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-40+23665C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971571 | ||||||
| chr3:14971574
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-40+23668C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971574 | ||||||
| chr3:14971670
|
A | G | 1 | a0001c0002t0005g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-40+23764A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971670 | ||||||
| chr3:14971730
|
A | C | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+23824A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971730 | ||||||
| chr3:14971810
|
C | CT | 45 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0129others(42): Show | 46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.-40+23919dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14971810 | |||||
| chr3:14971810
|
CT | C | 9 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0126others(6): Show | 9 | HG01433.hp1 NA18942.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40+23919delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14971810 | |||||
| chr3:14971841
|
T | G | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+23935T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971841 | ||||||
| chr3:14972128
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-40+24222A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972128 | ||||||
| chr3:14972129
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-40+24223G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972129 | ||||||
| chr3:14972132
|
A | G | 7 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0230others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40+24226A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972132 | ||||||
| chr3:14972286
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-40+24380T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972286 | ||||||
| chr3:14972310
|
G | A | 1 | a0001c0001t0003g0087 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-40+24404G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972310 | ||||||
| chr3:14972486
|
A | G | 4 | a0001c0003t0013g0246a0001c0003t0013g0247a0001c0003t0013g0248others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+24580A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972486 | ||||||
| chr3:14972602
|
T | G | 1 | a0001c0007t0014g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-40+24696T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972602 | ||||||
| chr3:14972669
|
G | A | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40+24763G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972669 | ||||||
| chr3:14972698
|
A | G | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+24792A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972698 | ||||||
| chr3:14972843
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-40+24937G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972843 | ||||||
| chr3:14972925
|
C | T | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+25019C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972925 | ||||||
| chr3:14972929
|
C | G | 1 | a0001c0001t0001g0214 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-40+25023C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972929 | ||||||
| chr3:14973047
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0129 | 2 | HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-40+25141T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973047 | ||||||
| chr3:14973235
|
G | A | 1 | a0001c0001t0035g0143 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-40+25329G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973235 | ||||||
| chr3:14973397
|
T | TA | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+25502dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14973397 | |||||
| chr3:14973408
|
A | T | 10 | a0001c0001t0003g0086a0001c0001t0041g0159a0001c0004t0007g0274others(7): Show | 10 | HG00408.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40+25502A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973408 | ||||||
| chr3:14973600
|
GTTA | G | 27 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(24): Show | 28 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-40+25696_-40+2569 others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14973600 | |||||
| chr3:14973606
|
C | T | 44 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(41): Show | 45 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-40+25700C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973606 | ||||||
| chr3:14973607
|
G | T | 27 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(24): Show | 28 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-40+25701G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973607 | ||||||
| chr3:14973725
|
A | C | 1 | a0001c0001t0003g0081 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-40+25819A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973725 | ||||||
| chr3:14973826
|
G | A | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+25920G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973826 | ||||||
| chr3:14973834
|
G | A | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+25928G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973834 | ||||||
| chr3:14973836
|
A | G | 1 | a0001c0001t0004g0241 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-40+25930A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973836 | ||||||
| chr3:14974020
|
C | T | 1 | a0001c0001t0012g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-40+26114C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974020 | ||||||
| chr3:14974068
|
A | T | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+26162A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974068 | ||||||
| chr3:14974133
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-40+26227A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974133 | ||||||
| chr3:14974189
|
T | C | 1 | a0001c0001t0003g0098 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-40+26283T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974189 | ||||||
| chr3:14974229
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0004g0238 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-40+26323G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974229 | ||||||
| chr3:14974564
|
A | G | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40+26658A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974564 | ||||||
| chr3:14974595
|
T | C | 2 | a0001c0001t0012g0300a0001c0001t0029g0299 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+26689T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974595 | ||||||
| chr3:14974609
|
G | GT | 20 | a0001c0001t0001g0107a0001c0001t0001g0129a0001c0001t0001g0142others(17): Show | 21 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-40+26717dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14974609 | |||||
| chr3:14974764
|
C | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0103others(18): Show | 22 | HG01255.hp1 HG01346.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-40+26858C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974764 | ||||||
| chr3:14975088
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0200 | 2 | HG00544.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.-40+27182A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14975088 | ||||||
| chr3:14975203
|
A | G | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+27297A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14975203 | ||||||
| chr3:14975408
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-40+27502C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14975408 | ||||||
| chr3:14975665
|
A | G | 104 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0187others(101): Show | 106 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.-40+27759A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14975665 | ||||||
| chr3:14975819
|
C | T | 2 | a0001c0001t0015g0001a0001c0001t0015g0059 | 3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-40+27913C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14975819 | ||||||
| chr3:14975870
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-40+27964C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14975870 | ||||||
| chr3:14976085
|
T | A | 49 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(46): Show | 50 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-39-27791T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976085 | ||||||
| chr3:14976187
|
T | C | 3 | a0001c0001t0003g0084a0001c0001t0003g0085a0001c0001t0003g0087 | 3 | NA18949.hp1 NA18978.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-39-27689T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976187 | ||||||
| chr3:14976291
|
A | G | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-27585A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976291 | ||||||
| chr3:14976388
|
A | C | 2 | a0001c0001t0012g0300a0001c0001t0029g0299 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-39-27488A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976388 | ||||||
| chr3:14976592
|
T | G | 3 | a0001c0001t0003g0088a0001c0001t0017g0294a0001c0001t0017g0295 | 3 | HG02809.hp1 HG06807.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.-39-27284T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976592 | ||||||
| chr3:14976602
|
C | CT | 9 | a0001c0001t0001g0117a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG01081.hp1 HG01109.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.-39-27252dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | |||||
| chr3:14976602
|
C | CTTTT | 7 | a0001c0001t0002g0050a0001c0001t0002g0074a0001c0001t0026g0034others(4): Show | 7 | HG01069.hp1 HG01081.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39-27255_-39-2725 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | |||||
| chr3:14976602
|
C | CTTTTT | 68 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(65): Show | 69 | HG00673.hp1 HG00733.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.-39-27256_-39-2725 others(9): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | |||||
| chr3:14976602
|
C | CTTTTTT | 15 | a0001c0001t0002g0058a0001c0001t0002g0262a0001c0001t0003g0080others(12): Show | 16 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.-39-27257_-39-2725 others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | |||||
| chr3:14976602
|
C | CTTTTTTT | 20 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0081others(17): Show | 21 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.-39-27258_-39-2725 others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | |||||
| chr3:14976602
|
C | CTTTTTTT others(1): Show |
6 | a0001c0001t0003g0086a0001c0001t0003g0094a0001c0001t0012g0284others(3): Show | 6 | HG00408.hp2 HG02129.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-27259_-39-2725 others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | |||||
| chr3:14976602
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0003g0096a0001c0004t0007g0274a0001c0004t0007g0278others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-27261_-39-2725 others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | |||||
| chr3:14976602
|
CT | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0125a0001c0001t0001g0146others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-27252delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | |||||
| chr3:14976705
|
T | C | 5 | a0001c0001t0001g0078a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG01106.hp2 HG01361.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39-27171T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976705 | ||||||
| chr3:14976833
|
T | C | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-27043T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976833 | ||||||
| chr3:14976897
|
A | G | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-26979A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976897 | ||||||
| chr3:14977115
|
T | G | 1 | a0001c0001t0002g0259 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-39-26761T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977115 | ||||||
| chr3:14977367
|
A | G | 3 | a0001c0005t0002g0296a0001c0005t0002g0297a0001c0005t0002g0298 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-39-26509A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977367 | ||||||
| chr3:14977370
|
GTGGCAGA others(13): Show |
G | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-39-26501_-39-2648 others(24): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14977370 | |||||
| chr3:14977378
|
T | C | 1 | a0001c0001t0012g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-39-26498T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977378 | ||||||
| chr3:14977825
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-39-26051C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977825 | ||||||
| chr3:14977948
|
C | CA | 60 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(57): Show | 61 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.-39-25913dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14977948 | |||||
| chr3:14977961
|
AAAG | A | 14 | a0001c0001t0021g0286a0001c0003t0006g0005a0001c0003t0006g0250others(11): Show | 15 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.-39-25897_-39-2589 others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14977961 | |||||
| chr3:14977964
|
G | A | 86 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(83): Show | 87 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.-39-25912G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977964 | ||||||
| chr3:14977967
|
G | A | 16 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(13): Show | 17 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.-39-25909G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977967 | ||||||
| chr3:14977967
|
G | T | 1 | a0001c0002t0005g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-39-25909G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977967 | ||||||
| chr3:14978005
|
AAATATGA others(6): Show |
A | 1 | a0001c0001t0001g0125 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-39-25870_-39-2585 others(17): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978005 | ||||||
| chr3:14978060
|
A | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-25816A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978060 | ||||||
| chr3:14978088
|
G | C | 8 | a0001c0003t0006g0005a0001c0003t0006g0251a0001c0003t0006g0252others(5): Show | 9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-39-25788G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978088 | ||||||
| chr3:14978182
|
C | T | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-25694C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978182 | ||||||
| chr3:14978399
|
G | A | 103 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(100): Show | 105 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.-39-25477G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978399 | ||||||
| chr3:14978589
|
C | A | 1 | a0001c0001t0002g0038 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-39-25287C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978589 | ||||||
| chr3:14978630
|
A | G | 1 | a0001c0001t0012g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39-25246A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978630 | ||||||
| chr3:14978713
|
A | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | NA18968.hp1 NA18990.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-39-25163A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978713 | ||||||
| chr3:14978800
|
T | C | 1 | a0001c0001t0012g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39-25076T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978800 | ||||||
| chr3:14978842
|
A | G | 30 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(27): Show | 31 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.-39-25034A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978842 | ||||||
| chr3:14978869
|
A | G | 103 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(100): Show | 105 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.-39-25007A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978869 | ||||||
| chr3:14979088
|
T | C | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-24788T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979088 | ||||||
| chr3:14979093
|
G | A | 3 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-39-24783G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979093 | ||||||
| chr3:14979199
|
TAAGGTGG others(7): Show |
T | 9 | a0001c0001t0001g0103a0001c0001t0001g0126a0001c0001t0001g0130others(6): Show | 9 | HG01433.hp1 NA18942.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39-24672_-39-2465 others(18): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14979199 | |||||
| chr3:14979233
|
G | A | 18 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0230others(15): Show | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-39-24643G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979233 | ||||||
| chr3:14979292
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-39-24584T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979292 | ||||||
| chr3:14979318
|
A | G | 2 | a0001c0001t0015g0001a0001c0001t0015g0059 | 3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-39-24558A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979318 | ||||||
| chr3:14979506
|
A | G | 54 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(51): Show | 55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-39-24370A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979506 | ||||||
| chr3:14979603
|
A | G | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-24273A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979603 | ||||||
| chr3:14979621
|
G | A | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-24255G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979621 | ||||||
| chr3:14979776
|
C | A | 1 | a0001c0001t0001g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-39-24100C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979776 | ||||||
| chr3:14979794
|
C | T | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-24082C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979794 | ||||||
| chr3:14979821
|
G | A | 1 | a0001c0003t0013g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-39-24055G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979821 | ||||||
| chr3:14979928
|
G | A | 1 | a0001c0007t0014g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-39-23948G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979928 | ||||||
| chr3:14980049
|
GA | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-23825delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14980049 | |||||
| chr3:14980087
|
T | C | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-23789T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980087 | ||||||
| chr3:14980317
|
T | TA | 16 | a0001c0001t0001g0121a0001c0001t0016g0275a0001c0001t0016g0276others(13): Show | 17 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.-39-23543dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14980317 | |||||
| chr3:14980318
|
A | T | 1 | a0001c0001t0001g0287 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-39-23558A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980318 | ||||||
| chr3:14980439
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-39-23437A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980439 | ||||||
| chr3:14980541
|
C | T | 1 | a0001c0003t0013g0246 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-39-23335C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980541 | ||||||
| chr3:14980558
|
TAAGA | T | 49 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(46): Show | 50 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-39-23314_-39-2331 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14980558 | |||||
| chr3:14980621
|
G | A | 1 | a0001c0001t0037g0147 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-39-23255G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980621 | ||||||
| chr3:14980667
|
A | C | 1 | a0001c0001t0021g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-39-23209A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980667 | ||||||
| chr3:14980756
|
C | T | 3 | a0001c0001t0038g0290a0001c0001t0039g0291a0001c0001t0040g0079 | 3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-39-23120C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980756 | ||||||
| chr3:14980804
|
A | G | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-23072A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980804 | ||||||
| chr3:14981126
|
G | C | 1 | a0001c0001t0001g0209 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-39-22750G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981126 | ||||||
| chr3:14981190
|
G | A | 1 | a0001c0001t0041g0159 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-39-22686G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981190 | ||||||
| chr3:14981236
|
G | A | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-22640G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981236 | ||||||
| chr3:14981275
|
C | T | 2 | a0001c0001t0038g0290a0001c0001t0039g0291 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-39-22601C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981275 | ||||||
| chr3:14981336
|
C | G | 131 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(128): Show | 134 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-39-22540C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981336 | ||||||
| chr3:14981374
|
C | T | 3 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG00438.hp1 HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.-39-22502C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981374 | ||||||
| chr3:14981593
|
G | A | 103 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(100): Show | 105 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.-39-22283G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981593 | ||||||
| chr3:14981597
|
T | C | 103 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(100): Show | 105 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.-39-22279T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981597 | ||||||
| chr3:14981602
|
C | CA | 12 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0111others(9): Show | 12 | HG01361.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-39-22253dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14981602 | |||||
| chr3:14981623
|
A | AAAG | 12 | a0001c0001t0016g0276a0001c0002t0014g0006a0001c0002t0014g0007others(9): Show | 12 | HG01081.hp2 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-39-22253_-39-2225 others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981623 | ||||||
| chr3:14981623
|
A | AAG | 34 | a0001c0001t0002g0038a0001c0001t0002g0041a0001c0001t0002g0051others(31): Show | 35 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.-39-22253_-39-2225 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981623 | ||||||
| chr3:14981623
|
A | AG | 57 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(54): Show | 58 | HG00609.hp1 HG00673.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.-39-22252dupG | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14981623 | |||||
| chr3:14981690
|
GA | G | 3 | a0001c0001t0004g0229a0001c0001t0004g0230a0001c0001t0042g0231 | 3 | HG02886.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-39-22184delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14981690 | |||||
| chr3:14981885
|
G | C | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-21991G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981885 | ||||||
| chr3:14981916
|
G | A | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-21960G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981916 | ||||||
| chr3:14981954
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-39-21922G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981954 | ||||||
| chr3:14981990
|
T | A | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-21886T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981990 | ||||||
| chr3:14982047
|
T | C | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-21829T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982047 | ||||||
| chr3:14982159
|
G | A | 5 | a0001c0001t0027g0072a0001c0001t0028g0065a0001c0005t0002g0296others(2): Show | 5 | HG03195.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39-21717G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982159 | ||||||
| chr3:14982243
|
C | T | 302 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(299): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-39-21633C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982243 | ||||||
| chr3:14982404
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-39-21472G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982404 | ||||||
| chr3:14982526
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-39-21350T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982526 | ||||||
| chr3:14982592
|
C | T | 9 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(6): Show | 9 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39-21284C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982592 | ||||||
| chr3:14982662
|
C | G | 3 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-39-21214C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982662 | ||||||
| chr3:14982764
|
C | T | 10 | a0001c0001t0001g0129a0001c0001t0001g0220a0001c0001t0001g0221others(7): Show | 10 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39-21112C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982764 | ||||||
| chr3:14983158
|
T | C | 2 | a0001c0002t0005g0027a0001c0002t0005g0029 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-39-20718T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983158 | ||||||
| chr3:14983304
|
G | A | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-20572G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983304 | ||||||
| chr3:14983318
|
CT | C | 8 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(5): Show | 8 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39-20549delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983318 | |||||
| chr3:14983462
|
T | TAC | 54 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0101others(51): Show | 54 | HG00140.hp2 HG01081.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.-39-20382_-39-2038 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | |||||
| chr3:14983462
|
T | TACAC | 46 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0106others(43): Show | 47 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.-39-20384_-39-2038 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | |||||
| chr3:14983462
|
T | TACACAC | 86 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0121others(83): Show | 88 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.-39-20386_-39-2038 others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | |||||
| chr3:14983462
|
T | TACACACA others(1): Show |
9 | a0001c0001t0001g0075a0001c0001t0002g0036a0001c0001t0002g0037others(6): Show | 9 | HG00408.hp2 HG00673.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39-20388_-39-2038 others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | |||||
| chr3:14983462
|
T | TACACACA others(3): Show |
4 | a0001c0001t0002g0051a0001c0001t0002g0070a0001c0001t0003g0083others(1): Show | 4 | HG00558.hp2 HG02165.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-20390_-39-2038 others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | |||||
| chr3:14983462
|
TAC | T | 3 | a0001c0001t0004g0237a0001c0001t0004g0243a0001c0003t0006g0255 | 3 | HG01934.hp1 HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-39-20382_-39-2038 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | |||||
| chr3:14983462
|
TACAC | T | 6 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-20384_-39-2038 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | |||||
| chr3:14983462
|
TACACACA others(13): Show |
T | 1 | a0001c0001t0041g0159 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-39-20400_-39-2038 others(24): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | |||||
| chr3:14983491
|
A | ACACG | 4 | a0001c0003t0013g0246a0001c0003t0013g0247a0001c0003t0013g0248others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-20382_-39-2038 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983491 | |||||
| chr3:14983491
|
A | ACG | 8 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(5): Show | 9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-39-20384_-39-2038 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983491 | |||||
| chr3:14983491
|
A | G | 1 | a0001c0003t0006g0255 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-39-20385A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983491 | ||||||
| chr3:14983548
|
G | T | 4 | a0001c0003t0013g0246a0001c0003t0013g0247a0001c0003t0013g0248others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-20328G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983548 | ||||||
| chr3:14983602
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-39-20274G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983602 | ||||||
| chr3:14983638
|
G | A | 8 | a0001c0003t0006g0005a0001c0003t0006g0251a0001c0003t0006g0252others(5): Show | 9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-39-20238G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983638 | ||||||
| chr3:14983756
|
G | A | 5 | a0001c0001t0002g0037a0001c0001t0012g0076a0001c0001t0012g0284others(2): Show | 5 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39-20120G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983756 | ||||||
| chr3:14983817
|
C | G | 54 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(51): Show | 55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-39-20059C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983817 | ||||||
| chr3:14983863
|
A | G | 3 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082 | 3 | HG02615.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-39-20013A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983863 | ||||||
| chr3:14983911
|
G | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-19965G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983911 | ||||||
| chr3:14983945
|
A | G | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-19931A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983945 | ||||||
| chr3:14983984
|
G | C | 1 | a0001c0001t0009g0197 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-39-19892G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983984 | ||||||
| chr3:14984118
|
C | T | 12 | a0001c0001t0001g0117a0001c0001t0001g0186a0001c0001t0001g0196others(9): Show | 12 | HG01123.hp1 HG01243.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.-39-19758C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984118 | ||||||
| chr3:14984169
|
T | C | 28 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(25): Show | 29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-39-19707T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984169 | ||||||
| chr3:14984324
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-39-19552A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984324 | ||||||
| chr3:14984361
|
A | G | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-19515A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984361 | ||||||
| chr3:14984376
|
T | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | NA18945.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-39-19500T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984376 | ||||||
| chr3:14984423
|
T | C | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-19453T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984423 | ||||||
| chr3:14984544
|
TAAAG | T | 54 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(51): Show | 55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-39-19328_-39-1932 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14984544 | |||||
| chr3:14984832
|
G | GT | 6 | a0001c0001t0001g0269a0001c0001t0008g0211a0001c0001t0012g0076others(3): Show | 6 | HG01258.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-19033dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14984832 | |||||
| chr3:14984935
|
C | T | 4 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-18941C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984935 | ||||||
| chr3:14985190
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-39-18686A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985190 | ||||||
| chr3:14985262
|
T | C | 1 | a0001c0007t0014g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-39-18614T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985262 | ||||||
| chr3:14985446
|
TCA | T | 3 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-39-18427_-39-1842 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14985446 | |||||
| chr3:14985463
|
G | A | 1 | a0001c0001t0012g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-39-18413G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985463 | ||||||
| chr3:14985613
|
C | T | 2 | a0001c0001t0020g0223a0001c0001t0020g0224 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-39-18263C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985613 | ||||||
| chr3:14985620
|
T | C | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-18256T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985620 | ||||||
| chr3:14985709
|
C | A | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-39-18167C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985709 | ||||||
| chr3:14985975
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-39-17901A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985975 | ||||||
| chr3:14986139
|
A | G | 1 | a0001c0003t0006g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-39-17737A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14986139 | ||||||
| chr3:14986865
|
A | G | 1 | a0001c0001t0029g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-39-17011A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14986865 | ||||||
| chr3:14986955
|
T | A | 54 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0002g0032others(51): Show | 55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-39-16921T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14986955 | ||||||
| chr3:14986971
|
A | G | 28 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(25): Show | 29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-39-16905A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14986971 | ||||||
| chr3:14987136
|
C | T | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG00438.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.-39-16740C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987136 | ||||||
| chr3:14987234
|
C | T | 1 | a0001c0003t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-39-16642C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987234 | ||||||
| chr3:14987274
|
G | A | 3 | a0001c0002t0005g0025a0001c0002t0005g0028a0001c0002t0005g0030 | 3 | HG03579.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-39-16602G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987274 | ||||||
| chr3:14987329
|
C | T | 1 | a0001c0003t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-39-16547C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987329 | ||||||
| chr3:14987453
|
G | C | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-16423G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987453 | ||||||
| chr3:14987625
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-39-16251T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987625 | ||||||
| chr3:14987626
|
C | T | 1 | a0001c0001t0021g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-39-16250C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987626 | ||||||
| chr3:14987646
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-39-16230A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987646 | ||||||
| chr3:14987826
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-39-16050C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987826 | ||||||
| chr3:14987861
|
C | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-16015C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987861 | ||||||
| chr3:14987867
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0034g0115 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-39-16009G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987867 | ||||||
| chr3:14987945
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-39-15931C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987945 | ||||||
| chr3:14988043
|
A | G | 1 | a0001c0001t0003g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-39-15833A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988043 | ||||||
| chr3:14988066
|
A | G | 1 | a0001c0001t0003g0098 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-39-15810A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988066 | ||||||
| chr3:14988248
|
C | G | 2 | a0001c0001t0016g0275a0001c0001t0016g0276 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-39-15628C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988248 | ||||||
| chr3:14988351
|
G | A | 1 | a0001c0001t0010g0271 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-39-15525G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988351 | ||||||
| chr3:14988384
|
A | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0220 | 2 | HG02683.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-39-15492A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988384 | ||||||
| chr3:14988502
|
G | A | 1 | a0001c0001t0039g0291 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-39-15374G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988502 | ||||||
| chr3:14988575
|
C | G | 3 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-39-15301C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988575 | ||||||
| chr3:14988763
|
C | T | 126 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(123): Show | 128 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-39-15113C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988763 | ||||||
| chr3:14988884
|
A | C | 1 | a0001c0003t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-39-14992A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988884 | ||||||
| chr3:14989038
|
T | A | 30 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(27): Show | 31 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.-39-14838T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14989038 | ||||||
| chr3:14989141
|
G | T | 1 | a0001c0001t0029g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-39-14735G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14989141 | ||||||
| chr3:14989307
|
G | A | 1 | a0001c0007t0014g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-39-14569G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14989307 | ||||||
| chr3:14989404
|
G | C | 2 | a0001c0002t0005g0027a0001c0002t0005g0029 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-39-14472G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14989404 | ||||||
| chr3:14989825
|
G | A | 1 | a0001c0001t0011g0217 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-39-14051G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14989825 | ||||||
| chr3:14989924
|
C | CA | 31 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0061others(28): Show | 31 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.-39-13923dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | |||||
| chr3:14989924
|
C | CAA | 13 | a0001c0001t0001g0105a0001c0001t0001g0186a0001c0001t0001g0213others(10): Show | 13 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.-39-13924_-39-1392 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | |||||
| chr3:14989924
|
CA | C | 76 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0103others(73): Show | 78 | HG00609.hp1 HG00673.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.-39-13923delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | |||||
| chr3:14989924
|
CAA | C | 24 | a0001c0001t0002g0055a0001c0001t0004g0228a0001c0001t0004g0230others(21): Show | 24 | HG01884.hp1 HG01934.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-39-13924_-39-1392 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | |||||
| chr3:14989924
|
CAAA | C | 7 | a0001c0001t0004g0237a0001c0001t0004g0240a0001c0001t0012g0300others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39-13925_-39-1392 others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | |||||
| chr3:14989924
|
CAAAAA | C | 11 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(8): Show | 11 | HG01109.hp1 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-39-13927_-39-1392 others(9): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | |||||
| chr3:14989924
|
CAAAAAAA others(1): Show |
C | 18 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0084others(15): Show | 20 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.-39-13930_-39-1392 others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | |||||
| chr3:14989924
|
CAAAAAAA others(5): Show |
C | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39-13934_-39-1392 others(16): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | |||||
| chr3:14989954
|
T | A | 4 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0182others(1): Show | 4 | NA18941.hp2 NA18960.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-13922T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14989954 | ||||||
| chr3:14990132
|
A | C | 4 | a0001c0003t0013g0246a0001c0003t0013g0247a0001c0003t0013g0248others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-13744A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990132 | ||||||
| chr3:14990216
|
A | C | 1 | a0001c0003t0006g0272 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-39-13660A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990216 | ||||||
| chr3:14990489
|
G | A | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-39-13387G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990489 | ||||||
| chr3:14990525
|
C | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-13351C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990525 | ||||||
| chr3:14990636
|
G | A | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-13240G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990636 | ||||||
| chr3:14990741
|
T | A | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-13135T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990741 | ||||||
| chr3:14990811
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0130 | 2 | NA18954.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-39-13065A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990811 | ||||||
| chr3:14991047
|
G | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-12829G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14991047 | ||||||
| chr3:14991345
|
C | T | 1 | a0001c0001t0008g0211 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-39-12531C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14991345 | ||||||
| chr3:14991445
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-39-12431G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14991445 | ||||||
| chr3:14991518
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-39-12358A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14991518 | ||||||
| chr3:14991533
|
A | G | 5 | a0001c0001t0011g0215a0001c0001t0011g0216a0001c0001t0011g0217others(2): Show | 5 | HG00642.hp1 HG01361.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39-12343A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14991533 | ||||||
| chr3:14991768
|
C | CT | 26 | a0001c0001t0001g0154a0001c0001t0001g0160a0001c0001t0001g0173others(23): Show | 26 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-39-12094dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14991768 | |||||
| chr3:14991971
|
A | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-11905A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14991971 | ||||||
| chr3:14992049
|
G | A | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-11827G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14992049 | ||||||
| chr3:14992364
|
C | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-11512C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14992364 | ||||||
| chr3:14992413
|
G | C | 2 | a0001c0001t0001g0157a0001c0001t0036g0174 | 2 | HG02027.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-39-11463G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14992413 | ||||||
| chr3:14992461
|
C | G | 2 | a0001c0001t0018g0067a0001c0001t0018g0068 | 2 | HG00733.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-39-11415C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14992461 | ||||||
| chr3:14992727
|
G | T | 1 | a0001c0001t0001g0185 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-39-11149G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14992727 | ||||||
| chr3:14992920
|
G | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0301 | 3 | HG00673.hp2 NA18991.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-39-10956G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14992920 | ||||||
| chr3:14993454
|
CA | C | 32 | a0001c0001t0001g0117a0001c0001t0001g0196a0001c0001t0012g0076others(29): Show | 33 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-39-10408delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14993454 | |||||
| chr3:14993631
|
A | G | 1 | a0001c0003t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-39-10245A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14993631 | ||||||
| chr3:14993673
|
AT | A | 18 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0230others(15): Show | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-39-10199delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14993673 | |||||
| chr3:14993840
|
A | G | 1 | a0001c0003t0006g0255 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-39-10036A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14993840 | ||||||
| chr3:14993932
|
G | A | 101 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(98): Show | 103 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.-39-9944G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14993932 | ||||||
| chr3:14994075
|
A | G | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-9801A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994075 | ||||||
| chr3:14994076
|
T | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39-9800T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994076 | ||||||
| chr3:14994154
|
ATT | A | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-9718_-39-9717d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994154 | |||||
| chr3:14994183
|
T | C | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-9693T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994183 | ||||||
| chr3:14994197
|
A | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0196 | 2 | NA18951.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-39-9679A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994197 | ||||||
| chr3:14994218
|
C | T | 1 | a0001c0001t0029g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-39-9658C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994218 | ||||||
| chr3:14994306
|
T | C | 4 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-9570T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994306 | ||||||
| chr3:14994419
|
G | T | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-9457G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994419 | ||||||
| chr3:14994427
|
T | C | 1 | a0001c0001t0008g0192 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-39-9449T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994427 | ||||||
| chr3:14994439
|
C | CT | 70 | a0001c0001t0001g0015a0001c0001t0001g0105a0001c0001t0001g0117others(67): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-39-9415dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994439 | |||||
| chr3:14994439
|
C | CTT | 78 | a0001c0001t0001g0149a0001c0001t0001g0301a0001c0001t0002g0032others(75): Show | 80 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.-39-9416_-39-9415d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994439 | |||||
| chr3:14994439
|
C | CTTT | 9 | a0001c0001t0002g0033a0001c0001t0002g0041a0001c0001t0002g0046others(6): Show | 9 | HG01175.hp2 HG01891.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-39-9417_-39-9415d others(5): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994439 | |||||
| chr3:14994547
|
A | G | 1 | a0001c0001t0035g0143 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-39-9329A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994547 | ||||||
| chr3:14994684
|
G | A | 1 | a0001c0002t0005g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-39-9192G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994684 | ||||||
| chr3:14994725
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-39-9151G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994725 | ||||||
| chr3:14994733
|
A | G | 155 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0301others(152): Show | 158 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.-39-9143A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994733 | ||||||
| chr3:14994752
|
T | TA | 96 | a0001c0001t0001g0078a0001c0001t0001g0110a0001c0001t0001g0111others(93): Show | 97 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.-39-9108dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994752 | |||||
| chr3:14994830
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-39-9046G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994830 | ||||||
| chr3:14994945
|
A | G | 31 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0301others(28): Show | 32 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.-39-8931A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994945 | ||||||
| chr3:14994977
|
C | CT | 32 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0114others(29): Show | 32 | HG01081.hp2 HG02027.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-39-8878dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994977 | |||||
| chr3:14994977
|
C | CTT | 22 | a0001c0001t0001g0209a0001c0002t0005g0019a0001c0002t0005g0020others(19): Show | 22 | HG01109.hp1 HG01168.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.-39-8879_-39-8878d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994977 | |||||
| chr3:14994977
|
CT | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 80 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.-39-8878delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994977 | |||||
| chr3:14995033
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-39-8843T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995033 | ||||||
| chr3:14995097
|
C | G | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-39-8779C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995097 | ||||||
| chr3:14995172
|
T | A | 5 | a0001c0001t0002g0039a0001c0001t0002g0042a0001c0001t0002g0043others(2): Show | 5 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39-8704T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995172 | ||||||
| chr3:14995255
|
C | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0110a0001c0001t0001g0111others(3): Show | 6 | HG01106.hp2 HG01361.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39-8621C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995255 | ||||||
| chr3:14995282
|
C | G | 4 | a0001c0001t0028g0065a0001c0005t0002g0296a0001c0005t0002g0297others(1): Show | 4 | HG03195.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-8594C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995282 | ||||||
| chr3:14995320
|
C | CA | 34 | a0001c0001t0001g0105a0001c0001t0001g0132a0001c0001t0001g0154others(31): Show | 34 | HG00642.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-39-8539dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995320 | |||||
| chr3:14995383
|
C | A | 258 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(255): Show | 262 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.-39-8493C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995383 | ||||||
| chr3:14995401
|
TA | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0009t0001g0016 | 3 | HG03139.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-39-8474delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995401 | ||||||
| chr3:14995498
|
A | G | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-8378A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995498 | ||||||
| chr3:14995668
|
C | CGCGTGTG others(9): Show |
1 | a0001c0002t0005g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-39-8207_-39-8206i others(18): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | |||||
| chr3:14995668
|
C | CGTGTGT | 8 | a0001c0001t0002g0037a0001c0001t0002g0041a0001c0001t0017g0294others(5): Show | 8 | HG01175.hp2 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39-8189_-39-8184d others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | |||||
| chr3:14995668
|
C | CGTGTGTG others(1): Show |
43 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(40): Show | 44 | HG00609.hp1 HG00642.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.-39-8191_-39-8184d others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | |||||
| chr3:14995668
|
C | CGTGTGTG others(3): Show |
26 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(23): Show | 26 | HG01192.hp1 HG01243.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-39-8193_-39-8184d others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | |||||
| chr3:14995668
|
C | CGTGTGTG others(5): Show |
9 | a0001c0001t0002g0036a0001c0001t0003g0080a0001c0001t0003g0081others(6): Show | 9 | HG00673.hp1 HG01192.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39-8195_-39-8184d others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | |||||
| chr3:14995668
|
C | CGTGTGTG others(7): Show |
11 | a0001c0001t0043g0236a0001c0003t0006g0005a0001c0003t0006g0250others(8): Show | 12 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.-39-8197_-39-8184d others(16): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | |||||
| chr3:14995668
|
C | CGTGTGTG others(9): Show |
13 | a0001c0001t0012g0076a0001c0002t0005g0019a0001c0002t0005g0020others(10): Show | 13 | HG01109.hp1 HG01168.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-39-8199_-39-8184d others(18): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | |||||
| chr3:14995668
|
C | CGTGTGTG others(11): Show |
14 | a0001c0001t0003g0083a0001c0001t0003g0085a0001c0001t0003g0094others(11): Show | 14 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-8201_-39-8184d others(20): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | |||||
| chr3:14995668
|
C | CGTGTGTG others(13): Show |
21 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0084others(18): Show | 22 | HG00408.hp2 HG00639.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-39-8203_-39-8184d others(22): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | |||||
| chr3:14995668
|
C | CGTGTGTG others(15): Show |
3 | a0001c0001t0003g0091a0001c0001t0003g0257a0001c0001t0003g0258 | 3 | HG01069.hp2 HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-39-8205_-39-8184d others(24): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | |||||
| chr3:14995668
|
C | CGTGTGTG others(17): Show |
2 | a0001c0001t0003g0088a0001c0001t0030g0077 | 2 | NA18951.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-39-8207_-39-8184d others(26): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | |||||
| chr3:14995668
|
C | CGTGTGTG others(19): Show |
1 | a0001c0001t0012g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39-8184_-39-8183i others(28): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | |||||
| chr3:14995669
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-39-8207G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995669 | ||||||
| chr3:14995670
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-39-8206T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995670 | ||||||
| chr3:14995824
|
T | G | 1 | a0001c0001t0021g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-39-8052T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995824 | ||||||
| chr3:14995894
|
C | T | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-39-7982C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995894 | ||||||
| chr3:14996084
|
G | A | 106 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(103): Show | 108 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.-39-7792G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996084 | ||||||
| chr3:14996192
|
G | T | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-7684G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996192 | ||||||
| chr3:14996278
|
A | G | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-7598A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996278 | ||||||
| chr3:14996344
|
C | G | 57 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(54): Show | 58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.-39-7532C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996344 | ||||||
| chr3:14996695
|
C | T | 24 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(21): Show | 25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.-39-7181C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996695 | ||||||
| chr3:14996708
|
C | T | 4 | a0001c0003t0013g0246a0001c0003t0013g0247a0001c0003t0013g0248others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-7168C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996708 | ||||||
| chr3:14996715
|
C | T | 1 | a0001c0007t0014g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-39-7161C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996715 | ||||||
| chr3:14996884
|
G | A | 18 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0230others(15): Show | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-39-6992G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996884 | ||||||
| chr3:14997024
|
G | T | 18 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0230others(15): Show | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-39-6852G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14997024 | ||||||
| chr3:14997075
|
G | T | 1 | a0001c0001t0021g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-39-6801G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14997075 | ||||||
| chr3:14997951
|
A | AC | 4 | a0001c0001t0001g0212a0001c0001t0001g0269a0001c0001t0009g0120others(1): Show | 4 | HG01109.hp2 HG02080.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-5921dupC | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14997951 | |||||
| chr3:14998061
|
C | T | 1 | a0001c0001t0027g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-39-5815C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998061 | ||||||
| chr3:14998062
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0144a0001c0001t0001g0145others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-5814G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998062 | ||||||
| chr3:14998569
|
G | T | 2 | a0001c0001t0004g0233a0001c0001t0004g0234 | 2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-39-5307G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998569 | ||||||
| chr3:14998659
|
T | C | 1 | a0001c0001t0002g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-39-5217T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998659 | ||||||
| chr3:14998774
|
G | T | 1 | a0001c0001t0001g0109 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-39-5102G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998774 | ||||||
| chr3:14998875
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-39-5001G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998875 | ||||||
| chr3:14998954
|
C | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0259others(3): Show | 6 | HG01070.hp1 HG01099.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39-4922C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998954 | ||||||
| chr3:14999025
|
T | A | 75 | a0001c0001t0001g0140a0001c0001t0002g0032a0001c0001t0002g0033others(72): Show | 76 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.-39-4851T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999025 | ||||||
| chr3:14999026
|
T | A | 1 | a0001c0001t0027g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-39-4850T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999026 | ||||||
| chr3:14999270
|
C | T | 2 | a0001c0001t0004g0244a0001c0001t0004g0245 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-39-4606C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999270 | ||||||
| chr3:14999281
|
A | AC | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-4594dupC | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14999281 | |||||
| chr3:14999455
|
C | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-4421C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999455 | ||||||
| chr3:14999460
|
T | C | 2 | a0001c0001t0020g0223a0001c0001t0020g0224 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-39-4416T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999460 | ||||||
| chr3:14999497
|
A | C | 1 | a0001c0007t0014g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-39-4379A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999497 | ||||||
| chr3:14999547
|
A | G | 1 | a0001c0001t0012g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39-4329A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999547 | ||||||
| chr3:14999592
|
T | C | 2 | a0001c0006t0001g0128a0001c0006t0001g0204 | 2 | NA18957.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-39-4284T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999592 | ||||||
| chr3:14999669
|
A | AT | 9 | a0001c0001t0001g0104a0001c0004t0007g0274a0001c0004t0007g0277others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39-4195dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14999669 | |||||
| chr3:14999669
|
AT | A | 71 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(68): Show | 73 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.-39-4195delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14999669 | |||||
| chr3:14999695
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-39-4181G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999695 | ||||||
| chr3:14999891
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-39-3985T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999891 | ||||||
| chr3:14999916
|
G | T | 2 | a0001c0001t0002g0058a0001c0001t0002g0069 | 2 | HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.-39-3960G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999916 | ||||||
| chr3:14999938
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-39-3938G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999938 | ||||||
| chr3:14999951
|
G | A | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-3925G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999951 | ||||||
| chr3:14999965
|
T | A | 1 | a0001c0001t0001g0266 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-39-3911T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999965 | ||||||
| chr3:14999984
|
A | G | 1 | a0001c0001t0041g0159 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-39-3892A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999984 | ||||||
| chr3:15000108
|
T | TA | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-3759dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15000108 | |||||
| chr3:15000108
|
T | TAA | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-3760_-39-3759d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15000108 | |||||
| chr3:15000158
|
C | G | 4 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-3718C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000158 | ||||||
| chr3:15000449
|
G | A | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-3427G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000449 | ||||||
| chr3:15000513
|
A | C | 1 | a0001c0001t0026g0034 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-39-3363A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000513 | ||||||
| chr3:15000529
|
C | T | 104 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(101): Show | 106 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.-39-3347C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000529 | ||||||
| chr3:15000571
|
C | T | 4 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-3305C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000571 | ||||||
| chr3:15000758
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-39-3118G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000758 | ||||||
| chr3:15000764
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-39-3112T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000764 | ||||||
| chr3:15000814
|
G | GT | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(69): Show | 75 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.-39-3042dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15000814 | |||||
| chr3:15000814
|
GT | G | 43 | a0001c0001t0002g0039a0001c0001t0002g0042a0001c0001t0002g0043others(40): Show | 43 | HG00609.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.-39-3042delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15000814 | |||||
| chr3:15000814
|
GTT | G | 13 | a0001c0003t0006g0005a0001c0003t0006g0251a0001c0003t0006g0252others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-3043_-39-3042d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15000814 | |||||
| chr3:15000818
|
T | G | 1 | a0001c0001t0001g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-39-3058T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000818 | ||||||
| chr3:15000884
|
G | A | 1 | a0001c0001t0033g0151 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-39-2992G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000884 | ||||||
| chr3:15000895
|
A | G | 1 | a0001c0001t0009g0118 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-39-2981A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000895 | ||||||
| chr3:15000959
|
C | T | 1 | a0001c0006t0001g0204 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-39-2917C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000959 | ||||||
| chr3:15000983
|
T | A | 57 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(54): Show | 58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.-39-2893T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000983 | ||||||
| chr3:15001094
|
G | A | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-39-2782G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15001094 | ||||||
| chr3:15001104
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-39-2772G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15001104 | ||||||
| chr3:15001151
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-39-2725T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15001151 | ||||||
| chr3:15001318
|
G | GT | 49 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0173others(46): Show | 50 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-39-2538dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15001318 | |||||
| chr3:15001318
|
GT | G | 42 | a0001c0001t0010g0048a0001c0001t0010g0060a0001c0001t0012g0076others(39): Show | 43 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.-39-2538delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15001318 | |||||
| chr3:15001318
|
GTT | G | 6 | a0001c0001t0012g0284a0001c0001t0012g0285a0001c0001t0012g0300others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39-2539_-39-2538d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15001318 | |||||
| chr3:15001328
|
TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0002g0045 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-39-2535_-39-2524d others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15001328 | |||||
| chr3:15001338
|
T | G | 1 | a0001c0001t0010g0047 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-39-2538T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15001338 | ||||||
| chr3:15001340
|
G | GT | 8 | a0001c0001t0001g0018a0001c0001t0001g0135a0001c0001t0001g0162others(5): Show | 8 | HG02165.hp2 HG02273.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-2526dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15001340 | |||||
| chr3:15001340
|
G | T | 1 | a0001c0001t0010g0047 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-39-2536G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15001340 | ||||||
| chr3:15001820
|
G | T | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-2056G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15001820 | ||||||
| chr3:15002187
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-39-1689G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002187 | ||||||
| chr3:15002195
|
T | C | 3 | a0001c0001t0003g0086a0001c0001t0003g0094a0001c0001t0023g0095 | 3 | HG00408.hp2 HG02129.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-39-1681T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002195 | ||||||
| chr3:15002198
|
T | C | 59 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(56): Show | 60 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.-39-1678T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002198 | ||||||
| chr3:15002278
|
T | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-1598T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002278 | ||||||
| chr3:15002364
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-39-1512G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002364 | ||||||
| chr3:15002433
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-39-1443C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002433 | ||||||
| chr3:15002477
|
A | T | 152 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(149): Show | 155 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.-39-1399A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002477 | ||||||
| chr3:15002542
|
G | T | 1 | a0001c0001t0012g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39-1334G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002542 | ||||||
| chr3:15002645
|
C | CT | 91 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0061others(88): Show | 92 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-39-1201dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002645 | |||||
| chr3:15002645
|
C | CTT | 21 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0121others(18): Show | 21 | HG00140.hp2 HG00609.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-39-1202_-39-1201d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002645 | |||||
| chr3:15002645
|
CT | C | 34 | a0001c0001t0001g0018a0001c0001t0001g0124a0001c0001t0001g0146others(31): Show | 35 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-39-1201delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002645 | |||||
| chr3:15002645
|
CTT | C | 12 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0038others(9): Show | 12 | HG00733.hp1 HG02683.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.-39-1202_-39-1201d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002645 | |||||
| chr3:15002645
|
CTTT | C | 57 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(54): Show | 59 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.-39-1203_-39-1201d others(5): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002645 | |||||
| chr3:15002645
|
CTTTTTTT others(8): Show |
C | 13 | a0001c0001t0012g0300a0001c0001t0016g0275a0001c0001t0016g0276others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-39-1215_-39-1201d others(17): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002645 | |||||
| chr3:15002863
|
G | C | 4 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-1013G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002863 | ||||||
| chr3:15002890
|
T | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0108others(27): Show | 31 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.-39-986T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002890 | ||||||
| chr3:15002909
|
C | T | 28 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(25): Show | 29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-39-967C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002909 | ||||||
| chr3:15002946
|
C | T | 4 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-930C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002946 | ||||||
| chr3:15002947
|
C | T | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-39-929C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002947 | ||||||
| chr3:15002953
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-39-923C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002953 | ||||||
| chr3:15002967
|
CT | C | 57 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(54): Show | 58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.-39-897delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002967 | |||||
| chr3:15003112
|
A | AT | 63 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0102others(60): Show | 64 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-39-747dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15003112 | |||||
| chr3:15003121
|
T | C | 3 | a0001c0001t0004g0228a0001c0001t0004g0233a0001c0001t0004g0234 | 3 | HG02109.hp1 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-39-755T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15003121 | ||||||
| chr3:15003143
|
A | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-733A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15003143 | ||||||
| chr3:15003258
|
C | T | 1 | a0001c0001t0027g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-39-618C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15003258 | ||||||
| chr3:15003534
|
A | G | 2 | a0001c0001t0002g0058a0001c0001t0002g0069 | 2 | HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.-39-342A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15003534 | ||||||
| chr3:15003816
|
A | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(1): Show | 4 | NA18946.hp1 NA18978.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-60A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15003816 | ||||||
| chr3:15004066
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.72+80A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004066 | ||||||
| chr3:15004206
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+220A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004206 | ||||||
| chr3:15004239
|
T | C | 1 | a0001c0001t0040g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.72+253T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004239 | ||||||
| chr3:15004581
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.72+595T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004581 | ||||||
| chr3:15004627
|
G | A | 4 | a0001c0001t0010g0047a0001c0001t0010g0048a0001c0001t0010g0060others(1): Show | 4 | HG00609.hp1 HG02071.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+641G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004627 | ||||||
| chr3:15004661
|
A | C | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.72+675A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004661 | ||||||
| chr3:15004758
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.72+772G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004758 | ||||||
| chr3:15004869
|
G | T | 4 | a0001c0001t0028g0065a0001c0005t0002g0296a0001c0005t0002g0297others(1): Show | 4 | HG03195.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+883G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004869 | ||||||
| chr3:15004927
|
A | G | 57 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(54): Show | 58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.72+941A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004927 | ||||||
| chr3:15004978
|
C | G | 1 | a0001c0001t0028g0065 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.72+992C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004978 | ||||||
| chr3:15005041
|
C | T | 3 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG00438.hp1 HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.72+1055C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15005041 | ||||||
| chr3:15005122
|
A | C | 4 | a0001c0003t0013g0246a0001c0003t0013g0247a0001c0003t0013g0248others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+1136A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15005122 | ||||||
| chr3:15005368
|
C | CT | 33 | a0001c0001t0001g0015a0001c0001t0001g0101a0001c0001t0001g0105others(30): Show | 33 | HG00438.hp2 HG01109.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.72+1407dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005368 | |||||
| chr3:15005368
|
CT | C | 43 | a0001c0001t0001g0185a0001c0001t0001g0199a0001c0001t0012g0300others(40): Show | 44 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.72+1407delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005368 | |||||
| chr3:15005368
|
CTTT | C | 54 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(51): Show | 55 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.72+1405_72+1407del others(3): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005368 | |||||
| chr3:15005519
|
C | CT | 103 | a0001c0001t0001g0134a0001c0001t0001g0152a0001c0001t0001g0165others(100): Show | 104 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(101): Show |
intron_variant | MODIFIER | c.72+1553dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005519 | |||||
| chr3:15005519
|
C | CTT | 49 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0301others(46): Show | 51 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.72+1552_72+1553dup others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005519 | |||||
| chr3:15005519
|
C | CTTT | 6 | a0001c0001t0002g0033a0001c0001t0003g0094a0001c0001t0016g0275others(3): Show | 6 | HG03098.hp1 HG03209.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+1551_72+1553dup others(3): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005519 | |||||
| chr3:15005519
|
CT | C | 12 | a0001c0001t0001g0117a0001c0001t0001g0132a0001c0001t0001g0196others(9): Show | 12 | HG01243.hp1 HG01496.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.72+1553delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005519 | |||||
| chr3:15005611
|
A | C | 1 | a0001c0001t0001g0200 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.72+1625A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15005611 | ||||||
| chr3:15005845
|
C | T | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+1859C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15005845 | ||||||
| chr3:15006067
|
C | A | 1 | a0001c0001t0001g0214 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.72+2081C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006067 | ||||||
| chr3:15006149
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.72+2163G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006149 | ||||||
| chr3:15006234
|
T | G | 2 | a0001c0001t0002g0071a0001c0001t0002g0263 | 2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.72+2248T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006234 | ||||||
| chr3:15006455
|
T | C | 28 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(25): Show | 29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.72+2469T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006455 | ||||||
| chr3:15006577
|
T | C | 1 | a0001c0001t0029g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.72+2591T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006577 | ||||||
| chr3:15006747
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.72+2761A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006747 | ||||||
| chr3:15006776
|
CT | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0142a0001c0001t0001g0165others(12): Show | 15 | HG01069.hp1 HG01169.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.72+2808delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15006776 | |||||
| chr3:15006811
|
T | C | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.72+2825T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006811 | ||||||
| chr3:15006845
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0225 | 2 | HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.72+2859G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006845 | ||||||
| chr3:15007151
|
G | A | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.72+3165G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15007151 | ||||||
| chr3:15007379
|
G | C | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+3393G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15007379 | ||||||
| chr3:15007717
|
G | A | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.72+3731G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15007717 | ||||||
| chr3:15007863
|
C | G | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.72+3877C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15007863 | ||||||
| chr3:15007967
|
G | A | 3 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.72+3981G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15007967 | ||||||
| chr3:15008029
|
G | A | 24 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(21): Show | 25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.72+4043G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008029 | ||||||
| chr3:15008035
|
C | T | 1 | a0001c0001t0004g0235 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.72+4049C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008035 | ||||||
| chr3:15008101
|
G | A | 12 | a0001c0001t0002g0039a0001c0001t0002g0042a0001c0001t0002g0043others(9): Show | 12 | HG00642.hp1 HG00735.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+4115G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008101 | ||||||
| chr3:15008134
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.72+4148A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008134 | ||||||
| chr3:15008181
|
C | T | 2 | a0001c0001t0008g0148a0001c0001t0008g0161 | 2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.72+4195C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008181 | ||||||
| chr3:15008214
|
TTG | T | 3 | a0001c0001t0012g0284a0001c0001t0012g0285a0001c0001t0030g0077 | 3 | HG02896.hp1 HG02897.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.72+4230_72+4231del others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15008214 | |||||
| chr3:15008219
|
TG | T | 100 | a0001c0001t0001g0113a0001c0001t0002g0032a0001c0001t0002g0033others(97): Show | 102 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.72+4234delG | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008219 | ||||||
| chr3:15008220
|
G | T | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(165): Show | 171 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.72+4234G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008220 | ||||||
| chr3:15008224
|
T | G | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.72+4238T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008224 | ||||||
| chr3:15008232
|
A | T | 10 | a0001c0001t0001g0105a0001c0001t0001g0178a0001c0001t0008g0148others(7): Show | 10 | HG00280.hp1 HG00639.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+4246A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008232 | ||||||
| chr3:15008382
|
C | T | 24 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(21): Show | 25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.72+4396C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008382 | ||||||
| chr3:15008383
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0184a0001c0001t0017g0294others(1): Show | 5 | HG02015.hp1 HG02155.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+4397G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008383 | ||||||
| chr3:15008392
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.72+4406C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008392 | ||||||
| chr3:15008524
|
GA | G | 76 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0198others(73): Show | 78 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.72+4550delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15008524 | |||||
| chr3:15008537
|
C | A | 1 | a0001c0001t0024g0053 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.72+4551C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008537 | ||||||
| chr3:15008568
|
C | G | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.72+4582C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008568 | ||||||
| chr3:15008644
|
C | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0149a0001c0001t0001g0153others(1): Show | 4 | HG02698.hp1 NA18946.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+4658C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008644 | ||||||
| chr3:15008690
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.72+4704A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008690 | ||||||
| chr3:15008963
|
A | G | 38 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0103others(35): Show | 39 | HG00140.hp2 HG01099.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.73-4626A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008963 | ||||||
| chr3:15008987
|
G | C | 1 | a0001c0001t0019g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.73-4602G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008987 | ||||||
| chr3:15009011
|
G | C | 1 | a0001c0007t0014g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-4578G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009011 | ||||||
| chr3:15009077
|
C | CG | 56 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(53): Show | 57 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.73-4508dupG | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15009077 | |||||
| chr3:15009178
|
T | C | 4 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-4411T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009178 | ||||||
| chr3:15009218
|
G | A | 4 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-4371G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009218 | ||||||
| chr3:15009271
|
A | T | 134 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(131): Show | 137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.73-4318A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009271 | ||||||
| chr3:15009281
|
G | C | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.73-4308G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009281 | ||||||
| chr3:15009558
|
T | TTGAGGGC others(21): Show |
1 | a0001c0001t0001g0158 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.73-4030_73-4003dup others(28): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15009558 | |||||
| chr3:15009615
|
C | G | 1 | a0001c0001t0034g0115 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73-3974C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009615 | ||||||
| chr3:15009619
|
C | G | 1 | a0001c0001t0002g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.73-3970C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009619 | ||||||
| chr3:15009621
|
G | A | 296 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(293): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.73-3968G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009621 | ||||||
| chr3:15009716
|
T | G | 8 | a0001c0003t0006g0005a0001c0003t0006g0251a0001c0003t0006g0252others(5): Show | 9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-3873T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009716 | ||||||
| chr3:15009908
|
G | C | 3 | a0001c0001t0038g0290a0001c0001t0039g0291a0001c0001t0040g0079 | 3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.73-3681G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009908 | ||||||
| chr3:15010045
|
G | A | 18 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0230others(15): Show | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-3544G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15010045 | ||||||
| chr3:15010103
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.73-3486C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15010103 | ||||||
| chr3:15010353
|
TA | T | 31 | a0001c0001t0002g0045a0001c0001t0012g0076a0001c0001t0012g0284others(28): Show | 32 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.73-3224delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15010353 | |||||
| chr3:15010563
|
A | T | 1 | a0001c0007t0014g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-3026A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15010563 | ||||||
| chr3:15010711
|
C | CA | 42 | a0001c0001t0001g0015a0001c0001t0001g0181a0001c0001t0015g0059others(39): Show | 43 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.73-2861dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15010711 | |||||
| chr3:15010998
|
T | C | 134 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(131): Show | 137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.73-2591T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15010998 | ||||||
| chr3:15011114
|
C | T | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.73-2475C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15011114 | ||||||
| chr3:15011211
|
C | T | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-2378C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15011211 | ||||||
| chr3:15011425
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0182 | 2 | NA18941.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.73-2164C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15011425 | ||||||
| chr3:15011472
|
T | C | 1 | a0001c0001t0004g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.73-2117T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15011472 | ||||||
| chr3:15011576
|
C | T | 32 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(29): Show | 33 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.73-2013C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15011576 | ||||||
| chr3:15011990
|
C | T | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-1599C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15011990 | ||||||
| chr3:15012054
|
A | T | 2 | a0001c0001t0012g0300a0001c0001t0029g0299 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.73-1535A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012054 | ||||||
| chr3:15012161
|
G | A | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.73-1428G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012161 | ||||||
| chr3:15012194
|
G | C | 1 | a0001c0003t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-1395G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012194 | ||||||
| chr3:15012230
|
C | CT | 57 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(54): Show | 58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.73-1347dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15012230 | |||||
| chr3:15012248
|
C | T | 10 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(7): Show | 10 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.73-1341C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012248 | ||||||
| chr3:15012382
|
C | T | 1 | a0001c0001t0003g0258 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.73-1207C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012382 | ||||||
| chr3:15012517
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.73-1072C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012517 | ||||||
| chr3:15012521
|
C | T | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.73-1068C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012521 | ||||||
| chr3:15012544
|
T | TCTGTCAA others(3): Show |
106 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(103): Show | 108 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.73-1045_73-1044ins others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012544 | ||||||
| chr3:15012584
|
T | G | 1 | a0001c0001t0012g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.73-1005T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012584 | ||||||
| chr3:15012614
|
A | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | HG01884.hp2 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.73-975A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012614 | ||||||
| chr3:15012643
|
C | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0169 | 2 | NA18990.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.73-946C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012643 | ||||||
| chr3:15013132
|
T | C | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-457T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15013132 | ||||||
| chr3:15013307
|
C | T | 106 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(103): Show | 108 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.73-282C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15013307 | ||||||
| chr3:15013337
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.73-252A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15013337 | ||||||
| chr3:15013463
|
G | T | 28 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(25): Show | 29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.73-126G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15013463 | ||||||
| chr3:15013916
|
C | T | 1 | a0001c0001t0003g0094 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.273+127C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15013916 | ||||||
| chr3:15013918
|
G | A | 2 | a0001c0002t0014g0006a0001c0002t0014g0007 | 2 | HG01081.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.273+129G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15013918 | ||||||
| chr3:15013972
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.273+183G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15013972 | ||||||
| chr3:15014073
|
T | C | 2 | a0001c0001t0020g0223a0001c0001t0020g0224 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.273+284T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014073 | ||||||
| chr3:15014147
|
G | A | 3 | a0001c0005t0002g0296a0001c0005t0002g0297a0001c0005t0002g0298 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.273+358G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014147 | ||||||
| chr3:15014392
|
A | C | 3 | a0001c0001t0018g0067a0001c0001t0018g0068a0001c0001t0025g0066 | 3 | HG00733.hp2 HG01192.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.273+603A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014392 | ||||||
| chr3:15014398
|
A | G | 49 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(46): Show | 50 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.273+609A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014398 | ||||||
| chr3:15014470
|
A | AT | 28 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(25): Show | 29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.273+692dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 15014470 | |||||
| chr3:15014470
|
A | T | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.273+681A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014470 | ||||||
| chr3:15014470
|
AT | A | 24 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(21): Show | 25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.273+692delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 15014470 | |||||
| chr3:15014604
|
C | T | 3 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.273+815C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014604 | ||||||
| chr3:15014971
|
C | G | 1 | a0001c0002t0005g0025 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.274-1181C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014971 | ||||||
| chr3:15015088
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.274-1064G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015088 | ||||||
| chr3:15015178
|
C | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.274-974C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015178 | ||||||
| chr3:15015351
|
G | A | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.274-801G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015351 | ||||||
| chr3:15015352
|
C | T | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.274-800C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015352 | ||||||
| chr3:15015464
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.274-688A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015464 | ||||||
| chr3:15015918
|
C | T | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-234C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015918 | ||||||
| chr3:15015968
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.274-184A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015968 | ||||||
| chr3:15016648
|
GTA | G | 8 | a0001c0001t0001g0061a0001c0001t0001g0152a0001c0001t0001g0165others(5): Show | 8 | HG02071.hp2 NA18942.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.376+395_376+396del others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15016648 | ||||||
| chr3:15016794
|
A | G | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.376+540A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15016794 | ||||||
| chr3:15016896
|
A | T | 24 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(21): Show | 25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.376+642A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15016896 | ||||||
| chr3:15016925
|
G | A | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.376+671G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15016925 | ||||||
| chr3:15017059
|
T | G | 1 | a0001c0001t0009g0270 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.376+805T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017059 | ||||||
| chr3:15017230
|
T | C | 1 | a0001c0001t0029g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.376+976T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017230 | ||||||
| chr3:15017408
|
T | C | 1 | a0001c0003t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376+1154T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017408 | ||||||
| chr3:15017412
|
G | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0103others(18): Show | 22 | HG01255.hp1 HG01346.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.376+1158G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017412 | ||||||
| chr3:15017449
|
A | G | 49 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(46): Show | 50 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.376+1195A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017449 | ||||||
| chr3:15017809
|
A | T | 1 | a0001c0001t0035g0143 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.376+1555A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017809 | ||||||
| chr3:15017823
|
T | C | 34 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(31): Show | 35 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.376+1569T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017823 | ||||||
| chr3:15018092
|
A | G | 296 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(293): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.376+1838A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018092 | ||||||
| chr3:15018277
|
A | G | 8 | a0001c0003t0006g0005a0001c0003t0006g0251a0001c0003t0006g0252others(5): Show | 9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.376+2023A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018277 | ||||||
| chr3:15018361
|
C | T | 1 | a0001c0001t0027g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.376+2107C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018361 | ||||||
| chr3:15018372
|
T | C | 2 | a0001c0002t0014g0006a0001c0002t0014g0007 | 2 | HG01081.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.376+2118T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018372 | ||||||
| chr3:15018381
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.376+2127C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018381 | ||||||
| chr3:15018388
|
C | T | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.376+2134C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018388 | ||||||
| chr3:15018488
|
C | T | 1 | a0001c0001t0028g0065 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.376+2234C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018488 | ||||||
| chr3:15018679
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.377-2074C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018679 | ||||||
| chr3:15019016
|
T | TA | 78 | a0001c0001t0001g0017a0001c0001t0001g0061a0001c0001t0001g0078others(75): Show | 80 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.377-1714dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 15019016 | |||||
| chr3:15019016
|
T | TAA | 8 | a0001c0001t0002g0035a0001c0001t0002g0038a0001c0001t0002g0041others(5): Show | 8 | HG01175.hp2 HG02129.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-1715_377-1714d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 15019016 | |||||
| chr3:15019016
|
TA | T | 28 | a0001c0001t0001g0185a0001c0001t0002g0054a0001c0001t0016g0275others(25): Show | 28 | HG01168.hp1 HG01255.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.377-1714delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 15019016 | |||||
| chr3:15019032
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.377-1721A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019032 | ||||||
| chr3:15019033
|
A | T | 6 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0132others(3): Show | 6 | NA18942.hp1 NA18948.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-1720A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019033 | ||||||
| chr3:15019035
|
AAAAAGAT others(9): Show |
A | 9 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0126others(6): Show | 9 | HG01433.hp1 NA18942.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.377-1716_377-1701d others(18): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 15019035 | |||||
| chr3:15019036
|
AAAAGATT others(8): Show |
A | 1 | a0001c0001t0001g0130 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.377-1715_377-1701d others(17): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 15019036 | |||||
| chr3:15019157
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0301 | 2 | NA18991.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.377-1596T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019157 | ||||||
| chr3:15019283
|
G | A | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.377-1470G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019283 | ||||||
| chr3:15019472
|
C | T | 1 | a0001c0001t0003g0083 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.377-1281C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019472 | ||||||
| chr3:15019714
|
T | C | 1 | a0001c0003t0006g0255 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.377-1039T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019714 | ||||||
| chr3:15019865
|
T | G | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.377-888T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019865 | ||||||
| chr3:15019981
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.377-772C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019981 | ||||||
| chr3:15020160
|
C | T | 3 | a0001c0001t0018g0067a0001c0001t0018g0068a0001c0001t0025g0066 | 3 | HG00733.hp2 HG01192.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.377-593C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15020160 | ||||||
| chr3:15020174
|
C | CT | 30 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(27): Show | 31 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.377-575dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 15020174 | |||||
| chr3:15020201
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0103others(34): Show | 38 | HG00140.hp2 HG01099.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.377-552G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15020201 | ||||||
| chr3:15020499
|
G | T | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.377-254G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15020499 | ||||||
| chr3:15020540
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.377-213C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15020540 | ||||||
| chr3:15021016
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.556+84G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15021016 | ||||||
| chr3:15021380
|
C | G | 6 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.556+448C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15021380 | ||||||
| chr3:15021396
|
C | A | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.556+464C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15021396 | ||||||
| chr3:15021665
|
GGCATGCA others(4): Show |
G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.556+750_556+760del others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 15021665 | |||||
| chr3:15021745
|
C | T | 2 | a0001c0001t0016g0275a0001c0001t0016g0276 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.556+813C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15021745 | ||||||
| chr3:15022019
|
A | G | 57 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(54): Show | 58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.556+1087A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022019 | ||||||
| chr3:15022335
|
C | T | 1 | a0001c0003t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.557-865C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022335 | ||||||
| chr3:15022382
|
TTTTTTC | T | 7 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.557-808_557-803del others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 15022382 | |||||
| chr3:15022392
|
T | C | 1 | a0001c0004t0007g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.557-808T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022392 | ||||||
| chr3:15022398
|
C | CCT | 3 | a0001c0001t0028g0065a0001c0005t0002g0296a0001c0005t0002g0297 | 3 | HG03471.hp2 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.557-802_557-801ins others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022398 | ||||||
| chr3:15022398
|
C | CT | 66 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(63): Show | 68 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.557-780dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 15022398 | |||||
| chr3:15022398
|
CT | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(138): Show | 143 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.557-780delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 15022398 | |||||
| chr3:15022398
|
CTT | C | 20 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0196others(17): Show | 20 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.557-781_557-780del others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 15022398 | |||||
| chr3:15022402
|
T | C | 3 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082 | 3 | HG02615.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.557-798T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022402 | ||||||
| chr3:15022403
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.557-797T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022403 | ||||||
| chr3:15022474
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0144a0001c0001t0001g0145others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-726G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022474 | ||||||
| chr3:15022491
|
G | A | 1 | a0001c0006t0001g0128 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.557-709G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022491 | ||||||
| chr3:15022685
|
G | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.557-515G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022685 | ||||||
| chr3:15022797
|
G | A | 1 | a0001c0001t0021g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.557-403G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022797 | ||||||
| chr3:15022976
|
G | A | 10 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0126others(7): Show | 10 | HG01433.hp1 NA18942.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.557-224G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022976 | ||||||
| chr3:15023045
|
T | G | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.557-155T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15023045 | ||||||
| chr3:15023485
|
C | A | 3 | a0001c0001t0004g0228a0001c0001t0004g0233a0001c0001t0004g0234 | 3 | HG02109.hp1 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.704+138C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 6/13 | chr3 | 15023485 | ||||||
| chr3:15023801
|
A | G | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.705-314A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 6/13 | chr3 | 15023801 | ||||||
| chr3:15024278
|
G | A | 16 | a0001c0001t0002g0039a0001c0001t0002g0042a0001c0001t0002g0043others(13): Show | 16 | HG00609.hp1 HG00642.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.798+70G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024278 | ||||||
| chr3:15024332
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.798+124C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024332 | ||||||
| chr3:15024463
|
G | T | 1 | a0001c0001t0002g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.798+255G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024463 | ||||||
| chr3:15024485
|
T | C | 3 | a0001c0001t0004g0228a0001c0001t0004g0233a0001c0001t0004g0234 | 3 | HG02109.hp1 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.798+277T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024485 | ||||||
| chr3:15024493
|
C | G | 3 | a0001c0001t0004g0228a0001c0001t0004g0233a0001c0001t0004g0234 | 3 | HG02109.hp1 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.798+285C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024493 | ||||||
| chr3:15024615
|
A | G | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.798+407A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024615 | ||||||
| chr3:15024672
|
A | G | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.798+464A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024672 | ||||||
| chr3:15024750
|
G | C | 16 | a0001c0001t0001g0141a0001c0001t0001g0201a0001c0001t0001g0202others(13): Show | 16 | HG00140.hp2 HG01099.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.798+542G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024750 | ||||||
| chr3:15024807
|
G | A | 3 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG00438.hp1 HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.798+599G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024807 | ||||||
| chr3:15024951
|
A | C | 1 | a0001c0001t0021g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.798+743A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024951 | ||||||
| chr3:15025081
|
T | A | 57 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(54): Show | 58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.798+873T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15025081 | ||||||
| chr3:15025121
|
T | G | 3 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.798+913T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15025121 | ||||||
| chr3:15025508
|
T | A | 16 | a0001c0001t0001g0141a0001c0001t0001g0201a0001c0001t0001g0202others(13): Show | 16 | HG00140.hp2 HG01099.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.798+1300T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15025508 | ||||||
| chr3:15025763
|
T | C | 3 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.798+1555T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15025763 | ||||||
| chr3:15025880
|
A | G | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.798+1672A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15025880 | ||||||
| chr3:15026025
|
C | CT | 21 | a0001c0001t0018g0067a0001c0001t0018g0068a0001c0001t0025g0066others(18): Show | 21 | HG00733.hp2 HG01081.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.798+1828dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | 15026025 | |||||
| chr3:15026159
|
T | C | 2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.798+1951T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026159 | ||||||
| chr3:15026303
|
G | A | 1 | a0001c0001t0012g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.798+2095G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026303 | ||||||
| chr3:15026426
|
A | G | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-2160A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026426 | ||||||
| chr3:15026705
|
GT | G | 74 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(71): Show | 75 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.799-1872delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | 15026705 | |||||
| chr3:15026721
|
A | G | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.799-1865A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026721 | ||||||
| chr3:15026726
|
T | C | 17 | a0001c0001t0001g0129a0001c0001t0001g0141a0001c0001t0001g0201others(14): Show | 17 | HG00140.hp2 HG01099.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.799-1860T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026726 | ||||||
| chr3:15026776
|
T | G | 5 | a0001c0001t0001g0154a0001c0001t0001g0160a0001c0001t0001g0173others(2): Show | 5 | HG01981.hp2 HG02148.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-1810T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026776 | ||||||
| chr3:15026824
|
C | T | 4 | a0001c0003t0013g0246a0001c0003t0013g0247a0001c0003t0013g0248others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-1762C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026824 | ||||||
| chr3:15026930
|
G | A | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.799-1656G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026930 | ||||||
| chr3:15027116
|
C | T | 6 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-1470C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15027116 | ||||||
| chr3:15027145
|
G | A | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.799-1441G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15027145 | ||||||
| chr3:15027222
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-1364C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15027222 | ||||||
| chr3:15027422
|
C | A | 1 | a0001c0001t0002g0046 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.799-1164C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15027422 | ||||||
| chr3:15027476
|
G | A | 2 | a0001c0001t0009g0116a0001c0001t0009g0120 | 2 | HG01081.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.799-1110G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15027476 | ||||||
| chr3:15027779
|
G | A | 3 | a0001c0002t0014g0006a0001c0002t0014g0007a0001c0007t0014g0273 | 3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.799-807G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15027779 | ||||||
| chr3:15028139
|
C | G | 1 | a0001c0001t0031g0219 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.799-447C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15028139 | ||||||
| chr3:15028425
|
G | C | 74 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(71): Show | 75 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.799-161G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15028425 | ||||||
| chr3:15028462
|
C | A | 1 | a0001c0001t0012g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.799-124C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15028462 | ||||||
| chr3:15028735
|
G | A | 1 | a0001c0001t0003g0093 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.932+16G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15028735 | ||||||
| chr3:15028750
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.932+31C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15028750 | ||||||
| chr3:15028867
|
G | C | 302 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(299): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.932+148G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15028867 | ||||||
| chr3:15029037
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.932+318T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029037 | ||||||
| chr3:15029066
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.932+347C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029066 | ||||||
| chr3:15029096
|
ATTTTTCT | A | 18 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0230others(15): Show | 18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.932+390_932+396del others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029096 | |||||
| chr3:15029164
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.932+445A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029164 | ||||||
| chr3:15029171
|
T | C | 134 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(131): Show | 137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.932+452T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029171 | ||||||
| chr3:15029287
|
A | C | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.932+568A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029287 | ||||||
| chr3:15029369
|
A | G | 1 | a0001c0001t0025g0066 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.932+650A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029369 | ||||||
| chr3:15029515
|
A | G | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.933-760A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029515 | ||||||
| chr3:15029627
|
A | G | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.933-648A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029627 | ||||||
| chr3:15029792
|
A | AATAC | 36 | a0001c0001t0002g0035a0001c0001t0002g0039a0001c0001t0002g0041others(33): Show | 36 | HG00438.hp1 HG00609.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.933-480_933-479ins others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | |||||
| chr3:15029792
|
A | AATACATA others(1): Show |
19 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0042others(16): Show | 21 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.933-480_933-479ins others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | |||||
| chr3:15029792
|
A | AATACATA others(5): Show |
1 | a0001c0001t0002g0045 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.933-480_933-479ins others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | |||||
| chr3:15029792
|
A | AATAG | 43 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(40): Show | 45 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.933-435_933-432dup others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | |||||
| chr3:15029792
|
A | AATAGATA others(1): Show |
9 | a0001c0001t0001g0017a0001c0001t0001g0130a0001c0001t0001g0142others(6): Show | 9 | HG00673.hp2 HG00735.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.933-439_933-432dup others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | |||||
| chr3:15029792
|
A | AATAGATA others(5): Show |
1 | a0001c0001t0001g0210 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.933-443_933-432dup others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | |||||
| chr3:15029792
|
AATAG | A | 33 | a0001c0001t0001g0078a0001c0001t0001g0101a0001c0001t0001g0103others(30): Show | 33 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.933-435_933-432del others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | |||||
| chr3:15029792
|
AATAGATA others(1): Show |
A | 8 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0188others(5): Show | 8 | HG00609.hp2 HG02698.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.933-439_933-432del others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | |||||
| chr3:15029796
|
G | C | 75 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0036others(72): Show | 76 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.933-479G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029796 | ||||||
| chr3:15029826
|
TAGATAGA others(3): Show |
T | 2 | a0001c0001t0012g0284a0001c0001t0012g0285 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.933-447_933-438del others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029826 | |||||
| chr3:15029830
|
TAGATAG | T | 3 | a0001c0001t0012g0076a0001c0001t0017g0294a0001c0001t0017g0295 | 3 | HG02055.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.933-443_933-438del others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029830 | |||||
| chr3:15029834
|
TAG | T | 8 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0004g0230others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.933-439_933-438del others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029834 | |||||
| chr3:15029840
|
G | T | 21 | a0001c0001t0003g0080a0001c0001t0003g0094a0001c0001t0004g0235others(18): Show | 21 | HG01109.hp1 HG01168.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.933-435G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029840 | ||||||
| chr3:15029840
|
GAT | G | 13 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0004g0230others(10): Show | 13 | HG02055.hp1 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.933-431_933-430del others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029840 | |||||
| chr3:15029842
|
T | G | 21 | a0001c0001t0003g0080a0001c0001t0003g0094a0001c0001t0004g0235others(18): Show | 21 | HG01109.hp1 HG01168.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.933-433T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029842 | ||||||
| chr3:15029842
|
T | TAGATAGA others(9): Show |
1 | a0001c0001t0004g0228 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.933-432_933-431ins others(16): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029842 | |||||
| chr3:15029842
|
T | TAGATAGA others(5): Show |
1 | a0001c0001t0004g0243 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.933-432_933-431ins others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029842 | |||||
| chr3:15029842
|
T | TAGATATA others(1): Show |
3 | a0001c0001t0004g0237a0001c0001t0004g0241a0001c0001t0004g0242 | 3 | HG02965.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.933-432_933-431ins others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029842 | |||||
| chr3:15029848
|
T | C | 39 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(36): Show | 39 | HG01109.hp1 HG01168.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.933-427T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029848 | ||||||
| chr3:15029848
|
T | TAGAC | 111 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(108): Show | 114 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.933-426_933-423dup others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029848 | |||||
| chr3:15029943
|
GAGAA | G | 7 | a0001c0001t0001g0103a0001c0001t0001g0126a0001c0001t0001g0131others(4): Show | 7 | HG01433.hp1 NA18954.hp2 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.933-326_933-323del others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029943 | |||||
| chr3:15029947
|
A | G | 3 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082 | 3 | HG02615.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.933-328A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029947 | ||||||
| chr3:15029975
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.933-300G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029975 | ||||||
| chr3:15030063
|
G | A | 1 | a0001c0001t0012g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.933-212G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15030063 | ||||||
| chr3:15030115
|
A | G | 2 | a0001c0001t0016g0275a0001c0001t0016g0276 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.933-160A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15030115 | ||||||
| chr3:15030459
|
G | A | 3 | a0001c0002t0014g0006a0001c0002t0014g0007a0001c0007t0014g0273 | 3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.1110+7G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15030459 | ||||||
| chr3:15030505
|
T | C | 1 | a0001c0001t0003g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1110+53T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15030505 | ||||||
| chr3:15030609
|
C | G | 3 | a0001c0002t0014g0006a0001c0002t0014g0007a0001c0007t0014g0273 | 3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1110+157C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15030609 | ||||||
| chr3:15030640
|
C | A | 34 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(31): Show | 35 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1110+188C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15030640 | ||||||
| chr3:15030729
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1110+277G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15030729 | ||||||
| chr3:15030839
|
A | G | 3 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1110+387A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15030839 | ||||||
| chr3:15031034
|
A | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0301 | 3 | HG00673.hp2 NA18991.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1110+582A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031034 | ||||||
| chr3:15031263
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1110+811G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031263 | ||||||
| chr3:15031370
|
AT | A | 150 | a0001c0001t0001g0061a0001c0001t0002g0032a0001c0001t0002g0033others(147): Show | 153 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1110+932delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr3 | 15031370 | |||||
| chr3:15031395
|
A | G | 1 | a0001c0001t0017g0294 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1110+943A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031395 | ||||||
| chr3:15031406
|
C | T | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1110+954C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031406 | ||||||
| chr3:15031416
|
T | A | 57 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(54): Show | 58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1111-963T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031416 | ||||||
| chr3:15031712
|
A | G | 5 | a0001c0001t0027g0072a0001c0001t0028g0065a0001c0005t0002g0296others(2): Show | 5 | HG03195.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-667A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031712 | ||||||
| chr3:15031723
|
C | G | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1111-656C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031723 | ||||||
| chr3:15031819
|
C | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1111-560C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031819 | ||||||
| chr3:15031832
|
A | G | 60 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(57): Show | 62 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1111-547A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031832 | ||||||
| chr3:15031876
|
A | G | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1111-503A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031876 | ||||||
| chr3:15032020
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1111-359G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15032020 | ||||||
| chr3:15032023
|
C | T | 4 | a0001c0003t0013g0246a0001c0003t0013g0247a0001c0003t0013g0248others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-356C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15032023 | ||||||
| chr3:15032042
|
A | G | 1 | a0001c0001t0003g0097 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1111-337A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15032042 | ||||||
| chr3:15032063
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0200 | 2 | HG00544.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.1111-316A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15032063 | ||||||
| chr3:15032541
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1232+41C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15032541 | ||||||
| chr3:15032548
|
C | T | 1 | a0001c0001t0043g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1232+48C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15032548 | ||||||
| chr3:15032816
|
C | T | 30 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(27): Show | 31 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1232+316C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15032816 | ||||||
| chr3:15032964
|
A | AC | 27 | a0001c0001t0001g0178a0001c0001t0003g0002a0001c0001t0003g0008others(24): Show | 28 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.1232+474dupC | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 15032964 | |||||
| chr3:15033014
|
C | T | 1 | a0001c0001t0001g0301 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1232+514C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033014 | ||||||
| chr3:15033262
|
C | T | 12 | a0001c0001t0001g0117a0001c0001t0001g0186a0001c0001t0001g0196others(9): Show | 12 | HG01123.hp1 HG01243.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1232+762C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033262 | ||||||
| chr3:15033351
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1232+851C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033351 | ||||||
| chr3:15033517
|
C | T | 134 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(131): Show | 137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1232+1017C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033517 | ||||||
| chr3:15033619
|
G | C | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1233-1051G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033619 | ||||||
| chr3:15033623
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1233-1047G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033623 | ||||||
| chr3:15033628
|
G | A | 24 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(21): Show | 25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1233-1042G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033628 | ||||||
| chr3:15033639
|
C | CT | 94 | a0001c0001t0001g0117a0001c0001t0001g0133a0001c0001t0001g0158others(91): Show | 97 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1233-1006dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 15033639 | |||||
| chr3:15033639
|
CT | C | 28 | a0001c0001t0001g0011a0001c0001t0001g0103a0001c0001t0001g0113others(25): Show | 28 | HG01109.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1233-1006delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 15033639 | |||||
| chr3:15033808
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1233-862G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033808 | ||||||
| chr3:15033853
|
A | G | 287 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(284): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1233-817A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033853 | ||||||
| chr3:15033970
|
T | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1233-700T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033970 | ||||||
| chr3:15034041
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1233-629C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034041 | ||||||
| chr3:15034046
|
G | A | 1 | a0001c0004t0007g0274 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1233-624G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034046 | ||||||
| chr3:15034291
|
T | A | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1233-379T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034291 | ||||||
| chr3:15034350
|
T | C | 134 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(131): Show | 137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1233-320T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034350 | ||||||
| chr3:15034390
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1233-280G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034390 | ||||||
| chr3:15034636
|
C | T | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1233-34C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034636 | ||||||
| chr3:15034669
|
G | A | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1233-1G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034669 | ||||||
| chr3:15034908
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1372+99C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15034908 | ||||||
| chr3:15035004
|
G | A | 286 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(283): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1372+195G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035004 | ||||||
| chr3:15035173
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1372+364G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035173 | ||||||
| chr3:15035183
|
C | T | 3 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082 | 3 | HG02615.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1372+374C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035183 | ||||||
| chr3:15035294
|
G | C | 17 | a0001c0001t0001g0129a0001c0001t0001g0141a0001c0001t0001g0201others(14): Show | 17 | HG00140.hp2 HG01099.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1372+485G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035294 | ||||||
| chr3:15035581
|
G | C | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1372+772G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035581 | ||||||
| chr3:15035657
|
G | T | 1 | a0001c0001t0001g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1372+848G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035657 | ||||||
| chr3:15035753
|
G | A | 1 | a0001c0001t0001g0009 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1372+944G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035753 | ||||||
| chr3:15035843
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1372+1034A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035843 | ||||||
| chr3:15035982
|
C | G | 4 | a0001c0003t0013g0246a0001c0003t0013g0247a0001c0003t0013g0248others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372+1173C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035982 | ||||||
| chr3:15036083
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1372+1274G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15036083 | ||||||
| chr3:15036133
|
T | G | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1372+1324T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15036133 | ||||||
| chr3:15036859
|
C | G | 12 | a0001c0001t0001g0117a0001c0001t0001g0186a0001c0001t0001g0196others(9): Show | 12 | HG01123.hp1 HG01243.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1373-1141C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15036859 | ||||||
| chr3:15036860
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1373-1140G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15036860 | ||||||
| chr3:15036982
|
CATG | C | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1373-1017_1373-101 others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15036982 | ||||||
| chr3:15037113
|
C | CA | 6 | a0001c0001t0001g0138a0001c0001t0003g0083a0001c0001t0024g0053others(3): Show | 6 | HG00558.hp2 HG01175.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1373-874dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037113 | |||||
| chr3:15037127
|
C | A | 11 | a0001c0001t0016g0275a0001c0001t0016g0276a0001c0001t0021g0286others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1373-873C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037127 | ||||||
| chr3:15037207
|
G | GTT | 17 | a0001c0001t0012g0076a0001c0001t0016g0275a0001c0001t0016g0276others(14): Show | 17 | HG01109.hp1 HG01168.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1373-791_1373-790d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037207 | |||||
| chr3:15037209
|
T | TTG | 37 | a0001c0001t0001g0061a0001c0001t0001g0166a0001c0001t0001g0172others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1373-761_1373-760d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | |||||
| chr3:15037209
|
T | TTGTG | 3 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG00438.hp1 HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1373-763_1373-760d others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | |||||
| chr3:15037209
|
T | TTTTGTG | 34 | a0001c0001t0002g0032a0001c0001t0002g0035a0001c0001t0002g0036others(31): Show | 34 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1373-790_1373-789i others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | |||||
| chr3:15037209
|
T | TTTTGTGT others(1): Show |
16 | a0001c0001t0002g0033a0001c0001t0002g0039a0001c0001t0002g0042others(13): Show | 16 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1373-790_1373-789i others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | |||||
| chr3:15037209
|
T | TTTTGTGT others(3): Show |
8 | a0001c0001t0002g0055a0001c0001t0002g0262a0001c0001t0011g0215others(5): Show | 9 | HG00642.hp1 HG01099.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1373-790_1373-789i others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | |||||
| chr3:15037209
|
T | TTTTGTGT others(5): Show |
1 | a0001c0001t0011g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1373-790_1373-789i others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | |||||
| chr3:15037209
|
TTG | T | 14 | a0001c0001t0001g0111a0001c0001t0001g0156a0001c0001t0012g0284others(11): Show | 15 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.1373-761_1373-760d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | |||||
| chr3:15037209
|
TTGTG | T | 7 | a0001c0001t0001g0017a0001c0001t0012g0300a0001c0001t0029g0299others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1373-763_1373-760d others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | |||||
| chr3:15037209
|
TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1373-769_1373-760d others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | |||||
| chr3:15037209
|
TTGTGTGT others(5): Show |
T | 8 | a0001c0001t0001g0114a0001c0001t0001g0144a0001c0001t0001g0145others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1373-771_1373-760d others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | |||||
| chr3:15037209
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1373-773_1373-760d others(16): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | |||||
| chr3:15037211
|
G | T | 11 | a0001c0002t0014g0006a0001c0002t0014g0007a0001c0004t0007g0274others(8): Show | 11 | HG01081.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1373-789G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037211 | ||||||
| chr3:15037213
|
G | T | 12 | a0001c0001t0012g0284a0001c0001t0012g0285a0001c0001t0030g0077others(9): Show | 13 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.1373-787G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037213 | ||||||
| chr3:15037215
|
G | T | 6 | a0001c0001t0012g0300a0001c0001t0029g0299a0001c0003t0013g0246others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1373-785G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037215 | ||||||
| chr3:15037239
|
G | T | 1 | a0001c0001t0004g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1373-761G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037239 | ||||||
| chr3:15037241
|
T | G | 4 | a0001c0001t0001g0101a0001c0001t0003g0093a0001c0001t0004g0233others(1): Show | 4 | HG02083.hp2 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1373-759T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037241 | ||||||
| chr3:15037523
|
C | T | 3 | a0001c0001t0038g0290a0001c0001t0039g0291a0001c0001t0040g0079 | 3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1373-477C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037523 | ||||||
| chr3:15037535
|
T | C | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1373-465T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037535 | ||||||
| chr3:15037581
|
A | C | 2 | a0001c0001t0016g0275a0001c0001t0016g0276 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1373-419A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037581 | ||||||
| chr3:15037661
|
T | C | 8 | a0001c0003t0006g0005a0001c0003t0006g0251a0001c0003t0006g0252others(5): Show | 9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.1373-339T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037661 | ||||||
| chr3:15037700
|
A | G | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1373-300A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037700 | ||||||
| chr3:15037726
|
T | C | 4 | a0001c0001t0012g0076a0001c0001t0012g0284a0001c0001t0012g0285others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1373-274T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037726 | ||||||
| chr3:15038192
|
T | C | 4 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0090others(1): Show | 5 | HG00639.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+55T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15038192 | ||||||
| chr3:15038543
|
A | G | 2 | a0001c0002t0014g0006a0001c0002t0014g0007 | 2 | HG01081.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1510+406A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15038543 | ||||||
| chr3:15038574
|
G | T | 1 | a0001c0001t0001g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1510+437G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15038574 | ||||||
| chr3:15038637
|
C | G | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1511-485C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15038637 | ||||||
| chr3:15038693
|
T | C | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1511-429T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15038693 | ||||||
| chr3:15038854
|
A | AG | 17 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1511-266dupG | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 15038854 | |||||
| chr3:15039095
|
T | TGG | 27 | a0001c0001t0003g0002a0001c0001t0003g0080a0001c0001t0003g0081others(24): Show | 28 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1511-19_1511-18dup others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 15039095 | |||||
| chr3:15039097
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1511-25G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15039097 | ||||||
| chr3:15039098
|
G | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0191a0001c0001t0001g0269 | 3 | HG02027.hp1 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1511-24G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15039098 | ||||||
| chr3:15039109
|
T | C | 1 | a0001c0001t0010g0271 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1511-13T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15039109 | ||||||
| chr3:15039233
|
G | A | 2 | a0001c0002t0014g0006a0001c0002t0014g0007 | 2 | HG01081.hp2 HG02970.hp2 |
splice_region_variant&intron_variant | LOW | c.1616+6G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039233 | ||||||
| chr3:15039364
|
C | T | 3 | a0001c0002t0014g0006a0001c0002t0014g0007a0001c0007t0014g0273 | 3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1616+137C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039364 | ||||||
| chr3:15039367
|
G | A | 1 | a0001c0001t0011g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1616+140G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039367 | ||||||
| chr3:15039568
|
G | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1616+341G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039568 | ||||||
| chr3:15039845
|
T | C | 60 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(57): Show | 62 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1616+618T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039845 | ||||||
| chr3:15039932
|
G | C | 152 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(149): Show | 155 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1616+705G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039932 | ||||||
| chr3:15039940
|
C | A | 134 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(131): Show | 137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1616+713C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039940 | ||||||
| chr3:15039977
|
C | T | 8 | a0001c0004t0007g0274a0001c0004t0007g0277a0001c0004t0007g0278others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1616+750C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039977 | ||||||
| chr3:15039997
|
A | T | 3 | a0001c0001t0001g0214a0001c0001t0016g0275a0001c0001t0016g0276 | 3 | HG03209.hp1 HG03516.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1616+770A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039997 | ||||||
| chr3:15040006
|
T | A | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1616+779T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040006 | ||||||
| chr3:15040018
|
G | A | 2 | a0001c0001t0019g0292a0001c0001t0019g0293 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1616+791G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040018 | ||||||
| chr3:15040116
|
C | T | 60 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(57): Show | 61 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1616+889C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040116 | ||||||
| chr3:15040166
|
C | CA | 65 | a0001c0001t0001g0061a0001c0001t0001g0078a0001c0001t0001g0110others(62): Show | 66 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.1616+950dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 15040166 | |||||
| chr3:15040178
|
C | A | 1 | a0001c0001t0004g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1616+951C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040178 | ||||||
| chr3:15040181
|
C | CA | 6 | a0001c0001t0001g0015a0001c0001t0001g0138a0001c0001t0001g0214others(3): Show | 6 | HG01981.hp1 HG04115.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1616+963dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 15040181 | |||||
| chr3:15040199
|
C | A | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1616+972C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040199 | ||||||
| chr3:15040200
|
G | C | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1616+973G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040200 | ||||||
| chr3:15040294
|
A | G | 3 | a0001c0001t0038g0290a0001c0001t0039g0291a0001c0001t0040g0079 | 3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1616+1067A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040294 | ||||||
| chr3:15040413
|
C | T | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1616+1186C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040413 | ||||||
| chr3:15040447
|
G | A | 3 | a0001c0001t0038g0290a0001c0001t0039g0291a0001c0001t0040g0079 | 3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1616+1220G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040447 | ||||||
| chr3:15040463
|
C | T | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1616+1236C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040463 | ||||||
| chr3:15040496
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1616+1269G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040496 | ||||||
| chr3:15040546
|
C | T | 57 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(54): Show | 58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1616+1319C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040546 | ||||||
| chr3:15040627
|
G | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0301 | 3 | HG00673.hp2 NA18991.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1616+1400G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040627 | ||||||
| chr3:15040689
|
G | A | 231 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(228): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1616+1462G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040689 | ||||||
| chr3:15040813
|
T | G | 5 | a0001c0001t0004g0235a0001c0001t0004g0237a0001c0001t0004g0238others(2): Show | 5 | HG01192.hp1 HG01934.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1616+1586T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040813 | ||||||
| chr3:15040959
|
G | A | 4 | a0001c0003t0013g0246a0001c0003t0013g0247a0001c0003t0013g0248others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1616+1732G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040959 | ||||||
| chr3:15041043
|
G | C | 30 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(27): Show | 31 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1617-1791G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15041043 | ||||||
| chr3:15041814
|
A | G | 134 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(131): Show | 137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1617-1020A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15041814 | ||||||
| chr3:15041870
|
C | T | 2 | a0001c0001t0009g0116a0001c0001t0009g0120 | 2 | HG01081.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1617-964C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15041870 | ||||||
| chr3:15041909
|
C | T | 28 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(25): Show | 29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1617-925C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15041909 | ||||||
| chr3:15041946
|
G | C | 13 | a0001c0003t0006g0005a0001c0003t0006g0250a0001c0003t0006g0251others(10): Show | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1617-888G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15041946 | ||||||
| chr3:15042105
|
G | C | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0021others(11): Show | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1617-729G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042105 | ||||||
| chr3:15042257
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1617-577T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042257 | ||||||
| chr3:15042277
|
C | G | 34 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(31): Show | 35 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1617-557C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042277 | ||||||
| chr3:15042417
|
C | T | 57 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0035others(54): Show | 58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1617-417C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042417 | ||||||
| chr3:15042507
|
C | T | 34 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0080others(31): Show | 35 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1617-327C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042507 | ||||||
| chr3:15042528
|
A | G | 2 | a0001c0001t0017g0294a0001c0001t0017g0295 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1617-306A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042528 | ||||||
| chr3:15042591
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1617-243G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042591 | ||||||
| chr3:15042710
|
G | T | 2 | a0001c0001t0009g0116a0001c0001t0009g0120 | 2 | HG01081.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1617-124G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042710 | ||||||
| chr3:15042755
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1617-79G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042755 |