Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2649 |
|---|---|
| ensemblid | ENSG00000148200.17 |
| hgncid | 7985 |
| symbol | NR6A1 |
| name | nuclear receptor subfamily 6 group A member 1 |
| refseq_nuc | NM_033334.4 |
| refseq_prot | NP_201591.2 |
| ensembl_nuc | ENST00000487099.7 |
| ensembl_prot | ENSP00000420267.1 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 124517275 |
| end | 124771311 |
| strand | - |
| ver | v1.2 |
| region | chr9:124517275-124771311 |
| region5000 | chr9:124512275-124776311 |
| regionname0 | NR6A1_chr9_124517275_124771311 |
| regionname5000 | NR6A1_chr9_124512275_124776311 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 480 | 231 | 79 | 20 | 97 | 6 | 27 | 71 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0002 | 0/0 | 480 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0003 | 0/0 | 480 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0004 | 0/0 | 480 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1443 | 219 | 69 | 20 | 95 | 6 | 27 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| c0002 | 0/0 | 1443 | 10 | 10 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| c0003 | 0/0 | 1443 | 2 | 0 | 0 | 2 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| c0004 | 0/0 | 1443 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| c0005 | 0/0 | 1443 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| c0006 | 0/0 | 1443 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 5623 | 56 | 7 | 7 | 25 | 2 | 13 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0002 | 0/0 | 5624 | 55 | 3 | 7 | 35 | 2 | 8 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0003 | 0/0 | 5625 | 10 | 0 | 1 | 7 | 1 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0004 | 0/0 | 5627 | 6 | 3 | 0 | 3 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0005 | 0/0 | 5622 | 5 | 5 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0006 | 0/0 | 5623 | 4 | 1 | 0 | 3 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0007 | 0/0 | 5622 | 4 | 4 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0008 | 0/0 | 5624 | 4 | 4 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0009 | 0/0 | 5622 | 4 | 0 | 0 | 3 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0010 | 0/0 | 5623 | 4 | 4 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0011 | 0/0 | 5624 | 3 | 0 | 0 | 3 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0012 | 0/0 | 5625 | 3 | 0 | 0 | 3 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0013 | 0/0 | 5628 | 3 | 3 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0014 | 0/0 | 5623 | 3 | 2 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0015 | 0/0 | 5623 | 3 | 0 | 0 | 3 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0016 | 0/0 | 5623 | 3 | 3 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0017 | 0/0 | 5630 | 3 | 3 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0018 | 0/0 | 5627 | 2 | 2 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0019 | 0/0 | 5629 | 2 | 2 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0020 | 0/0 | 5630 | 2 | 2 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0021 | 0/0 | 5624 | 2 | 1 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0022 | 0/0 | 5624 | 2 | 2 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0023 | 0/0 | 5626 | 2 | 0 | 1 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0024 | 0/0 | 5630 | 2 | 2 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0025 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0026 | 0/0 | 5611 | 2 | 0 | 1 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0027 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0028 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0029 | 0/0 | 5627 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0030 | 0/0 | 5626 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0031 | 0/0 | 5627 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0032 | 0/0 | 5625 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0033 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0034 | 0/0 | 5626 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0035 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0036 | 0/0 | 5609 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0037 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0038 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0039 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0040 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0041 | 0/0 | 5626 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0042 | 0/0 | 5630 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0043 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0044 | 0/0 | 5626 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0045 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0046 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0047 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0048 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0049 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0050 | 0/0 | 5625 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0051 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0052 | 0/0 | 5624 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0053 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0054 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0055 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0056 | 0/0 | 5625 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0057 | 0/0 | 5626 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0058 | 0/0 | 5627 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0059 | 0/0 | 5627 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0060 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0061 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0062 | 0/0 | 5644 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0063 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0064 | 0/0 | 5622 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0065 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0066 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0067 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0068 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| t0069 | 0/0 | 5634 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0115 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1443 | 219 | 69 | 20 | 95 | 6 | 27 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0002 | 0/0 | 1443 | 10 | 10 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0003 | 0/0 | 1443 | 2 | 0 | 0 | 2 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0002c0006 | 0/0 | 1443 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0003c0005 | 0/0 | 1443 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0004c0004 | 0/0 | 1443 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 7065 | 56 | 7 | 7 | 25 | 2 | 13 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0002 | 0/0 | 7066 | 54 | 3 | 7 | 34 | 2 | 8 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0003 | 0/0 | 7067 | 10 | 0 | 1 | 7 | 1 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0004 | 0/0 | 7069 | 6 | 3 | 0 | 3 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0006 | 0/0 | 7065 | 4 | 1 | 0 | 3 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0007 | 0/0 | 7064 | 4 | 4 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0008 | 0/0 | 7066 | 4 | 4 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0009 | 0/0 | 7064 | 4 | 0 | 0 | 3 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0011 | 0/0 | 7066 | 3 | 0 | 0 | 3 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0012 | 0/0 | 7067 | 3 | 0 | 0 | 3 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0013 | 0/0 | 7070 | 3 | 3 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0014 | 0/0 | 7065 | 3 | 2 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0015 | 0/0 | 7065 | 3 | 0 | 0 | 3 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0016 | 0/0 | 7065 | 3 | 3 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0017 | 0/0 | 7072 | 3 | 3 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0018 | 0/0 | 7069 | 2 | 2 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0019 | 0/0 | 7071 | 2 | 2 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0020 | 0/0 | 7072 | 2 | 2 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0021 | 0/0 | 7066 | 2 | 1 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0022 | 0/0 | 7066 | 2 | 2 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0023 | 0/0 | 7068 | 2 | 0 | 1 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0024 | 0/0 | 7072 | 2 | 2 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0025 | 0/0 | 7073 | 2 | 2 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0026 | 0/0 | 7053 | 2 | 0 | 1 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0027 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0028 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0029 | 0/0 | 7069 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0030 | 0/0 | 7068 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0031 | 0/0 | 7069 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0032 | 0/0 | 7067 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0033 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0034 | 0/0 | 7068 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0035 | 0/0 | 7065 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0037 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0038 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0039 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0040 | 0/0 | 7067 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0041 | 0/0 | 7068 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0042 | 0/0 | 7072 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0043 | 0/0 | 7066 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0044 | 0/0 | 7068 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0045 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0046 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0047 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0049 | 0/0 | 7067 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0050 | 0/0 | 7067 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0051 | 0/0 | 7066 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0052 | 0/0 | 7066 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0053 | 0/0 | 7066 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0054 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0056 | 0/0 | 7067 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0057 | 0/0 | 7068 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0058 | 0/0 | 7069 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0059 | 0/0 | 7069 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0060 | 0/0 | 7071 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0061 | 0/0 | 7071 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0062 | 0/0 | 7086 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0063 | 0/0 | 7065 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0064 | 0/0 | 7064 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0065 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0066 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0001t0068 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0002t0005 | 0/0 | 7064 | 5 | 5 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0002t0010 | 0/0 | 7065 | 4 | 4 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0002t0067 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0003t0048 | 0/0 | 7065 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0001c0003t0055 | 0/0 | 7066 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0002c0006t0069 | 0/0 | 7076 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0003c0005t0002 | 0/0 | 7066 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| a0004c0004t0036 | 0/0 | 7051 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | copy fasta | chr9 | 124512275 | 124776311 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0115 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0009g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0009g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0011g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0011g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0011g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0012g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0012g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0012g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0013g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0014g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0014g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0014g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0015g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0015g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0015g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0016g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0016g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0016g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0017g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0017g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0018g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0018g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0019g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0019g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0020g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0020g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0021g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0021g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0022g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0022g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0023g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0023g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0024g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0024g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0025g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0025g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0026g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0026g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0027g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0028g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0029g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0030g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0031g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0032g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0033g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0034g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0035g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0037g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0038g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0039g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0040g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0041g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0042g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0043g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0044g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0045g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0046g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0047g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0049g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0050g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0051g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0052g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0053g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0054g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0056g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0057g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0058g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0059g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0060g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0061g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0062g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0063g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0064g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0065g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0066g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0001t0068g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0002t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0002t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0002t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0002t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0002t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0002t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0002t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0002t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0002t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0002t0067g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0003t0048g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0001c0003t0055g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0002c0006t0069g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0003c0005t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| a0004c0004t0036g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | FIN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00323 | hp2 | a0001 | c0001 | t0064 | g0124 | EUR | FIN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00423 | hp2 | a0001 | c0003 | t0055 | g0181 | EAS | CHS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00544 | hp2 | a0001 | c0001 | t0057 | g0192 | EAS | CHS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00558 | hp1 | a0001 | c0003 | t0048 | g0102 | EAS | CHS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00609 | hp1 | a0001 | c0001 | t0043 | g0107 | EAS | CHS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00639 | hp1 | a0001 | c0001 | t0029 | g0003 | AMR | PUR | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00642 | hp1 | a0001 | c0001 | t0026 | g0233 | AMR | PUR | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG00642 | hp2 | a0001 | c0001 | t0023 | g0043 | AMR | PUR | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01106 | hp2 | a0001 | c0001 | t0063 | g0135 | AMR | PUR | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01167 | hp2 | a0001 | c0001 | t0014 | g0071 | AMR | PUR | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0035 | EUR | IBS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0131 | EUR | IBS | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01884 | hp1 | a0001 | c0001 | t0016 | g0075 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01884 | hp2 | a0001 | c0001 | t0028 | g0002 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02015 | hp1 | a0001 | c0001 | t0015 | g0127 | EAS | KHV | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02015 | hp2 | a0001 | c0001 | t0011 | g0200 | EAS | KHV | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | KHV | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02055 | hp1 | a0001 | c0001 | t0018 | g0030 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02055 | hp2 | a0001 | c0001 | t0021 | g0148 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0203 | EAS | KHV | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02145 | hp1 | a0001 | c0001 | t0047 | g0105 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02145 | hp2 | a0001 | c0002 | t0067 | g0221 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02155 | hp1 | a0001 | c0001 | t0011 | g0201 | EAS | CDX | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | CDX | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02257 | hp1 | a0001 | c0001 | t0049 | g0231 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02257 | hp2 | a0001 | c0001 | t0065 | g0041 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02258 | hp1 | a0001 | c0001 | t0042 | g0099 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0086 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02451 | hp1 | a0001 | c0002 | t0005 | g0227 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02451 | hp2 | a0001 | c0001 | t0013 | g0196 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02572 | hp2 | a0004 | c0004 | t0036 | g0010 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02602 | hp2 | a0001 | c0001 | t0035 | g0016 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02615 | hp1 | a0001 | c0001 | t0019 | g0074 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02622 | hp1 | a0001 | c0001 | t0031 | g0005 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02622 | hp2 | a0001 | c0001 | t0025 | g0015 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02630 | hp1 | a0001 | c0001 | t0018 | g0028 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02630 | hp2 | a0001 | c0001 | t0022 | g0217 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0069 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02647 | hp2 | a0001 | c0002 | t0010 | g0225 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02698 | hp1 | a0001 | c0001 | t0026 | g0232 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02717 | hp1 | a0001 | c0002 | t0010 | g0222 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0096 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0090 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02723 | hp2 | a0001 | c0001 | t0068 | g0006 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02809 | hp1 | a0001 | c0002 | t0005 | g0226 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02809 | hp2 | a0001 | c0001 | t0040 | g0029 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02818 | hp2 | a0001 | c0001 | t0046 | g0008 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0095 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02895 | hp2 | a0001 | c0002 | t0005 | g0230 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02896 | hp1 | a0001 | c0001 | t0038 | g0093 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0094 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02922 | hp1 | a0001 | c0001 | t0016 | g0077 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02965 | hp1 | a0001 | c0001 | t0041 | g0031 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02965 | hp2 | a0001 | c0001 | t0066 | g0007 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02970 | hp1 | a0001 | c0001 | t0025 | g0014 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02970 | hp2 | a0001 | c0001 | t0030 | g0004 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02976 | hp1 | a0001 | c0001 | t0017 | g0066 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02976 | hp2 | a0001 | c0001 | t0013 | g0190 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03017 | hp1 | a0002 | c0006 | t0069 | g0234 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03041 | hp1 | a0001 | c0001 | t0016 | g0078 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03041 | hp2 | a0001 | c0001 | t0024 | g0013 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03130 | hp1 | a0001 | c0001 | t0034 | g0210 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03130 | hp2 | a0001 | c0002 | t0010 | g0223 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03139 | hp1 | a0001 | c0002 | t0010 | g0224 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03139 | hp2 | a0001 | c0001 | t0039 | g0092 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03195 | hp1 | a0001 | c0002 | t0005 | g0228 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0072 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03225 | hp1 | a0001 | c0001 | t0017 | g0068 | AFR | MSL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0212 | AFR | MSL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0198 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03516 | hp2 | a0001 | c0001 | t0045 | g0070 | AFR | ESN | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03540 | hp1 | a0001 | c0001 | t0033 | g0097 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | BEB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03831 | hp2 | a0001 | c0001 | t0044 | g0175 | SAS | BEB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03834 | hp2 | a0001 | c0001 | t0009 | g0150 | SAS | BEB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03927 | hp1 | a0001 | c0001 | t0052 | g0179 | SAS | BEB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | BEB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18522 | hp1 | a0001 | c0002 | t0005 | g0229 | AFR | YRI | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0089 | AFR | YRI | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18906 | hp1 | a0001 | c0001 | t0019 | g0091 | AFR | YRI | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0197 | AFR | YRI | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18939 | hp1 | a0001 | c0001 | t0009 | g0060 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18943 | hp1 | a0001 | c0001 | t0059 | g0125 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18943 | hp2 | a0001 | c0001 | t0009 | g0101 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18945 | hp2 | a0001 | c0001 | t0032 | g0214 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18963 | hp1 | a0003 | c0005 | t0002 | g0146 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18975 | hp1 | a0001 | c0001 | t0009 | g0168 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18977 | hp1 | a0001 | c0001 | t0012 | g0207 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18977 | hp2 | a0001 | c0001 | t0021 | g0213 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18978 | hp1 | a0001 | c0001 | t0058 | g0208 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18978 | hp2 | a0001 | c0001 | t0050 | g0024 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18993 | hp2 | a0001 | c0001 | t0011 | g0205 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18995 | hp2 | a0001 | c0001 | t0012 | g0206 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19000 | hp2 | a0001 | c0001 | t0023 | g0188 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19007 | hp2 | a0001 | c0001 | t0051 | g0140 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19010 | hp1 | a0001 | c0001 | t0015 | g0156 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19010 | hp2 | a0001 | c0001 | t0056 | g0081 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19011 | hp2 | a0001 | c0001 | t0012 | g0204 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19030 | hp1 | a0001 | c0001 | t0027 | g0001 | AFR | LWK | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19030 | hp2 | a0001 | c0001 | t0020 | g0025 | AFR | LWK | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | LWK | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0087 | AFR | LWK | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19057 | hp2 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19080 | hp2 | a0001 | c0001 | t0053 | g0082 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0088 | AFR | YRI | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA19240 | hp2 | a0001 | c0001 | t0054 | g0076 | AFR | YRI | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ASW | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA20129 | hp2 | a0001 | c0001 | t0024 | g0012 | AFR | ASW | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02559 | hp1 | a0001 | c0001 | t0020 | g0026 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG02559 | hp2 | a0001 | c0001 | t0022 | g0220 | AFR | ACB | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03471 | hp1 | a0001 | c0001 | t0017 | g0067 | AFR | MSL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG03471 | hp2 | a0001 | c0001 | t0062 | g0104 | AFR | MSL | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | USA | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| HG06807 | hp2 | a0001 | c0001 | t0060 | g0027 | AFR | USA | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA18955 | hp2 | a0001 | c0001 | t0015 | g0155 | EAS | JPT | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA20300 | hp1 | a0001 | c0001 | t0037 | g0032 | AFR | USA | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | USA | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| NA21309 | hp2 | a0001 | c0001 | t0061 | g0100 | AFR | LWK | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0119 | REF | REF | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0115 | REF | REF | NR6A1_chr9_124512275_124776311 | NR6A1 | chr9 | 124512275 | 124776311 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:124522721
|
C | T | 1 | a0004 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1427G>A | p.Ser476Asn | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 1619/7065 | 1427/1443 | 476/480 | chr9 | 124522721 | ||
| chr9:124524868
|
T | C | 1 | a0003 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.1207A>G | p.Arg403Gly | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 9/10 | 1399/7065 | 1207/1443 | 403/480 | chr9 | 124524868 | ||
| chr9:124538194
|
T | G | 1 | a0002 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.722A>C | p.Gln241Pro | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/10 | 914/7065 | 722/1443 | 241/480 | chr9 | 124538194 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:124522726
|
C | T | 1 | a0001c0003 | 2 | HG00423.hp2 HG00558.hp1 |
synonymous_variant | LOW | c.1422G>A | p.Lys474Lys | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 1614/7065 | 1422/1443 | 474/480 | chr9 | 124522726 | ||
| chr9:124522753
|
G | A | 1 | a0002c0006 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.1395C>T | p.Leu465Leu | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 1587/7065 | 1395/1443 | 465/480 | chr9 | 124522753 | ||
| chr9:124536084
|
G | A | 1 | a0001c0002 | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
synonymous_variant | LOW | c.873C>T | p.Ala291Ala | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/10 | 1065/7065 | 873/1443 | 291/480 | chr9 | 124536084 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:124517432
|
C | CT | 16 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(13): Show | 32 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*5272dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 5272 | chr9 | 124517432 | |||||
| chr9:124517555
|
T | C | 1 | a0001c0001t0056 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5150A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 5150 | chr9 | 124517555 | |||||
| chr9:124517712
|
G | C | 1 | a0001c0001t0052 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4993C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 4993 | chr9 | 124517712 | |||||
| chr9:124517757
|
G | T | 2 | a0001c0001t0046a0001c0001t0060 | 2 | HG02818.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4948C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 4948 | chr9 | 124517757 | |||||
| chr9:124517864
|
A | G | 1 | a0002c0006t0069 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4841T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 4841 | chr9 | 124517864 | |||||
| chr9:124518089
|
A | G | 3 | a0001c0001t0015a0001c0001t0051a0001c0001t0059 | 5 | HG02015.hp1 NA18943.hp1 NA18955.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4616T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 4616 | chr9 | 124518089 | |||||
| chr9:124518139
|
C | T | 1 | a0001c0001t0065 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4566G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 4566 | chr9 | 124518139 | |||||
| chr9:124518218
|
G | C | 3 | a0001c0002t0005a0001c0002t0010a0001c0002t0067 | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4487C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 4487 | chr9 | 124518218 | |||||
| chr9:124518401
|
A | C | 1 | a0001c0001t0049 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4304T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 4304 | chr9 | 124518401 | |||||
| chr9:124518647
|
T | C | 3 | a0001c0001t0007a0001c0001t0038a0001c0001t0039 | 6 | HG02723.hp1 HG02896.hp1 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4058A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 4058 | chr9 | 124518647 | |||||
| chr9:124518724
|
G | A | 2 | a0001c0001t0028a0001c0001t0029 | 2 | HG00639.hp1 HG01884.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3981C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 3981 | chr9 | 124518724 | |||||
| chr9:124518757
|
G | GT | 7 | a0001c0001t0021a0001c0001t0028a0001c0001t0029others(4): Show | 8 | HG00639.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3947dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 3947 | chr9 | 124518757 | |||||
| chr9:124519069
|
G | C | 1 | a0002c0006t0069 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3636C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 3636 | chr9 | 124519069 | |||||
| chr9:124519221
|
A | G | 15 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(12): Show | 31 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*3484T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 3484 | chr9 | 124519221 | |||||
| chr9:124519304
|
C | T | 1 | a0001c0001t0022 | 2 | HG02559.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3401G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 3401 | chr9 | 124519304 | |||||
| chr9:124519386
|
T | C | 1 | a0001c0001t0053 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3319A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 3319 | chr9 | 124519386 | |||||
| chr9:124519441
|
G | A | 2 | a0001c0001t0016a0001c0001t0054 | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3264C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 3264 | chr9 | 124519441 | |||||
| chr9:124519453
|
G | C | 2 | a0001c0001t0016a0001c0001t0054 | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3252C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 3252 | chr9 | 124519453 | |||||
| chr9:124519532
|
A | T | 18 | a0001c0001t0007a0001c0001t0008a0001c0001t0014others(15): Show | 31 | HG01167.hp2 HG02055.hp1 HG02258.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*3173T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 3173 | chr9 | 124519532 | |||||
| chr9:124519667
|
G | A | 1 | a0001c0001t0068 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3038C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 3038 | chr9 | 124519667 | |||||
| chr9:124519696
|
G | C | 45 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(42): Show | 83 | HG00544.hp2 HG00639.hp1 HG01167.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*3009C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 3009 | chr9 | 124519696 | |||||
| chr9:124519859
|
A | G | 22 | a0001c0001t0007a0001c0001t0008a0001c0001t0014others(19): Show | 42 | HG01167.hp2 HG02055.hp1 HG02145.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2846T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2846 | chr9 | 124519859 | |||||
| chr9:124519889
|
G | A | 2 | a0001c0003t0048a0001c0003t0055 | 2 | HG00423.hp2 HG00558.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2816C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2816 | chr9 | 124519889 | |||||
| chr9:124519897
|
G | A | 1 | a0002c0006t0069 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2808C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2808 | chr9 | 124519897 | |||||
| chr9:124519901
|
C | CA | 17 | a0001c0001t0002a0001c0001t0008a0001c0001t0012others(14): Show | 77 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2803dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2803 | chr9 | 124519901 | |||||
| chr9:124519901
|
C | CAA | 7 | a0001c0001t0003a0001c0001t0032a0001c0001t0034others(4): Show | 16 | HG00544.hp1 HG00544.hp2 HG01167.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2802_*2803dupTT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2803 | chr9 | 124519901 | |||||
| chr9:124519901
|
C | CAAA | 5 | a0001c0001t0004a0001c0001t0023a0001c0001t0030others(2): Show | 11 | HG00642.hp2 HG02027.hp1 HG02818.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2801_*2803dupTTT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2803 | chr9 | 124519901 | |||||
| chr9:124519901
|
C | CAAAA | 4 | a0001c0001t0013a0001c0001t0018a0001c0001t0031others(1): Show | 7 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2800_*2803dupTTTT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2803 | chr9 | 124519901 | |||||
| chr9:124519901
|
C | CAAAAAA | 5 | a0001c0001t0019a0001c0001t0024a0001c0001t0042others(2): Show | 7 | HG02258.hp1 HG02615.hp1 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2798_*2803dupTTTT others(2): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2803 | chr9 | 124519901 | |||||
| chr9:124519901
|
C | CAAAAAAA | 4 | a0001c0001t0017a0001c0001t0020a0001c0001t0025others(1): Show | 8 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2797_*2803dupTTTT others(3): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2803 | chr9 | 124519901 | |||||
| chr9:124519901
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0029 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2791_*2803dupTTTT others(9): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2803 | chr9 | 124519901 | |||||
| chr9:124519901
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0062 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2784_*2803dupTTTT others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2803 | chr9 | 124519901 | |||||
| chr9:124519901
|
CA | C | 5 | a0001c0001t0006a0001c0001t0007a0001c0001t0009others(2): Show | 18 | HG00323.hp2 HG02083.hp1 HG02451.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2803delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2803 | chr9 | 124519901 | |||||
| chr9:124519901
|
CAAAAAAA others(7): Show |
C | 1 | a0004c0004t0036 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2790_*2803delTTTT others(10): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2790 | chr9 | 124519901 | |||||
| chr9:124520031
|
A | G | 1 | a0002c0006t0069 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2674T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2674 | chr9 | 124520031 | |||||
| chr9:124520105
|
T | C | 1 | a0001c0001t0063 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2600A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2600 | chr9 | 124520105 | |||||
| chr9:124520123
|
A | C | 1 | a0001c0001t0033 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2582T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2582 | chr9 | 124520123 | |||||
| chr9:124520322
|
A | G | 4 | a0001c0002t0005a0001c0002t0010a0001c0002t0067others(1): Show | 11 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2383T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2383 | chr9 | 124520322 | |||||
| chr9:124520330
|
T | G | 1 | a0002c0006t0069 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2375 | chr9 | 124520330 | |||||
| chr9:124520535
|
C | T | 1 | a0001c0001t0044 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2170G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2170 | chr9 | 124520535 | |||||
| chr9:124520597
|
A | G | 4 | a0001c0002t0005a0001c0002t0010a0001c0002t0067others(1): Show | 11 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2108T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 2108 | chr9 | 124520597 | |||||
| chr9:124520758
|
C | T | 1 | a0001c0001t0043 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1947G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 1947 | chr9 | 124520758 | |||||
| chr9:124521056
|
C | G | 21 | a0001c0001t0007a0001c0001t0008a0001c0001t0018others(18): Show | 37 | HG00639.hp1 HG01884.hp2 HG02055.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1649G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 1649 | chr9 | 124521056 | |||||
| chr9:124521186
|
A | C | 1 | a0001c0001t0035 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1519T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 1519 | chr9 | 124521186 | |||||
| chr9:124521223
|
C | T | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(6): Show | 23 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1482G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 1482 | chr9 | 124521223 | |||||
| chr9:124521232
|
A | G | 1 | a0001c0001t0033 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1473T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 1473 | chr9 | 124521232 | |||||
| chr9:124521528
|
G | T | 1 | a0001c0001t0032 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1177C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 1177 | chr9 | 124521528 | |||||
| chr9:124521671
|
T | C | 1 | a0001c0001t0064 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1034A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 1034 | chr9 | 124521671 | |||||
| chr9:124522026
|
T | A | 1 | a0001c0001t0065 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*679A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 679 | chr9 | 124522026 | |||||
| chr9:124522195
|
G | A | 1 | a0001c0001t0066 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*510C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 510 | chr9 | 124522195 | |||||
| chr9:124522231
|
T | C | 3 | a0001c0002t0005a0001c0002t0010a0001c0002t0067 | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*474A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 474 | chr9 | 124522231 | |||||
| chr9:124522458
|
T | C | 1 | a0001c0001t0068 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*247A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 10/10 | 247 | chr9 | 124522458 | |||||
| chr9:124771173
|
C | G | 2 | a0001c0001t0030a0001c0001t0031 | 2 | HG02622.hp1 HG02970.hp2 |
5_prime_UTR_variant | MODIFIER | c.-54G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/10 | 54 | chr9 | 124771173 | |||||
| chr9:124771200
|
G | A | 2 | a0001c0001t0028a0001c0001t0029 | 2 | HG00639.hp1 HG01884.hp2 |
5_prime_UTR_variant | MODIFIER | c.-81C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/10 | 81 | chr9 | 124771200 | |||||
| chr9:124771226
|
AGCTCCCG others(6): Show |
A | 1 | a0001c0001t0026 | 2 | HG00642.hp1 HG02698.hp1 |
5_prime_UTR_variant | MODIFIER | c.-120_-108delCGCGGC others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/10 | 108 | chr9 | 124771226 | |||||
| chr9:124771276
|
G | GCTCCGCG others(3): Show |
1 | a0002c0006t0069 | 1 | HG03017.hp1 | 5_prime_UTR_variant | MODIFIER | c.-167_-158dupGGGCGC others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/10 | 158 | chr9 | 124771276 | |||||
| chr9:124771276
|
GCTCCGCG others(3): Show |
G | 2 | a0001c0001t0028a0001c0001t0029 | 2 | HG00639.hp1 HG01884.hp2 |
5_prime_UTR_variant | MODIFIER | c.-167_-158delGGGCGC others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/10 | 158 | chr9 | 124771276 | |||||
| chr9:124771290
|
C | T | 1 | a0001c0001t0027 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-171G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/10 | 171 | chr9 | 124771290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:124522805
|
G | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1355-12C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 9/9 | chr9 | 124522805 | ||||||
| chr9:124522805
|
G | T | 2 | a0001c0003t0048g0102a0001c0003t0055g0181 | 2 | HG00423.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.1355-12C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 9/9 | chr9 | 124522805 | ||||||
| chr9:124523518
|
A | AT | 9 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0024g0012others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1355-726dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 9/9 | chr9 | 124523518 | ||||||
| chr9:124523518
|
AT | A | 52 | a0001c0001t0001g0009a0001c0001t0001g0160a0001c0001t0001g0161others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1355-726delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 9/9 | chr9 | 124523518 | ||||||
| chr9:124523701
|
T | C | 1 | a0001c0001t0009g0168 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1355-908A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 9/9 | chr9 | 124523701 | ||||||
| chr9:124524134
|
A | T | 11 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(8): Show | 11 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1354+587T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 9/9 | chr9 | 124524134 | ||||||
| chr9:124524239
|
G | T | 1 | a0001c0001t0017g0066 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1354+482C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 9/9 | chr9 | 124524239 | ||||||
| chr9:124524262
|
T | C | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1354+459A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 9/9 | chr9 | 124524262 | ||||||
| chr9:124524405
|
ACT | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1354+314_1354+315d others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 9/9 | chr9 | 124524405 | ||||||
| chr9:124524879
|
G | GA | 27 | a0001c0001t0002g0103a0001c0001t0002g0166a0001c0001t0003g0050others(24): Show | 27 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(24): Show |
splice_region_variant&intron_variant | LOW | c.1202-7dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124524879 | ||||||
| chr9:124524890
|
A | AC | 12 | a0001c0001t0004g0209a0001c0001t0006g0212a0001c0001t0024g0012others(9): Show | 12 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1202-18_1202-17ins others(1): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124524890 | ||||||
| chr9:124524890
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1202-17T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124524890 | ||||||
| chr9:124525050
|
G | A | 46 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(43): Show | 46 | HG00639.hp1 HG01167.hp2 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.1202-177C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525050 | ||||||
| chr9:124525213
|
A | G | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202-340T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525213 | ||||||
| chr9:124525284
|
A | AAC | 20 | a0001c0001t0001g0120a0001c0001t0001g0219a0001c0001t0002g0080others(17): Show | 20 | HG00609.hp2 HG01167.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1202-413_1202-412d others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
A | AACAC | 94 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0022others(91): Show | 94 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.1202-415_1202-412d others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
A | AACACAC | 37 | a0001c0001t0001g0064a0001c0001t0001g0113a0001c0001t0001g0118others(34): Show | 37 | HG00621.hp2 HG01106.hp2 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.1202-417_1202-412d others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
A | AACACACA others(1): Show |
26 | a0001c0001t0001g0058a0001c0001t0001g0112a0001c0001t0001g0163others(23): Show | 26 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1202-419_1202-412d others(10): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
A | AACACACA others(3): Show |
14 | a0001c0001t0001g0136a0001c0001t0002g0033a0001c0001t0002g0142others(11): Show | 14 | HG00423.hp2 HG00621.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1202-421_1202-412d others(12): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
A | AACACACA others(5): Show |
14 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0180others(11): Show | 14 | HG00558.hp1 HG00642.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.1202-423_1202-412d others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
A | AACACACA others(7): Show |
6 | a0001c0001t0001g0161a0001c0001t0001g0173a0001c0001t0001g0182others(3): Show | 6 | HG02165.hp2 HG02523.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202-425_1202-412d others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
A | AACACACA others(9): Show |
4 | a0001c0001t0001g0164a0001c0001t0002g0170a0001c0001t0003g0171others(1): Show | 4 | HG03139.hp2 HG04199.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202-427_1202-412d others(18): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
A | AACACACA others(11): Show |
1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1202-429_1202-412d others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
A | AACACACA others(13): Show |
1 | a0001c0001t0008g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1202-431_1202-412d others(22): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0002g0187 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1202-412_1202-411i others(13): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
A | C | 1 | a0001c0001t0001g0019 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1202-411T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
AAC | A | 4 | a0001c0001t0001g0065a0001c0001t0002g0109a0001c0001t0006g0212others(1): Show | 4 | HG01978.hp1 HG02572.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202-413_1202-412d others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525284
|
AACACACA others(5): Show |
A | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1202-423_1202-412d others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525284 | ||||||
| chr9:124525324
|
G | C | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1202-451C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525324 | ||||||
| chr9:124525599
|
C | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202-726G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525599 | ||||||
| chr9:124525650
|
C | T | 29 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(26): Show | 29 | HG01167.hp2 HG02055.hp1 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.1202-777G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525650 | ||||||
| chr9:124525677
|
A | ATC | 3 | a0001c0001t0001g0116a0001c0001t0002g0157a0001c0001t0002g0159 | 3 | HG00639.hp2 HG02683.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1202-806_1202-805d others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525677 | ||||||
| chr9:124525677
|
A | ATCTC | 2 | a0001c0002t0010g0222a0001c0002t0010g0225 | 2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1202-808_1202-805d others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525677 | ||||||
| chr9:124525691
|
C | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1202-818G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525691 | ||||||
| chr9:124525693
|
C | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1202-820G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525693 | ||||||
| chr9:124525695
|
C | A | 6 | a0001c0001t0006g0212a0001c0001t0028g0002a0001c0001t0029g0003others(3): Show | 6 | HG00639.hp1 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202-822G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525695 | ||||||
| chr9:124525697
|
C | A | 19 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0141others(16): Show | 19 | HG00639.hp1 HG01433.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1202-824G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525697 | ||||||
| chr9:124525697
|
C | CTA | 6 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0002g0170others(3): Show | 6 | HG03239.hp1 HG03831.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202-825_1202-824i others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525697 | ||||||
| chr9:124525699
|
C | A | 102 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0023others(99): Show | 102 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1202-826G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525699 | ||||||
| chr9:124525699
|
C | CTA | 26 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(23): Show | 26 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.1202-828_1202-827d others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525699 | ||||||
| chr9:124525701
|
A | C | 2 | a0001c0001t0001g0045a0001c0001t0003g0215 | 2 | HG02735.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1202-828T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525701 | ||||||
| chr9:124525706
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1202-833A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525706 | ||||||
| chr9:124525708
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1202-835A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525708 | ||||||
| chr9:124525710
|
T | C | 2 | a0001c0001t0029g0003a0002c0006t0069g0234 | 2 | HG00639.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1202-837A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525710 | ||||||
| chr9:124525712
|
C | T | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1202-839G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525712 | ||||||
| chr9:124525880
|
C | T | 1 | a0001c0001t0022g0217 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1201+899G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525880 | ||||||
| chr9:124525903
|
T | C | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201+876A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124525903 | ||||||
| chr9:124526138
|
T | C | 1 | a0001c0001t0022g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1201+641A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124526138 | ||||||
| chr9:124526272
|
T | TTGTGTGT others(3): Show |
1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1201+506_1201+507i others(12): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124526272 | ||||||
| chr9:124526280
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1201+499T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124526280 | ||||||
| chr9:124526288
|
A | ATG | 6 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0129others(3): Show | 6 | HG02647.hp1 HG02683.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201+489_1201+490d others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124526288 | ||||||
| chr9:124526288
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1201+491T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124526288 | ||||||
| chr9:124526288
|
ATG | A | 26 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0143others(23): Show | 26 | HG01106.hp2 HG01361.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.1201+489_1201+490d others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124526288 | ||||||
| chr9:124526288
|
ATGTG | A | 58 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0001g0161others(55): Show | 58 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1201+487_1201+490d others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124526288 | ||||||
| chr9:124526288
|
ATGTGTG | A | 12 | a0001c0001t0002g0037a0001c0001t0004g0193a0001c0001t0004g0195others(9): Show | 12 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1201+485_1201+490d others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124526288 | ||||||
| chr9:124526356
|
C | T | 2 | a0001c0001t0066g0007a0004c0004t0036g0010 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1201+423G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124526356 | ||||||
| chr9:124526538
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0009g0060 | 2 | NA18939.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1201+241A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 8/9 | chr9 | 124526538 | ||||||
| chr9:124526939
|
A | C | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.1080-39T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124526939 | ||||||
| chr9:124527011
|
G | A | 1 | a0001c0001t0063g0135 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1080-111C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124527011 | ||||||
| chr9:124527456
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1080-556A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124527456 | ||||||
| chr9:124527476
|
G | A | 1 | a0001c0001t0002g0133 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1080-576C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124527476 | ||||||
| chr9:124527556
|
T | C | 1 | a0001c0001t0059g0125 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1080-656A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124527556 | ||||||
| chr9:124527757
|
TAGGAGTG others(9): Show |
T | 11 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(8): Show | 11 | HG02258.hp2 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1080-873_1080-858d others(18): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124527757 | ||||||
| chr9:124527961
|
T | C | 2 | a0001c0001t0066g0007a0004c0004t0036g0010 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1080-1061A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124527961 | ||||||
| chr9:124527988
|
C | T | 4 | a0001c0001t0006g0191a0001c0001t0006g0202a0001c0001t0006g0203others(1): Show | 4 | HG02015.hp2 HG02083.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080-1088G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124527988 | ||||||
| chr9:124528063
|
C | T | 30 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(27): Show | 30 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.1080-1163G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124528063 | ||||||
| chr9:124528768
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1080-1868T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124528768 | ||||||
| chr9:124528769
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1080-1869C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124528769 | ||||||
| chr9:124528777
|
AC | A | 2 | a0001c0003t0048g0102a0001c0003t0055g0181 | 2 | HG00423.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.1080-1878delG | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124528777 | ||||||
| chr9:124528833
|
C | T | 81 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(78): Show | 81 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.1080-1933G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124528833 | ||||||
| chr9:124528979
|
C | T | 1 | a0001c0001t0002g0211 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1080-2079G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124528979 | ||||||
| chr9:124529031
|
C | G | 2 | a0001c0001t0047g0105a0001c0001t0062g0104 | 2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1080-2131G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124529031 | ||||||
| chr9:124529104
|
G | A | 1 | a0001c0001t0028g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1080-2204C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124529104 | ||||||
| chr9:124529284
|
T | C | 1 | a0001c0001t0030g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1080-2384A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124529284 | ||||||
| chr9:124529514
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1080-2614C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124529514 | ||||||
| chr9:124529554
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0044g0175 | 2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1080-2654G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124529554 | ||||||
| chr9:124529714
|
C | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1080-2814G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124529714 | ||||||
| chr9:124529728
|
C | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1080-2828G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124529728 | ||||||
| chr9:124530208
|
C | G | 71 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(68): Show | 71 | HG00639.hp1 HG01167.hp2 HG01884.hp2 others(68): Show |
intron_variant | MODIFIER | c.1080-3308G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124530208 | ||||||
| chr9:124530256
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1080-3356C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124530256 | ||||||
| chr9:124530666
|
T | C | 1 | a0001c0001t0008g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1080-3766A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124530666 | ||||||
| chr9:124531451
|
C | G | 8 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0143others(5): Show | 8 | HG01106.hp2 HG01361.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1079+4427G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124531451 | ||||||
| chr9:124531526
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1079+4352C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124531526 | ||||||
| chr9:124531755
|
C | T | 7 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079+4123G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124531755 | ||||||
| chr9:124531906
|
G | T | 31 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(28): Show | 31 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1079+3972C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124531906 | ||||||
| chr9:124532306
|
A | G | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.1079+3572T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124532306 | ||||||
| chr9:124532332
|
A | C | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1079+3546T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124532332 | ||||||
| chr9:124532556
|
C | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1079+3322G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124532556 | ||||||
| chr9:124532567
|
T | G | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.1079+3311A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124532567 | ||||||
| chr9:124532633
|
G | A | 5 | a0001c0001t0004g0197a0001c0001t0004g0199a0001c0001t0013g0190others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079+3245C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124532633 | ||||||
| chr9:124532813
|
T | C | 1 | a0001c0001t0002g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1079+3065A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124532813 | ||||||
| chr9:124532821
|
G | A | 8 | a0001c0001t0002g0211a0001c0001t0002g0216a0001c0001t0003g0215others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1079+3057C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124532821 | ||||||
| chr9:124533035
|
A | G | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1079+2843T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124533035 | ||||||
| chr9:124533417
|
C | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079+2461G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124533417 | ||||||
| chr9:124533469
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1079+2409G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124533469 | ||||||
| chr9:124533582
|
A | G | 2 | a0001c0001t0008g0094a0001c0001t0008g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1079+2296T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124533582 | ||||||
| chr9:124533583
|
T | G | 2 | a0001c0001t0008g0094a0001c0001t0008g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1079+2295A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124533583 | ||||||
| chr9:124533622
|
T | G | 2 | a0001c0001t0022g0217a0001c0001t0022g0220 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1079+2256A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124533622 | ||||||
| chr9:124533655
|
C | CT | 32 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(29): Show | 32 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1079+2222dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124533655 | ||||||
| chr9:124533849
|
C | T | 1 | a0001c0001t0028g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1079+2029G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124533849 | ||||||
| chr9:124533859
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1079+2019G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124533859 | ||||||
| chr9:124534072
|
C | CT | 8 | a0001c0001t0001g0038a0001c0001t0002g0051a0001c0001t0002g0137others(5): Show | 8 | HG01106.hp2 HG01361.hp2 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.1079+1805dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124534072 | ||||||
| chr9:124534072
|
CT | C | 54 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(51): Show | 54 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1079+1805delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124534072 | ||||||
| chr9:124534072
|
CTT | C | 23 | a0001c0001t0004g0193a0001c0001t0004g0195a0001c0001t0004g0197others(20): Show | 23 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.1079+1804_1079+180 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124534072 | ||||||
| chr9:124534111
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1079+1767G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124534111 | ||||||
| chr9:124534112
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1079+1766C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124534112 | ||||||
| chr9:124534647
|
A | C | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1079+1231T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124534647 | ||||||
| chr9:124534670
|
C | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079+1208G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124534670 | ||||||
| chr9:124534812
|
C | T | 1 | a0001c0001t0051g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1079+1066G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124534812 | ||||||
| chr9:124534847
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1079+1031A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124534847 | ||||||
| chr9:124534981
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0009g0060 | 2 | NA18939.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1079+897C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124534981 | ||||||
| chr9:124535025
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1079+853C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124535025 | ||||||
| chr9:124535055
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079+823G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124535055 | ||||||
| chr9:124535103
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1079+775C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124535103 | ||||||
| chr9:124535477
|
C | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079+401G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124535477 | ||||||
| chr9:124535503
|
G | A | 7 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079+375C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124535503 | ||||||
| chr9:124535531
|
C | T | 80 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(77): Show | 80 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1079+347G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124535531 | ||||||
| chr9:124535533
|
G | T | 1 | a0001c0001t0023g0043 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1079+345C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124535533 | ||||||
| chr9:124535556
|
C | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079+322G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124535556 | ||||||
| chr9:124535556
|
C | T | 1 | a0001c0001t0022g0217 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1079+322G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124535556 | ||||||
| chr9:124535629
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0219 | 2 | HG02165.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1079+249C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 7/9 | chr9 | 124535629 | ||||||
| chr9:124536203
|
T | C | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.825-71A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124536203 | ||||||
| chr9:124536623
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.825-491G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124536623 | ||||||
| chr9:124536631
|
C | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.825-499G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124536631 | ||||||
| chr9:124536663
|
T | TA | 7 | a0001c0001t0001g0161a0001c0001t0002g0051a0001c0001t0002g0158others(4): Show | 7 | HG02572.hp2 HG02602.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.825-532dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124536663 | ||||||
| chr9:124536794
|
T | C | 6 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.825-662A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124536794 | ||||||
| chr9:124536912
|
G | A | 1 | a0001c0001t0061g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.825-780C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124536912 | ||||||
| chr9:124537059
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0002g0137a0001c0001t0063g0135 | 3 | HG01106.hp2 HG01361.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.825-927G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124537059 | ||||||
| chr9:124537070
|
A | AT | 8 | a0001c0001t0001g0019a0001c0001t0001g0163a0001c0001t0001g0182others(5): Show | 8 | HG00438.hp2 HG02523.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.825-939dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124537070 | ||||||
| chr9:124537070
|
AT | A | 41 | a0001c0001t0001g0114a0001c0001t0002g0211a0001c0001t0002g0216others(38): Show | 41 | HG00609.hp2 HG01167.hp2 HG01516.hp1 others(38): Show |
intron_variant | MODIFIER | c.825-939delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124537070 | ||||||
| chr9:124537070
|
ATTTTTTT others(1): Show |
A | 19 | a0001c0001t0004g0193a0001c0001t0004g0195a0001c0001t0004g0197others(16): Show | 19 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.825-946_825-939del others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124537070 | ||||||
| chr9:124537148
|
A | G | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.824+944T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124537148 | ||||||
| chr9:124537218
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.824+874A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124537218 | ||||||
| chr9:124537303
|
C | T | 4 | a0001c0001t0001g0178a0001c0001t0002g0176a0001c0001t0002g0177others(1): Show | 4 | HG02698.hp2 HG03927.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.824+789G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124537303 | ||||||
| chr9:124537313
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.824+779A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124537313 | ||||||
| chr9:124537315
|
G | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.824+777C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124537315 | ||||||
| chr9:124537426
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.824+666A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124537426 | ||||||
| chr9:124537495
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0002g0167 | 2 | NA18957.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.824+597A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124537495 | ||||||
| chr9:124537876
|
C | T | 5 | a0001c0001t0001g0122a0001c0001t0002g0121a0001c0001t0002g0157others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.824+216G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124537876 | ||||||
| chr9:124538025
|
C | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.824+67G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 6/9 | chr9 | 124538025 | ||||||
| chr9:124538536
|
C | A | 3 | a0001c0001t0002g0080a0001c0001t0002g0083a0001c0001t0053g0082 | 3 | NA19011.hp1 NA19060.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.597-217G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124538536 | ||||||
| chr9:124538722
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.597-403G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124538722 | ||||||
| chr9:124538736
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.597-417G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124538736 | ||||||
| chr9:124538777
|
T | C | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-458A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124538777 | ||||||
| chr9:124538905
|
TA | T | 232 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(229): Show | 232 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.597-587delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124538905 | ||||||
| chr9:124539047
|
T | A | 6 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.597-728A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124539047 | ||||||
| chr9:124539048
|
T | A | 31 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(28): Show | 31 | HG01167.hp2 HG02055.hp1 HG02258.hp2 others(28): Show |
intron_variant | MODIFIER | c.597-729A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124539048 | ||||||
| chr9:124539049
|
A | T | 14 | a0001c0001t0001g0047a0001c0001t0001g0120a0001c0001t0001g0219others(11): Show | 14 | HG02145.hp1 HG02165.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.597-730T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124539049 | ||||||
| chr9:124539255
|
A | C | 1 | a0001c0001t0001g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.596+778T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124539255 | ||||||
| chr9:124539369
|
C | T | 1 | a0004c0004t0036g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.596+664G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124539369 | ||||||
| chr9:124539886
|
T | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.596+147A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124539886 | ||||||
| chr9:124539996
|
C | CCAAAGCT others(17): Show |
1 | a0001c0001t0001g0161 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.596+36_596+37insCA others(22): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124539996 | ||||||
| chr9:124540000
|
A | T | 38 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(35): Show | 38 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(35): Show |
intron_variant | MODIFIER | c.596+33T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124540000 | ||||||
| chr9:124540001
|
G | A | 38 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(35): Show | 38 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(35): Show |
intron_variant | MODIFIER | c.596+32C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124540001 | ||||||
| chr9:124540003
|
T | A | 38 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(35): Show | 38 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(35): Show |
intron_variant | MODIFIER | c.596+30A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124540003 | ||||||
| chr9:124540005
|
A | C | 38 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(35): Show | 38 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(35): Show |
intron_variant | MODIFIER | c.596+28T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124540005 | ||||||
| chr9:124540007
|
G | C | 38 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(35): Show | 38 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(35): Show |
intron_variant | MODIFIER | c.596+26C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124540007 | ||||||
| chr9:124540009
|
C | CCTTTAAG others(19): Show |
37 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(34): Show | 37 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(34): Show |
intron_variant | MODIFIER | c.596+23_596+24insTG others(24): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124540009 | ||||||
| chr9:124540011
|
A | C | 37 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(34): Show | 37 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(34): Show |
intron_variant | MODIFIER | c.596+22T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 5/9 | chr9 | 124540011 | ||||||
| chr9:124540271
|
T | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-84A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124540271 | ||||||
| chr9:124540342
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-155C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124540342 | ||||||
| chr9:124540491
|
A | G | 1 | a0001c0001t0035g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.442-304T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124540491 | ||||||
| chr9:124540549
|
A | G | 4 | a0001c0001t0001g0118a0001c0001t0002g0145a0001c0001t0002g0149others(1): Show | 4 | HG00438.hp2 NA18961.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-362T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124540549 | ||||||
| chr9:124540686
|
C | T | 21 | a0001c0001t0004g0193a0001c0001t0004g0195a0001c0001t0004g0197others(18): Show | 21 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.442-499G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124540686 | ||||||
| chr9:124540820
|
C | T | 1 | a0001c0001t0002g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.442-633G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124540820 | ||||||
| chr9:124541219
|
T | C | 119 | a0001c0001t0001g0129a0001c0001t0001g0160a0001c0001t0001g0161others(116): Show | 119 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.442-1032A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124541219 | ||||||
| chr9:124541296
|
A | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.442-1109T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124541296 | ||||||
| chr9:124541316
|
C | A | 5 | a0001c0001t0001g0122a0001c0001t0002g0121a0001c0001t0002g0157others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-1129G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124541316 | ||||||
| chr9:124541363
|
G | A | 1 | a0001c0001t0003g0056 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.442-1176C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124541363 | ||||||
| chr9:124541478
|
A | G | 33 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(30): Show | 33 | HG01167.hp2 HG02055.hp1 HG02258.hp2 others(30): Show |
intron_variant | MODIFIER | c.442-1291T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124541478 | ||||||
| chr9:124541528
|
T | C | 1 | a0001c0001t0035g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.442-1341A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124541528 | ||||||
| chr9:124541631
|
T | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.442-1444A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124541631 | ||||||
| chr9:124541745
|
G | C | 12 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0002t0005g0226others(9): Show | 12 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-1558C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124541745 | ||||||
| chr9:124541861
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.442-1674A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124541861 | ||||||
| chr9:124542073
|
G | A | 79 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(76): Show | 79 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.441+1729C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124542073 | ||||||
| chr9:124542089
|
T | G | 1 | a0001c0001t0043g0107 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.441+1713A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124542089 | ||||||
| chr9:124542125
|
G | A | 1 | a0001c0001t0064g0124 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.441+1677C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124542125 | ||||||
| chr9:124542338
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.441+1464G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124542338 | ||||||
| chr9:124542362
|
C | T | 3 | a0001c0001t0014g0071a0001c0001t0014g0072a0001c0001t0045g0070 | 3 | HG01167.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.441+1440G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124542362 | ||||||
| chr9:124542681
|
C | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.441+1121G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124542681 | ||||||
| chr9:124542977
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.441+825G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124542977 | ||||||
| chr9:124542996
|
C | T | 80 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(77): Show | 80 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.441+806G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124542996 | ||||||
| chr9:124543404
|
C | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.441+398G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124543404 | ||||||
| chr9:124543413
|
C | T | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.441+389G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124543413 | ||||||
| chr9:124543665
|
A | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+137T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124543665 | ||||||
| chr9:124543754
|
G | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.441+48C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 4/9 | chr9 | 124543754 | ||||||
| chr9:124544010
|
C | G | 1 | a0001c0001t0017g0067 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.386-153G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124544010 | ||||||
| chr9:124544061
|
A | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.386-204T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124544061 | ||||||
| chr9:124544102
|
T | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.386-245A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124544102 | ||||||
| chr9:124544172
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.386-315A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124544172 | ||||||
| chr9:124544244
|
C | G | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.386-387G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124544244 | ||||||
| chr9:124544304
|
A | G | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.386-447T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124544304 | ||||||
| chr9:124544355
|
T | G | 2 | a0001c0001t0002g0189a0001c0001t0023g0188 | 2 | NA18959.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.386-498A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124544355 | ||||||
| chr9:124544709
|
T | C | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-852A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124544709 | ||||||
| chr9:124544851
|
G | C | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.386-994C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124544851 | ||||||
| chr9:124544970
|
A | C | 2 | a0001c0001t0002g0189a0001c0001t0023g0188 | 2 | NA18959.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.386-1113T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124544970 | ||||||
| chr9:124545104
|
AG | A | 35 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(32): Show | 35 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.386-1248delC | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124545104 | ||||||
| chr9:124545421
|
G | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.386-1564C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124545421 | ||||||
| chr9:124545933
|
T | C | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.386-2076A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124545933 | ||||||
| chr9:124546097
|
A | G | 1 | a0001c0001t0061g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.386-2240T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124546097 | ||||||
| chr9:124546165
|
G | A | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.386-2308C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124546165 | ||||||
| chr9:124546362
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.386-2505A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124546362 | ||||||
| chr9:124546376
|
A | G | 1 | a0001c0001t0040g0029 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.386-2519T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124546376 | ||||||
| chr9:124546594
|
A | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.386-2737T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124546594 | ||||||
| chr9:124546689
|
A | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.386-2832T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124546689 | ||||||
| chr9:124546741
|
G | A | 1 | a0001c0001t0002g0018 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.386-2884C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124546741 | ||||||
| chr9:124546915
|
A | G | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.386-3058T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124546915 | ||||||
| chr9:124547053
|
A | G | 2 | a0001c0001t0001g0174a0001c0001t0044g0175 | 2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.386-3196T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124547053 | ||||||
| chr9:124547069
|
A | G | 1 | a0001c0001t0016g0077 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.386-3212T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124547069 | ||||||
| chr9:124547276
|
C | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.386-3419G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124547276 | ||||||
| chr9:124547321
|
C | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.386-3464G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124547321 | ||||||
| chr9:124547588
|
A | G | 4 | a0001c0001t0015g0127a0001c0001t0015g0155a0001c0001t0015g0156others(1): Show | 4 | HG02015.hp1 NA18943.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-3731T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124547588 | ||||||
| chr9:124547809
|
C | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.386-3952G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124547809 | ||||||
| chr9:124547833
|
C | A | 1 | a0001c0001t0003g0056 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.386-3976G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124547833 | ||||||
| chr9:124547963
|
C | T | 68 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(65): Show | 68 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(65): Show |
intron_variant | MODIFIER | c.386-4106G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124547963 | ||||||
| chr9:124548087
|
T | C | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.386-4230A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124548087 | ||||||
| chr9:124548230
|
C | T | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.386-4373G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124548230 | ||||||
| chr9:124548388
|
G | A | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.386-4531C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124548388 | ||||||
| chr9:124548451
|
G | A | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.386-4594C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124548451 | ||||||
| chr9:124548583
|
T | A | 1 | a0001c0001t0002g0133 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.386-4726A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124548583 | ||||||
| chr9:124548653
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.386-4796C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124548653 | ||||||
| chr9:124548803
|
A | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.386-4946T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124548803 | ||||||
| chr9:124548880
|
C | T | 7 | a0001c0001t0014g0069a0001c0001t0014g0071a0001c0001t0014g0072others(4): Show | 7 | HG01167.hp2 HG02647.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-5023G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124548880 | ||||||
| chr9:124549016
|
C | G | 1 | a0003c0005t0002g0146 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.386-5159G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124549016 | ||||||
| chr9:124549179
|
AGGATGTT others(10): Show |
A | 2 | a0001c0002t0005g0226a0001c0002t0005g0230 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.385+5132_385+5148d others(19): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124549179 | ||||||
| chr9:124549205
|
T | G | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.385+5123A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124549205 | ||||||
| chr9:124549235
|
GTTT | G | 112 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(109): Show | 112 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.385+5090_385+5092d others(5): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124549235 | ||||||
| chr9:124549478
|
A | G | 1 | a0001c0001t0025g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.385+4850T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124549478 | ||||||
| chr9:124549488
|
G | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.385+4840C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124549488 | ||||||
| chr9:124549776
|
A | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0219 | 2 | HG02165.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.385+4552T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124549776 | ||||||
| chr9:124550277
|
T | C | 1 | a0001c0001t0054g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.385+4051A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124550277 | ||||||
| chr9:124550375
|
A | AT | 33 | a0001c0001t0001g0044a0001c0001t0002g0011a0001c0001t0002g0054others(30): Show | 33 | HG00544.hp2 HG01884.hp2 HG02015.hp2 others(30): Show |
intron_variant | MODIFIER | c.385+3952dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124550375 | ||||||
| chr9:124550375
|
AT | A | 10 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0114others(7): Show | 10 | HG01884.hp1 HG02735.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.385+3952delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124550375 | ||||||
| chr9:124550375
|
ATTTTTTT | A | 11 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(8): Show | 11 | HG02145.hp2 HG02451.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.385+3946_385+3952d others(9): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124550375 | ||||||
| chr9:124550652
|
C | G | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+3676G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124550652 | ||||||
| chr9:124550807
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.385+3521T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124550807 | ||||||
| chr9:124550919
|
A | C | 1 | a0004c0004t0036g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.385+3409T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124550919 | ||||||
| chr9:124550958
|
C | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+3370G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124550958 | ||||||
| chr9:124551101
|
AT | A | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.385+3226delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124551101 | ||||||
| chr9:124551147
|
A | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.385+3181T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124551147 | ||||||
| chr9:124551290
|
C | G | 1 | a0001c0001t0002g0218 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.385+3038G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124551290 | ||||||
| chr9:124551329
|
G | A | 30 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(27): Show | 30 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.385+2999C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124551329 | ||||||
| chr9:124551520
|
G | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.385+2808C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124551520 | ||||||
| chr9:124551697
|
C | A | 1 | a0004c0004t0036g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.385+2631G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124551697 | ||||||
| chr9:124551754
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0002g0169 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.385+2574G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124551754 | ||||||
| chr9:124551943
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0009g0060 | 2 | NA18939.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.385+2385G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124551943 | ||||||
| chr9:124552137
|
C | G | 1 | a0001c0001t0002g0167 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.385+2191G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124552137 | ||||||
| chr9:124552227
|
A | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385+2101T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124552227 | ||||||
| chr9:124552250
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.385+2078G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124552250 | ||||||
| chr9:124552422
|
C | T | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.385+1906G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124552422 | ||||||
| chr9:124552489
|
A | G | 25 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(22): Show | 25 | HG00544.hp2 HG00639.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.385+1839T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124552489 | ||||||
| chr9:124552559
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.385+1769C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124552559 | ||||||
| chr9:124552581
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.385+1747G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124552581 | ||||||
| chr9:124552596
|
C | A | 2 | a0001c0001t0011g0201a0001c0001t0012g0206 | 2 | HG02155.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.385+1732G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124552596 | ||||||
| chr9:124552637
|
A | C | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.385+1691T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124552637 | ||||||
| chr9:124552665
|
T | C | 1 | a0001c0001t0021g0213 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.385+1663A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124552665 | ||||||
| chr9:124552785
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.385+1543G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124552785 | ||||||
| chr9:124552795
|
A | G | 31 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(28): Show | 31 | HG01167.hp2 HG02055.hp1 HG02258.hp2 others(28): Show |
intron_variant | MODIFIER | c.385+1533T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124552795 | ||||||
| chr9:124553266
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.385+1062G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124553266 | ||||||
| chr9:124553535
|
G | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.385+793C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124553535 | ||||||
| chr9:124553549
|
C | CT | 14 | a0001c0001t0001g0063a0001c0001t0001g0118a0001c0001t0001g0120others(11): Show | 14 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(11): Show |
intron_variant | MODIFIER | c.385+778dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124553549 | ||||||
| chr9:124553549
|
CT | C | 44 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0128others(41): Show | 44 | HG00558.hp1 HG00639.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.385+778delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124553549 | ||||||
| chr9:124553549
|
CTT | C | 30 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(27): Show | 30 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.385+777_385+778del others(2): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124553549 | ||||||
| chr9:124553549
|
CTTT | C | 5 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(2): Show | 5 | HG01884.hp1 HG02922.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+776_385+778del others(3): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124553549 | ||||||
| chr9:124553588
|
C | T | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.385+740G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124553588 | ||||||
| chr9:124553704
|
T | C | 24 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(21): Show | 24 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.385+624A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124553704 | ||||||
| chr9:124553792
|
T | A | 1 | a0001c0001t0001g0178 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.385+536A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124553792 | ||||||
| chr9:124553793
|
T | A | 1 | a0001c0001t0001g0178 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.385+535A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124553793 | ||||||
| chr9:124553873
|
A | G | 1 | a0001c0001t0034g0210 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.385+455T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124553873 | ||||||
| chr9:124554043
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.385+285T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124554043 | ||||||
| chr9:124554283
|
G | A | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.385+45C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124554283 | ||||||
| chr9:124554316
|
A | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.385+12T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 3/9 | chr9 | 124554316 | ||||||
| chr9:124554895
|
A | C | 1 | a0001c0001t0001g0178 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.143-325T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124554895 | ||||||
| chr9:124554986
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-416G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124554986 | ||||||
| chr9:124555167
|
G | T | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-597C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124555167 | ||||||
| chr9:124555194
|
C | T | 17 | a0001c0001t0004g0193a0001c0001t0004g0195a0001c0001t0004g0197others(14): Show | 17 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.143-624G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124555194 | ||||||
| chr9:124555232
|
T | A | 1 | a0001c0001t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.143-662A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124555232 | ||||||
| chr9:124555670
|
G | A | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-1100C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124555670 | ||||||
| chr9:124555722
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.143-1152A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124555722 | ||||||
| chr9:124555769
|
C | G | 1 | a0001c0001t0014g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.143-1199G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124555769 | ||||||
| chr9:124555847
|
T | C | 22 | a0001c0001t0004g0193a0001c0001t0004g0195a0001c0001t0004g0197others(19): Show | 22 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.143-1277A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124555847 | ||||||
| chr9:124555937
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-1367C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124555937 | ||||||
| chr9:124555942
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-1372G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124555942 | ||||||
| chr9:124556131
|
T | G | 1 | a0001c0001t0013g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.143-1561A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556131 | ||||||
| chr9:124556279
|
A | T | 1 | a0001c0001t0002g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.143-1709T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556279 | ||||||
| chr9:124556293
|
C | A | 81 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(78): Show | 81 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.143-1723G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556293 | ||||||
| chr9:124556296
|
A | G | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-1726T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556296 | ||||||
| chr9:124556299
|
C | A | 5 | a0001c0001t0018g0028a0001c0001t0018g0030a0001c0001t0037g0032others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-1729G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556299 | ||||||
| chr9:124556424
|
C | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(84): Show | 87 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.143-1854G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556424 | ||||||
| chr9:124556455
|
T | A | 1 | a0001c0001t0002g0216 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.143-1885A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556455 | ||||||
| chr9:124556460
|
A | AT | 10 | a0001c0001t0001g0113a0001c0001t0001g0141a0001c0001t0002g0033others(7): Show | 10 | HG01433.hp2 HG01884.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-1891dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556460 | ||||||
| chr9:124556460
|
AT | A | 51 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(48): Show | 51 | HG00423.hp2 HG00558.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.143-1891delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556460 | ||||||
| chr9:124556604
|
G | C | 6 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-2034C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556604 | ||||||
| chr9:124556800
|
A | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-2230T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556800 | ||||||
| chr9:124556867
|
CT | C | 58 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(55): Show | 58 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-2298delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556867 | ||||||
| chr9:124556867
|
CTT | C | 21 | a0001c0001t0004g0193a0001c0001t0004g0195a0001c0001t0004g0197others(18): Show | 21 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.143-2299_143-2298d others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124556867 | ||||||
| chr9:124557113
|
G | A | 2 | a0001c0001t0003g0048a0001c0001t0003g0050 | 2 | HG02027.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.143-2543C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124557113 | ||||||
| chr9:124557196
|
T | G | 2 | a0001c0001t0001g0064a0001c0001t0002g0054 | 2 | HG02056.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.143-2626A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124557196 | ||||||
| chr9:124557207
|
C | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-2637G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124557207 | ||||||
| chr9:124557223
|
G | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-2653C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124557223 | ||||||
| chr9:124557282
|
G | A | 168 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(165): Show | 168 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.143-2712C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124557282 | ||||||
| chr9:124557401
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-2831C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124557401 | ||||||
| chr9:124557877
|
T | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-3307A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124557877 | ||||||
| chr9:124557925
|
C | T | 79 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(76): Show | 79 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.143-3355G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124557925 | ||||||
| chr9:124558041
|
G | A | 4 | a0001c0001t0001g0178a0001c0001t0002g0176a0001c0001t0002g0177others(1): Show | 4 | HG02698.hp2 HG03927.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-3471C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124558041 | ||||||
| chr9:124558325
|
C | T | 2 | a0001c0001t0033g0097a0002c0006t0069g0234 | 2 | HG03017.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.143-3755G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124558325 | ||||||
| chr9:124558416
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.143-3846T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124558416 | ||||||
| chr9:124558477
|
T | C | 1 | a0001c0001t0059g0125 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.143-3907A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124558477 | ||||||
| chr9:124558591
|
A | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-4021T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124558591 | ||||||
| chr9:124558596
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-4026A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124558596 | ||||||
| chr9:124558683
|
C | T | 1 | a0001c0001t0025g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.143-4113G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124558683 | ||||||
| chr9:124558741
|
T | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0053others(4): Show | 7 | HG00558.hp2 HG02056.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-4171A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124558741 | ||||||
| chr9:124558852
|
AC | A | 10 | a0001c0001t0014g0069a0001c0001t0014g0071a0001c0001t0014g0072others(7): Show | 10 | HG01167.hp2 HG02647.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-4283delG | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124558852 | ||||||
| chr9:124558971
|
T | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-4401A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124558971 | ||||||
| chr9:124559113
|
A | T | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-4543T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124559113 | ||||||
| chr9:124559115
|
A | G | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-4545T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124559115 | ||||||
| chr9:124559143
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-4573T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124559143 | ||||||
| chr9:124559208
|
T | A | 13 | a0001c0001t0033g0097a0001c0001t0068g0006a0001c0002t0005g0226others(10): Show | 13 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-4638A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124559208 | ||||||
| chr9:124559227
|
C | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-4657G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124559227 | ||||||
| chr9:124559327
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0002g0018others(1): Show | 4 | HG00621.hp2 NA18983.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-4757G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124559327 | ||||||
| chr9:124559781
|
G | T | 1 | a0001c0001t0002g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.143-5211C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124559781 | ||||||
| chr9:124559959
|
C | A | 1 | a0001c0001t0002g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.143-5389G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124559959 | ||||||
| chr9:124560025
|
A | T | 1 | a0001c0001t0002g0158 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.143-5455T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124560025 | ||||||
| chr9:124560074
|
C | G | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.143-5504G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124560074 | ||||||
| chr9:124560582
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.143-6012G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124560582 | ||||||
| chr9:124560599
|
C | T | 2 | a0001c0001t0065g0041a0001c0001t0066g0007 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.143-6029G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124560599 | ||||||
| chr9:124560744
|
A | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-6174T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124560744 | ||||||
| chr9:124560903
|
C | G | 1 | a0001c0001t0062g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.143-6333G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124560903 | ||||||
| chr9:124561362
|
C | A | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-6792G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124561362 | ||||||
| chr9:124561366
|
T | G | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-6796A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124561366 | ||||||
| chr9:124561420
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.143-6850C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124561420 | ||||||
| chr9:124561497
|
C | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(84): Show | 87 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.143-6927G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124561497 | ||||||
| chr9:124561537
|
T | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-6967A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124561537 | ||||||
| chr9:124561764
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-7194G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124561764 | ||||||
| chr9:124561794
|
A | C | 169 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(166): Show | 169 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.143-7224T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124561794 | ||||||
| chr9:124561844
|
A | G | 1 | a0001c0001t0002g0189 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.143-7274T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124561844 | ||||||
| chr9:124561856
|
G | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(84): Show | 87 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.143-7286C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124561856 | ||||||
| chr9:124561995
|
A | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-7425T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124561995 | ||||||
| chr9:124562241
|
T | C | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-7671A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124562241 | ||||||
| chr9:124562490
|
T | C | 1 | a0001c0001t0003g0042 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.143-7920A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124562490 | ||||||
| chr9:124562514
|
T | C | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-7944A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124562514 | ||||||
| chr9:124562671
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.143-8101G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124562671 | ||||||
| chr9:124562860
|
T | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-8290A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124562860 | ||||||
| chr9:124563274
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-8704G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124563274 | ||||||
| chr9:124563676
|
T | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-9106A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124563676 | ||||||
| chr9:124563778
|
G | A | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-9208C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124563778 | ||||||
| chr9:124563911
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.143-9341T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124563911 | ||||||
| chr9:124564131
|
A | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-9561T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564131 | ||||||
| chr9:124564134
|
T | C | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-9564A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564134 | ||||||
| chr9:124564260
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-9690T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564260 | ||||||
| chr9:124564458
|
T | C | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-9888A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564458 | ||||||
| chr9:124564681
|
C | CTG | 27 | a0001c0001t0001g0163a0001c0001t0001g0180a0001c0001t0002g0033others(24): Show | 27 | HG00544.hp2 HG01433.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.143-10113_143-1011 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564681 | ||||||
| chr9:124564681
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-10123_143-1011 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564681 | ||||||
| chr9:124564681
|
C | CTGTGTGT others(7): Show |
1 | a0001c0002t0010g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.143-10125_143-1011 others(18): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564681 | ||||||
| chr9:124564681
|
C | CTGTGTGT others(9): Show |
3 | a0001c0002t0005g0226a0001c0002t0005g0230a0001c0002t0010g0222 | 3 | HG02717.hp1 HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.143-10127_143-1011 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564681 | ||||||
| chr9:124564681
|
C | CTGTGTGT others(11): Show |
3 | a0001c0002t0010g0223a0001c0002t0010g0224a0001c0002t0067g0221 | 3 | HG02145.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.143-10129_143-1011 others(22): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564681 | ||||||
| chr9:124564681
|
C | CTGTGTGT others(15): Show |
1 | a0001c0002t0005g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.143-10133_143-1011 others(26): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564681 | ||||||
| chr9:124564681
|
C | CTGTGTGT others(21): Show |
2 | a0001c0002t0005g0228a0001c0002t0005g0229 | 2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.143-10139_143-1011 others(32): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564681 | ||||||
| chr9:124564681
|
CTG | C | 148 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(145): Show | 148 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.143-10113_143-1011 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564681 | ||||||
| chr9:124564742
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0002g0145 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.143-10172G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564742 | ||||||
| chr9:124564753
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-10183T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564753 | ||||||
| chr9:124564938
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-10368C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564938 | ||||||
| chr9:124564996
|
T | A | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.143-10426A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124564996 | ||||||
| chr9:124565071
|
T | C | 2 | a0001c0001t0047g0105a0001c0001t0062g0104 | 2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.143-10501A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565071 | ||||||
| chr9:124565146
|
A | C | 4 | a0001c0001t0008g0094a0001c0001t0008g0095a0001c0001t0008g0096others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-10576T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565146 | ||||||
| chr9:124565200
|
G | A | 43 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(40): Show | 43 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.143-10630C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565200 | ||||||
| chr9:124565291
|
G | T | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-10721C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565291 | ||||||
| chr9:124565298
|
G | A | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-10728C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565298 | ||||||
| chr9:124565458
|
TA | T | 79 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(76): Show | 79 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.143-10889delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565458 | ||||||
| chr9:124565484
|
A | G | 43 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(40): Show | 43 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.143-10914T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565484 | ||||||
| chr9:124565487
|
A | G | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.143-10917T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565487 | ||||||
| chr9:124565538
|
T | G | 2 | a0001c0001t0011g0205a0001c0001t0012g0207 | 2 | NA18977.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.143-10968A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565538 | ||||||
| chr9:124565541
|
AAAGGC | A | 10 | a0001c0001t0014g0069a0001c0001t0014g0071a0001c0001t0014g0072others(7): Show | 10 | HG01167.hp2 HG02647.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-10976_143-1097 others(9): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565541 | ||||||
| chr9:124565654
|
A | G | 1 | a0001c0001t0016g0075 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.143-11084T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565654 | ||||||
| chr9:124565668
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.143-11098G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565668 | ||||||
| chr9:124565674
|
T | C | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-11104A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565674 | ||||||
| chr9:124565929
|
A | G | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-11359T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124565929 | ||||||
| chr9:124566147
|
T | C | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-11577A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124566147 | ||||||
| chr9:124566174
|
A | T | 2 | a0001c0001t0001g0173a0001c0001t0009g0168 | 2 | NA18975.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.143-11604T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124566174 | ||||||
| chr9:124566366
|
C | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0002g0018others(4): Show | 7 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-11796G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124566366 | ||||||
| chr9:124566757
|
C | A | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-12187G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124566757 | ||||||
| chr9:124566852
|
T | C | 4 | a0001c0001t0008g0094a0001c0001t0008g0095a0001c0001t0008g0096others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-12282A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124566852 | ||||||
| chr9:124566875
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-12305T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124566875 | ||||||
| chr9:124566904
|
A | C | 2 | a0001c0001t0001g0152a0002c0006t0069g0234 | 2 | HG03017.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.143-12334T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124566904 | ||||||
| chr9:124566916
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.143-12346C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124566916 | ||||||
| chr9:124566924
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.143-12354G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124566924 | ||||||
| chr9:124566988
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.143-12418C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124566988 | ||||||
| chr9:124567040
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.143-12470C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567040 | ||||||
| chr9:124567107
|
C | CA | 12 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0143others(9): Show | 12 | HG00438.hp2 HG01106.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-12538dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567107 | ||||||
| chr9:124567115
|
A | T | 10 | a0001c0001t0007g0088a0001c0001t0007g0089a0001c0001t0007g0090others(7): Show | 10 | HG02258.hp2 HG02717.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.143-12545T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567115 | ||||||
| chr9:124567145
|
C | T | 80 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(77): Show | 80 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.143-12575G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567145 | ||||||
| chr9:124567448
|
C | T | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-12878G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567448 | ||||||
| chr9:124567584
|
A | G | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-13014T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567584 | ||||||
| chr9:124567593
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-13023A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567593 | ||||||
| chr9:124567663
|
T | C | 2 | a0001c0001t0002g0170a0001c0001t0002g0172 | 2 | NA18939.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.143-13093A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567663 | ||||||
| chr9:124567686
|
G | C | 1 | a0001c0001t0001g0106 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.143-13116C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567686 | ||||||
| chr9:124567831
|
C | CT | 17 | a0001c0001t0001g0065a0001c0001t0001g0106a0001c0001t0001g0152others(14): Show | 17 | HG01884.hp2 HG01978.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.143-13262dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567831 | ||||||
| chr9:124567831
|
CT | C | 6 | a0001c0001t0001g0009a0001c0001t0002g0062a0001c0001t0003g0110others(3): Show | 6 | HG01167.hp1 HG02451.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-13262delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567831 | ||||||
| chr9:124567831
|
CTTTTTT | C | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-13267_143-1326 others(10): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567831 | ||||||
| chr9:124567831
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0018g0028a0001c0001t0018g0030a0001c0001t0037g0032others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-13273_143-1326 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567831 | ||||||
| chr9:124567854
|
T | A | 8 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0143others(5): Show | 8 | HG01106.hp2 HG01361.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-13284A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567854 | ||||||
| chr9:124567863
|
C | G | 80 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(77): Show | 80 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.143-13293G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124567863 | ||||||
| chr9:124568007
|
C | T | 1 | a0001c0001t0028g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.143-13437G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568007 | ||||||
| chr9:124568169
|
C | CA | 20 | a0001c0001t0001g0063a0001c0001t0001g0139a0001c0001t0002g0109others(17): Show | 20 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.143-13600dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568169 | ||||||
| chr9:124568169
|
C | CAA | 44 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0036others(41): Show | 44 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.143-13601_143-1360 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568169 | ||||||
| chr9:124568169
|
C | CAAA | 21 | a0001c0001t0001g0017a0001c0001t0002g0011a0001c0001t0002g0051others(18): Show | 21 | HG00609.hp1 HG01361.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-13602_143-1360 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568169 | ||||||
| chr9:124568169
|
C | CAAAA | 8 | a0001c0001t0001g0106a0001c0001t0003g0050a0001c0001t0018g0028others(5): Show | 8 | HG02027.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-13603_143-1360 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568169 | ||||||
| chr9:124568169
|
CA | C | 44 | a0001c0001t0001g0136a0001c0001t0001g0160a0001c0001t0001g0161others(41): Show | 44 | HG00558.hp1 HG02056.hp1 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.143-13600delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568169 | ||||||
| chr9:124568169
|
CAA | C | 6 | a0001c0001t0002g0183a0001c0001t0016g0075a0001c0001t0016g0077others(3): Show | 6 | HG01884.hp1 HG02922.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-13601_143-1360 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568169 | ||||||
| chr9:124568195
|
A | AC | 2 | a0001c0001t0001g0118a0001c0001t0002g0145 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.143-13626_143-1362 others(5): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568195 | ||||||
| chr9:124568212
|
G | A | 17 | a0001c0001t0004g0193a0001c0001t0004g0195a0001c0001t0004g0197others(14): Show | 17 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.143-13642C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568212 | ||||||
| chr9:124568257
|
G | A | 68 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(65): Show | 68 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.143-13687C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568257 | ||||||
| chr9:124568415
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.143-13845C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568415 | ||||||
| chr9:124568442
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-13872G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568442 | ||||||
| chr9:124568446
|
GCACTCCA others(623): Show |
G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-14506_143-1387 others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568446 | ||||||
| chr9:124568482
|
C | CA | 14 | a0001c0001t0001g0063a0001c0001t0004g0195a0001c0001t0006g0191others(11): Show | 14 | HG00323.hp1 HG02015.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.143-13913dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568482 | ||||||
| chr9:124568885
|
G | A | 11 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(8): Show | 11 | HG02258.hp2 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.143-14315C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568885 | ||||||
| chr9:124568915
|
C | T | 6 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-14345G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124568915 | ||||||
| chr9:124569238
|
G | C | 1 | a0001c0001t0037g0032 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.143-14668C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124569238 | ||||||
| chr9:124569260
|
C | G | 1 | a0001c0001t0002g0185 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.143-14690G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124569260 | ||||||
| chr9:124569268
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-14698G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124569268 | ||||||
| chr9:124569351
|
T | C | 30 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(27): Show | 30 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.143-14781A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124569351 | ||||||
| chr9:124569690
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-15120G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124569690 | ||||||
| chr9:124569955
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-15385A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124569955 | ||||||
| chr9:124569965
|
T | C | 1 | a0001c0002t0010g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.143-15395A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124569965 | ||||||
| chr9:124570034
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-15464A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124570034 | ||||||
| chr9:124570108
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-15538A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124570108 | ||||||
| chr9:124570236
|
C | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-15666G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124570236 | ||||||
| chr9:124570267
|
CGTTTCAA | C | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-15704_143-1569 others(11): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124570267 | ||||||
| chr9:124570390
|
A | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-15820T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124570390 | ||||||
| chr9:124570611
|
T | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-16041A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124570611 | ||||||
| chr9:124570689
|
CT | C | 3 | a0001c0001t0002g0170a0001c0001t0002g0172a0001c0001t0003g0171 | 3 | NA18939.hp2 NA19004.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.143-16120delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124570689 | ||||||
| chr9:124570808
|
C | A | 163 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(160): Show | 163 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.143-16238G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124570808 | ||||||
| chr9:124571170
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.143-16600T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124571170 | ||||||
| chr9:124571319
|
G | A | 1 | a0001c0001t0021g0148 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.143-16749C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124571319 | ||||||
| chr9:124571360
|
G | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-16790C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124571360 | ||||||
| chr9:124571548
|
C | T | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-16978G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124571548 | ||||||
| chr9:124571761
|
G | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-17191C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124571761 | ||||||
| chr9:124571772
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-17202A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124571772 | ||||||
| chr9:124571989
|
C | G | 2 | a0001c0001t0001g0061a0001c0001t0009g0060 | 2 | NA18939.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.143-17419G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124571989 | ||||||
| chr9:124572109
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-17539G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124572109 | ||||||
| chr9:124572209
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0009g0060 | 3 | NA18939.hp1 NA18975.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.143-17639G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124572209 | ||||||
| chr9:124572308
|
C | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-17738G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124572308 | ||||||
| chr9:124572439
|
TAG | T | 18 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(15): Show | 18 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.143-17871_143-1787 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124572439 | ||||||
| chr9:124572530
|
T | C | 1 | a0001c0001t0002g0166 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.143-17960A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124572530 | ||||||
| chr9:124572747
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-18177C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124572747 | ||||||
| chr9:124573112
|
A | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-18542T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124573112 | ||||||
| chr9:124573166
|
T | A | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-18596A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124573166 | ||||||
| chr9:124573403
|
C | A | 1 | a0001c0001t0002g0137 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.143-18833G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124573403 | ||||||
| chr9:124573475
|
C | T | 99 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(96): Show | 99 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.143-18905G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124573475 | ||||||
| chr9:124573501
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.143-18931T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124573501 | ||||||
| chr9:124573616
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.143-19046A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124573616 | ||||||
| chr9:124574278
|
G | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-19708C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124574278 | ||||||
| chr9:124574289
|
T | C | 1 | a0001c0001t0038g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.143-19719A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124574289 | ||||||
| chr9:124574633
|
T | C | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-20063A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124574633 | ||||||
| chr9:124574634
|
G | A | 170 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(167): Show | 170 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.143-20064C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124574634 | ||||||
| chr9:124574837
|
T | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-20267A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124574837 | ||||||
| chr9:124574879
|
A | G | 8 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0106others(5): Show | 8 | HG00609.hp1 HG02027.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-20309T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124574879 | ||||||
| chr9:124575019
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0047others(1): Show | 4 | NA18954.hp1 NA18957.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-20449G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575019 | ||||||
| chr9:124575125
|
T | C | 1 | a0001c0001t0011g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.143-20555A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575125 | ||||||
| chr9:124575192
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.143-20622G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575192 | ||||||
| chr9:124575248
|
C | T | 24 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(21): Show | 24 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(21): Show |
intron_variant | MODIFIER | c.143-20678G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575248 | ||||||
| chr9:124575296
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-20726C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575296 | ||||||
| chr9:124575331
|
T | C | 21 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(18): Show | 21 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.143-20761A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575331 | ||||||
| chr9:124575372
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-20802C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575372 | ||||||
| chr9:124575589
|
A | T | 4 | a0001c0001t0019g0074a0001c0001t0020g0025a0001c0001t0020g0026others(1): Show | 4 | HG02559.hp1 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-21019T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575589 | ||||||
| chr9:124575634
|
G | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-21064C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575634 | ||||||
| chr9:124575649
|
C | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-21079G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575649 | ||||||
| chr9:124575721
|
TATCACAT others(11): Show |
T | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.143-21169_143-2115 others(22): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575721 | ||||||
| chr9:124575850
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-21280A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575850 | ||||||
| chr9:124575894
|
C | A | 135 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(132): Show | 135 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.143-21324G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575894 | ||||||
| chr9:124575983
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-21413G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575983 | ||||||
| chr9:124575984
|
G | A | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-21414C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124575984 | ||||||
| chr9:124576131
|
C | T | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-21561G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124576131 | ||||||
| chr9:124576357
|
G | A | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-21787C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124576357 | ||||||
| chr9:124576434
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-21864G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124576434 | ||||||
| chr9:124576797
|
G | T | 81 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(78): Show | 81 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.143-22227C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124576797 | ||||||
| chr9:124576840
|
C | T | 1 | a0001c0001t0063g0135 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.143-22270G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124576840 | ||||||
| chr9:124576884
|
C | T | 88 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(85): Show | 88 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.143-22314G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124576884 | ||||||
| chr9:124576959
|
G | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-22389C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124576959 | ||||||
| chr9:124577490
|
A | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-22920T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124577490 | ||||||
| chr9:124577611
|
T | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-23041A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124577611 | ||||||
| chr9:124577732
|
C | A | 1 | a0001c0001t0051g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.143-23162G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124577732 | ||||||
| chr9:124577787
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.143-23217T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124577787 | ||||||
| chr9:124577862
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-23292A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124577862 | ||||||
| chr9:124577866
|
T | C | 89 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(86): Show | 89 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.143-23296A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124577866 | ||||||
| chr9:124577978
|
A | T | 1 | a0001c0001t0021g0213 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.143-23408T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124577978 | ||||||
| chr9:124578076
|
C | T | 1 | a0001c0001t0002g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.143-23506G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124578076 | ||||||
| chr9:124578137
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-23567A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124578137 | ||||||
| chr9:124578609
|
A | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-24039T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124578609 | ||||||
| chr9:124578612
|
T | C | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-24042A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124578612 | ||||||
| chr9:124578831
|
C | T | 168 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(165): Show | 168 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.143-24261G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124578831 | ||||||
| chr9:124579091
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-24521C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124579091 | ||||||
| chr9:124579144
|
ATGGTGGC others(127): Show |
A | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-24708_143-2457 others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124579144 | ||||||
| chr9:124579633
|
G | A | 1 | a0001c0002t0005g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.143-25063C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124579633 | ||||||
| chr9:124579686
|
C | A | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-25116G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124579686 | ||||||
| chr9:124579711
|
T | A | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-25141A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124579711 | ||||||
| chr9:124579739
|
G | A | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-25169C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124579739 | ||||||
| chr9:124579901
|
T | C | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-25331A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124579901 | ||||||
| chr9:124579967
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-25397T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124579967 | ||||||
| chr9:124579999
|
A | G | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-25429T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124579999 | ||||||
| chr9:124580187
|
T | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-25617A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124580187 | ||||||
| chr9:124580375
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.143-25805C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124580375 | ||||||
| chr9:124580384
|
T | C | 1 | a0001c0001t0002g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.143-25814A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124580384 | ||||||
| chr9:124580511
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-25941T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124580511 | ||||||
| chr9:124580536
|
T | C | 127 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(124): Show | 127 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.143-25966A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124580536 | ||||||
| chr9:124580644
|
T | C | 1 | a0001c0001t0029g0003 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.143-26074A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124580644 | ||||||
| chr9:124580823
|
A | AAAT | 15 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(12): Show | 15 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.143-26256_143-2625 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124580823 | ||||||
| chr9:124580930
|
G | A | 88 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(85): Show | 88 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.143-26360C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124580930 | ||||||
| chr9:124581043
|
G | A | 2 | a0001c0001t0003g0048a0001c0001t0003g0050 | 2 | HG02027.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.143-26473C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124581043 | ||||||
| chr9:124581093
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-26523G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124581093 | ||||||
| chr9:124581233
|
T | C | 2 | a0001c0001t0006g0212a0001c0001t0068g0006 | 2 | HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.143-26663A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124581233 | ||||||
| chr9:124581245
|
C | T | 89 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(86): Show | 89 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.143-26675G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124581245 | ||||||
| chr9:124581251
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-26681A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124581251 | ||||||
| chr9:124581316
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0050g0024 | 2 | HG00558.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.143-26746G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124581316 | ||||||
| chr9:124581748
|
T | C | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-27178A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124581748 | ||||||
| chr9:124581779
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-27209C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124581779 | ||||||
| chr9:124581806
|
C | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-27236G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124581806 | ||||||
| chr9:124581806
|
C | T | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.143-27236G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124581806 | ||||||
| chr9:124581870
|
G | A | 5 | a0001c0001t0018g0028a0001c0001t0018g0030a0001c0001t0037g0032others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-27300C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124581870 | ||||||
| chr9:124582262
|
G | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-27692C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124582262 | ||||||
| chr9:124582579
|
T | TA | 7 | a0001c0001t0006g0212a0001c0001t0015g0127a0001c0001t0015g0155others(4): Show | 7 | HG02015.hp1 HG02723.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-28010dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124582579 | ||||||
| chr9:124582665
|
C | T | 81 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(78): Show | 81 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.143-28095G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124582665 | ||||||
| chr9:124582670
|
T | C | 14 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.143-28100A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124582670 | ||||||
| chr9:124582825
|
T | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-28255A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124582825 | ||||||
| chr9:124582968
|
T | TC | 24 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(21): Show | 24 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.143-28399dupG | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124582968 | ||||||
| chr9:124583159
|
C | A | 1 | a0001c0001t0002g0142 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.143-28589G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124583159 | ||||||
| chr9:124583230
|
A | C | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-28660T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124583230 | ||||||
| chr9:124583266
|
T | C | 2 | a0001c0001t0002g0049a0001c0001t0040g0029 | 2 | HG02809.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.143-28696A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124583266 | ||||||
| chr9:124583515
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.143-28945G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124583515 | ||||||
| chr9:124583846
|
A | G | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-29276T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124583846 | ||||||
| chr9:124583910
|
T | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-29340A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124583910 | ||||||
| chr9:124584002
|
T | C | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-29432A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584002 | ||||||
| chr9:124584086
|
T | C | 5 | a0001c0001t0018g0028a0001c0001t0018g0030a0001c0001t0037g0032others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-29516A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584086 | ||||||
| chr9:124584096
|
C | CT | 25 | a0001c0001t0001g0040a0001c0001t0001g0058a0001c0001t0001g0144others(22): Show | 25 | HG00423.hp1 HG00423.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.143-29527dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584096 | ||||||
| chr9:124584140
|
G | T | 1 | a0001c0001t0002g0051 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.143-29570C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584140 | ||||||
| chr9:124584200
|
C | T | 1 | a0001c0002t0005g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.143-29630G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584200 | ||||||
| chr9:124584208
|
A | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-29638T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584208 | ||||||
| chr9:124584299
|
G | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-29729C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584299 | ||||||
| chr9:124584302
|
T | TCAACACT others(164): Show |
1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-29733_143-2973 others(175): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584302 | ||||||
| chr9:124584303
|
T | C | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-29733A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584303 | ||||||
| chr9:124584327
|
G | A | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-29757C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584327 | ||||||
| chr9:124584356
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-29786G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584356 | ||||||
| chr9:124584408
|
T | C | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-29838A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584408 | ||||||
| chr9:124584436
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-29866C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584436 | ||||||
| chr9:124584817
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-30247G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124584817 | ||||||
| chr9:124585045
|
AGAAAGGC others(20): Show |
A | 1 | a0001c0001t0002g0011 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.143-30502_143-3047 others(31): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585045 | ||||||
| chr9:124585079
|
C | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-30509G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585079 | ||||||
| chr9:124585177
|
G | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-30607C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585177 | ||||||
| chr9:124585431
|
C | G | 1 | a0001c0001t0002g0137 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.143-30861G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585431 | ||||||
| chr9:124585543
|
CA | C | 111 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(108): Show | 111 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.143-30974delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585543 | ||||||
| chr9:124585543
|
CAA | C | 6 | a0001c0001t0024g0013a0001c0001t0025g0014a0001c0001t0025g0015others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-30975_143-3097 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585543 | ||||||
| chr9:124585556
|
A | AG | 3 | a0001c0002t0005g0229a0001c0002t0010g0224a0001c0002t0067g0221 | 3 | HG02145.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.143-30987_143-3098 others(5): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585556 | ||||||
| chr9:124585557
|
A | AG | 8 | a0001c0001t0001g0174a0001c0001t0002g0166a0001c0001t0002g0167others(5): Show | 8 | HG00423.hp2 HG02165.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-30988_143-3098 others(5): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585557 | ||||||
| chr9:124585557
|
A | AGG | 11 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0002g0162others(8): Show | 11 | HG02056.hp1 HG03831.hp2 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.143-30988_143-3098 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585557 | ||||||
| chr9:124585557
|
A | AGGG | 3 | a0001c0001t0001g0178a0001c0001t0002g0176a0001c0001t0002g0177 | 3 | HG02698.hp2 NA18994.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.143-30988_143-3098 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585557 | ||||||
| chr9:124585557
|
A | G | 9 | a0001c0001t0027g0001a0001c0002t0005g0226a0001c0002t0005g0227others(6): Show | 9 | HG02145.hp2 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-30987T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585557 | ||||||
| chr9:124585557
|
AAGG | A | 16 | a0001c0001t0004g0193a0001c0001t0004g0195a0001c0001t0004g0197others(13): Show | 16 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.143-30990_143-3098 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585557 | ||||||
| chr9:124585558
|
A | AG | 30 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0057others(27): Show | 30 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.143-30989dupC | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585558 | ||||||
| chr9:124585558
|
A | G | 43 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(40): Show | 43 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(40): Show |
intron_variant | MODIFIER | c.143-30988T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585558 | ||||||
| chr9:124585558
|
AG | A | 31 | a0001c0001t0002g0062a0001c0001t0004g0209a0001c0001t0007g0087others(28): Show | 31 | HG01167.hp2 HG02559.hp1 HG02559.hp2 others(28): Show |
intron_variant | MODIFIER | c.143-30989delC | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585558 | ||||||
| chr9:124585560
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-30990C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585560 | ||||||
| chr9:124585563
|
G | C | 13 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(10): Show | 13 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-30993C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585563 | ||||||
| chr9:124585700
|
A | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-31130T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585700 | ||||||
| chr9:124585976
|
A | C | 5 | a0001c0001t0002g0211a0001c0001t0002g0216a0001c0001t0003g0215others(2): Show | 5 | HG00609.hp2 NA18942.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-31406T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124585976 | ||||||
| chr9:124586075
|
A | G | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-31505T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124586075 | ||||||
| chr9:124586189
|
T | C | 1 | a0001c0001t0002g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.143-31619A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124586189 | ||||||
| chr9:124586445
|
A | AT | 14 | a0001c0001t0001g0061a0001c0001t0001g0118a0001c0001t0002g0080others(11): Show | 14 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.143-31876dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124586445 | ||||||
| chr9:124586554
|
T | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-31984A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124586554 | ||||||
| chr9:124586588
|
G | A | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-32018C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124586588 | ||||||
| chr9:124586602
|
T | C | 169 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(166): Show | 169 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.143-32032A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124586602 | ||||||
| chr9:124586915
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-32345A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124586915 | ||||||
| chr9:124586943
|
T | G | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.143-32373A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124586943 | ||||||
| chr9:124587155
|
T | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-32585A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124587155 | ||||||
| chr9:124587427
|
G | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-32857C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124587427 | ||||||
| chr9:124587428
|
A | G | 1 | a0001c0001t0064g0124 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.143-32858T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124587428 | ||||||
| chr9:124587493
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-32923G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124587493 | ||||||
| chr9:124587506
|
C | T | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.143-32936G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124587506 | ||||||
| chr9:124587533
|
G | T | 81 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(78): Show | 81 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.143-32963C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124587533 | ||||||
| chr9:124587790
|
T | C | 2 | a0001c0001t0008g0094a0001c0001t0008g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143-33220A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124587790 | ||||||
| chr9:124587795
|
A | G | 1 | a0001c0001t0002g0133 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.143-33225T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124587795 | ||||||
| chr9:124588028
|
C | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-33458G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588028 | ||||||
| chr9:124588029
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-33459G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588029 | ||||||
| chr9:124588037
|
C | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-33467G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588037 | ||||||
| chr9:124588353
|
A | G | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-33783T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588353 | ||||||
| chr9:124588367
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.143-33797C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588367 | ||||||
| chr9:124588399
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-33829G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588399 | ||||||
| chr9:124588498
|
C | G | 233 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(230): Show | 233 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.143-33928G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588498 | ||||||
| chr9:124588518
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.143-33948G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588518 | ||||||
| chr9:124588583
|
A | C | 7 | a0001c0001t0002g0211a0001c0001t0002g0216a0001c0001t0003g0215others(4): Show | 7 | HG00609.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-34013T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588583 | ||||||
| chr9:124588643
|
G | A | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-34073C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588643 | ||||||
| chr9:124588671
|
G | A | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-34101C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588671 | ||||||
| chr9:124588781
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-34211T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588781 | ||||||
| chr9:124588793
|
G | A | 2 | a0001c0001t0013g0190a0001c0001t0013g0196 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.143-34223C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588793 | ||||||
| chr9:124588919
|
CA | C | 33 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.143-34350delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588919 | ||||||
| chr9:124588934
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-34364C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588934 | ||||||
| chr9:124588934
|
G | GA | 3 | a0001c0001t0001g0079a0001c0001t0008g0086a0001c0001t0046g0008 | 3 | HG02258.hp2 HG02818.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.143-34365dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588934 | ||||||
| chr9:124588935
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-34365T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588935 | ||||||
| chr9:124588936
|
AAG | A | 49 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(46): Show | 49 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.143-34368_143-3436 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588936 | ||||||
| chr9:124588937
|
AG | A | 32 | a0001c0001t0002g0185a0001c0001t0004g0193a0001c0001t0004g0194others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.143-34368delC | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588937 | ||||||
| chr9:124588938
|
G | A | 89 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(86): Show | 89 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.143-34368C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588938 | ||||||
| chr9:124588955
|
A | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-34385T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124588955 | ||||||
| chr9:124589212
|
T | C | 180 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(177): Show | 180 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.143-34642A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124589212 | ||||||
| chr9:124589253
|
T | G | 1 | a0001c0001t0002g0021 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.143-34683A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124589253 | ||||||
| chr9:124589263
|
G | A | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-34693C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124589263 | ||||||
| chr9:124589303
|
G | A | 1 | a0001c0001t0003g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.143-34733C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124589303 | ||||||
| chr9:124589339
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.143-34769C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124589339 | ||||||
| chr9:124589403
|
A | G | 138 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(135): Show | 138 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.143-34833T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124589403 | ||||||
| chr9:124589440
|
C | T | 1 | a0001c0001t0064g0124 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.143-34870G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124589440 | ||||||
| chr9:124589447
|
AAAAC | A | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-34881_143-3487 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124589447 | ||||||
| chr9:124589551
|
A | G | 1 | a0001c0001t0064g0124 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.143-34981T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124589551 | ||||||
| chr9:124589674
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-35104T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124589674 | ||||||
| chr9:124589926
|
G | A | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-35356C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124589926 | ||||||
| chr9:124589991
|
A | G | 134 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(131): Show | 134 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.143-35421T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124589991 | ||||||
| chr9:124590026
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.143-35456G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590026 | ||||||
| chr9:124590041
|
G | A | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-35471C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590041 | ||||||
| chr9:124590061
|
C | CA | 66 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0116others(63): Show | 66 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.143-35492dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590061 | ||||||
| chr9:124590061
|
C | CAA | 21 | a0001c0001t0001g0120a0001c0001t0001g0160a0001c0001t0001g0161others(18): Show | 21 | HG00423.hp2 HG01981.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.143-35493_143-3549 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590061 | ||||||
| chr9:124590061
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0067g0221 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.143-35501_143-3549 others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590061 | ||||||
| chr9:124590061
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0027g0001a0001c0002t0010g0222a0001c0002t0010g0225 | 3 | HG02647.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.143-35502_143-3549 others(15): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590061 | ||||||
| chr9:124590061
|
C | CAAAAAAA others(7): Show |
2 | a0001c0002t0005g0228a0001c0002t0005g0229 | 2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.143-35505_143-3549 others(18): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590061 | ||||||
| chr9:124590061
|
C | CAAAAAAA others(9): Show |
2 | a0001c0002t0005g0226a0001c0002t0005g0230 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.143-35507_143-3549 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590061 | ||||||
| chr9:124590061
|
C | CAAAAAAA others(13): Show |
1 | a0001c0002t0005g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.143-35511_143-3549 others(24): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590061 | ||||||
| chr9:124590061
|
CA | C | 54 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(51): Show | 54 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.143-35492delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590061 | ||||||
| chr9:124590061
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0143 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.143-35503_143-3549 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590061 | ||||||
| chr9:124590061
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0058g0208 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.143-35504_143-3549 others(17): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590061 | ||||||
| chr9:124590061
|
CAAAAAAA others(7): Show |
C | 18 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(15): Show | 18 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.143-35505_143-3549 others(18): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590061 | ||||||
| chr9:124590061
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-35506_143-3549 others(19): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590061 | ||||||
| chr9:124590111
|
C | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-35541G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590111 | ||||||
| chr9:124590179
|
G | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-35609C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590179 | ||||||
| chr9:124590186
|
G | A | 1 | a0001c0001t0008g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.143-35616C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590186 | ||||||
| chr9:124590186
|
G | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-35616C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590186 | ||||||
| chr9:124590305
|
G | A | 1 | a0001c0002t0010g0222 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.143-35735C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590305 | ||||||
| chr9:124590346
|
T | TA | 12 | a0001c0001t0001g0118a0001c0001t0002g0145a0001c0001t0002g0149others(9): Show | 12 | HG00438.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.143-35777dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590346 | ||||||
| chr9:124590436
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.143-35866T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590436 | ||||||
| chr9:124590449
|
A | T | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-35879T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590449 | ||||||
| chr9:124590456
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.143-35886G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590456 | ||||||
| chr9:124590860
|
C | A | 1 | a0001c0001t0008g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.143-36290G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124590860 | ||||||
| chr9:124591308
|
C | A | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-36738G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124591308 | ||||||
| chr9:124591617
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.143-37047T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124591617 | ||||||
| chr9:124591629
|
C | A | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-37059G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124591629 | ||||||
| chr9:124591976
|
G | A | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-37406C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124591976 | ||||||
| chr9:124592257
|
CT | C | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-37688delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124592257 | ||||||
| chr9:124592400
|
G | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-37830C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124592400 | ||||||
| chr9:124592908
|
T | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-38338A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124592908 | ||||||
| chr9:124593190
|
T | G | 1 | a0001c0001t0001g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.143-38620A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124593190 | ||||||
| chr9:124593240
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0043g0107 | 2 | HG00609.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.143-38670T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124593240 | ||||||
| chr9:124593343
|
T | C | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-38773A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124593343 | ||||||
| chr9:124593499
|
C | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-38929G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124593499 | ||||||
| chr9:124593666
|
G | C | 2 | a0001c0001t0001g0144a0001c0001t0002g0142 | 2 | HG00621.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.143-39096C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124593666 | ||||||
| chr9:124593920
|
C | T | 1 | a0001c0001t0002g0162 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.143-39350G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124593920 | ||||||
| chr9:124594149
|
C | CT | 85 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(82): Show | 85 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.143-39580_143-3957 others(5): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124594149 | ||||||
| chr9:124594171
|
C | A | 80 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(77): Show | 80 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.143-39601G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124594171 | ||||||
| chr9:124594243
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.143-39673T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124594243 | ||||||
| chr9:124594610
|
G | T | 8 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0143others(5): Show | 8 | HG01106.hp2 HG01361.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-40040C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124594610 | ||||||
| chr9:124594697
|
G | C | 33 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(30): Show | 33 | HG00544.hp2 HG00639.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.143-40127C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124594697 | ||||||
| chr9:124594771
|
C | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-40201G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124594771 | ||||||
| chr9:124594814
|
G | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-40244C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124594814 | ||||||
| chr9:124595038
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.143-40468G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124595038 | ||||||
| chr9:124595085
|
C | T | 1 | a0001c0001t0064g0124 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.143-40515G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124595085 | ||||||
| chr9:124595099
|
T | C | 1 | a0001c0001t0003g0215 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.143-40529A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124595099 | ||||||
| chr9:124595279
|
G | A | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-40709C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124595279 | ||||||
| chr9:124595284
|
C | T | 18 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(15): Show | 18 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.143-40714G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124595284 | ||||||
| chr9:124595303
|
C | T | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-40733G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124595303 | ||||||
| chr9:124595313
|
G | T | 18 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(15): Show | 18 | HG02015.hp2 HG02027.hp1 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.143-40743C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124595313 | ||||||
| chr9:124595399
|
C | T | 125 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(122): Show | 125 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.143-40829G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124595399 | ||||||
| chr9:124595543
|
T | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-40973A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124595543 | ||||||
| chr9:124595794
|
T | C | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-41224A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124595794 | ||||||
| chr9:124595910
|
G | C | 1 | a0001c0001t0004g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.143-41340C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124595910 | ||||||
| chr9:124596193
|
G | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-41623C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124596193 | ||||||
| chr9:124596357
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-41787G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124596357 | ||||||
| chr9:124596378
|
A | T | 1 | a0001c0001t0002g0054 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.143-41808T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124596378 | ||||||
| chr9:124596530
|
T | C | 1 | a0001c0001t0021g0213 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.143-41960A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124596530 | ||||||
| chr9:124596671
|
T | C | 8 | a0001c0002t0005g0227a0001c0002t0005g0228a0001c0002t0005g0229others(5): Show | 8 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-42101A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124596671 | ||||||
| chr9:124596673
|
C | T | 1 | a0001c0001t0035g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.143-42103G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124596673 | ||||||
| chr9:124596730
|
C | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-42160G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124596730 | ||||||
| chr9:124596794
|
G | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.143-42224C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124596794 | ||||||
| chr9:124596888
|
C | G | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.143-42318G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124596888 | ||||||
| chr9:124596903
|
T | C | 14 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.143-42333A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124596903 | ||||||
| chr9:124596997
|
C | T | 1 | a0001c0001t0008g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.143-42427G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124596997 | ||||||
| chr9:124597048
|
G | C | 1 | a0001c0001t0019g0091 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.143-42478C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124597048 | ||||||
| chr9:124597127
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0002g0183 | 2 | HG02523.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.143-42557T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124597127 | ||||||
| chr9:124597336
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-42766C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124597336 | ||||||
| chr9:124597824
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0002g0169 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.143-43254T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124597824 | ||||||
| chr9:124597835
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.143-43265A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124597835 | ||||||
| chr9:124597861
|
G | C | 2 | a0001c0003t0048g0102a0001c0003t0055g0181 | 2 | HG00423.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.143-43291C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124597861 | ||||||
| chr9:124597996
|
C | T | 2 | a0001c0001t0013g0190a0001c0001t0013g0196 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.143-43426G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124597996 | ||||||
| chr9:124598148
|
C | A | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-43578G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124598148 | ||||||
| chr9:124598221
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-43651G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124598221 | ||||||
| chr9:124598576
|
C | A | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-44006G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124598576 | ||||||
| chr9:124598647
|
T | TA | 102 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0036others(99): Show | 102 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.143-44078dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124598647 | ||||||
| chr9:124598647
|
T | TAA | 15 | a0001c0001t0001g0022a0001c0001t0001g0058a0001c0001t0001g0085others(12): Show | 15 | HG00423.hp1 HG00609.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.143-44079_143-4407 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124598647 | ||||||
| chr9:124598647
|
T | TAAA | 18 | a0001c0001t0016g0075a0001c0001t0016g0078a0001c0001t0024g0012others(15): Show | 18 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.143-44080_143-4407 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124598647 | ||||||
| chr9:124598647
|
TA | T | 7 | a0001c0001t0001g0063a0001c0001t0001g0108a0001c0001t0001g0128others(4): Show | 7 | HG00323.hp1 HG00438.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-44078delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124598647 | ||||||
| chr9:124598858
|
T | C | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-44288A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124598858 | ||||||
| chr9:124598977
|
C | T | 1 | a0001c0001t0004g0195 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.143-44407G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124598977 | ||||||
| chr9:124598988
|
T | C | 1 | a0001c0002t0010g0222 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.143-44418A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124598988 | ||||||
| chr9:124599024
|
C | T | 1 | a0001c0001t0008g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.143-44454G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599024 | ||||||
| chr9:124599093
|
T | C | 1 | a0001c0001t0001g0017 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.143-44523A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599093 | ||||||
| chr9:124599112
|
T | G | 1 | a0001c0001t0002g0165 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.143-44542A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599112 | ||||||
| chr9:124599113
|
C | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-44543G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599113 | ||||||
| chr9:124599304
|
G | A | 1 | a0001c0001t0020g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.143-44734C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599304 | ||||||
| chr9:124599380
|
T | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-44810A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599380 | ||||||
| chr9:124599419
|
C | CA | 9 | a0001c0001t0001g0180a0001c0001t0002g0149a0001c0001t0006g0212others(6): Show | 9 | HG00438.hp2 HG02723.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-44850dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599419 | ||||||
| chr9:124599419
|
CA | C | 14 | a0001c0001t0002g0073a0001c0001t0003g0042a0001c0001t0015g0155others(11): Show | 14 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.143-44850delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599419 | ||||||
| chr9:124599425
|
A | G | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-44855T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599425 | ||||||
| chr9:124599478
|
C | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-44908G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599478 | ||||||
| chr9:124599643
|
C | T | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-45073G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599643 | ||||||
| chr9:124599836
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-45266A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599836 | ||||||
| chr9:124599958
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-45388C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599958 | ||||||
| chr9:124599968
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-45398C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124599968 | ||||||
| chr9:124600166
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-45596T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124600166 | ||||||
| chr9:124600431
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.143-45861C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124600431 | ||||||
| chr9:124600468
|
G | T | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.143-45898C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124600468 | ||||||
| chr9:124600523
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-45953G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124600523 | ||||||
| chr9:124600523
|
C | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-45953G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124600523 | ||||||
| chr9:124600662
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-46092T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124600662 | ||||||
| chr9:124600690
|
A | G | 2 | a0001c0001t0002g0034a0001c0001t0003g0035 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.143-46120T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124600690 | ||||||
| chr9:124600706
|
A | C | 5 | a0001c0001t0001g0120a0001c0001t0001g0219a0001c0001t0003g0056others(2): Show | 5 | HG00544.hp2 HG02165.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-46136T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124600706 | ||||||
| chr9:124600905
|
T | A | 1 | a0001c0001t0002g0176 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.143-46335A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124600905 | ||||||
| chr9:124600951
|
G | GAA | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-46383_143-4638 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124600951 | ||||||
| chr9:124600988
|
A | C | 1 | a0001c0001t0039g0092 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.143-46418T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124600988 | ||||||
| chr9:124601025
|
C | T | 2 | a0001c0001t0047g0105a0001c0001t0062g0104 | 2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.143-46455G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124601025 | ||||||
| chr9:124601168
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-46598A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124601168 | ||||||
| chr9:124601203
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.143-46633C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124601203 | ||||||
| chr9:124601254
|
C | T | 1 | a0001c0001t0008g0096 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.143-46684G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124601254 | ||||||
| chr9:124601583
|
C | CAA | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-47015_143-4701 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124601583 | ||||||
| chr9:124601583
|
CA | C | 104 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(101): Show | 104 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.143-47014delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124601583 | ||||||
| chr9:124601606
|
AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0002g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.143-47046_143-4703 others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124601606 | ||||||
| chr9:124601626
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.143-47056T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124601626 | ||||||
| chr9:124601666
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-47096C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124601666 | ||||||
| chr9:124601689
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.143-47119T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124601689 | ||||||
| chr9:124601702
|
C | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-47132G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124601702 | ||||||
| chr9:124601798
|
T | C | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-47228A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124601798 | ||||||
| chr9:124602236
|
T | C | 69 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(66): Show | 69 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.143-47666A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124602236 | ||||||
| chr9:124602376
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.143-47806G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124602376 | ||||||
| chr9:124602709
|
C | T | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-48139G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124602709 | ||||||
| chr9:124602768
|
T | C | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-48198A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124602768 | ||||||
| chr9:124602791
|
G | C | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-48221C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124602791 | ||||||
| chr9:124602856
|
T | C | 1 | a0001c0001t0039g0092 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.143-48286A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124602856 | ||||||
| chr9:124602927
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.143-48357C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124602927 | ||||||
| chr9:124603824
|
G | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-49254C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124603824 | ||||||
| chr9:124604030
|
G | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-49460C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124604030 | ||||||
| chr9:124604100
|
T | C | 1 | a0001c0001t0025g0015 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.143-49530A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124604100 | ||||||
| chr9:124604167
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0002g0142 | 2 | HG00621.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.143-49597A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124604167 | ||||||
| chr9:124604391
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-49821A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124604391 | ||||||
| chr9:124604538
|
G | A | 1 | a0001c0002t0010g0222 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.143-49968C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124604538 | ||||||
| chr9:124604571
|
C | T | 5 | a0001c0001t0018g0028a0001c0001t0018g0030a0001c0001t0037g0032others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-50001G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124604571 | ||||||
| chr9:124604589
|
G | A | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-50019C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124604589 | ||||||
| chr9:124604751
|
T | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-50181A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124604751 | ||||||
| chr9:124604754
|
C | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-50184G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124604754 | ||||||
| chr9:124604936
|
A | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-50366T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124604936 | ||||||
| chr9:124604981
|
ACACCGTG others(9): Show |
A | 1 | a0001c0001t0019g0091 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.143-50427_143-5041 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124604981 | ||||||
| chr9:124604998
|
A | T | 1 | a0001c0001t0019g0091 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.143-50428T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124604998 | ||||||
| chr9:124605020
|
C | T | 1 | a0001c0001t0040g0029 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.143-50450G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124605020 | ||||||
| chr9:124605202
|
C | T | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-50632G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124605202 | ||||||
| chr9:124605297
|
G | T | 2 | a0001c0001t0004g0193a0001c0001t0004g0194 | 2 | NA18969.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.143-50727C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124605297 | ||||||
| chr9:124605359
|
T | A | 4 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(1): Show | 4 | HG02723.hp1 NA18522.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-50789A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124605359 | ||||||
| chr9:124605537
|
G | A | 4 | a0001c0001t0008g0094a0001c0001t0008g0095a0001c0001t0028g0002others(1): Show | 4 | HG00639.hp1 HG01884.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-50967C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124605537 | ||||||
| chr9:124605542
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.143-50972T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124605542 | ||||||
| chr9:124605631
|
T | C | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-51061A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124605631 | ||||||
| chr9:124605781
|
C | T | 231 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(228): Show | 231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.143-51211G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124605781 | ||||||
| chr9:124605937
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-51367C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124605937 | ||||||
| chr9:124606340
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-51770A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124606340 | ||||||
| chr9:124606504
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-51934C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124606504 | ||||||
| chr9:124607000
|
T | C | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-52430A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607000 | ||||||
| chr9:124607015
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-52445T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607015 | ||||||
| chr9:124607200
|
G | A | 1 | a0001c0001t0002g0103 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.143-52630C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607200 | ||||||
| chr9:124607216
|
G | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-52646C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607216 | ||||||
| chr9:124607296
|
T | A | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-52726A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607296 | ||||||
| chr9:124607400
|
C | T | 170 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(167): Show | 170 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.143-52830G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607400 | ||||||
| chr9:124607412
|
G | A | 1 | a0001c0001t0028g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.143-52842C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607412 | ||||||
| chr9:124607422
|
G | T | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-52852C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607422 | ||||||
| chr9:124607430
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-52860G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607430 | ||||||
| chr9:124607566
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-52996A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607566 | ||||||
| chr9:124607777
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.143-53207C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607777 | ||||||
| chr9:124607852
|
C | T | 1 | a0001c0001t0058g0208 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.143-53282G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607852 | ||||||
| chr9:124607886
|
A | G | 1 | a0001c0001t0003g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.143-53316T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124607886 | ||||||
| chr9:124608028
|
C | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(84): Show | 87 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.143-53458G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124608028 | ||||||
| chr9:124608091
|
T | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-53521A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124608091 | ||||||
| chr9:124608301
|
A | G | 233 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(230): Show | 233 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.143-53731T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124608301 | ||||||
| chr9:124608550
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.143-53980C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124608550 | ||||||
| chr9:124608835
|
T | A | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-54265A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124608835 | ||||||
| chr9:124609056
|
T | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-54486A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124609056 | ||||||
| chr9:124609260
|
T | C | 1 | a0001c0001t0002g0185 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.143-54690A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124609260 | ||||||
| chr9:124609494
|
C | T | 1 | a0001c0001t0035g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.143-54924G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124609494 | ||||||
| chr9:124609591
|
G | C | 30 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(27): Show | 30 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.143-55021C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124609591 | ||||||
| chr9:124609927
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.143-55357A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124609927 | ||||||
| chr9:124610015
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-55445C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124610015 | ||||||
| chr9:124610135
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-55565T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124610135 | ||||||
| chr9:124610165
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.143-55595G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124610165 | ||||||
| chr9:124610187
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-55617C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124610187 | ||||||
| chr9:124610692
|
T | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-56122A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124610692 | ||||||
| chr9:124610784
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-56214A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124610784 | ||||||
| chr9:124610864
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0002g0018 | 2 | NA18983.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.143-56294C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124610864 | ||||||
| chr9:124610934
|
C | T | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-56364G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124610934 | ||||||
| chr9:124611173
|
C | CA | 15 | a0001c0001t0002g0109a0001c0001t0023g0043a0001c0001t0028g0002others(12): Show | 15 | HG00639.hp1 HG00642.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.143-56604dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611173 | ||||||
| chr9:124611184
|
C | A | 126 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(123): Show | 126 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.143-56614G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611184 | ||||||
| chr9:124611265
|
G | C | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.143-56695C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611265 | ||||||
| chr9:124611445
|
A | G | 2 | a0001c0001t0003g0048a0001c0001t0003g0050 | 2 | HG02027.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.143-56875T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611445 | ||||||
| chr9:124611553
|
T | C | 24 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(21): Show | 24 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.143-56983A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611553 | ||||||
| chr9:124611681
|
C | T | 1 | a0001c0001t0002g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.143-57111G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611681 | ||||||
| chr9:124611693
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-57123C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611693 | ||||||
| chr9:124611716
|
T | A | 91 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(88): Show | 91 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.143-57146A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611716 | ||||||
| chr9:124611749
|
T | TAG | 29 | a0001c0001t0001g0144a0001c0001t0001g0160a0001c0001t0001g0163others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.143-57181_143-5718 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611749 | ||||||
| chr9:124611749
|
T | TAGAG | 3 | a0001c0001t0001g0180a0001c0001t0009g0150a0001c0001t0023g0188 | 3 | HG02922.hp2 HG03834.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.143-57183_143-5718 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611749 | ||||||
| chr9:124611749
|
T | TAGAGAGA others(5): Show |
1 | a0001c0001t0001g0052 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.143-57191_143-5718 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611749 | ||||||
| chr9:124611751
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-57181C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611751 | ||||||
| chr9:124611774
|
A | AGAGAGAA others(1): Show |
41 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(38): Show | 41 | HG00544.hp2 HG01884.hp1 HG02015.hp2 others(38): Show |
intron_variant | MODIFIER | c.143-57205_143-5720 others(12): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(3): Show |
4 | a0001c0001t0006g0212a0001c0001t0027g0001a0001c0001t0065g0041others(1): Show | 4 | HG02257.hp2 HG02723.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-57214_143-5720 others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(15): Show |
1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-57205_143-5720 others(26): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(9): Show |
5 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0002g0055others(2): Show | 5 | HG00639.hp1 HG01106.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-57205_143-5720 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(13): Show |
36 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0036others(33): Show | 36 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.143-57205_143-5720 others(24): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(23): Show |
1 | a0001c0001t0014g0071 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.143-57205_143-5720 others(34): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(15): Show |
8 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0002g0049others(5): Show | 8 | HG00558.hp2 HG00609.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-57205_143-5720 others(26): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(17): Show |
8 | a0001c0001t0001g0053a0001c0001t0002g0033a0001c0001t0002g0080others(5): Show | 8 | HG00544.hp1 HG01433.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-57205_143-5720 others(28): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(19): Show |
10 | a0001c0001t0001g0019a0001c0001t0002g0018a0001c0001t0002g0073others(7): Show | 10 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.143-57205_143-5720 others(30): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(21): Show |
2 | a0001c0001t0039g0092a0001c0001t0061g0100 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.143-57205_143-5720 others(32): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(31): Show |
1 | a0001c0001t0017g0067 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.143-57205_143-5720 others(42): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(23): Show |
4 | a0001c0001t0020g0025a0001c0001t0020g0026a0001c0001t0034g0210others(1): Show | 4 | HG02559.hp1 HG03130.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-57205_143-5720 others(34): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(25): Show |
7 | a0001c0001t0001g0064a0001c0001t0007g0090a0001c0001t0008g0086others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-57205_143-5720 others(36): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(35): Show |
3 | a0001c0001t0014g0072a0001c0001t0017g0066a0001c0001t0045g0070 | 3 | HG02976.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.143-57205_143-5720 others(46): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(27): Show |
1 | a0001c0001t0060g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.143-57205_143-5720 others(38): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(37): Show |
2 | a0001c0001t0014g0069a0001c0001t0017g0068 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.143-57205_143-5720 others(48): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(29): Show |
1 | a0001c0001t0004g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.143-57205_143-5720 others(40): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(31): Show |
1 | a0001c0001t0008g0096 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.143-57205_143-5720 others(42): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(37): Show |
1 | a0001c0001t0008g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.143-57205_143-5720 others(48): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611774
|
A | AGAGAGAG others(39): Show |
1 | a0001c0001t0008g0094 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.143-57205_143-5720 others(50): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611774 | ||||||
| chr9:124611947
|
T | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-57377A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611947 | ||||||
| chr9:124611950
|
A | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-57380T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124611950 | ||||||
| chr9:124612054
|
A | G | 14 | a0001c0001t0027g0001a0001c0001t0028g0002a0001c0001t0029g0003others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.143-57484T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124612054 | ||||||
| chr9:124612080
|
G | C | 1 | a0001c0001t0002g0218 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.143-57510C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124612080 | ||||||
| chr9:124612152
|
T | C | 1 | a0001c0001t0015g0127 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.143-57582A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124612152 | ||||||
| chr9:124612192
|
G | C | 1 | a0001c0001t0004g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.143-57622C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124612192 | ||||||
| chr9:124612278
|
C | A | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-57708G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124612278 | ||||||
| chr9:124612586
|
T | C | 6 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-58016A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124612586 | ||||||
| chr9:124612751
|
C | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-58181G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124612751 | ||||||
| chr9:124612793
|
T | TTTTC | 28 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0106others(25): Show | 28 | HG00544.hp2 HG00609.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.143-58227_143-5822 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124612793 | ||||||
| chr9:124612793
|
T | TTTTCTTT others(1): Show |
23 | a0001c0001t0001g0161a0001c0001t0001g0174a0001c0001t0001g0178others(20): Show | 23 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-58231_143-5822 others(12): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124612793 | ||||||
| chr9:124612793
|
T | TTTTCTTT others(5): Show |
5 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0002g0176others(2): Show | 5 | HG02698.hp2 HG04228.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-58235_143-5822 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124612793 | ||||||
| chr9:124612793
|
T | TTTTCTTT others(9): Show |
1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-58239_143-5822 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124612793 | ||||||
| chr9:124612793
|
T | TTTTCTTT others(13): Show |
1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.143-58243_143-5822 others(24): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124612793 | ||||||
| chr9:124613077
|
C | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-58507G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124613077 | ||||||
| chr9:124613116
|
G | A | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-58546C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124613116 | ||||||
| chr9:124613135
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-58565T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124613135 | ||||||
| chr9:124613299
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-58729G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124613299 | ||||||
| chr9:124613718
|
C | T | 2 | a0001c0001t0003g0048a0001c0001t0003g0050 | 2 | HG02027.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.143-59148G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124613718 | ||||||
| chr9:124613878
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-59308G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124613878 | ||||||
| chr9:124614023
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-59453A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124614023 | ||||||
| chr9:124614181
|
G | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-59611C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124614181 | ||||||
| chr9:124614596
|
C | G | 12 | a0001c0001t0033g0097a0001c0002t0005g0226a0001c0002t0005g0227others(9): Show | 12 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-60026G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124614596 | ||||||
| chr9:124614869
|
A | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-60299T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124614869 | ||||||
| chr9:124614952
|
T | C | 27 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(24): Show | 27 | HG00544.hp2 HG00639.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.143-60382A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124614952 | ||||||
| chr9:124615161
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.143-60591G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124615161 | ||||||
| chr9:124615241
|
T | C | 1 | a0001c0001t0002g0051 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.143-60671A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124615241 | ||||||
| chr9:124615316
|
T | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.143-60746A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124615316 | ||||||
| chr9:124615369
|
G | A | 1 | a0001c0001t0002g0166 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.143-60799C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124615369 | ||||||
| chr9:124615501
|
T | A | 139 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(136): Show | 139 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.143-60931A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124615501 | ||||||
| chr9:124615884
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-61314G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124615884 | ||||||
| chr9:124616011
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-61441G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616011 | ||||||
| chr9:124616027
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-61457A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616027 | ||||||
| chr9:124616063
|
A | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-61493T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616063 | ||||||
| chr9:124616153
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-61583A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616153 | ||||||
| chr9:124616266
|
G | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-61696C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616266 | ||||||
| chr9:124616283
|
T | A | 3 | a0001c0001t0001g0023a0001c0001t0002g0051a0001c0001t0050g0024 | 3 | HG00558.hp2 NA18978.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.143-61713A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616283 | ||||||
| chr9:124616284
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0002g0051a0001c0001t0050g0024 | 3 | HG00558.hp2 NA18978.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.143-61714G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616284 | ||||||
| chr9:124616293
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0009g0060 | 3 | NA18939.hp1 NA18975.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.143-61723G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616293 | ||||||
| chr9:124616327
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-61757G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616327 | ||||||
| chr9:124616381
|
C | T | 1 | a0001c0001t0016g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.143-61811G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616381 | ||||||
| chr9:124616402
|
CA | C | 71 | a0001c0001t0001g0036a0001c0001t0001g0128a0001c0001t0001g0160others(68): Show | 71 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.143-61833delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616402 | ||||||
| chr9:124616402
|
CAA | C | 12 | a0001c0001t0002g0189a0001c0001t0033g0097a0001c0002t0005g0226others(9): Show | 12 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-61834_143-6183 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616402 | ||||||
| chr9:124616438
|
A | C | 1 | a0001c0001t0028g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.143-61868T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616438 | ||||||
| chr9:124616835
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-62265C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124616835 | ||||||
| chr9:124617085
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-62515C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124617085 | ||||||
| chr9:124617229
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-62659T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124617229 | ||||||
| chr9:124617480
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0002g0051a0001c0001t0050g0024 | 3 | HG00558.hp2 NA18978.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.143-62910G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124617480 | ||||||
| chr9:124617715
|
A | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-63145T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124617715 | ||||||
| chr9:124617721
|
C | T | 2 | a0001c0001t0008g0094a0001c0001t0008g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143-63151G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124617721 | ||||||
| chr9:124618019
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-63449G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124618019 | ||||||
| chr9:124618180
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-63610T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124618180 | ||||||
| chr9:124618895
|
G | A | 13 | a0001c0001t0014g0069a0001c0001t0014g0071a0001c0001t0014g0072others(10): Show | 13 | HG01167.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-64325C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124618895 | ||||||
| chr9:124618939
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.143-64369G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124618939 | ||||||
| chr9:124619197
|
G | A | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-64627C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124619197 | ||||||
| chr9:124619260
|
A | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-64690T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124619260 | ||||||
| chr9:124619273
|
A | T | 2 | a0001c0001t0046g0008a0001c0001t0060g0027 | 2 | HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.143-64703T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124619273 | ||||||
| chr9:124619303
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-64733C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124619303 | ||||||
| chr9:124619623
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0009g0060 | 3 | NA18939.hp1 NA18975.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.143-65053T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124619623 | ||||||
| chr9:124619711
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-65141A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124619711 | ||||||
| chr9:124619827
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-65257G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124619827 | ||||||
| chr9:124619850
|
C | A | 4 | a0001c0001t0001g0178a0001c0001t0002g0176a0001c0001t0002g0177others(1): Show | 4 | HG02698.hp2 HG03927.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-65280G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124619850 | ||||||
| chr9:124619859
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.143-65289G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124619859 | ||||||
| chr9:124620004
|
T | A | 1 | a0001c0001t0015g0127 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.143-65434A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124620004 | ||||||
| chr9:124620049
|
G | A | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-65479C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124620049 | ||||||
| chr9:124620407
|
T | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-65837A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124620407 | ||||||
| chr9:124620527
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-65957C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124620527 | ||||||
| chr9:124620528
|
G | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-65958C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124620528 | ||||||
| chr9:124620584
|
T | C | 1 | a0001c0001t0002g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.143-66014A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124620584 | ||||||
| chr9:124620763
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-66193G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124620763 | ||||||
| chr9:124620809
|
TA | T | 15 | a0001c0001t0006g0212a0001c0001t0008g0086a0001c0001t0024g0012others(12): Show | 15 | HG00639.hp1 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.143-66240delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124620809 | ||||||
| chr9:124620881
|
T | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-66311A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124620881 | ||||||
| chr9:124621225
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-66655T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124621225 | ||||||
| chr9:124621483
|
T | TAAAAAAA others(3): Show |
1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-66923_143-6691 others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124621483 | ||||||
| chr9:124621483
|
TA | T | 135 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(132): Show | 135 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.143-66914delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124621483 | ||||||
| chr9:124621736
|
A | G | 1 | a0001c0001t0058g0208 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.143-67166T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124621736 | ||||||
| chr9:124621752
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-67182A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124621752 | ||||||
| chr9:124621823
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-67253G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124621823 | ||||||
| chr9:124621935
|
C | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-67365G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124621935 | ||||||
| chr9:124621984
|
C | T | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-67414G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124621984 | ||||||
| chr9:124622122
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-67552C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124622122 | ||||||
| chr9:124622175
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.143-67605G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124622175 | ||||||
| chr9:124622418
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-67848A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124622418 | ||||||
| chr9:124622730
|
T | C | 1 | a0001c0001t0003g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.143-68160A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124622730 | ||||||
| chr9:124622866
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0002g0145 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.143-68296G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124622866 | ||||||
| chr9:124622970
|
A | G | 1 | a0001c0001t0011g0205 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.143-68400T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124622970 | ||||||
| chr9:124622991
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-68421C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124622991 | ||||||
| chr9:124623010
|
G | T | 1 | a0001c0001t0002g0054 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.143-68440C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124623010 | ||||||
| chr9:124623209
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-68639A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124623209 | ||||||
| chr9:124623330
|
T | C | 170 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(167): Show | 170 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.143-68760A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124623330 | ||||||
| chr9:124623361
|
A | ATTAT | 34 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0144others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.143-68795_143-6879 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124623361 | ||||||
| chr9:124623506
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-68936A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124623506 | ||||||
| chr9:124623526
|
AT | A | 88 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(85): Show | 88 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.143-68957delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124623526 | ||||||
| chr9:124623592
|
G | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-69022C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124623592 | ||||||
| chr9:124623764
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-69194C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124623764 | ||||||
| chr9:124623929
|
T | A | 1 | a0001c0001t0002g0021 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.143-69359A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124623929 | ||||||
| chr9:124623956
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-69386G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124623956 | ||||||
| chr9:124623992
|
G | T | 2 | a0001c0001t0026g0232a0001c0001t0026g0233 | 2 | HG00642.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.143-69422C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124623992 | ||||||
| chr9:124624198
|
A | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-69628T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124624198 | ||||||
| chr9:124624397
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.143-69827C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124624397 | ||||||
| chr9:124624566
|
G | A | 12 | a0001c0001t0033g0097a0001c0002t0005g0226a0001c0002t0005g0227others(9): Show | 12 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-69996C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124624566 | ||||||
| chr9:124624585
|
A | C | 14 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(11): Show | 14 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.143-70015T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124624585 | ||||||
| chr9:124624912
|
G | GT | 146 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(143): Show | 146 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.143-70343dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124624912 | ||||||
| chr9:124624912
|
G | GTT | 5 | a0001c0001t0001g0044a0001c0001t0002g0054a0001c0001t0008g0094others(2): Show | 5 | HG00609.hp1 HG02056.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-70344_143-7034 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124624912 | ||||||
| chr9:124624963
|
A | G | 1 | a0001c0001t0028g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.143-70393T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124624963 | ||||||
| chr9:124624979
|
G | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-70409C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124624979 | ||||||
| chr9:124625161
|
T | C | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-70591A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124625161 | ||||||
| chr9:124625196
|
C | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-70626G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124625196 | ||||||
| chr9:124625350
|
T | C | 1 | a0001c0001t0025g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.143-70780A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124625350 | ||||||
| chr9:124625530
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-70960G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124625530 | ||||||
| chr9:124625689
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-71119C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124625689 | ||||||
| chr9:124626120
|
G | A | 2 | a0001c0001t0013g0190a0001c0001t0013g0196 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.143-71550C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124626120 | ||||||
| chr9:124626379
|
T | G | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.143-71809A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124626379 | ||||||
| chr9:124626588
|
C | T | 10 | a0001c0001t0014g0069a0001c0001t0014g0071a0001c0001t0014g0072others(7): Show | 10 | HG01167.hp2 HG02647.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-72018G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124626588 | ||||||
| chr9:124626615
|
G | A | 14 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(11): Show | 14 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.143-72045C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124626615 | ||||||
| chr9:124626692
|
T | C | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-72122A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124626692 | ||||||
| chr9:124626820
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-72250C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124626820 | ||||||
| chr9:124626946
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-72376A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124626946 | ||||||
| chr9:124627161
|
G | A | 2 | a0001c0001t0013g0190a0001c0001t0013g0196 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.143-72591C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627161 | ||||||
| chr9:124627180
|
G | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-72610C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627180 | ||||||
| chr9:124627198
|
C | G | 231 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(228): Show | 231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.143-72628G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627198 | ||||||
| chr9:124627292
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-72722G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627292 | ||||||
| chr9:124627318
|
T | TA | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-72749dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627318 | ||||||
| chr9:124627882
|
C | CT | 5 | a0001c0001t0001g0120a0001c0001t0002g0131a0001c0001t0002g0158others(2): Show | 5 | HG01517.hp2 HG02055.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-73313dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627882 | ||||||
| chr9:124627882
|
C | CTT | 5 | a0001c0001t0001g0122a0001c0001t0002g0103a0001c0001t0002g0121others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-73314_143-7331 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627882 | ||||||
| chr9:124627882
|
CT | C | 34 | a0001c0001t0001g0123a0001c0001t0001g0161a0001c0001t0001g0163others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.143-73313delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627882 | ||||||
| chr9:124627882
|
CTT | C | 42 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0064others(39): Show | 42 | HG00544.hp2 HG01361.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.143-73314_143-7331 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627882 | ||||||
| chr9:124627882
|
CTTT | C | 70 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(67): Show | 70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.143-73315_143-7331 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627882 | ||||||
| chr9:124627882
|
CTTTTTTT others(2): Show |
C | 16 | a0001c0001t0004g0209a0001c0001t0006g0212a0001c0001t0016g0075others(13): Show | 16 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.143-73321_143-7331 others(13): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627882 | ||||||
| chr9:124627882
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-73322_143-7331 others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627882 | ||||||
| chr9:124627882
|
CTTTTTTT others(13): Show |
C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-73332_143-7331 others(24): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627882 | ||||||
| chr9:124627895
|
T | C | 20 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(17): Show | 20 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.143-73325A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627895 | ||||||
| chr9:124627910
|
T | C | 25 | a0001c0001t0002g0133a0001c0001t0004g0193a0001c0001t0004g0194others(22): Show | 25 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.143-73340A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627910 | ||||||
| chr9:124627951
|
A | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-73381T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627951 | ||||||
| chr9:124627974
|
C | T | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-73404G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627974 | ||||||
| chr9:124627985
|
G | C | 1 | a0001c0001t0021g0148 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.143-73415C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124627985 | ||||||
| chr9:124628041
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.143-73471C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124628041 | ||||||
| chr9:124628153
|
G | A | 1 | a0001c0001t0029g0003 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.143-73583C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124628153 | ||||||
| chr9:124628273
|
C | T | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-73703G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124628273 | ||||||
| chr9:124628474
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-73904C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124628474 | ||||||
| chr9:124628575
|
C | T | 29 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.143-74005G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124628575 | ||||||
| chr9:124628801
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-74231G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124628801 | ||||||
| chr9:124628865
|
T | G | 2 | a0001c0001t0033g0097a0002c0006t0069g0234 | 2 | HG03017.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.143-74295A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124628865 | ||||||
| chr9:124628880
|
G | A | 1 | a0001c0001t0037g0032 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.143-74310C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124628880 | ||||||
| chr9:124628895
|
G | C | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-74325C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124628895 | ||||||
| chr9:124628952
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-74382G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124628952 | ||||||
| chr9:124629127
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.143-74557C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124629127 | ||||||
| chr9:124629192
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-74622T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124629192 | ||||||
| chr9:124629210
|
C | T | 5 | a0001c0001t0008g0086a0001c0001t0008g0094a0001c0001t0008g0095others(2): Show | 5 | HG02258.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-74640G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124629210 | ||||||
| chr9:124629333
|
A | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-74763T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124629333 | ||||||
| chr9:124629409
|
TTTC | T | 85 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(82): Show | 85 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.143-74842_143-7484 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124629409 | ||||||
| chr9:124629487
|
T | C | 13 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(10): Show | 13 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-74917A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124629487 | ||||||
| chr9:124629616
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-75046C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124629616 | ||||||
| chr9:124630210
|
G | GT | 102 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(99): Show | 102 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.143-75641dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630210 | ||||||
| chr9:124630210
|
G | GTT | 15 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0065others(12): Show | 15 | HG01106.hp1 HG01978.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.143-75642_143-7564 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630210 | ||||||
| chr9:124630315
|
A | G | 1 | a0001c0001t0002g0046 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.143-75745T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630315 | ||||||
| chr9:124630445
|
C | T | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-75875G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630445 | ||||||
| chr9:124630503
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.143-75933A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630503 | ||||||
| chr9:124630543
|
G | A | 2 | a0001c0001t0013g0190a0001c0001t0013g0196 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.143-75973C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630543 | ||||||
| chr9:124630577
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-76007C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630577 | ||||||
| chr9:124630578
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-76008C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630578 | ||||||
| chr9:124630647
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0009g0168 | 2 | NA18975.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.143-76077G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630647 | ||||||
| chr9:124630670
|
C | CT | 80 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0022others(77): Show | 80 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.143-76101dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630670 | ||||||
| chr9:124630670
|
C | CTT | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0044others(12): Show | 15 | HG00621.hp2 HG01081.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.143-76102_143-7610 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630670 | ||||||
| chr9:124630670
|
C | CTTT | 5 | a0001c0001t0007g0088a0001c0001t0007g0089a0001c0001t0007g0090others(2): Show | 5 | HG02723.hp1 HG02896.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-76103_143-7610 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630670 | ||||||
| chr9:124630670
|
C | CTTTT | 29 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(26): Show | 29 | HG01884.hp1 HG02027.hp1 HG02083.hp1 others(26): Show |
intron_variant | MODIFIER | c.143-76104_143-7610 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630670 | ||||||
| chr9:124630670
|
C | CTTTTT | 7 | a0001c0001t0006g0202a0001c0001t0011g0200a0001c0001t0011g0205others(4): Show | 7 | HG00544.hp2 HG00639.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-76105_143-7610 others(9): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630670 | ||||||
| chr9:124630670
|
CT | C | 9 | a0001c0001t0002g0189a0001c0002t0005g0226a0001c0002t0005g0227others(6): Show | 9 | HG02451.hp1 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-76101delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630670 | ||||||
| chr9:124630709
|
G | A | 1 | a0001c0001t0025g0015 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.143-76139C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630709 | ||||||
| chr9:124630968
|
G | C | 4 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0015others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-76398C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124630968 | ||||||
| chr9:124631009
|
T | TAAGAATA others(3003): Show |
1 | a0001c0001t0021g0148 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.143-76440_143-7643 others(3014): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124631009 | ||||||
| chr9:124631161
|
C | T | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-76591G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124631161 | ||||||
| chr9:124631196
|
C | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-76626G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124631196 | ||||||
| chr9:124631657
|
T | C | 7 | a0001c0001t0014g0069a0001c0001t0014g0071a0001c0001t0014g0072others(4): Show | 7 | HG01167.hp2 HG02647.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-77087A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124631657 | ||||||
| chr9:124631664
|
T | C | 1 | a0001c0001t0031g0005 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.143-77094A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124631664 | ||||||
| chr9:124631669
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-77099G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124631669 | ||||||
| chr9:124631679
|
CA | C | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-77110delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124631679 | ||||||
| chr9:124631763
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.143-77193G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124631763 | ||||||
| chr9:124631857
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-77287G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124631857 | ||||||
| chr9:124631870
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-77300G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124631870 | ||||||
| chr9:124631871
|
G | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-77301C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124631871 | ||||||
| chr9:124632398
|
T | C | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-77828A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124632398 | ||||||
| chr9:124632559
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.143-77989A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124632559 | ||||||
| chr9:124632619
|
A | G | 25 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(22): Show | 25 | HG00544.hp2 HG00639.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.143-78049T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124632619 | ||||||
| chr9:124632624
|
T | A | 13 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(10): Show | 13 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-78054A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124632624 | ||||||
| chr9:124632955
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-78385A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124632955 | ||||||
| chr9:124633066
|
T | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-78496A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633066 | ||||||
| chr9:124633131
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.143-78561C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633131 | ||||||
| chr9:124633176
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-78606C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633176 | ||||||
| chr9:124633272
|
G | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-78702C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633272 | ||||||
| chr9:124633295
|
C | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-78725G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633295 | ||||||
| chr9:124633327
|
C | A | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-78757G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633327 | ||||||
| chr9:124633330
|
G | A | 1 | a0001c0001t0021g0148 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.143-78760C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633330 | ||||||
| chr9:124633335
|
G | T | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.143-78765C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633335 | ||||||
| chr9:124633340
|
T | C | 1 | a0001c0001t0003g0215 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.143-78770A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633340 | ||||||
| chr9:124633365
|
T | C | 2 | a0001c0001t0003g0048a0001c0001t0003g0050 | 2 | HG02027.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.143-78795A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633365 | ||||||
| chr9:124633382
|
G | A | 1 | a0001c0001t0025g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.143-78812C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633382 | ||||||
| chr9:124633402
|
C | CA | 7 | a0001c0001t0002g0138a0001c0001t0002g0162a0001c0001t0016g0075others(4): Show | 7 | HG01884.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-78833dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633402 | ||||||
| chr9:124633402
|
C | CAA | 33 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(30): Show | 33 | HG00438.hp1 HG02056.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.143-78834_143-7883 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633402 | ||||||
| chr9:124633402
|
C | CAAA | 7 | a0001c0001t0001g0164a0001c0001t0001g0173a0001c0001t0002g0170others(4): Show | 7 | HG00423.hp2 HG00558.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-78835_143-7883 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633402 | ||||||
| chr9:124633402
|
CA | C | 105 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0022others(102): Show | 105 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.143-78833delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633402 | ||||||
| chr9:124633402
|
CAA | C | 11 | a0001c0001t0001g0009a0001c0002t0005g0226a0001c0002t0005g0227others(8): Show | 11 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-78834_143-7883 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633402 | ||||||
| chr9:124633402
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-78844_143-7883 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633402 | ||||||
| chr9:124633427
|
T | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-78857A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633427 | ||||||
| chr9:124633428
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-78858A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633428 | ||||||
| chr9:124633588
|
C | T | 1 | a0001c0001t0060g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.143-79018G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633588 | ||||||
| chr9:124633644
|
T | C | 4 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(1): Show | 4 | HG02723.hp1 NA18522.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-79074A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633644 | ||||||
| chr9:124633720
|
T | C | 1 | a0001c0001t0038g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.143-79150A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633720 | ||||||
| chr9:124633744
|
T | C | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-79174A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633744 | ||||||
| chr9:124633842
|
G | T | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-79272C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124633842 | ||||||
| chr9:124634066
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-79496T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124634066 | ||||||
| chr9:124634095
|
G | T | 1 | a0001c0001t0002g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.143-79525C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124634095 | ||||||
| chr9:124634501
|
A | T | 3 | a0001c0001t0004g0197a0001c0001t0004g0199a0001c0001t0013g0198 | 3 | HG03516.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-79931T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124634501 | ||||||
| chr9:124634770
|
C | A | 1 | a0001c0001t0021g0213 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.143-80200G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124634770 | ||||||
| chr9:124634770
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-80200G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124634770 | ||||||
| chr9:124634852
|
C | A | 7 | a0001c0001t0006g0191a0001c0001t0006g0202a0001c0001t0006g0203others(4): Show | 7 | HG02015.hp2 HG02083.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-80282G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124634852 | ||||||
| chr9:124635113
|
T | C | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-80543A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124635113 | ||||||
| chr9:124635121
|
A | G | 169 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(166): Show | 169 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.143-80551T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124635121 | ||||||
| chr9:124635164
|
G | A | 81 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(78): Show | 81 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.143-80594C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124635164 | ||||||
| chr9:124635201
|
C | T | 2 | a0001c0002t0005g0226a0001c0002t0005g0230 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.143-80631G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124635201 | ||||||
| chr9:124635226
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.143-80656G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124635226 | ||||||
| chr9:124635290
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.143-80720C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124635290 | ||||||
| chr9:124635317
|
C | T | 1 | a0001c0001t0057g0192 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.143-80747G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124635317 | ||||||
| chr9:124635409
|
C | T | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-80839G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124635409 | ||||||
| chr9:124635500
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-80930G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124635500 | ||||||
| chr9:124635745
|
G | A | 12 | a0001c0001t0033g0097a0001c0002t0005g0226a0001c0002t0005g0227others(9): Show | 12 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-81175C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124635745 | ||||||
| chr9:124635775
|
T | C | 1 | a0001c0001t0002g0021 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.143-81205A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124635775 | ||||||
| chr9:124635862
|
A | T | 1 | a0001c0001t0002g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.143-81292T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124635862 | ||||||
| chr9:124636059
|
T | C | 3 | a0001c0001t0019g0074a0001c0001t0020g0025a0001c0001t0020g0026 | 3 | HG02559.hp1 HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.143-81489A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124636059 | ||||||
| chr9:124636283
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.143-81713A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124636283 | ||||||
| chr9:124636429
|
T | C | 1 | a0001c0001t0057g0192 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.143-81859A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124636429 | ||||||
| chr9:124636759
|
C | T | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-82189G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124636759 | ||||||
| chr9:124637008
|
A | G | 1 | a0001c0001t0002g0167 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.143-82438T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637008 | ||||||
| chr9:124637022
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-82452T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637022 | ||||||
| chr9:124637366
|
G | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-82796C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637366 | ||||||
| chr9:124637368
|
A | C | 2 | a0001c0001t0020g0025a0001c0001t0020g0026 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.143-82798T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637368 | ||||||
| chr9:124637534
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-82964C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637534 | ||||||
| chr9:124637655
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-83085A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637655 | ||||||
| chr9:124637715
|
A | G | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.143-83145T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637715 | ||||||
| chr9:124637757
|
T | C | 1 | a0001c0001t0061g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.143-83187A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637757 | ||||||
| chr9:124637789
|
G | A | 1 | a0001c0001t0022g0217 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.143-83219C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637789 | ||||||
| chr9:124637817
|
G | C | 1 | a0001c0001t0003g0215 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.143-83247C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637817 | ||||||
| chr9:124637871
|
G | A | 3 | a0001c0001t0001g0113a0001c0001t0009g0150a0002c0006t0069g0234 | 3 | HG03017.hp1 HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.143-83301C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637871 | ||||||
| chr9:124637892
|
C | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-83322G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637892 | ||||||
| chr9:124637892
|
C | CA | 48 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0047others(45): Show | 48 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.143-83323dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637892 | ||||||
| chr9:124637892
|
CA | C | 52 | a0001c0001t0001g0058a0001c0001t0001g0160a0001c0001t0001g0161others(49): Show | 52 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.143-83323delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637892 | ||||||
| chr9:124637892
|
CAAAAAAA others(2): Show |
C | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-83331_143-8332 others(13): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637892 | ||||||
| chr9:124637906
|
A | G | 1 | a0001c0001t0019g0091 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.143-83336T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637906 | ||||||
| chr9:124637907
|
A | AAAAAAAG others(12): Show |
1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-83338_143-8333 others(23): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637907 | ||||||
| chr9:124637907
|
A | G | 3 | a0001c0001t0003g0215a0001c0001t0028g0002a0001c0001t0029g0003 | 3 | HG00639.hp1 HG01884.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.143-83337T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637907 | ||||||
| chr9:124637909
|
A | G | 44 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(41): Show | 44 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.143-83339T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637909 | ||||||
| chr9:124637913
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-83343C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637913 | ||||||
| chr9:124637922
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-83352C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124637922 | ||||||
| chr9:124638108
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.143-83538C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124638108 | ||||||
| chr9:124638202
|
G | A | 5 | a0001c0001t0018g0028a0001c0001t0018g0030a0001c0001t0037g0032others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-83632C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124638202 | ||||||
| chr9:124638253
|
C | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-83683G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124638253 | ||||||
| chr9:124638263
|
TA | T | 24 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(21): Show | 24 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.143-83694delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124638263 | ||||||
| chr9:124638331
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0002g0037 | 2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.143-83761A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124638331 | ||||||
| chr9:124638475
|
G | C | 22 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(19): Show | 22 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.143-83905C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124638475 | ||||||
| chr9:124638485
|
G | T | 83 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(80): Show | 83 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.143-83915C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124638485 | ||||||
| chr9:124639147
|
C | T | 3 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195 | 3 | HG02027.hp1 NA18969.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.143-84577G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124639147 | ||||||
| chr9:124639533
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-84963G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124639533 | ||||||
| chr9:124639678
|
G | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-85108C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124639678 | ||||||
| chr9:124639695
|
TC | T | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-85126delG | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124639695 | ||||||
| chr9:124639869
|
G | T | 1 | a0001c0001t0002g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.143-85299C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124639869 | ||||||
| chr9:124639883
|
A | T | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-85313T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124639883 | ||||||
| chr9:124639909
|
A | G | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.143-85339T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124639909 | ||||||
| chr9:124639996
|
T | G | 9 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-85426A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124639996 | ||||||
| chr9:124640150
|
C | T | 1 | a0001c0001t0052g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.143-85580G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124640150 | ||||||
| chr9:124640384
|
C | T | 1 | a0001c0001t0003g0056 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.143-85814G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124640384 | ||||||
| chr9:124640714
|
T | C | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-86144A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124640714 | ||||||
| chr9:124640944
|
A | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-86374T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124640944 | ||||||
| chr9:124640990
|
T | C | 1 | a0001c0001t0016g0075 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.143-86420A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124640990 | ||||||
| chr9:124641022
|
A | G | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-86452T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124641022 | ||||||
| chr9:124641259
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.143-86689A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124641259 | ||||||
| chr9:124641272
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-86702A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124641272 | ||||||
| chr9:124641298
|
GCCGTGAG others(9): Show |
G | 1 | a0001c0001t0029g0003 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.143-86744_143-8672 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124641298 | ||||||
| chr9:124641307
|
C | A | 2 | a0001c0001t0002g0211a0001c0001t0032g0214 | 2 | NA18942.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.143-86737G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124641307 | ||||||
| chr9:124641359
|
C | CA | 15 | a0001c0001t0001g0022a0001c0001t0002g0103a0001c0001t0023g0188others(12): Show | 15 | HG02145.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.143-86790dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124641359 | ||||||
| chr9:124641372
|
A | G | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-86802T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124641372 | ||||||
| chr9:124641427
|
G | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-86857C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124641427 | ||||||
| chr9:124641561
|
A | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.143-86991T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124641561 | ||||||
| chr9:124641656
|
C | T | 90 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(87): Show | 90 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.143-87086G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124641656 | ||||||
| chr9:124641832
|
C | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-87262G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124641832 | ||||||
| chr9:124642006
|
C | T | 1 | a0001c0001t0002g0021 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.143-87436G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124642006 | ||||||
| chr9:124642055
|
T | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-87485A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124642055 | ||||||
| chr9:124642097
|
G | A | 22 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(19): Show | 22 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.143-87527C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124642097 | ||||||
| chr9:124642110
|
G | A | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-87540C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124642110 | ||||||
| chr9:124642111
|
C | T | 1 | a0001c0001t0002g0103 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.143-87541G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124642111 | ||||||
| chr9:124642126
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-87556C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124642126 | ||||||
| chr9:124642860
|
A | G | 1 | a0001c0001t0034g0210 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.143-88290T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124642860 | ||||||
| chr9:124643101
|
T | TG | 44 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0112others(41): Show | 44 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.143-88532dupC | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643101 | ||||||
| chr9:124643102
|
G | A | 2 | a0001c0001t0006g0191a0001c0001t0006g0202 | 2 | NA18955.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.143-88532C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643102 | ||||||
| chr9:124643102
|
G | T | 11 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(8): Show | 11 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-88532C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643102 | ||||||
| chr9:124643104
|
G | C | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-88534C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643104 | ||||||
| chr9:124643104
|
G | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-88534C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643104 | ||||||
| chr9:124643289
|
G | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143-88719C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643289 | ||||||
| chr9:124643353
|
C | T | 84 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.143-88783G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643353 | ||||||
| chr9:124643513
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-88943A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643513 | ||||||
| chr9:124643600
|
C | CA | 35 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(32): Show | 35 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.143-89031dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643600 | ||||||
| chr9:124643648
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-89078G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643648 | ||||||
| chr9:124643678
|
T | C | 4 | a0001c0001t0001g0178a0001c0001t0002g0176a0001c0001t0002g0177others(1): Show | 4 | HG02698.hp2 HG03927.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-89108A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643678 | ||||||
| chr9:124643692
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-89122C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643692 | ||||||
| chr9:124643760
|
C | CA | 9 | a0001c0001t0001g0057a0001c0001t0001g0129a0001c0001t0002g0172others(6): Show | 9 | HG01106.hp1 HG02056.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-89191dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643760 | ||||||
| chr9:124643770
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-89200T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643770 | ||||||
| chr9:124643775
|
AG | A | 39 | a0001c0001t0002g0021a0001c0001t0004g0193a0001c0001t0004g0194others(36): Show | 39 | HG00544.hp2 HG00639.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.143-89206delC | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643775 | ||||||
| chr9:124643776
|
G | A | 119 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.143-89206C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643776 | ||||||
| chr9:124643925
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.143-89355C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643925 | ||||||
| chr9:124643978
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+89330T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124643978 | ||||||
| chr9:124644048
|
G | A | 22 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(19): Show | 22 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.142+89260C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644048 | ||||||
| chr9:124644271
|
C | CTTCTTTT others(3): Show |
1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+89036_142+8903 others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644271 | ||||||
| chr9:124644271
|
C | CTTT | 14 | a0001c0001t0001g0132a0001c0001t0004g0209a0001c0001t0013g0196others(11): Show | 14 | HG01081.hp1 HG01167.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+89034_142+8903 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644271 | ||||||
| chr9:124644271
|
C | CTTTT | 155 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(152): Show | 155 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.142+89033_142+8903 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644271 | ||||||
| chr9:124644271
|
C | CTTTTT | 48 | a0001c0001t0001g0038a0001c0001t0001g0112a0001c0001t0001g0141others(45): Show | 48 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.142+89032_142+8903 others(9): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644271 | ||||||
| chr9:124644271
|
C | CTTTTTT | 6 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0185others(3): Show | 6 | HG00438.hp1 HG03225.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+89031_142+8903 others(10): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644271 | ||||||
| chr9:124644271
|
C | CTTTTTTT | 6 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+89030_142+8903 others(11): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644271 | ||||||
| chr9:124644303
|
C | T | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+89005G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644303 | ||||||
| chr9:124644309
|
A | G | 231 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(228): Show | 231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.142+88999T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644309 | ||||||
| chr9:124644352
|
A | G | 1 | a0001c0001t0002g0187 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.142+88956T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644352 | ||||||
| chr9:124644448
|
C | T | 3 | a0001c0002t0005g0227a0001c0002t0005g0228a0001c0002t0005g0229 | 3 | HG02451.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142+88860G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644448 | ||||||
| chr9:124644449
|
A | G | 3 | a0001c0002t0005g0227a0001c0002t0005g0228a0001c0002t0005g0229 | 3 | HG02451.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142+88859T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644449 | ||||||
| chr9:124644472
|
G | A | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+88836C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644472 | ||||||
| chr9:124644658
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.142+88650T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644658 | ||||||
| chr9:124644682
|
T | C | 56 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.142+88626A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644682 | ||||||
| chr9:124644809
|
A | C | 1 | a0001c0001t0029g0003 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.142+88499T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644809 | ||||||
| chr9:124644842
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+88466T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644842 | ||||||
| chr9:124644909
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0128 | 2 | HG03490.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.142+88399T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124644909 | ||||||
| chr9:124645148
|
A | G | 1 | a0001c0001t0002g0177 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.142+88160T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124645148 | ||||||
| chr9:124645500
|
A | G | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+87808T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124645500 | ||||||
| chr9:124645615
|
C | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(84): Show | 87 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.142+87693G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124645615 | ||||||
| chr9:124645780
|
C | T | 171 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(168): Show | 171 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.142+87528G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124645780 | ||||||
| chr9:124645825
|
C | A | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+87483G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124645825 | ||||||
| chr9:124645857
|
C | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+87451G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124645857 | ||||||
| chr9:124645905
|
T | C | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+87403A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124645905 | ||||||
| chr9:124645907
|
G | T | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+87401C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124645907 | ||||||
| chr9:124645931
|
G | A | 1 | a0001c0002t0005g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.142+87377C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124645931 | ||||||
| chr9:124646067
|
A | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+87241T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124646067 | ||||||
| chr9:124646114
|
A | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+87194T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124646114 | ||||||
| chr9:124646164
|
C | T | 1 | a0001c0001t0004g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142+87144G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124646164 | ||||||
| chr9:124646187
|
G | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+87121C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124646187 | ||||||
| chr9:124646595
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.142+86713A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124646595 | ||||||
| chr9:124646654
|
C | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+86654G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124646654 | ||||||
| chr9:124646715
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+86593G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124646715 | ||||||
| chr9:124646889
|
A | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+86419T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124646889 | ||||||
| chr9:124646991
|
C | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+86317G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124646991 | ||||||
| chr9:124647260
|
A | G | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+86048T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124647260 | ||||||
| chr9:124647284
|
T | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+86024A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124647284 | ||||||
| chr9:124647297
|
C | T | 2 | a0001c0001t0003g0048a0001c0001t0003g0050 | 2 | HG02027.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.142+86011G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124647297 | ||||||
| chr9:124647547
|
G | A | 1 | a0001c0001t0002g0011 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.142+85761C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124647547 | ||||||
| chr9:124647724
|
CA | C | 70 | a0001c0001t0001g0040a0001c0001t0001g0139a0001c0001t0001g0160others(67): Show | 70 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.142+85583delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124647724 | ||||||
| chr9:124647754
|
G | A | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+85554C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124647754 | ||||||
| chr9:124647759
|
G | A | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+85549C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124647759 | ||||||
| chr9:124647759
|
G | GA | 170 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(167): Show | 170 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.142+85548dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124647759 | ||||||
| chr9:124647841
|
A | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+85467T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124647841 | ||||||
| chr9:124647892
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+85416G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124647892 | ||||||
| chr9:124648046
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.142+85262T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124648046 | ||||||
| chr9:124648059
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+85249A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124648059 | ||||||
| chr9:124648236
|
C | A | 42 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0117others(39): Show | 42 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.142+85072G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124648236 | ||||||
| chr9:124648236
|
C | T | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+85072G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124648236 | ||||||
| chr9:124648315
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+84993A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124648315 | ||||||
| chr9:124648497
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+84811G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124648497 | ||||||
| chr9:124648673
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+84635T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124648673 | ||||||
| chr9:124648707
|
T | TA | 5 | a0001c0001t0001g0009a0001c0001t0001g0180a0001c0001t0028g0002others(2): Show | 5 | HG00639.hp1 HG01884.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+84600dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124648707 | ||||||
| chr9:124648720
|
G | A | 12 | a0001c0001t0033g0097a0001c0002t0005g0226a0001c0002t0005g0227others(9): Show | 12 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.142+84588C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124648720 | ||||||
| chr9:124648741
|
A | G | 1 | a0001c0001t0004g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142+84567T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124648741 | ||||||
| chr9:124648948
|
T | A | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+84360A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124648948 | ||||||
| chr9:124649105
|
A | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+84203T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649105 | ||||||
| chr9:124649124
|
C | T | 3 | a0001c0001t0014g0071a0001c0001t0014g0072a0001c0001t0045g0070 | 3 | HG01167.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.142+84184G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649124 | ||||||
| chr9:124649233
|
C | CA | 32 | a0001c0001t0001g0058a0001c0001t0001g0065a0001c0001t0001g0118others(29): Show | 32 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.142+84074dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649233 | ||||||
| chr9:124649233
|
C | CAA | 9 | a0001c0001t0002g0149a0001c0001t0004g0197a0001c0001t0004g0199others(6): Show | 9 | HG00438.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+84073_142+8407 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649233 | ||||||
| chr9:124649233
|
C | CAAAAA | 8 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(5): Show | 8 | HG02451.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.142+84070_142+8407 others(9): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649233 | ||||||
| chr9:124649233
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+84060_142+8407 others(19): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649233 | ||||||
| chr9:124649233
|
CA | C | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.142+84074delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649233 | ||||||
| chr9:124649268
|
G | A | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+84040C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649268 | ||||||
| chr9:124649273
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+84035T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649273 | ||||||
| chr9:124649298
|
T | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(84): Show | 87 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.142+84010A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649298 | ||||||
| chr9:124649328
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+83980A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649328 | ||||||
| chr9:124649349
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.142+83959A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649349 | ||||||
| chr9:124649404
|
T | C | 2 | a0001c0001t0037g0032a0001c0001t0041g0031 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.142+83904A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649404 | ||||||
| chr9:124649443
|
A | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+83865T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649443 | ||||||
| chr9:124649663
|
G | C | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+83645C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649663 | ||||||
| chr9:124649737
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+83571C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649737 | ||||||
| chr9:124649741
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+83567G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124649741 | ||||||
| chr9:124650024
|
T | C | 1 | a0001c0001t0029g0003 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.142+83284A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124650024 | ||||||
| chr9:124650332
|
C | T | 1 | a0001c0001t0034g0210 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.142+82976G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124650332 | ||||||
| chr9:124650362
|
T | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+82946A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124650362 | ||||||
| chr9:124650415
|
G | C | 1 | a0001c0001t0029g0003 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.142+82893C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124650415 | ||||||
| chr9:124650912
|
T | TC | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+82395dupG | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124650912 | ||||||
| chr9:124651063
|
T | C | 2 | a0001c0001t0006g0191a0001c0001t0006g0202 | 2 | NA18955.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.142+82245A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651063 | ||||||
| chr9:124651169
|
G | T | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+82139C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651169 | ||||||
| chr9:124651192
|
G | T | 1 | a0001c0001t0008g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.142+82116C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651192 | ||||||
| chr9:124651263
|
C | T | 84 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(81): Show | 84 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.142+82045G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651263 | ||||||
| chr9:124651272
|
T | C | 56 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.142+82036A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651272 | ||||||
| chr9:124651283
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+82025A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651283 | ||||||
| chr9:124651352
|
C | G | 3 | a0001c0001t0014g0069a0001c0001t0017g0066a0001c0001t0017g0068 | 3 | HG02647.hp1 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.142+81956G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651352 | ||||||
| chr9:124651492
|
A | T | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+81816T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651492 | ||||||
| chr9:124651576
|
G | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+81732C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651576 | ||||||
| chr9:124651664
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142+81644G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651664 | ||||||
| chr9:124651708
|
T | C | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.142+81600A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651708 | ||||||
| chr9:124651770
|
C | T | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+81538G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651770 | ||||||
| chr9:124651941
|
CTTGACAG others(9): Show |
C | 1 | a0001c0001t0009g0101 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.142+81351_142+8136 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651941 | ||||||
| chr9:124651951
|
A | C | 1 | a0001c0001t0057g0192 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.142+81357T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651951 | ||||||
| chr9:124651965
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+81343G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651965 | ||||||
| chr9:124651988
|
C | T | 11 | a0001c0001t0033g0097a0001c0002t0005g0226a0001c0002t0005g0227others(8): Show | 11 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+81320G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124651988 | ||||||
| chr9:124652176
|
G | A | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+81132C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124652176 | ||||||
| chr9:124652510
|
G | A | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+80798C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124652510 | ||||||
| chr9:124652535
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+80773G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124652535 | ||||||
| chr9:124652835
|
G | C | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+80473C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124652835 | ||||||
| chr9:124653082
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+80226T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124653082 | ||||||
| chr9:124653096
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+80212C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124653096 | ||||||
| chr9:124653274
|
C | CT | 9 | a0001c0001t0001g0163a0001c0001t0024g0012a0001c0001t0024g0013others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+80033dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124653274 | ||||||
| chr9:124653274
|
CT | C | 11 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(8): Show | 11 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+80033delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124653274 | ||||||
| chr9:124653383
|
T | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+79925A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124653383 | ||||||
| chr9:124653589
|
T | C | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+79719A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124653589 | ||||||
| chr9:124653765
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+79543T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124653765 | ||||||
| chr9:124654110
|
C | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+79198G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654110 | ||||||
| chr9:124654155
|
G | A | 2 | a0001c0001t0001g0141a0002c0006t0069g0234 | 2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.142+79153C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654155 | ||||||
| chr9:124654239
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+79069C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654239 | ||||||
| chr9:124654278
|
C | T | 3 | a0001c0001t0014g0069a0001c0001t0017g0066a0001c0001t0017g0068 | 3 | HG02647.hp1 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.142+79030G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654278 | ||||||
| chr9:124654330
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142+78978A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654330 | ||||||
| chr9:124654602
|
G | T | 1 | a0001c0001t0003g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.142+78706C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654602 | ||||||
| chr9:124654621
|
T | C | 82 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.142+78687A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654621 | ||||||
| chr9:124654724
|
T | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+78584A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654724 | ||||||
| chr9:124654727
|
T | C | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+78581A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654727 | ||||||
| chr9:124654872
|
T | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+78436A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654872 | ||||||
| chr9:124654872
|
T | TG | 2 | a0001c0001t0002g0142a0001c0001t0004g0209 | 2 | HG00621.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.142+78435_142+7843 others(5): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654872 | ||||||
| chr9:124654874
|
G | A | 3 | a0001c0001t0002g0142a0001c0001t0004g0209a0002c0006t0069g0234 | 3 | HG00621.hp1 HG02818.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.142+78434C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654874 | ||||||
| chr9:124654875
|
T | C | 3 | a0001c0001t0002g0142a0001c0001t0004g0209a0002c0006t0069g0234 | 3 | HG00621.hp1 HG02818.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.142+78433A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654875 | ||||||
| chr9:124654875
|
T | TAC | 75 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0112others(72): Show | 75 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.142+78431_142+7843 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654875 | ||||||
| chr9:124654875
|
T | TACAC | 22 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0174others(19): Show | 22 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.142+78429_142+7843 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654875 | ||||||
| chr9:124654875
|
T | TACACAC | 26 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0160others(23): Show | 26 | HG00609.hp1 HG01081.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.142+78427_142+7843 others(10): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654875 | ||||||
| chr9:124654875
|
T | TACACACA others(1): Show |
36 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0023others(33): Show | 36 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.142+78425_142+7843 others(12): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654875 | ||||||
| chr9:124654875
|
T | TACACACA others(3): Show |
26 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0064others(23): Show | 26 | HG00639.hp1 HG01106.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.142+78423_142+7843 others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654875 | ||||||
| chr9:124654875
|
T | TACACACA others(5): Show |
12 | a0001c0001t0001g0038a0001c0001t0001g0063a0001c0001t0001g0065others(9): Show | 12 | HG00323.hp1 HG01978.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.142+78421_142+7843 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654875 | ||||||
| chr9:124654875
|
T | TACACACA others(7): Show |
7 | a0001c0001t0001g0044a0001c0001t0002g0033a0001c0001t0002g0037others(4): Show | 7 | HG01433.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+78419_142+7843 others(18): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654875 | ||||||
| chr9:124654875
|
TAC | T | 5 | a0001c0001t0001g0117a0001c0001t0001g0130a0001c0001t0002g0131others(2): Show | 5 | HG01517.hp2 HG01981.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+78431_142+7843 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654875 | ||||||
| chr9:124654875
|
TACAC | T | 3 | a0001c0001t0001g0120a0001c0001t0001g0219a0001c0001t0002g0166 | 3 | HG02165.hp1 NA19005.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.142+78429_142+7843 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654875 | ||||||
| chr9:124654875
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+78423_142+7843 others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124654875 | ||||||
| chr9:124655280
|
C | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+78028G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124655280 | ||||||
| chr9:124655363
|
T | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+77945A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124655363 | ||||||
| chr9:124655659
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+77649A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124655659 | ||||||
| chr9:124655660
|
G | A | 1 | a0001c0001t0009g0101 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.142+77648C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124655660 | ||||||
| chr9:124655724
|
G | C | 101 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(98): Show | 101 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.142+77584C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124655724 | ||||||
| chr9:124655942
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.142+77366A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124655942 | ||||||
| chr9:124656002
|
T | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+77306A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124656002 | ||||||
| chr9:124656134
|
T | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+77174A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124656134 | ||||||
| chr9:124656194
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+77114G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124656194 | ||||||
| chr9:124656319
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+76989G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124656319 | ||||||
| chr9:124656427
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.142+76881C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124656427 | ||||||
| chr9:124656499
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.142+76809A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124656499 | ||||||
| chr9:124656588
|
T | G | 1 | a0001c0001t0002g0020 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.142+76720A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124656588 | ||||||
| chr9:124657089
|
G | GA | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.142+76218dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124657089 | ||||||
| chr9:124657203
|
CAA | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+76103_142+7610 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124657203 | ||||||
| chr9:124657251
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+76057T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124657251 | ||||||
| chr9:124657299
|
T | G | 2 | a0001c0001t0003g0048a0001c0001t0003g0050 | 2 | HG02027.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.142+76009A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124657299 | ||||||
| chr9:124657471
|
T | C | 2 | a0001c0001t0026g0232a0001c0001t0026g0233 | 2 | HG00642.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.142+75837A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124657471 | ||||||
| chr9:124657703
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+75605G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124657703 | ||||||
| chr9:124657748
|
C | CT | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+75559_142+7556 others(5): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124657748 | ||||||
| chr9:124657748
|
C | T | 3 | a0001c0002t0005g0227a0001c0002t0005g0228a0001c0002t0005g0229 | 3 | HG02451.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142+75560G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124657748 | ||||||
| chr9:124657750
|
C | G | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+75558G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124657750 | ||||||
| chr9:124657804
|
G | C | 1 | a0001c0001t0016g0077 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.142+75504C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124657804 | ||||||
| chr9:124657835
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+75473T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124657835 | ||||||
| chr9:124658471
|
G | A | 2 | a0001c0003t0048g0102a0001c0003t0055g0181 | 2 | HG00423.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.142+74837C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124658471 | ||||||
| chr9:124658930
|
T | A | 1 | a0001c0001t0022g0217 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.142+74378A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124658930 | ||||||
| chr9:124658966
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.142+74342G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124658966 | ||||||
| chr9:124659094
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+74214A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124659094 | ||||||
| chr9:124659134
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+74174A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124659134 | ||||||
| chr9:124659233
|
G | A | 1 | a0001c0001t0016g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142+74075C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124659233 | ||||||
| chr9:124659301
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+74007C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124659301 | ||||||
| chr9:124659472
|
C | T | 1 | a0004c0004t0036g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+73836G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124659472 | ||||||
| chr9:124659731
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+73577G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124659731 | ||||||
| chr9:124659900
|
C | G | 170 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(167): Show | 170 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.142+73408G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124659900 | ||||||
| chr9:124660047
|
A | T | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+73261T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660047 | ||||||
| chr9:124660212
|
T | C | 3 | a0001c0001t0014g0071a0001c0001t0014g0072a0001c0001t0045g0070 | 3 | HG01167.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.142+73096A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660212 | ||||||
| chr9:124660247
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0047others(1): Show | 4 | NA18954.hp1 NA18957.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+73061T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660247 | ||||||
| chr9:124660577
|
C | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+72731G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660577 | ||||||
| chr9:124660620
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+72688G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660620 | ||||||
| chr9:124660648
|
C | CA | 90 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(87): Show | 90 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.142+72659dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660648 | ||||||
| chr9:124660648
|
C | CAA | 62 | a0001c0001t0001g0023a0001c0001t0001g0038a0001c0001t0001g0045others(59): Show | 62 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.142+72658_142+7265 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660648 | ||||||
| chr9:124660648
|
C | CAAA | 11 | a0001c0001t0006g0212a0001c0001t0013g0198a0001c0001t0024g0012others(8): Show | 11 | HG00639.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+72657_142+7265 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660648 | ||||||
| chr9:124660713
|
T | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+72595A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660713 | ||||||
| chr9:124660778
|
C | T | 1 | a0001c0001t0028g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+72530G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660778 | ||||||
| chr9:124660832
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+72476A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660832 | ||||||
| chr9:124660834
|
A | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+72474T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660834 | ||||||
| chr9:124660842
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+72466G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660842 | ||||||
| chr9:124660923
|
C | G | 1 | a0001c0001t0004g0195 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.142+72385G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660923 | ||||||
| chr9:124660994
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+72314G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124660994 | ||||||
| chr9:124661065
|
A | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+72243T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124661065 | ||||||
| chr9:124661324
|
C | T | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+71984G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124661324 | ||||||
| chr9:124661325
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0002g0034a0001c0001t0003g0035 | 3 | HG01516.hp1 HG01517.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.142+71983C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124661325 | ||||||
| chr9:124661363
|
C | T | 6 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+71945G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124661363 | ||||||
| chr9:124661443
|
T | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+71865A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124661443 | ||||||
| chr9:124661582
|
A | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+71726T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124661582 | ||||||
| chr9:124661632
|
T | A | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+71676A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124661632 | ||||||
| chr9:124661726
|
A | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+71582T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124661726 | ||||||
| chr9:124661892
|
T | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+71416A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124661892 | ||||||
| chr9:124662135
|
G | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+71173C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124662135 | ||||||
| chr9:124662183
|
G | A | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+71125C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124662183 | ||||||
| chr9:124662371
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+70937C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124662371 | ||||||
| chr9:124662477
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+70831C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124662477 | ||||||
| chr9:124662491
|
A | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+70817T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124662491 | ||||||
| chr9:124662662
|
G | A | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+70646C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124662662 | ||||||
| chr9:124662914
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.142+70394C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124662914 | ||||||
| chr9:124663275
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+70033G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124663275 | ||||||
| chr9:124663327
|
T | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+69981A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124663327 | ||||||
| chr9:124663373
|
T | A | 1 | a0001c0001t0013g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.142+69935A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124663373 | ||||||
| chr9:124663377
|
T | A | 1 | a0001c0001t0013g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.142+69931A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124663377 | ||||||
| chr9:124663383
|
AAGAAACA others(2): Show |
A | 2 | a0001c0001t0001g0106a0001c0001t0043g0107 | 2 | HG00609.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.142+69916_142+6992 others(13): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124663383 | ||||||
| chr9:124663516
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+69792A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124663516 | ||||||
| chr9:124663517
|
C | A | 14 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+69791G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124663517 | ||||||
| chr9:124663696
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+69612A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124663696 | ||||||
| chr9:124663848
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+69460C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124663848 | ||||||
| chr9:124663876
|
A | G | 1 | a0001c0001t0002g0187 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.142+69432T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124663876 | ||||||
| chr9:124664440
|
T | A | 1 | a0001c0001t0031g0005 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.142+68868A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124664440 | ||||||
| chr9:124664583
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+68725G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124664583 | ||||||
| chr9:124664692
|
G | A | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+68616C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124664692 | ||||||
| chr9:124664739
|
T | C | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142+68569A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124664739 | ||||||
| chr9:124664750
|
A | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+68558T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124664750 | ||||||
| chr9:124664858
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+68450C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124664858 | ||||||
| chr9:124664871
|
A | G | 1 | a0001c0001t0019g0091 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.142+68437T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124664871 | ||||||
| chr9:124665008
|
T | TA | 29 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0113others(26): Show | 29 | HG00609.hp2 HG01361.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.142+68299_142+6830 others(5): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665008 | ||||||
| chr9:124665009
|
C | A | 202 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(199): Show | 202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.142+68299G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665009 | ||||||
| chr9:124665010
|
C | A | 29 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0113others(26): Show | 29 | HG00609.hp2 HG01361.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.142+68298G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665010 | ||||||
| chr9:124665010
|
CA | C | 26 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(23): Show | 26 | HG00438.hp1 HG00558.hp1 HG02165.hp2 others(23): Show |
intron_variant | MODIFIER | c.142+68297delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665010 | ||||||
| chr9:124665017
|
A | C | 2 | a0001c0001t0001g0045a0001c0001t0013g0198 | 2 | HG02735.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.142+68291T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665017 | ||||||
| chr9:124665111
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+68197A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665111 | ||||||
| chr9:124665155
|
C | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+68153G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665155 | ||||||
| chr9:124665395
|
A | C | 4 | a0001c0001t0008g0094a0001c0001t0008g0095a0001c0001t0008g0096others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+67913T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665395 | ||||||
| chr9:124665604
|
G | A | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+67704C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665604 | ||||||
| chr9:124665749
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+67559G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665749 | ||||||
| chr9:124665842
|
C | T | 1 | a0001c0001t0009g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.142+67466G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665842 | ||||||
| chr9:124665956
|
C | T | 86 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(83): Show | 86 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.142+67352G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665956 | ||||||
| chr9:124665983
|
T | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+67325A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124665983 | ||||||
| chr9:124666254
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+67054G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666254 | ||||||
| chr9:124666275
|
C | CT | 13 | a0001c0001t0001g0112a0001c0001t0001g0141a0001c0001t0002g0021others(10): Show | 13 | HG00609.hp2 HG01981.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.142+67032dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666275
|
C | CTTTT | 24 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0006g0202others(21): Show | 24 | HG00544.hp2 HG02015.hp2 HG02083.hp1 others(21): Show |
intron_variant | MODIFIER | c.142+67029_142+6703 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666275
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+67024_142+6703 others(13): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666275
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0062g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.142+67023_142+6703 others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666275
|
C | CTTTTTTT others(4): Show |
1 | a0004c0004t0036g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+67022_142+6703 others(15): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666275
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142+67020_142+6703 others(17): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666275
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0002g0218 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.142+67018_142+6703 others(19): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666275
|
C | CTTTTTTT others(9): Show |
5 | a0001c0001t0001g0163a0001c0001t0001g0174a0001c0001t0002g0170others(2): Show | 5 | HG00558.hp1 HG03239.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+67017_142+6703 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666275
|
C | CTTTTTTT others(10): Show |
18 | a0001c0001t0001g0161a0001c0001t0001g0173a0001c0001t0001g0178others(15): Show | 18 | HG00423.hp2 HG00438.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.142+67016_142+6703 others(21): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666275
|
C | CTTTTTTT others(11): Show |
7 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0002g0169others(4): Show | 7 | HG01884.hp1 HG02922.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+67015_142+6703 others(22): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666275
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0052g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.142+67014_142+6703 others(23): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666275
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0002g0187a0001c0001t0054g0076 | 2 | HG02056.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142+67013_142+6703 others(24): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666275
|
CT | C | 30 | a0001c0001t0001g0106a0001c0001t0007g0087a0001c0001t0007g0088others(27): Show | 30 | HG01167.hp2 HG02055.hp1 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.142+67032delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666275 | ||||||
| chr9:124666399
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.142+66909G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666399 | ||||||
| chr9:124666570
|
T | G | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+66738A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666570 | ||||||
| chr9:124666669
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+66639C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666669 | ||||||
| chr9:124666720
|
G | A | 8 | a0001c0002t0005g0227a0001c0002t0005g0228a0001c0002t0005g0229others(5): Show | 8 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+66588C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666720 | ||||||
| chr9:124666780
|
A | T | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+66528T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666780 | ||||||
| chr9:124666802
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+66506T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666802 | ||||||
| chr9:124666890
|
C | T | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+66418G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666890 | ||||||
| chr9:124666895
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0043g0107 | 2 | HG00609.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.142+66413C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666895 | ||||||
| chr9:124666989
|
T | G | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+66319A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124666989 | ||||||
| chr9:124667475
|
A | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+65833T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124667475 | ||||||
| chr9:124667637
|
T | C | 1 | a0001c0001t0003g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.142+65671A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124667637 | ||||||
| chr9:124667668
|
G | A | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+65640C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124667668 | ||||||
| chr9:124667727
|
T | C | 1 | a0001c0001t0002g0103 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.142+65581A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124667727 | ||||||
| chr9:124668200
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+65108C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124668200 | ||||||
| chr9:124668278
|
G | C | 41 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(38): Show | 41 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.142+65030C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124668278 | ||||||
| chr9:124668280
|
G | A | 1 | a0001c0001t0052g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.142+65028C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124668280 | ||||||
| chr9:124668311
|
T | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+64997A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124668311 | ||||||
| chr9:124668332
|
T | TGGCAGAA others(14): Show |
10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+64955_142+6497 others(25): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124668332 | ||||||
| chr9:124668630
|
G | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+64678C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124668630 | ||||||
| chr9:124668684
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+64624C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124668684 | ||||||
| chr9:124668733
|
T | C | 82 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.142+64575A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124668733 | ||||||
| chr9:124668813
|
T | C | 24 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(21): Show | 24 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.142+64495A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124668813 | ||||||
| chr9:124669177
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+64131A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124669177 | ||||||
| chr9:124669358
|
C | A | 2 | a0001c0001t0026g0232a0001c0001t0026g0233 | 2 | HG00642.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.142+63950G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124669358 | ||||||
| chr9:124669521
|
T | C | 1 | a0001c0001t0052g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.142+63787A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124669521 | ||||||
| chr9:124669785
|
T | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+63523A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124669785 | ||||||
| chr9:124669801
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.142+63507A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124669801 | ||||||
| chr9:124669886
|
C | T | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+63422G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124669886 | ||||||
| chr9:124669995
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+63313A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124669995 | ||||||
| chr9:124670059
|
T | C | 7 | a0001c0001t0006g0191a0001c0001t0006g0202a0001c0001t0006g0203others(4): Show | 7 | HG02015.hp2 HG02083.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+63249A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670059 | ||||||
| chr9:124670064
|
T | C | 3 | a0001c0001t0004g0197a0001c0001t0004g0199a0001c0001t0013g0198 | 3 | HG03516.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+63244A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670064 | ||||||
| chr9:124670172
|
G | A | 1 | a0001c0001t0035g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.142+63136C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670172 | ||||||
| chr9:124670216
|
C | CA | 5 | a0001c0001t0001g0112a0001c0001t0003g0171a0001c0001t0006g0212others(2): Show | 5 | HG03225.hp2 HG03831.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+63091dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670216 | ||||||
| chr9:124670216
|
CA | C | 35 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(32): Show | 35 | HG00544.hp2 HG01884.hp1 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.142+63091delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670216 | ||||||
| chr9:124670231
|
A | T | 1 | a0001c0001t0002g0133 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.142+63077T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670231 | ||||||
| chr9:124670346
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+62962C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670346 | ||||||
| chr9:124670466
|
G | C | 2 | a0001c0001t0047g0105a0001c0001t0062g0104 | 2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.142+62842C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670466 | ||||||
| chr9:124670519
|
A | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+62789T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670519 | ||||||
| chr9:124670520
|
T | TATATTAT others(104): Show |
1 | a0001c0002t0005g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.142+62787_142+6278 others(115): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670520 | ||||||
| chr9:124670520
|
T | TATATTAT others(104): Show |
9 | a0001c0002t0005g0227a0001c0002t0005g0228a0001c0002t0005g0229others(6): Show | 9 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+62787_142+6278 others(115): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670520 | ||||||
| chr9:124670522
|
C | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+62786G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670522 | ||||||
| chr9:124670524
|
G | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+62784C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670524 | ||||||
| chr9:124670526
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+62782G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670526 | ||||||
| chr9:124670602
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+62706C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670602 | ||||||
| chr9:124670906
|
G | A | 5 | a0001c0001t0002g0211a0001c0001t0002g0216a0001c0001t0003g0215others(2): Show | 5 | HG00609.hp2 NA18942.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+62402C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124670906 | ||||||
| chr9:124671044
|
A | G | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+62264T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124671044 | ||||||
| chr9:124671223
|
T | C | 1 | a0001c0001t0003g0215 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.142+62085A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124671223 | ||||||
| chr9:124672106
|
C | T | 3 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097 | 3 | HG00639.hp1 HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142+61202G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124672106 | ||||||
| chr9:124672148
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.142+61160G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124672148 | ||||||
| chr9:124672165
|
G | A | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+61143C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124672165 | ||||||
| chr9:124672273
|
A | T | 1 | a0001c0001t0061g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.142+61035T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124672273 | ||||||
| chr9:124672594
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+60714C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124672594 | ||||||
| chr9:124672614
|
C | CA | 10 | a0001c0001t0004g0209a0001c0001t0024g0012a0001c0001t0024g0013others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+60693dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124672614 | ||||||
| chr9:124672642
|
A | G | 1 | a0001c0001t0008g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.142+60666T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124672642 | ||||||
| chr9:124672828
|
G | A | 1 | a0001c0001t0009g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.142+60480C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124672828 | ||||||
| chr9:124672995
|
C | A | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+60313G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124672995 | ||||||
| chr9:124673207
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0009g0150 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.142+60101T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124673207 | ||||||
| chr9:124673303
|
A | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+60005T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124673303 | ||||||
| chr9:124673403
|
C | T | 8 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0143others(5): Show | 8 | HG01106.hp2 HG01361.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+59905G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124673403 | ||||||
| chr9:124673583
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+59725G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124673583 | ||||||
| chr9:124673630
|
C | T | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+59678G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124673630 | ||||||
| chr9:124673771
|
C | T | 5 | a0001c0001t0015g0127a0001c0001t0015g0155a0001c0001t0015g0156others(2): Show | 5 | HG02015.hp1 HG03017.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+59537G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124673771 | ||||||
| chr9:124673813
|
T | C | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+59495A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124673813 | ||||||
| chr9:124674312
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+58996T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124674312 | ||||||
| chr9:124674312
|
A | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+58996T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124674312 | ||||||
| chr9:124674376
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.142+58932T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124674376 | ||||||
| chr9:124674486
|
AAGTATCT others(5): Show |
A | 1 | a0001c0001t0001g0141 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142+58810_142+5882 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124674486 | ||||||
| chr9:124674647
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+58661T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124674647 | ||||||
| chr9:124674977
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0128 | 2 | HG03490.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.142+58331C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124674977 | ||||||
| chr9:124675127
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+58181A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675127 | ||||||
| chr9:124675318
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0128 | 2 | HG03490.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.142+57990A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675318 | ||||||
| chr9:124675347
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+57961G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675347 | ||||||
| chr9:124675555
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.142+57753G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675555 | ||||||
| chr9:124675598
|
A | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+57710T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675598 | ||||||
| chr9:124675694
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+57614A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675694 | ||||||
| chr9:124675712
|
T | C | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+57596A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675712 | ||||||
| chr9:124675738
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.142+57570A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675738 | ||||||
| chr9:124675785
|
A | G | 1 | a0001c0001t0002g0080 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.142+57523T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675785 | ||||||
| chr9:124675854
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+57454G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675854 | ||||||
| chr9:124675880
|
G | T | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.142+57428C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675880 | ||||||
| chr9:124675918
|
G | T | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+57390C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675918 | ||||||
| chr9:124675993
|
G | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+57315C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124675993 | ||||||
| chr9:124676015
|
C | T | 55 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(52): Show | 55 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.142+57293G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124676015 | ||||||
| chr9:124676036
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+57272C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124676036 | ||||||
| chr9:124676441
|
A | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0002g0169 | 3 | HG03490.hp1 HG03492.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.142+56867T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124676441 | ||||||
| chr9:124676446
|
A | C | 3 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097 | 3 | HG00639.hp1 HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142+56862T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124676446 | ||||||
| chr9:124676652
|
A | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0219 | 2 | HG02165.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.142+56656T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124676652 | ||||||
| chr9:124676921
|
T | C | 170 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(167): Show | 170 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.142+56387A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124676921 | ||||||
| chr9:124676984
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+56324T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124676984 | ||||||
| chr9:124676984
|
A | G | 1 | a0001c0003t0055g0181 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.142+56324T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124676984 | ||||||
| chr9:124677168
|
G | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+56140C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124677168 | ||||||
| chr9:124677287
|
C | G | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+56021G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124677287 | ||||||
| chr9:124677448
|
G | A | 1 | a0001c0001t0034g0210 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.142+55860C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124677448 | ||||||
| chr9:124677451
|
G | A | 1 | a0001c0001t0028g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+55857C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124677451 | ||||||
| chr9:124677544
|
T | C | 1 | a0001c0001t0002g0046 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.142+55764A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124677544 | ||||||
| chr9:124677670
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+55638T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124677670 | ||||||
| chr9:124677671
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+55637T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124677671 | ||||||
| chr9:124677770
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+55538G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124677770 | ||||||
| chr9:124677816
|
G | T | 1 | a0001c0001t0004g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142+55492C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124677816 | ||||||
| chr9:124677832
|
A | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+55476T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124677832 | ||||||
| chr9:124677835
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142+55473T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124677835 | ||||||
| chr9:124677952
|
C | G | 83 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.142+55356G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124677952 | ||||||
| chr9:124678331
|
T | G | 3 | a0001c0001t0019g0074a0001c0001t0020g0025a0001c0001t0020g0026 | 3 | HG02559.hp1 HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.142+54977A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124678331 | ||||||
| chr9:124678354
|
G | A | 6 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+54954C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124678354 | ||||||
| chr9:124678463
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+54845C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124678463 | ||||||
| chr9:124678486
|
G | C | 1 | a0001c0001t0039g0092 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142+54822C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124678486 | ||||||
| chr9:124678869
|
G | A | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+54439C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124678869 | ||||||
| chr9:124678881
|
A | T | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.142+54427T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124678881 | ||||||
| chr9:124678952
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.142+54356C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124678952 | ||||||
| chr9:124679000
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+54308C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124679000 | ||||||
| chr9:124679167
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.142+54141A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124679167 | ||||||
| chr9:124679198
|
G | A | 1 | a0001c0001t0018g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.142+54110C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124679198 | ||||||
| chr9:124679240
|
G | C | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142+54068C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124679240 | ||||||
| chr9:124679531
|
A | C | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+53777T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124679531 | ||||||
| chr9:124679550
|
T | C | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+53758A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124679550 | ||||||
| chr9:124679735
|
C | CA | 6 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0036others(3): Show | 6 | HG03017.hp2 NA18954.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+53572dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124679735 | ||||||
| chr9:124679789
|
T | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+53519A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124679789 | ||||||
| chr9:124679810
|
T | C | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+53498A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124679810 | ||||||
| chr9:124679902
|
GA | G | 13 | a0001c0001t0002g0187a0001c0001t0007g0087a0001c0001t0007g0088others(10): Show | 13 | HG02056.hp1 HG02258.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.142+53405delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124679902 | ||||||
| chr9:124680029
|
A | T | 7 | a0001c0001t0002g0162a0001c0001t0002g0185a0001c0001t0002g0186others(4): Show | 7 | HG00438.hp1 HG02056.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.142+53279T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680029 | ||||||
| chr9:124680034
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+53274A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680034 | ||||||
| chr9:124680057
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+53251G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680057 | ||||||
| chr9:124680082
|
G | GTGTA | 2 | a0001c0001t0037g0032a0001c0001t0041g0031 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.142+53222_142+5322 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680082 | ||||||
| chr9:124680090
|
A | ATG | 11 | a0001c0001t0001g0038a0001c0001t0001g0064a0001c0001t0001g0126others(8): Show | 11 | HG00639.hp1 HG01884.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+53216_142+5321 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680090 | ||||||
| chr9:124680090
|
ATG | A | 61 | a0001c0001t0001g0143a0001c0001t0001g0160a0001c0001t0001g0161others(58): Show | 61 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.142+53216_142+5321 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680090 | ||||||
| chr9:124680090
|
ATGTG | A | 12 | a0001c0001t0001g0036a0001c0001t0004g0197a0001c0001t0004g0199others(9): Show | 12 | HG01884.hp1 HG02818.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+53214_142+5321 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680090 | ||||||
| chr9:124680090
|
ATGTGTG | A | 25 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(22): Show | 25 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.142+53212_142+5321 others(10): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680090 | ||||||
| chr9:124680092
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+53216C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680092 | ||||||
| chr9:124680094
|
G | A | 44 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(41): Show | 44 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.142+53214C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680094 | ||||||
| chr9:124680096
|
G | A | 6 | a0001c0001t0004g0209a0001c0001t0016g0075a0001c0001t0016g0077others(3): Show | 6 | HG01884.hp1 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+53212C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680096 | ||||||
| chr9:124680098
|
G | A | 8 | a0001c0002t0005g0227a0001c0002t0005g0228a0001c0002t0005g0229others(5): Show | 8 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+53210C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680098 | ||||||
| chr9:124680100
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+53208C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680100 | ||||||
| chr9:124680102
|
G | A | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.142+53206C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680102 | ||||||
| chr9:124680121
|
T | TG | 2 | a0001c0001t0003g0042a0001c0001t0009g0101 | 2 | HG03927.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.142+53186_142+5318 others(5): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680121 | ||||||
| chr9:124680266
|
A | G | 1 | a0001c0002t0005g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.142+53042T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680266 | ||||||
| chr9:124680455
|
T | C | 2 | a0001c0001t0026g0232a0001c0001t0026g0233 | 2 | HG00642.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.142+52853A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680455 | ||||||
| chr9:124680469
|
T | G | 2 | a0001c0001t0006g0212a0001c0001t0068g0006 | 2 | HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.142+52839A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680469 | ||||||
| chr9:124680582
|
C | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+52726G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124680582 | ||||||
| chr9:124681096
|
A | G | 1 | a0001c0001t0022g0217 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.142+52212T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681096 | ||||||
| chr9:124681117
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.142+52191G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681117 | ||||||
| chr9:124681220
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.142+52088T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681220 | ||||||
| chr9:124681304
|
G | C | 34 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(31): Show | 34 | HG00544.hp2 HG00639.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.142+52004C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681304 | ||||||
| chr9:124681338
|
C | CT | 15 | a0001c0001t0001g0053a0001c0001t0002g0049a0001c0001t0002g0051others(12): Show | 15 | HG00438.hp2 HG00642.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.142+51969dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681338 | ||||||
| chr9:124681338
|
CT | C | 12 | a0001c0001t0001g0129a0001c0001t0002g0176a0001c0001t0016g0077others(9): Show | 12 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+51969delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681338 | ||||||
| chr9:124681387
|
G | A | 4 | a0001c0001t0008g0094a0001c0001t0008g0095a0001c0001t0008g0096others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+51921C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681387 | ||||||
| chr9:124681435
|
G | A | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+51873C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681435 | ||||||
| chr9:124681591
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.142+51717G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681591 | ||||||
| chr9:124681668
|
G | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+51640C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681668 | ||||||
| chr9:124681893
|
T | C | 1 | a0001c0001t0052g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.142+51415A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681893 | ||||||
| chr9:124681918
|
G | C | 1 | a0001c0001t0002g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.142+51390C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681918 | ||||||
| chr9:124681975
|
T | TTTTTG | 3 | a0001c0001t0001g0117a0001c0001t0002g0211a0001c0001t0032g0214 | 3 | HG02615.hp2 NA18942.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.142+51328_142+5133 others(9): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681975 | ||||||
| chr9:124681975
|
TTTTTG | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+51328_142+5133 others(9): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681975 | ||||||
| chr9:124681991
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+51317A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124681991 | ||||||
| chr9:124682033
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+51275A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124682033 | ||||||
| chr9:124682099
|
A | T | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.142+51209T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124682099 | ||||||
| chr9:124682140
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.142+51168C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124682140 | ||||||
| chr9:124682156
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+51152T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124682156 | ||||||
| chr9:124682263
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+51045C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124682263 | ||||||
| chr9:124682291
|
C | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+51017G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124682291 | ||||||
| chr9:124682600
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+50708G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124682600 | ||||||
| chr9:124682714
|
G | C | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+50594C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124682714 | ||||||
| chr9:124682933
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+50375G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124682933 | ||||||
| chr9:124682934
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+50374T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124682934 | ||||||
| chr9:124682936
|
T | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+50372A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124682936 | ||||||
| chr9:124683025
|
A | C | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.142+50283T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683025 | ||||||
| chr9:124683124
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+50184G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683124 | ||||||
| chr9:124683207
|
A | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+50101T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683207 | ||||||
| chr9:124683216
|
A | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+50092T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683216 | ||||||
| chr9:124683235
|
G | GGGAAAA | 16 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0053others(13): Show | 16 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.142+50067_142+5007 others(10): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683235 | ||||||
| chr9:124683235
|
G | GGGAAAAG others(5): Show |
4 | a0001c0001t0001g0120a0001c0001t0001g0130a0001c0001t0001g0219others(1): Show | 4 | HG01517.hp2 HG02165.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+50061_142+5007 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683235 | ||||||
| chr9:124683235
|
GGGAAAA | G | 46 | a0001c0001t0001g0040a0001c0001t0001g0079a0001c0001t0001g0117others(43): Show | 46 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.142+50067_142+5007 others(10): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683235 | ||||||
| chr9:124683235
|
GGGAAAAG others(5): Show |
G | 33 | a0001c0001t0001g0112a0001c0001t0002g0046a0001c0001t0004g0193others(30): Show | 33 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.142+50061_142+5007 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683235 | ||||||
| chr9:124683247
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+50061T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683247 | ||||||
| chr9:124683405
|
T | A | 2 | a0001c0001t0001g0118a0001c0001t0002g0145 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.142+49903A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683405 | ||||||
| chr9:124683412
|
A | C | 1 | a0001c0001t0018g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.142+49896T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683412 | ||||||
| chr9:124683546
|
C | A | 6 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+49762G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683546 | ||||||
| chr9:124683583
|
C | T | 55 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(52): Show | 55 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.142+49725G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683583 | ||||||
| chr9:124683782
|
A | G | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+49526T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683782 | ||||||
| chr9:124683827
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+49481G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683827 | ||||||
| chr9:124683949
|
G | A | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+49359C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124683949 | ||||||
| chr9:124684009
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+49299G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124684009 | ||||||
| chr9:124684017
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+49291G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124684017 | ||||||
| chr9:124684078
|
C | T | 2 | a0001c0001t0040g0029a0001c0001t0049g0231 | 2 | HG02257.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.142+49230G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124684078 | ||||||
| chr9:124684128
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.142+49180T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124684128 | ||||||
| chr9:124684471
|
C | T | 2 | a0001c0001t0026g0232a0001c0001t0026g0233 | 2 | HG00642.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.142+48837G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124684471 | ||||||
| chr9:124684606
|
T | C | 84 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(81): Show | 84 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.142+48702A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124684606 | ||||||
| chr9:124684608
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.142+48700G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124684608 | ||||||
| chr9:124684990
|
C | CA | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.142+48317dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124684990 | ||||||
| chr9:124685227
|
T | C | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+48081A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124685227 | ||||||
| chr9:124685394
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+47914C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124685394 | ||||||
| chr9:124685394
|
G | T | 3 | a0001c0001t0001g0038a0001c0001t0002g0037a0001c0001t0002g0055 | 3 | HG03831.hp1 HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.142+47914C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124685394 | ||||||
| chr9:124685453
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+47855A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124685453 | ||||||
| chr9:124685489
|
G | A | 4 | a0001c0001t0008g0094a0001c0001t0008g0095a0001c0001t0008g0096others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+47819C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124685489 | ||||||
| chr9:124685855
|
A | G | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+47453T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124685855 | ||||||
| chr9:124686359
|
A | C | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+46949T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124686359 | ||||||
| chr9:124686704
|
C | CT | 9 | a0001c0001t0001g0130a0001c0001t0002g0055a0001c0001t0002g0158others(6): Show | 9 | HG02602.hp1 HG02735.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.142+46603dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124686704 | ||||||
| chr9:124686704
|
CT | C | 12 | a0001c0001t0030g0004a0001c0001t0031g0005a0001c0001t0049g0231others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+46603delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124686704 | ||||||
| chr9:124686751
|
T | A | 2 | a0001c0001t0001g0117a0001c0001t0002g0153 | 2 | HG01981.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.142+46557A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124686751 | ||||||
| chr9:124686855
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.142+46453G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124686855 | ||||||
| chr9:124686877
|
A | AT | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+46430dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124686877 | ||||||
| chr9:124686906
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.142+46402C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124686906 | ||||||
| chr9:124686965
|
A | G | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.142+46343T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124686965 | ||||||
| chr9:124687007
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+46301T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687007 | ||||||
| chr9:124687284
|
C | CTAATTAA others(5): Show |
4 | a0001c0001t0008g0094a0001c0001t0008g0095a0001c0001t0008g0096others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+46023_142+4602 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687284 | ||||||
| chr9:124687284
|
C | CTAATTAA others(9): Show |
2 | a0001c0001t0020g0025a0001c0001t0020g0026 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.142+46023_142+4602 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687284 | ||||||
| chr9:124687287
|
A | ATTATTTA others(5): Show |
1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+46020_142+4602 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687287 | ||||||
| chr9:124687287
|
A | ATTATTTA others(9): Show |
3 | a0001c0001t0027g0001a0001c0001t0029g0003a0001c0001t0033g0097 | 3 | HG00639.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.142+46020_142+4602 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687287 | ||||||
| chr9:124687287
|
A | ATTATTTA others(13): Show |
4 | a0001c0001t0016g0077a0001c0001t0016g0078a0001c0001t0028g0002others(1): Show | 4 | HG01884.hp2 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+46020_142+4602 others(24): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687287 | ||||||
| chr9:124687287
|
A | ATTATTTA others(17): Show |
6 | a0001c0001t0016g0075a0001c0002t0005g0226a0001c0002t0005g0229others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+46020_142+4602 others(28): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687287 | ||||||
| chr9:124687287
|
A | ATTATTTA others(21): Show |
5 | a0001c0002t0005g0227a0001c0002t0005g0228a0001c0002t0005g0230others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+46020_142+4602 others(32): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687287 | ||||||
| chr9:124687291
|
A | ATTAATTA others(9): Show |
9 | a0001c0001t0014g0069a0001c0001t0014g0071a0001c0001t0014g0072others(6): Show | 9 | HG01167.hp2 HG02615.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.142+46016_142+4601 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTAATTA others(13): Show |
2 | a0001c0001t0006g0203a0001c0001t0011g0200 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.142+46016_142+4601 others(24): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTAATTA others(17): Show |
1 | a0001c0001t0057g0192 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.142+46016_142+4601 others(28): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTAATTA others(5): Show |
6 | a0001c0001t0001g0019a0001c0001t0001g0085a0001c0001t0002g0020others(3): Show | 6 | HG00621.hp2 HG01361.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+46016_142+4601 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTAATTA others(9): Show |
8 | a0001c0001t0006g0191a0001c0001t0007g0087a0001c0001t0007g0088others(5): Show | 8 | HG02723.hp1 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.142+46016_142+4601 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTAATTA others(13): Show |
7 | a0001c0001t0006g0202a0001c0001t0008g0086a0001c0001t0011g0201others(4): Show | 7 | HG02155.hp1 HG02258.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+46016_142+4601 others(24): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTAATTA others(17): Show |
1 | a0001c0001t0004g0195 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.142+46016_142+4601 others(28): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTAATTA others(1): Show |
2 | a0001c0001t0001g0036a0001c0001t0001g0040 | 2 | HG01081.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.142+46016_142+4601 others(12): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTAATTA others(5): Show |
41 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0022others(38): Show | 41 | HG00558.hp2 HG00609.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.142+46016_142+4601 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTAATTA others(9): Show |
11 | a0001c0001t0002g0073a0001c0001t0003g0098a0001c0001t0004g0194others(8): Show | 11 | HG00544.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.142+46016_142+4601 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTAATTA others(13): Show |
6 | a0001c0001t0004g0193a0001c0001t0004g0197a0001c0001t0004g0199others(3): Show | 6 | HG02451.hp2 HG02976.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+46016_142+4601 others(24): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTATTTA others(5): Show |
5 | a0001c0001t0001g0053a0001c0001t0001g0063a0001c0001t0002g0049others(2): Show | 5 | HG00323.hp1 HG02965.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+46005_142+4601 others(16): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTATTTA others(9): Show |
2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142+46016_142+4601 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTATTTA others(9): Show |
9 | a0001c0001t0001g0058a0001c0001t0024g0012a0001c0001t0024g0013others(6): Show | 9 | HG00423.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.142+46001_142+4601 others(20): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | ATTATTTA others(17): Show |
1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+45993_142+4601 others(28): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687291
|
A | T | 21 | a0001c0001t0002g0134a0001c0001t0003g0215a0001c0001t0016g0075others(18): Show | 21 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.142+46017T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687291 | ||||||
| chr9:124687295
|
T | A | 34 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(31): Show | 34 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.142+46013A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687295 | ||||||
| chr9:124687834
|
C | T | 2 | a0001c0001t0002g0103a0001c0001t0009g0101 | 2 | NA18943.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.142+45474G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687834 | ||||||
| chr9:124687859
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0002g0051a0001c0001t0050g0024 | 3 | HG00558.hp2 NA18978.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.142+45449C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687859 | ||||||
| chr9:124687884
|
C | T | 24 | a0001c0001t0003g0056a0001c0001t0004g0193a0001c0001t0004g0194others(21): Show | 24 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.142+45424G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124687884 | ||||||
| chr9:124688292
|
C | T | 170 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(167): Show | 170 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.142+45016G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124688292 | ||||||
| chr9:124688375
|
A | G | 1 | a0001c0001t0058g0208 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.142+44933T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124688375 | ||||||
| chr9:124688423
|
C | A | 1 | a0001c0001t0029g0003 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.142+44885G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124688423 | ||||||
| chr9:124688778
|
C | T | 170 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(167): Show | 170 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.142+44530G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124688778 | ||||||
| chr9:124688896
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0002g0018 | 3 | NA18983.hp2 NA18995.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.142+44412T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124688896 | ||||||
| chr9:124688898
|
T | C | 3 | a0001c0001t0004g0197a0001c0001t0004g0199a0001c0001t0013g0198 | 3 | HG03516.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+44410A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124688898 | ||||||
| chr9:124688912
|
T | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+44396A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124688912 | ||||||
| chr9:124689047
|
A | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+44261T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124689047 | ||||||
| chr9:124689226
|
T | C | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.142+44082A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124689226 | ||||||
| chr9:124689346
|
T | A | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+43962A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124689346 | ||||||
| chr9:124689414
|
GA | G | 125 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(122): Show | 125 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.142+43893delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124689414 | ||||||
| chr9:124689694
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+43614T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124689694 | ||||||
| chr9:124689996
|
A | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+43312T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124689996 | ||||||
| chr9:124690024
|
C | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+43284G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124690024 | ||||||
| chr9:124690042
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.142+43266G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124690042 | ||||||
| chr9:124690098
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0172a0001c0001t0003g0171 | 3 | NA18939.hp2 NA19004.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.142+43210G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124690098 | ||||||
| chr9:124690127
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+43181A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124690127 | ||||||
| chr9:124690143
|
A | T | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.142+43165T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124690143 | ||||||
| chr9:124690450
|
T | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+42858A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124690450 | ||||||
| chr9:124690513
|
G | T | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+42795C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124690513 | ||||||
| chr9:124690698
|
T | G | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(84): Show | 87 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.142+42610A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124690698 | ||||||
| chr9:124690922
|
A | C | 1 | a0001c0001t0001g0113 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.142+42386T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124690922 | ||||||
| chr9:124690925
|
T | C | 55 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(52): Show | 55 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.142+42383A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124690925 | ||||||
| chr9:124690987
|
G | T | 1 | a0001c0001t0002g0054 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.142+42321C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124690987 | ||||||
| chr9:124691085
|
G | A | 1 | a0001c0001t0021g0148 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.142+42223C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124691085 | ||||||
| chr9:124691108
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.142+42200C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124691108 | ||||||
| chr9:124691398
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+41910A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124691398 | ||||||
| chr9:124691546
|
T | A | 6 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+41762A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124691546 | ||||||
| chr9:124691580
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+41728T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124691580 | ||||||
| chr9:124691868
|
G | A | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+41440C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124691868 | ||||||
| chr9:124691917
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.142+41391A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124691917 | ||||||
| chr9:124691925
|
C | T | 22 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(19): Show | 22 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.142+41383G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124691925 | ||||||
| chr9:124692129
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+41179A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124692129 | ||||||
| chr9:124692158
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+41150G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124692158 | ||||||
| chr9:124692327
|
A | T | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.142+40981T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124692327 | ||||||
| chr9:124692564
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+40744G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124692564 | ||||||
| chr9:124692591
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+40717A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124692591 | ||||||
| chr9:124692827
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+40481C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124692827 | ||||||
| chr9:124692981
|
T | C | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+40327A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124692981 | ||||||
| chr9:124693184
|
A | G | 14 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+40124T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124693184 | ||||||
| chr9:124693299
|
A | T | 13 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097others(10): Show | 13 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.142+40009T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124693299 | ||||||
| chr9:124693394
|
A | G | 14 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+39914T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124693394 | ||||||
| chr9:124693458
|
C | T | 1 | a0001c0001t0028g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+39850G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124693458 | ||||||
| chr9:124693557
|
T | C | 3 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097 | 3 | HG00639.hp1 HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142+39751A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124693557 | ||||||
| chr9:124693960
|
T | C | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+39348A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124693960 | ||||||
| chr9:124693988
|
A | G | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+39320T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124693988 | ||||||
| chr9:124694012
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+39296G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124694012 | ||||||
| chr9:124694288
|
T | C | 1 | a0001c0001t0039g0092 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142+39020A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124694288 | ||||||
| chr9:124694427
|
A | T | 37 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(34): Show | 37 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.142+38881T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124694427 | ||||||
| chr9:124694669
|
C | T | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+38639G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124694669 | ||||||
| chr9:124694917
|
T | C | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+38391A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124694917 | ||||||
| chr9:124695009
|
G | C | 1 | a0001c0001t0004g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.142+38299C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124695009 | ||||||
| chr9:124695071
|
A | T | 1 | a0001c0002t0010g0222 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.142+38237T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124695071 | ||||||
| chr9:124695127
|
T | G | 1 | a0001c0001t0002g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142+38181A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124695127 | ||||||
| chr9:124695310
|
C | T | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(28): Show | 31 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.142+37998G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124695310 | ||||||
| chr9:124695368
|
G | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+37940C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124695368 | ||||||
| chr9:124695437
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+37871G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124695437 | ||||||
| chr9:124695662
|
G | A | 1 | a0001c0001t0053g0082 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.142+37646C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124695662 | ||||||
| chr9:124695730
|
C | A | 1 | a0001c0001t0002g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142+37578G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124695730 | ||||||
| chr9:124695861
|
C | T | 1 | a0001c0001t0002g0103 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.142+37447G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124695861 | ||||||
| chr9:124695978
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.142+37330G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124695978 | ||||||
| chr9:124696049
|
T | C | 1 | a0001c0001t0025g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+37259A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696049 | ||||||
| chr9:124696112
|
G | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+37196C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696112 | ||||||
| chr9:124696160
|
C | T | 1 | a0001c0001t0061g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.142+37148G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696160 | ||||||
| chr9:124696165
|
A | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+37143T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696165 | ||||||
| chr9:124696189
|
G | A | 137 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(134): Show | 137 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.142+37119C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696189 | ||||||
| chr9:124696520
|
C | CT | 44 | a0001c0001t0001g0044a0001c0001t0001g0119a0001c0001t0001g0128others(41): Show | 44 | HG00544.hp2 HG01081.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.142+36787dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696520 | ||||||
| chr9:124696520
|
C | CTT | 83 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(80): Show | 83 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.142+36786_142+3678 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696520 | ||||||
| chr9:124696520
|
C | CTTT | 16 | a0001c0001t0001g0038a0001c0001t0001g0053a0001c0001t0001g0085others(13): Show | 16 | HG02145.hp2 HG02273.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.142+36785_142+3678 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696520 | ||||||
| chr9:124696592
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+36716C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696592 | ||||||
| chr9:124696604
|
C | T | 1 | a0001c0001t0001g0119 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.142+36704G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696604 | ||||||
| chr9:124696803
|
C | T | 1 | a0001c0001t0015g0127 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.142+36505G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696803 | ||||||
| chr9:124696927
|
G | A | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+36381C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696927 | ||||||
| chr9:124696999
|
T | C | 33 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(30): Show | 33 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.142+36309A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124696999 | ||||||
| chr9:124697246
|
T | A | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+36062A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697246 | ||||||
| chr9:124697264
|
C | T | 1 | a0001c0001t0025g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+36044G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697264 | ||||||
| chr9:124697271
|
T | C | 11 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(8): Show | 11 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+36037A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697271 | ||||||
| chr9:124697382
|
C | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+35926G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697382 | ||||||
| chr9:124697505
|
G | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+35803C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697505 | ||||||
| chr9:124697550
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+35758A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697550 | ||||||
| chr9:124697583
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+35725T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697583 | ||||||
| chr9:124697672
|
G | A | 2 | a0001c0001t0013g0190a0001c0001t0013g0196 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.142+35636C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697672 | ||||||
| chr9:124697676
|
T | A | 1 | a0001c0001t0002g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.142+35632A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697676 | ||||||
| chr9:124697676
|
T | TA | 18 | a0001c0001t0001g0079a0001c0001t0024g0012a0001c0001t0024g0013others(15): Show | 18 | HG02145.hp2 HG02258.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.142+35631dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697676 | ||||||
| chr9:124697676
|
TA | T | 5 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(2): Show | 5 | HG01884.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+35631delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697676 | ||||||
| chr9:124697798
|
T | C | 4 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(1): Show | 4 | HG02723.hp1 NA18522.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+35510A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697798 | ||||||
| chr9:124697870
|
T | C | 1 | a0001c0001t0002g0165 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.142+35438A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124697870 | ||||||
| chr9:124698338
|
C | T | 138 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(135): Show | 138 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.142+34970G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124698338 | ||||||
| chr9:124698701
|
G | C | 1 | a0001c0001t0008g0096 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.142+34607C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124698701 | ||||||
| chr9:124698736
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+34572G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124698736 | ||||||
| chr9:124698745
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+34563A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124698745 | ||||||
| chr9:124698897
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.142+34411A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124698897 | ||||||
| chr9:124699373
|
A | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+33935T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124699373 | ||||||
| chr9:124699785
|
C | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+33523G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124699785 | ||||||
| chr9:124699813
|
G | A | 1 | a0001c0001t0003g0056 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.142+33495C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124699813 | ||||||
| chr9:124699885
|
T | C | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+33423A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124699885 | ||||||
| chr9:124700030
|
A | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+33278T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700030 | ||||||
| chr9:124700040
|
G | T | 1 | a0001c0001t0002g0154 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.142+33268C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700040 | ||||||
| chr9:124700201
|
G | T | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+33107C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700201 | ||||||
| chr9:124700376
|
T | A | 5 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(2): Show | 5 | HG02723.hp1 HG02818.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+32932A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700376 | ||||||
| chr9:124700393
|
A | AT | 4 | a0001c0001t0006g0191a0001c0001t0006g0202a0001c0001t0006g0203others(1): Show | 4 | HG02015.hp2 HG02083.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+32914dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700393 | ||||||
| chr9:124700422
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142+32886A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700422 | ||||||
| chr9:124700433
|
C | G | 1 | a0001c0001t0038g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.142+32875G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700433 | ||||||
| chr9:124700434
|
T | G | 1 | a0001c0001t0038g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.142+32874A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700434 | ||||||
| chr9:124700662
|
C | G | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+32646G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700662 | ||||||
| chr9:124700665
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+32643A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700665 | ||||||
| chr9:124700754
|
C | CT | 12 | a0001c0001t0001g0061a0001c0001t0001g0118a0001c0001t0001g0123others(9): Show | 12 | HG00438.hp2 HG01361.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.142+32553dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700754 | ||||||
| chr9:124700754
|
CT | C | 93 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0120others(90): Show | 93 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.142+32553delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700754 | ||||||
| chr9:124700754
|
CTT | C | 16 | a0001c0001t0001g0180a0001c0001t0016g0075a0001c0001t0016g0077others(13): Show | 16 | HG01884.hp1 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.142+32552_142+3255 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700754 | ||||||
| chr9:124700844
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+32464A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700844 | ||||||
| chr9:124700856
|
G | T | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+32452C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700856 | ||||||
| chr9:124700863
|
C | A | 2 | a0001c0001t0046g0008a0001c0001t0060g0027 | 2 | HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142+32445G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700863 | ||||||
| chr9:124700973
|
C | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(84): Show | 87 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.142+32335G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700973 | ||||||
| chr9:124700977
|
T | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+32331A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124700977 | ||||||
| chr9:124701135
|
G | A | 1 | a0001c0001t0008g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.142+32173C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124701135 | ||||||
| chr9:124701232
|
C | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+32076G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124701232 | ||||||
| chr9:124701259
|
C | T | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+32049G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124701259 | ||||||
| chr9:124701574
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+31734A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124701574 | ||||||
| chr9:124701674
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.142+31634A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124701674 | ||||||
| chr9:124701699
|
G | A | 33 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(30): Show | 33 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.142+31609C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124701699 | ||||||
| chr9:124701745
|
C | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+31563G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124701745 | ||||||
| chr9:124701869
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0043g0107 | 2 | HG00609.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.142+31439C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124701869 | ||||||
| chr9:124701887
|
G | C | 138 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(135): Show | 138 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.142+31421C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124701887 | ||||||
| chr9:124701977
|
G | A | 1 | a0001c0002t0010g0224 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.142+31331C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124701977 | ||||||
| chr9:124701993
|
A | G | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+31315T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124701993 | ||||||
| chr9:124702261
|
C | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+31047G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124702261 | ||||||
| chr9:124702284
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+31024A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124702284 | ||||||
| chr9:124702362
|
A | G | 11 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(8): Show | 11 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+30946T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124702362 | ||||||
| chr9:124702569
|
G | A | 1 | a0001c0001t0025g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+30739C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124702569 | ||||||
| chr9:124702617
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.142+30691T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124702617 | ||||||
| chr9:124702673
|
C | T | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+30635G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124702673 | ||||||
| chr9:124702717
|
T | A | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+30591A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124702717 | ||||||
| chr9:124702727
|
T | G | 2 | a0001c0001t0001g0117a0001c0001t0002g0153 | 2 | HG01981.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.142+30581A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124702727 | ||||||
| chr9:124702778
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.142+30530A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124702778 | ||||||
| chr9:124702807
|
G | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0053others(4): Show | 7 | HG00558.hp2 HG02056.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+30501C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124702807 | ||||||
| chr9:124703132
|
T | G | 3 | a0001c0001t0014g0069a0001c0001t0017g0066a0001c0001t0017g0068 | 3 | HG02647.hp1 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.142+30176A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703132 | ||||||
| chr9:124703207
|
A | AT | 44 | a0001c0001t0001g0064a0001c0001t0001g0160a0001c0001t0001g0163others(41): Show | 44 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.142+30100dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703207 | ||||||
| chr9:124703207
|
A | ATTTTT | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+30096_142+3010 others(9): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703207 | ||||||
| chr9:124703207
|
AT | A | 8 | a0001c0001t0001g0063a0001c0001t0002g0037a0001c0001t0002g0159others(5): Show | 8 | HG00323.hp1 HG01884.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.142+30100delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703207 | ||||||
| chr9:124703207
|
ATTT | A | 6 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+30098_142+3010 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703207 | ||||||
| chr9:124703247
|
C | T | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+30061G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703247 | ||||||
| chr9:124703293
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+30015A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703293 | ||||||
| chr9:124703356
|
G | A | 1 | a0001c0001t0002g0011 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.142+29952C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703356 | ||||||
| chr9:124703416
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+29892G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703416 | ||||||
| chr9:124703536
|
G | A | 14 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(11): Show | 14 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.142+29772C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703536 | ||||||
| chr9:124703816
|
T | A | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.142+29492A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703816 | ||||||
| chr9:124703830
|
AT | A | 88 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(85): Show | 88 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.142+29477delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703830 | ||||||
| chr9:124703907
|
C | T | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.142+29401G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703907 | ||||||
| chr9:124703958
|
C | G | 8 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0143others(5): Show | 8 | HG01106.hp2 HG01361.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+29350G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124703958 | ||||||
| chr9:124704043
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+29265A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704043 | ||||||
| chr9:124704182
|
T | C | 1 | a0003c0005t0002g0146 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.142+29126A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704182 | ||||||
| chr9:124704286
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+29022C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704286 | ||||||
| chr9:124704605
|
C | T | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142+28703G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704605 | ||||||
| chr9:124704606
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+28702C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704606 | ||||||
| chr9:124704612
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+28696C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704612 | ||||||
| chr9:124704743
|
T | G | 1 | a0001c0001t0002g0177 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.142+28565A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704743 | ||||||
| chr9:124704751
|
G | T | 1 | a0001c0001t0002g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.142+28557C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704751 | ||||||
| chr9:124704854
|
C | G | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+28454G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704854 | ||||||
| chr9:124704884
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+28424C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704884 | ||||||
| chr9:124704963
|
T | C | 3 | a0001c0001t0014g0071a0001c0001t0014g0072a0001c0001t0045g0070 | 3 | HG01167.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.142+28345A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704963 | ||||||
| chr9:124704978
|
C | T | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+28330G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704978 | ||||||
| chr9:124704999
|
G | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+28309C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124704999 | ||||||
| chr9:124705163
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+28145T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705163 | ||||||
| chr9:124705566
|
C | G | 1 | a0001c0001t0002g0049 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.142+27742G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705566 | ||||||
| chr9:124705614
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.142+27694C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705614 | ||||||
| chr9:124705706
|
C | T | 1 | a0003c0005t0002g0146 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.142+27602G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705706 | ||||||
| chr9:124705782
|
C | CT | 10 | a0001c0001t0021g0148a0001c0001t0024g0012a0001c0001t0024g0013others(7): Show | 10 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.142+27525dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705782 | ||||||
| chr9:124705782
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+27526G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705782 | ||||||
| chr9:124705782
|
CT | C | 62 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(59): Show | 62 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.142+27525delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705782 | ||||||
| chr9:124705783
|
T | C | 40 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(37): Show | 40 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.142+27525A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705783 | ||||||
| chr9:124705831
|
A | G | 1 | a0001c0001t0002g0177 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.142+27477T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705831 | ||||||
| chr9:124705880
|
A | C | 1 | a0001c0001t0038g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.142+27428T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705880 | ||||||
| chr9:124705925
|
G | A | 86 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(83): Show | 86 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.142+27383C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705925 | ||||||
| chr9:124705937
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0002g0039 | 2 | HG01081.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.142+27371C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705937 | ||||||
| chr9:124705941
|
A | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+27367T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705941 | ||||||
| chr9:124705951
|
T | A | 5 | a0001c0001t0018g0028a0001c0001t0018g0030a0001c0001t0037g0032others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+27357A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124705951 | ||||||
| chr9:124706004
|
G | A | 1 | a0001c0001t0031g0005 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.142+27304C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124706004 | ||||||
| chr9:124706218
|
C | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+27090G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124706218 | ||||||
| chr9:124706443
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.142+26865T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124706443 | ||||||
| chr9:124706519
|
A | AT | 6 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0120others(3): Show | 6 | HG00639.hp2 HG02165.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+26788dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124706519 | ||||||
| chr9:124706521
|
T | C | 1 | a0001c0001t0022g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.142+26787A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124706521 | ||||||
| chr9:124706537
|
T | C | 171 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(168): Show | 171 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.142+26771A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124706537 | ||||||
| chr9:124706587
|
T | A | 5 | a0001c0001t0018g0028a0001c0001t0018g0030a0001c0001t0037g0032others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+26721A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124706587 | ||||||
| chr9:124706760
|
C | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+26548G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124706760 | ||||||
| chr9:124707017
|
G | A | 2 | a0001c0001t0046g0008a0001c0001t0060g0027 | 2 | HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142+26291C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707017 | ||||||
| chr9:124707117
|
TCTC | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+26188_142+2619 others(7): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707117 | ||||||
| chr9:124707183
|
T | C | 1 | a0001c0001t0065g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.142+26125A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707183 | ||||||
| chr9:124707214
|
T | C | 3 | a0001c0002t0005g0227a0001c0002t0005g0228a0001c0002t0005g0229 | 3 | HG02451.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142+26094A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707214 | ||||||
| chr9:124707224
|
T | A | 1 | a0001c0001t0051g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.142+26084A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707224 | ||||||
| chr9:124707230
|
C | G | 12 | a0001c0001t0033g0097a0001c0002t0005g0226a0001c0002t0005g0227others(9): Show | 12 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.142+26078G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707230 | ||||||
| chr9:124707271
|
C | T | 82 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.142+26037G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707271 | ||||||
| chr9:124707330
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.142+25978G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707330 | ||||||
| chr9:124707358
|
T | C | 1 | a0001c0001t0002g0049 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.142+25950A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707358 | ||||||
| chr9:124707486
|
T | G | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.142+25822A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707486 | ||||||
| chr9:124707515
|
G | GT | 10 | a0001c0001t0002g0051a0001c0001t0021g0213a0001c0001t0024g0012others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+25792dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707515 | ||||||
| chr9:124707515
|
G | GTT | 5 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+25791_142+2579 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707515 | ||||||
| chr9:124707515
|
GT | G | 35 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(32): Show | 35 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.142+25792delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707515 | ||||||
| chr9:124707522
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+25786A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707522 | ||||||
| chr9:124707570
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.142+25738A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707570 | ||||||
| chr9:124707839
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0009g0060 | 2 | NA18939.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.142+25469G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124707839 | ||||||
| chr9:124708382
|
A | G | 1 | a0001c0001t0002g0049 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.142+24926T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124708382 | ||||||
| chr9:124708452
|
A | G | 5 | a0001c0001t0001g0120a0001c0001t0001g0152a0001c0001t0001g0219others(2): Show | 5 | HG02055.hp2 HG02165.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+24856T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124708452 | ||||||
| chr9:124708564
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.142+24744C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124708564 | ||||||
| chr9:124708615
|
C | T | 33 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(30): Show | 33 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.142+24693G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124708615 | ||||||
| chr9:124708711
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+24597A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124708711 | ||||||
| chr9:124708921
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+24387G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124708921 | ||||||
| chr9:124708990
|
G | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+24318C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124708990 | ||||||
| chr9:124709065
|
C | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+24243G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124709065 | ||||||
| chr9:124709206
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+24102G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124709206 | ||||||
| chr9:124709496
|
C | A | 1 | a0001c0001t0002g0157 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.142+23812G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124709496 | ||||||
| chr9:124709622
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+23686A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124709622 | ||||||
| chr9:124709722
|
T | C | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+23586A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124709722 | ||||||
| chr9:124709732
|
G | C | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+23576C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124709732 | ||||||
| chr9:124709744
|
AC | A | 84 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.142+23563delG | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124709744 | ||||||
| chr9:124710174
|
G | A | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+23134C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124710174 | ||||||
| chr9:124710422
|
G | A | 1 | a0001c0001t0007g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142+22886C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124710422 | ||||||
| chr9:124710798
|
G | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0009g0060 | 3 | NA18939.hp1 NA18975.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.142+22510C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124710798 | ||||||
| chr9:124710859
|
G | T | 1 | a0001c0001t0002g0037 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.142+22449C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124710859 | ||||||
| chr9:124711045
|
T | C | 1 | a0001c0001t0002g0049 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.142+22263A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711045 | ||||||
| chr9:124711062
|
G | A | 2 | a0001c0001t0017g0066a0001c0001t0017g0068 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.142+22246C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711062 | ||||||
| chr9:124711186
|
TTAAAAAA others(6): Show |
T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+22109_142+2212 others(17): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711186 | ||||||
| chr9:124711187
|
T | TA | 19 | a0001c0001t0001g0120a0001c0001t0001g0126a0001c0001t0001g0219others(16): Show | 19 | HG00609.hp2 HG01433.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.142+22120dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711187 | ||||||
| chr9:124711187
|
T | TAAAA | 7 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(4): Show | 7 | HG02451.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+22117_142+2212 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711187 | ||||||
| chr9:124711187
|
TA | T | 58 | a0001c0001t0001g0009a0001c0001t0001g0160a0001c0001t0001g0161others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.142+22120delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711187 | ||||||
| chr9:124711187
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0003g0215 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.142+22110_142+2212 others(15): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711187 | ||||||
| chr9:124711187
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0001g0114 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.142+22108_142+2212 others(17): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711187 | ||||||
| chr9:124711299
|
T | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+22009A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711299 | ||||||
| chr9:124711302
|
CT | C | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+22005delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711302 | ||||||
| chr9:124711318
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142+21990G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711318 | ||||||
| chr9:124711389
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+21919A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711389 | ||||||
| chr9:124711433
|
T | A | 4 | a0001c0001t0009g0101a0001c0001t0015g0127a0001c0001t0015g0155others(1): Show | 4 | HG02015.hp1 NA18943.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+21875A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711433 | ||||||
| chr9:124711433
|
T | TA | 5 | a0001c0001t0001g0023a0001c0001t0019g0074a0001c0001t0020g0025others(2): Show | 5 | HG00558.hp2 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+21874dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711433 | ||||||
| chr9:124711483
|
T | A | 1 | a0001c0001t0022g0217 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.142+21825A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711483 | ||||||
| chr9:124711522
|
G | A | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+21786C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711522 | ||||||
| chr9:124711595
|
T | C | 5 | a0001c0001t0018g0028a0001c0001t0018g0030a0001c0001t0037g0032others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+21713A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711595 | ||||||
| chr9:124711805
|
T | G | 1 | a0001c0001t0012g0207 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.142+21503A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711805 | ||||||
| chr9:124711886
|
T | C | 1 | a0001c0001t0040g0029 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.142+21422A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124711886 | ||||||
| chr9:124712117
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.142+21191G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712117 | ||||||
| chr9:124712226
|
T | C | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+21082A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712226 | ||||||
| chr9:124712315
|
A | G | 88 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(85): Show | 88 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.142+20993T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712315 | ||||||
| chr9:124712325
|
G | A | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+20983C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712325 | ||||||
| chr9:124712376
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+20932T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712376 | ||||||
| chr9:124712401
|
G | C | 1 | a0001c0001t0002g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.142+20907C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712401 | ||||||
| chr9:124712430
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+20878C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712430 | ||||||
| chr9:124712460
|
T | G | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142+20848A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712460 | ||||||
| chr9:124712587
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+20721C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712587 | ||||||
| chr9:124712607
|
CA | C | 88 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(85): Show | 88 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.142+20700delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712607 | ||||||
| chr9:124712696
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+20612A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712696 | ||||||
| chr9:124712832
|
C | T | 84 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.142+20476G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712832 | ||||||
| chr9:124712939
|
C | A | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+20369G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712939 | ||||||
| chr9:124712989
|
C | G | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+20319G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124712989 | ||||||
| chr9:124713184
|
T | C | 1 | a0001c0001t0002g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.142+20124A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124713184 | ||||||
| chr9:124713550
|
A | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+19758T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124713550 | ||||||
| chr9:124713858
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+19450T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124713858 | ||||||
| chr9:124713972
|
C | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+19336G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124713972 | ||||||
| chr9:124714529
|
C | A | 1 | a0001c0001t0002g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.142+18779G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124714529 | ||||||
| chr9:124714895
|
C | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+18413G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124714895 | ||||||
| chr9:124714959
|
G | A | 13 | a0001c0001t0014g0069a0001c0001t0014g0071a0001c0001t0014g0072others(10): Show | 13 | HG01167.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+18349C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124714959 | ||||||
| chr9:124714966
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+18342C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124714966 | ||||||
| chr9:124714977
|
T | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+18331A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124714977 | ||||||
| chr9:124715035
|
T | C | 33 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(30): Show | 33 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.142+18273A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124715035 | ||||||
| chr9:124715043
|
A | C | 83 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.142+18265T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124715043 | ||||||
| chr9:124715202
|
G | GA | 5 | a0001c0001t0002g0145a0001c0001t0016g0075a0001c0001t0016g0077others(2): Show | 5 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+18105dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124715202 | ||||||
| chr9:124715301
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+18007A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124715301 | ||||||
| chr9:124715352
|
G | A | 1 | a0001c0001t0003g0215 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.142+17956C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124715352 | ||||||
| chr9:124715858
|
G | A | 83 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.142+17450C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124715858 | ||||||
| chr9:124715902
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+17406C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124715902 | ||||||
| chr9:124715947
|
A | C | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+17361T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124715947 | ||||||
| chr9:124716238
|
A | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+17070T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124716238 | ||||||
| chr9:124716372
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+16936C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124716372 | ||||||
| chr9:124716377
|
T | C | 3 | a0001c0001t0001g0023a0001c0001t0002g0051a0001c0001t0050g0024 | 3 | HG00558.hp2 NA18978.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.142+16931A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124716377 | ||||||
| chr9:124716482
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+16826G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124716482 | ||||||
| chr9:124716557
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+16751G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124716557 | ||||||
| chr9:124716754
|
C | T | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+16554G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124716754 | ||||||
| chr9:124716788
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.142+16520G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124716788 | ||||||
| chr9:124717053
|
T | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+16255A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124717053 | ||||||
| chr9:124717185
|
C | T | 82 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.142+16123G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124717185 | ||||||
| chr9:124717287
|
G | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+16021C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124717287 | ||||||
| chr9:124717452
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.142+15856T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124717452 | ||||||
| chr9:124717471
|
T | C | 68 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(65): Show | 68 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.142+15837A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124717471 | ||||||
| chr9:124717549
|
C | T | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.142+15759G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124717549 | ||||||
| chr9:124717635
|
G | C | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+15673C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124717635 | ||||||
| chr9:124717659
|
T | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+15649A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124717659 | ||||||
| chr9:124717716
|
C | T | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142+15592G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124717716 | ||||||
| chr9:124717870
|
A | T | 1 | a0001c0001t0002g0131 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.142+15438T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124717870 | ||||||
| chr9:124718126
|
A | G | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+15182T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718126 | ||||||
| chr9:124718330
|
T | G | 1 | a0001c0001t0002g0021 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.142+14978A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718330 | ||||||
| chr9:124718346
|
T | C | 2 | a0001c0001t0011g0205a0001c0001t0012g0207 | 2 | NA18977.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.142+14962A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718346 | ||||||
| chr9:124718380
|
C | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+14928G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718380 | ||||||
| chr9:124718658
|
T | G | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+14650A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718658 | ||||||
| chr9:124718731
|
A | G | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+14577T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718731 | ||||||
| chr9:124718801
|
A | C | 1 | a0001c0001t0014g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.142+14507T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718801 | ||||||
| chr9:124718803
|
CT | C | 106 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0116others(103): Show | 106 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.142+14504delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718803 | ||||||
| chr9:124718803
|
CTT | C | 85 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0022others(82): Show | 85 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.142+14503_142+1450 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718803 | ||||||
| chr9:124718803
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0028g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+14494_142+1450 others(15): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718803 | ||||||
| chr9:124718839
|
G | A | 1 | a0001c0001t0004g0195 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.142+14469C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718839 | ||||||
| chr9:124718875
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0002g0142 | 2 | HG00621.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.142+14433G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718875 | ||||||
| chr9:124718937
|
C | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+14371G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124718937 | ||||||
| chr9:124719107
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+14201G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124719107 | ||||||
| chr9:124719184
|
C | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+14124G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124719184 | ||||||
| chr9:124719378
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.142+13930T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124719378 | ||||||
| chr9:124719692
|
G | A | 2 | a0001c0002t0005g0226a0001c0002t0005g0230 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.142+13616C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124719692 | ||||||
| chr9:124719780
|
C | T | 1 | a0001c0002t0010g0222 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.142+13528G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124719780 | ||||||
| chr9:124719784
|
G | T | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+13524C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124719784 | ||||||
| chr9:124719927
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0002g0142 | 2 | HG00621.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.142+13381A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124719927 | ||||||
| chr9:124719986
|
AAT | A | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+13320_142+1332 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124719986 | ||||||
| chr9:124720040
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+13268G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124720040 | ||||||
| chr9:124720065
|
G | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+13243C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124720065 | ||||||
| chr9:124720163
|
T | C | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+13145A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124720163 | ||||||
| chr9:124720192
|
C | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(84): Show | 87 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.142+13116G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124720192 | ||||||
| chr9:124720216
|
T | A | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+13092A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124720216 | ||||||
| chr9:124720413
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.142+12895G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124720413 | ||||||
| chr9:124720483
|
A | T | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+12825T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124720483 | ||||||
| chr9:124720669
|
G | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+12639C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124720669 | ||||||
| chr9:124720960
|
C | A | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142+12348G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124720960 | ||||||
| chr9:124720978
|
T | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+12330A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124720978 | ||||||
| chr9:124721099
|
C | A | 5 | a0001c0001t0018g0028a0001c0001t0018g0030a0001c0001t0037g0032others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+12209G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124721099 | ||||||
| chr9:124721184
|
T | C | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+12124A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124721184 | ||||||
| chr9:124721203
|
C | G | 1 | a0001c0001t0004g0193 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.142+12105G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124721203 | ||||||
| chr9:124721257
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+12051C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124721257 | ||||||
| chr9:124721473
|
G | T | 3 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097 | 3 | HG00639.hp1 HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142+11835C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124721473 | ||||||
| chr9:124721592
|
A | G | 3 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097 | 3 | HG00639.hp1 HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142+11716T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124721592 | ||||||
| chr9:124721668
|
C | G | 1 | a0001c0001t0038g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.142+11640G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124721668 | ||||||
| chr9:124721726
|
A | G | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+11582T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124721726 | ||||||
| chr9:124721858
|
ATTAT | A | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+11446_142+1144 others(8): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124721858 | ||||||
| chr9:124722301
|
A | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+11007T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124722301 | ||||||
| chr9:124722379
|
A | C | 1 | a0001c0001t0002g0189 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.142+10929T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124722379 | ||||||
| chr9:124722686
|
C | T | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+10622G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124722686 | ||||||
| chr9:124722765
|
T | C | 1 | a0001c0001t0022g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.142+10543A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124722765 | ||||||
| chr9:124723067
|
T | C | 6 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+10241A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124723067 | ||||||
| chr9:124723166
|
T | A | 85 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(82): Show | 85 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.142+10142A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124723166 | ||||||
| chr9:124723709
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+9599T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124723709 | ||||||
| chr9:124723737
|
A | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+9571T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124723737 | ||||||
| chr9:124723834
|
T | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+9474A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124723834 | ||||||
| chr9:124723845
|
T | C | 2 | a0001c0001t0008g0094a0001c0001t0008g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.142+9463A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124723845 | ||||||
| chr9:124724283
|
G | A | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.142+9025C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124724283 | ||||||
| chr9:124724296
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142+9012C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124724296 | ||||||
| chr9:124724440
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+8868T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124724440 | ||||||
| chr9:124724534
|
C | CA | 5 | a0001c0001t0001g0085a0001c0001t0001g0132a0001c0001t0002g0051others(2): Show | 5 | HG01081.hp1 HG02273.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+8773dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124724534 | ||||||
| chr9:124724617
|
G | A | 83 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.142+8691C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124724617 | ||||||
| chr9:124724802
|
T | A | 1 | a0001c0001t0020g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.142+8506A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124724802 | ||||||
| chr9:124724840
|
T | C | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.142+8468A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124724840 | ||||||
| chr9:124725119
|
C | T | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+8189G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124725119 | ||||||
| chr9:124725120
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0002g0039 | 2 | HG01081.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.142+8188C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124725120 | ||||||
| chr9:124725249
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+8059A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124725249 | ||||||
| chr9:124725386
|
G | A | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+7922C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124725386 | ||||||
| chr9:124725393
|
A | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+7915T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124725393 | ||||||
| chr9:124725402
|
G | GA | 9 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+7905dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124725402 | ||||||
| chr9:124725402
|
GA | G | 6 | a0001c0001t0018g0028a0001c0001t0018g0030a0001c0001t0027g0001others(3): Show | 6 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+7905delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124725402 | ||||||
| chr9:124725557
|
G | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+7751C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124725557 | ||||||
| chr9:124725754
|
A | G | 41 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(38): Show | 41 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.142+7554T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124725754 | ||||||
| chr9:124726418
|
T | C | 1 | a0001c0001t0003g0215 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.142+6890A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124726418 | ||||||
| chr9:124726547
|
T | C | 3 | a0001c0001t0014g0071a0001c0001t0014g0072a0001c0001t0045g0070 | 3 | HG01167.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.142+6761A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124726547 | ||||||
| chr9:124726639
|
C | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+6669G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124726639 | ||||||
| chr9:124726688
|
C | A | 1 | a0001c0001t0057g0192 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.142+6620G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124726688 | ||||||
| chr9:124726691
|
CTCACTTC others(1): Show |
C | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | NA18969.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.142+6609_142+6616d others(10): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124726691 | ||||||
| chr9:124726727
|
C | T | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+6581G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124726727 | ||||||
| chr9:124726937
|
G | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+6371C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124726937 | ||||||
| chr9:124727101
|
A | T | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+6207T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124727101 | ||||||
| chr9:124727120
|
TCCTATGT others(2): Show |
T | 86 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(83): Show | 86 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.142+6179_142+6187d others(11): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124727120 | ||||||
| chr9:124727366
|
A | G | 1 | a0001c0001t0002g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.142+5942T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124727366 | ||||||
| chr9:124727481
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+5827T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124727481 | ||||||
| chr9:124727669
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+5639C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124727669 | ||||||
| chr9:124727759
|
A | T | 1 | a0001c0001t0001g0119 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.142+5549T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124727759 | ||||||
| chr9:124727760
|
C | T | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+5548G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124727760 | ||||||
| chr9:124727798
|
C | T | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+5510G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124727798 | ||||||
| chr9:124727841
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142+5467A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124727841 | ||||||
| chr9:124727873
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+5435G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124727873 | ||||||
| chr9:124727885
|
A | G | 14 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+5423T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124727885 | ||||||
| chr9:124728006
|
A | T | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+5302T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728006 | ||||||
| chr9:124728020
|
T | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+5288A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728020 | ||||||
| chr9:124728042
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+5266G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728042 | ||||||
| chr9:124728112
|
T | A | 1 | a0001c0001t0004g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142+5196A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728112 | ||||||
| chr9:124728116
|
T | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+5192A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728116 | ||||||
| chr9:124728495
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0044g0175 | 2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.142+4813G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728495 | ||||||
| chr9:124728550
|
G | T | 1 | a0001c0001t0063g0135 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.142+4758C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728550 | ||||||
| chr9:124728621
|
C | T | 1 | a0004c0004t0036g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+4687G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728621 | ||||||
| chr9:124728622
|
G | A | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142+4686C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728622 | ||||||
| chr9:124728637
|
A | AAAAT | 89 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(86): Show | 89 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.142+4667_142+4670d others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728637 | ||||||
| chr9:124728637
|
A | AAAATAAA others(1): Show |
18 | a0001c0001t0001g0044a0001c0001t0001g0144a0001c0001t0002g0142others(15): Show | 18 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.142+4663_142+4670d others(10): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728637 | ||||||
| chr9:124728637
|
A | AAAATAAA others(5): Show |
37 | a0001c0001t0001g0161a0001c0001t0001g0164a0001c0001t0001g0173others(34): Show | 37 | HG00544.hp2 HG01884.hp1 HG02015.hp2 others(34): Show |
intron_variant | MODIFIER | c.142+4659_142+4670d others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728637 | ||||||
| chr9:124728637
|
A | AAAATAAA others(9): Show |
27 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0174others(24): Show | 27 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.142+4655_142+4670d others(18): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728637 | ||||||
| chr9:124728637
|
A | AAAATAAA others(13): Show |
3 | a0001c0001t0002g0176a0001c0001t0002g0189a0001c0001t0023g0188 | 3 | NA18959.hp2 NA19000.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.142+4651_142+4670d others(22): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728637 | ||||||
| chr9:124728637
|
A | AAAATAAA others(17): Show |
1 | a0001c0001t0002g0185 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.142+4647_142+4670d others(26): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728637 | ||||||
| chr9:124728750
|
AG | A | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+4557delC | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728750 | ||||||
| chr9:124728815
|
T | C | 1 | a0001c0001t0046g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.142+4493A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728815 | ||||||
| chr9:124728818
|
C | T | 1 | a0001c0001t0063g0135 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.142+4490G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728818 | ||||||
| chr9:124728845
|
G | A | 2 | a0001c0001t0006g0212a0001c0001t0033g0097 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142+4463C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728845 | ||||||
| chr9:124728908
|
C | A | 231 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(228): Show | 231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.142+4400G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124728908 | ||||||
| chr9:124729207
|
G | A | 1 | a0001c0001t0051g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.142+4101C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124729207 | ||||||
| chr9:124729213
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+4095C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124729213 | ||||||
| chr9:124729244
|
A | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+4064T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124729244 | ||||||
| chr9:124729443
|
G | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.142+3865C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124729443 | ||||||
| chr9:124729811
|
A | AT | 8 | a0001c0001t0002g0133a0001c0001t0002g0153a0001c0001t0002g0185others(5): Show | 8 | HG00438.hp1 HG01106.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+3496dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124729811 | ||||||
| chr9:124729843
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+3465C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124729843 | ||||||
| chr9:124729876
|
G | A | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+3432C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124729876 | ||||||
| chr9:124729882
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+3426C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124729882 | ||||||
| chr9:124729906
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+3402T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124729906 | ||||||
| chr9:124729937
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.142+3371G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124729937 | ||||||
| chr9:124730219
|
G | A | 84 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(81): Show | 84 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.142+3089C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124730219 | ||||||
| chr9:124730322
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0002g0054 | 2 | HG02056.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.142+2986A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124730322 | ||||||
| chr9:124730371
|
G | A | 2 | a0001c0001t0013g0190a0001c0001t0013g0196 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.142+2937C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124730371 | ||||||
| chr9:124730396
|
T | C | 1 | a0001c0001t0003g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.142+2912A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124730396 | ||||||
| chr9:124730555
|
C | CT | 76 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(73): Show | 76 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.142+2752dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124730555 | ||||||
| chr9:124730555
|
C | CTT | 11 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0106others(8): Show | 11 | HG00609.hp1 HG01081.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.142+2751_142+2752d others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124730555 | ||||||
| chr9:124730608
|
T | A | 1 | a0001c0001t0001g0132 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.142+2700A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124730608 | ||||||
| chr9:124730801
|
G | A | 1 | a0001c0001t0030g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.142+2507C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124730801 | ||||||
| chr9:124730883
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0044g0175 | 2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.142+2425G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124730883 | ||||||
| chr9:124730954
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+2354C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124730954 | ||||||
| chr9:124730994
|
A | C | 1 | a0001c0001t0021g0213 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.142+2314T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124730994 | ||||||
| chr9:124731126
|
C | T | 1 | a0001c0001t0004g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142+2182G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731126 | ||||||
| chr9:124731199
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+2109C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731199 | ||||||
| chr9:124731243
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+2065C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731243 | ||||||
| chr9:124731295
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+2013C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731295 | ||||||
| chr9:124731370
|
G | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+1938C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731370 | ||||||
| chr9:124731370
|
GA | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+1937delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731370 | ||||||
| chr9:124731475
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.142+1833C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731475 | ||||||
| chr9:124731480
|
C | T | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+1828G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731480 | ||||||
| chr9:124731517
|
G | A | 1 | a0004c0004t0036g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+1791C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731517 | ||||||
| chr9:124731518
|
CAG | C | 13 | a0001c0001t0014g0069a0001c0001t0014g0071a0001c0001t0014g0072others(10): Show | 13 | HG01167.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+1788_142+1789d others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731518 | ||||||
| chr9:124731605
|
T | C | 14 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+1703A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731605 | ||||||
| chr9:124731749
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.142+1559A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731749 | ||||||
| chr9:124731827
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0051g0140 | 2 | HG02155.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.142+1481C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731827 | ||||||
| chr9:124731867
|
T | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0219 | 2 | HG02165.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.142+1441A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731867 | ||||||
| chr9:124731868
|
T | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0002g0169 | 3 | HG03490.hp1 HG03492.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.142+1440A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731868 | ||||||
| chr9:124731950
|
G | A | 82 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.142+1358C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731950 | ||||||
| chr9:124731954
|
T | C | 2 | a0001c0003t0048g0102a0001c0003t0055g0181 | 2 | HG00423.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.142+1354A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124731954 | ||||||
| chr9:124732082
|
T | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+1226A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124732082 | ||||||
| chr9:124732332
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.142+976C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124732332 | ||||||
| chr9:124732423
|
C | T | 4 | a0001c0001t0001g0178a0001c0001t0002g0176a0001c0001t0002g0177others(1): Show | 4 | HG02698.hp2 HG03927.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+885G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124732423 | ||||||
| chr9:124732694
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.142+614G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124732694 | ||||||
| chr9:124732697
|
A | AT | 19 | a0001c0001t0001g0164a0001c0001t0002g0153a0001c0001t0002g0170others(16): Show | 19 | HG01981.hp2 HG02145.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.142+610dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124732697 | ||||||
| chr9:124732784
|
C | T | 9 | a0001c0001t0002g0109a0001c0001t0002g0111a0001c0001t0002g0211others(6): Show | 9 | HG00609.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.142+524G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124732784 | ||||||
| chr9:124732789
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142+519G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124732789 | ||||||
| chr9:124732858
|
G | A | 2 | a0001c0002t0005g0226a0001c0002t0005g0230 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.142+450C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124732858 | ||||||
| chr9:124733229
|
C | T | 90 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(87): Show | 90 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.142+79G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 2/9 | chr9 | 124733229 | ||||||
| chr9:124733368
|
GA | G | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-20delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124733368 | ||||||
| chr9:124733381
|
A | G | 8 | a0001c0002t0005g0227a0001c0002t0005g0228a0001c0002t0005g0229others(5): Show | 8 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-32T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124733381 | ||||||
| chr9:124733429
|
T | C | 21 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(18): Show | 21 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.101-80A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124733429 | ||||||
| chr9:124733701
|
T | C | 1 | a0001c0001t0014g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.101-352A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124733701 | ||||||
| chr9:124733788
|
A | G | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-439T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124733788 | ||||||
| chr9:124733808
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-459G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124733808 | ||||||
| chr9:124733813
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.101-464T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124733813 | ||||||
| chr9:124733985
|
A | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-636T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124733985 | ||||||
| chr9:124734078
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-729G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124734078 | ||||||
| chr9:124734119
|
T | C | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.101-770A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124734119 | ||||||
| chr9:124734247
|
T | A | 1 | a0001c0001t0002g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.101-898A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124734247 | ||||||
| chr9:124734302
|
C | T | 2 | a0001c0003t0048g0102a0001c0003t0055g0181 | 2 | HG00423.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.101-953G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124734302 | ||||||
| chr9:124734348
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.101-999C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124734348 | ||||||
| chr9:124734558
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0001g0130a0001c0001t0002g0131others(1): Show | 4 | HG01517.hp2 HG01981.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-1209A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124734558 | ||||||
| chr9:124734656
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.101-1307C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124734656 | ||||||
| chr9:124734680
|
G | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.101-1331C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124734680 | ||||||
| chr9:124734865
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-1516G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124734865 | ||||||
| chr9:124734931
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.101-1582C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124734931 | ||||||
| chr9:124735192
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101-1843A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124735192 | ||||||
| chr9:124735211
|
T | C | 1 | a0001c0001t0002g0103 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.101-1862A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124735211 | ||||||
| chr9:124735294
|
T | C | 86 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(83): Show | 86 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.101-1945A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124735294 | ||||||
| chr9:124735474
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.101-2125C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124735474 | ||||||
| chr9:124735747
|
T | A | 2 | a0001c0001t0026g0232a0001c0001t0026g0233 | 2 | HG00642.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.101-2398A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124735747 | ||||||
| chr9:124735757
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-2408T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124735757 | ||||||
| chr9:124736095
|
T | C | 62 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(59): Show | 62 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.101-2746A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124736095 | ||||||
| chr9:124736237
|
C | T | 1 | a0001c0001t0004g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.101-2888G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124736237 | ||||||
| chr9:124736238
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.101-2889C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124736238 | ||||||
| chr9:124736381
|
G | C | 1 | a0001c0001t0003g0056 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.101-3032C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124736381 | ||||||
| chr9:124736533
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0002g0034a0001c0001t0003g0035 | 3 | HG01516.hp1 HG01517.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.101-3184G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124736533 | ||||||
| chr9:124736544
|
G | A | 1 | a0001c0002t0010g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.101-3195C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124736544 | ||||||
| chr9:124736610
|
G | A | 17 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(14): Show | 17 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-3261C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124736610 | ||||||
| chr9:124736688
|
A | G | 1 | a0001c0001t0002g0216 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.101-3339T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124736688 | ||||||
| chr9:124737162
|
A | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.101-3813T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124737162 | ||||||
| chr9:124737454
|
G | A | 1 | a0001c0001t0026g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.101-4105C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124737454 | ||||||
| chr9:124737592
|
G | A | 14 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.101-4243C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124737592 | ||||||
| chr9:124737640
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-4291A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124737640 | ||||||
| chr9:124737676
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-4327C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124737676 | ||||||
| chr9:124737811
|
G | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.101-4462C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124737811 | ||||||
| chr9:124737871
|
C | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-4522G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124737871 | ||||||
| chr9:124737892
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0141 | 2 | HG01081.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.101-4543C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124737892 | ||||||
| chr9:124737896
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-4547C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124737896 | ||||||
| chr9:124737981
|
C | T | 1 | a0001c0001t0002g0018 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.101-4632G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124737981 | ||||||
| chr9:124738056
|
C | A | 1 | a0001c0001t0002g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.101-4707G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124738056 | ||||||
| chr9:124738186
|
G | A | 1 | a0001c0001t0044g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.101-4837C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124738186 | ||||||
| chr9:124738201
|
C | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.101-4852G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124738201 | ||||||
| chr9:124738231
|
G | A | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.101-4882C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124738231 | ||||||
| chr9:124738357
|
TCAGGAAA others(14): Show |
T | 2 | a0001c0001t0046g0008a0001c0001t0060g0027 | 2 | HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.101-5029_101-5009d others(23): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124738357 | ||||||
| chr9:124738448
|
A | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.101-5099T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124738448 | ||||||
| chr9:124738565
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.101-5216G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124738565 | ||||||
| chr9:124738653
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.101-5304C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124738653 | ||||||
| chr9:124738760
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.101-5411A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124738760 | ||||||
| chr9:124738864
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0002g0145 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.101-5515C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124738864 | ||||||
| chr9:124738934
|
G | A | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-5585C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124738934 | ||||||
| chr9:124738983
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-5634G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124738983 | ||||||
| chr9:124739000
|
T | TA | 151 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(148): Show | 151 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.101-5652dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124739000 | ||||||
| chr9:124739125
|
T | C | 8 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0143others(5): Show | 8 | HG01106.hp2 HG01361.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-5776A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124739125 | ||||||
| chr9:124739187
|
C | CA | 15 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0141others(12): Show | 15 | HG01978.hp1 HG02145.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.101-5839dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124739187 | ||||||
| chr9:124739425
|
G | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.101-6076C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124739425 | ||||||
| chr9:124739749
|
T | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.101-6400A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124739749 | ||||||
| chr9:124739798
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0002g0142 | 2 | HG00621.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.101-6449C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124739798 | ||||||
| chr9:124739889
|
A | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101-6540T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124739889 | ||||||
| chr9:124739894
|
C | A | 1 | a0001c0001t0001g0161 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.101-6545G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124739894 | ||||||
| chr9:124739941
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.101-6592G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124739941 | ||||||
| chr9:124740062
|
T | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.101-6713A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124740062 | ||||||
| chr9:124740239
|
A | G | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.101-6890T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124740239 | ||||||
| chr9:124740273
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-6924G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124740273 | ||||||
| chr9:124740321
|
G | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0172a0001c0001t0003g0171 | 3 | NA18939.hp2 NA19004.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.101-6972C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124740321 | ||||||
| chr9:124740456
|
TTTTA | T | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.101-7111_101-7108d others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124740456 | ||||||
| chr9:124740597
|
T | C | 1 | a0001c0001t0061g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.101-7248A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124740597 | ||||||
| chr9:124740643
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-7294A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124740643 | ||||||
| chr9:124740665
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.101-7316C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124740665 | ||||||
| chr9:124741073
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0049g0231 | 2 | HG02257.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.101-7724G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741073 | ||||||
| chr9:124741094
|
CTGTCCAA others(20): Show |
C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101-7772_101-7746d others(29): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741094 | ||||||
| chr9:124741131
|
T | C | 11 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(8): Show | 11 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-7782A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741131 | ||||||
| chr9:124741151
|
G | A | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.101-7802C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741151 | ||||||
| chr9:124741234
|
A | G | 1 | a0001c0001t0016g0075 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.101-7885T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741234 | ||||||
| chr9:124741242
|
C | T | 1 | a0001c0001t0001g0009 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.101-7893G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741242 | ||||||
| chr9:124741264
|
ACAC | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.101-7918_101-7916d others(5): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741264 | ||||||
| chr9:124741432
|
G | A | 1 | a0001c0001t0030g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.101-8083C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741432 | ||||||
| chr9:124741433
|
T | C | 3 | a0001c0001t0019g0074a0001c0001t0020g0025a0001c0001t0020g0026 | 3 | HG02559.hp1 HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.101-8084A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741433 | ||||||
| chr9:124741645
|
T | C | 24 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(21): Show | 24 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.101-8296A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741645 | ||||||
| chr9:124741687
|
T | C | 12 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0002t0005g0226others(9): Show | 12 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.101-8338A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741687 | ||||||
| chr9:124741715
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-8366C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741715 | ||||||
| chr9:124741897
|
C | A | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-8548G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124741897 | ||||||
| chr9:124742071
|
T | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-8722A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124742071 | ||||||
| chr9:124742333
|
T | C | 14 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.101-8984A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124742333 | ||||||
| chr9:124742453
|
C | T | 7 | a0001c0001t0014g0069a0001c0001t0014g0071a0001c0001t0014g0072others(4): Show | 7 | HG01167.hp2 HG02647.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-9104G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124742453 | ||||||
| chr9:124742631
|
T | C | 171 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(168): Show | 171 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.101-9282A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124742631 | ||||||
| chr9:124742658
|
C | T | 5 | a0001c0001t0001g0122a0001c0001t0002g0121a0001c0001t0002g0157others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-9309G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124742658 | ||||||
| chr9:124742803
|
G | A | 1 | a0001c0002t0010g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.101-9454C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124742803 | ||||||
| chr9:124742925
|
A | G | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.101-9576T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124742925 | ||||||
| chr9:124743026
|
G | A | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.101-9677C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124743026 | ||||||
| chr9:124743196
|
A | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-9847T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124743196 | ||||||
| chr9:124743329
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.101-9980C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124743329 | ||||||
| chr9:124743362
|
T | C | 14 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.101-10013A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124743362 | ||||||
| chr9:124743452
|
G | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101-10103C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124743452 | ||||||
| chr9:124743700
|
G | A | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-10351C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124743700 | ||||||
| chr9:124744141
|
G | A | 1 | a0001c0001t0003g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.101-10792C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124744141 | ||||||
| chr9:124744277
|
C | T | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-10928G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124744277 | ||||||
| chr9:124744401
|
T | C | 1 | a0001c0001t0038g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.101-11052A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124744401 | ||||||
| chr9:124744487
|
T | C | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.101-11138A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124744487 | ||||||
| chr9:124744542
|
A | T | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.101-11193T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124744542 | ||||||
| chr9:124744564
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-11215G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124744564 | ||||||
| chr9:124744580
|
A | C | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-11231T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124744580 | ||||||
| chr9:124744883
|
T | C | 1 | a0001c0001t0002g0186 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.101-11534A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124744883 | ||||||
| chr9:124744933
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-11584A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124744933 | ||||||
| chr9:124745144
|
G | A | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.101-11795C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745144 | ||||||
| chr9:124745257
|
G | GA | 84 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.101-11909dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745257 | ||||||
| chr9:124745316
|
T | C | 33 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(30): Show | 33 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.101-11967A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745316 | ||||||
| chr9:124745379
|
A | T | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.101-12030T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745379 | ||||||
| chr9:124745501
|
G | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101-12152C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745501 | ||||||
| chr9:124745527
|
C | T | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.101-12178G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745527 | ||||||
| chr9:124745529
|
G | A | 2 | a0001c0001t0011g0205a0001c0001t0012g0207 | 2 | NA18977.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.101-12180C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745529 | ||||||
| chr9:124745586
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.101-12237C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745586 | ||||||
| chr9:124745606
|
G | C | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.101-12257C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745606 | ||||||
| chr9:124745671
|
TA | T | 85 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(82): Show | 85 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.101-12323delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745671 | ||||||
| chr9:124745715
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0044g0175 | 2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.101-12366C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745715 | ||||||
| chr9:124745943
|
G | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101-12594C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745943 | ||||||
| chr9:124745987
|
C | CA | 21 | a0001c0001t0001g0065a0001c0001t0001g0113a0001c0001t0001g0118others(18): Show | 21 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.101-12639dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745987 | ||||||
| chr9:124745987
|
C | CAA | 9 | a0001c0001t0012g0207a0001c0002t0005g0227a0001c0002t0005g0228others(6): Show | 9 | HG02451.hp1 HG02647.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.101-12640_101-1263 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745987 | ||||||
| chr9:124745987
|
CA | C | 44 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0160others(41): Show | 44 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.101-12639delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124745987 | ||||||
| chr9:124746016
|
A | G | 171 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(168): Show | 171 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.101-12667T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124746016 | ||||||
| chr9:124746364
|
G | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.101-13015C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124746364 | ||||||
| chr9:124746398
|
G | A | 1 | a0001c0001t0023g0188 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.101-13049C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124746398 | ||||||
| chr9:124746406
|
C | A | 1 | a0001c0001t0002g0158 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.101-13057G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124746406 | ||||||
| chr9:124746950
|
G | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101-13601C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124746950 | ||||||
| chr9:124747187
|
C | CT | 79 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(76): Show | 79 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.101-13839dupA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124747187 | ||||||
| chr9:124747187
|
C | CTT | 17 | a0001c0001t0002g0033a0001c0001t0002g0083a0001c0001t0009g0060others(14): Show | 17 | HG01433.hp2 HG02145.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-13840_101-1383 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124747187 | ||||||
| chr9:124747187
|
CT | C | 21 | a0001c0001t0001g0143a0001c0001t0003g0110a0001c0001t0004g0193others(18): Show | 21 | HG00544.hp2 HG01167.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.101-13839delA | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124747187 | ||||||
| chr9:124747498
|
C | T | 1 | a0001c0001t0035g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.101-14149G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124747498 | ||||||
| chr9:124747518
|
G | A | 2 | a0001c0001t0037g0032a0001c0001t0041g0031 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.101-14169C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124747518 | ||||||
| chr9:124747661
|
T | G | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.101-14312A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124747661 | ||||||
| chr9:124747775
|
T | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.101-14426A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124747775 | ||||||
| chr9:124747814
|
C | T | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.101-14465G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124747814 | ||||||
| chr9:124747886
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.101-14537C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124747886 | ||||||
| chr9:124747961
|
C | T | 83 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.101-14612G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124747961 | ||||||
| chr9:124748165
|
T | G | 1 | a0001c0001t0001g0144 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.101-14816A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748165 | ||||||
| chr9:124748328
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.101-14979G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748328 | ||||||
| chr9:124748349
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.101-15000A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748349 | ||||||
| chr9:124748351
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0002g0145 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.101-15002C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748351 | ||||||
| chr9:124748390
|
T | A | 33 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(30): Show | 33 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.101-15041A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748390 | ||||||
| chr9:124748523
|
T | C | 11 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(8): Show | 11 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-15174A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748523 | ||||||
| chr9:124748627
|
G | A | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.101-15278C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748627 | ||||||
| chr9:124748686
|
C | T | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.101-15337G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748686 | ||||||
| chr9:124748695
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-15346A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748695 | ||||||
| chr9:124748728
|
G | A | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-15379C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748728 | ||||||
| chr9:124748740
|
C | G | 1 | a0001c0001t0008g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101-15391G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748740 | ||||||
| chr9:124748861
|
T | C | 24 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(21): Show | 24 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.101-15512A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748861 | ||||||
| chr9:124748864
|
C | CA | 8 | a0001c0001t0001g0180a0001c0001t0012g0207a0001c0001t0016g0075others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-15516dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124748864 | ||||||
| chr9:124749035
|
G | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-15686C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124749035 | ||||||
| chr9:124749256
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.101-15907G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124749256 | ||||||
| chr9:124749617
|
A | G | 1 | a0001c0001t0061g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.101-16268T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124749617 | ||||||
| chr9:124749645
|
T | G | 86 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(83): Show | 86 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.101-16296A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124749645 | ||||||
| chr9:124749761
|
G | A | 138 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(135): Show | 138 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.101-16412C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124749761 | ||||||
| chr9:124749857
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-16508T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124749857 | ||||||
| chr9:124749885
|
T | C | 1 | a0001c0001t0046g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.101-16536A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124749885 | ||||||
| chr9:124750216
|
A | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.101-16867T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124750216 | ||||||
| chr9:124750358
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.101-17009G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124750358 | ||||||
| chr9:124750381
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-17032G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124750381 | ||||||
| chr9:124750397
|
T | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-17048A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124750397 | ||||||
| chr9:124750529
|
G | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.101-17180C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124750529 | ||||||
| chr9:124750570
|
C | A | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.101-17221G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124750570 | ||||||
| chr9:124750617
|
G | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101-17268C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124750617 | ||||||
| chr9:124750755
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-17406C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124750755 | ||||||
| chr9:124750842
|
A | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101-17493T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124750842 | ||||||
| chr9:124750973
|
A | G | 3 | a0001c0001t0001g0118a0001c0001t0002g0145a0001c0001t0002g0149 | 3 | HG00438.hp2 NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.101-17624T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124750973 | ||||||
| chr9:124751067
|
TC | T | 231 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(228): Show | 231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.101-17719delG | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124751067 | ||||||
| chr9:124751255
|
A | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.101-17906T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124751255 | ||||||
| chr9:124751357
|
T | C | 13 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(10): Show | 13 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.101-18008A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124751357 | ||||||
| chr9:124751553
|
G | A | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.101-18204C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124751553 | ||||||
| chr9:124751870
|
C | T | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.101-18521G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124751870 | ||||||
| chr9:124752161
|
C | T | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.101-18812G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124752161 | ||||||
| chr9:124752255
|
C | A | 2 | a0001c0001t0001g0061a0001c0001t0009g0060 | 2 | NA18939.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.100+18765G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124752255 | ||||||
| chr9:124752274
|
A | G | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.100+18746T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124752274 | ||||||
| chr9:124752331
|
T | G | 1 | a0001c0001t0028g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100+18689A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124752331 | ||||||
| chr9:124752399
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.100+18621T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124752399 | ||||||
| chr9:124752550
|
C | T | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100+18470G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124752550 | ||||||
| chr9:124752558
|
A | G | 1 | a0001c0001t0008g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100+18462T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124752558 | ||||||
| chr9:124752815
|
T | TA | 14 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0030g0004others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.100+18204dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124752815 | ||||||
| chr9:124752816
|
A | T | 4 | a0001c0001t0008g0094a0001c0001t0008g0095a0001c0001t0008g0096others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+18204T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124752816 | ||||||
| chr9:124752946
|
G | C | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.100+18074C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124752946 | ||||||
| chr9:124753753
|
G | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.100+17267C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124753753 | ||||||
| chr9:124753809
|
A | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100+17211T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124753809 | ||||||
| chr9:124753898
|
T | C | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(84): Show | 87 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.100+17122A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124753898 | ||||||
| chr9:124754037
|
G | A | 4 | a0001c0001t0001g0178a0001c0001t0002g0176a0001c0001t0002g0177others(1): Show | 4 | HG02698.hp2 HG03927.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+16983C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124754037 | ||||||
| chr9:124754287
|
C | A | 1 | a0001c0001t0001g0022 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.100+16733G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124754287 | ||||||
| chr9:124754405
|
C | T | 2 | a0001c0001t0004g0209a0001c0001t0034g0210 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.100+16615G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124754405 | ||||||
| chr9:124754506
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+16514C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124754506 | ||||||
| chr9:124754558
|
G | A | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+16462C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124754558 | ||||||
| chr9:124754583
|
G | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100+16437C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124754583 | ||||||
| chr9:124754591
|
C | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+16429G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124754591 | ||||||
| chr9:124754744
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+16276A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124754744 | ||||||
| chr9:124755174
|
G | GTAAGACT others(3): Show |
231 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(228): Show | 231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.100+15845_100+1584 others(14): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124755174 | ||||||
| chr9:124755195
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.100+15825C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124755195 | ||||||
| chr9:124755316
|
C | T | 1 | a0001c0001t0013g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100+15704G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124755316 | ||||||
| chr9:124755409
|
T | C | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+15611A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124755409 | ||||||
| chr9:124755770
|
A | C | 14 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0001t0033g0097others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.100+15250T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124755770 | ||||||
| chr9:124756034
|
CTT | C | 3 | a0001c0001t0014g0071a0001c0001t0014g0072a0001c0001t0045g0070 | 3 | HG01167.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100+14984_100+1498 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124756034 | ||||||
| chr9:124756272
|
T | C | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100+14748A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124756272 | ||||||
| chr9:124756284
|
T | C | 1 | a0001c0001t0015g0156 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.100+14736A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124756284 | ||||||
| chr9:124756855
|
G | A | 55 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(52): Show | 55 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.100+14165C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124756855 | ||||||
| chr9:124757239
|
T | G | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100+13781A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124757239 | ||||||
| chr9:124757268
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+13752A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124757268 | ||||||
| chr9:124757345
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.100+13675C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124757345 | ||||||
| chr9:124757461
|
C | CA | 74 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0118others(71): Show | 74 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.100+13558dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124757461 | ||||||
| chr9:124757461
|
C | CAA | 11 | a0001c0001t0001g0152a0001c0001t0002g0145a0001c0001t0002g0147others(8): Show | 11 | HG00544.hp2 HG03516.hp1 HG03540.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+13557_100+1355 others(6): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124757461 | ||||||
| chr9:124757461
|
CA | C | 12 | a0001c0001t0001g0180a0001c0001t0068g0006a0001c0002t0005g0226others(9): Show | 12 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.100+13558delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124757461 | ||||||
| chr9:124757462
|
A | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0002g0018others(2): Show | 5 | HG00621.hp2 NA18983.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+13558T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124757462 | ||||||
| chr9:124757591
|
A | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100+13429T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124757591 | ||||||
| chr9:124758165
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.100+12855A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124758165 | ||||||
| chr9:124758175
|
TC | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(84): Show | 87 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.100+12844delG | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124758175 | ||||||
| chr9:124758282
|
C | T | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100+12738G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124758282 | ||||||
| chr9:124758297
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.100+12723C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124758297 | ||||||
| chr9:124758356
|
T | C | 14 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(11): Show | 14 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.100+12664A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124758356 | ||||||
| chr9:124758450
|
T | C | 61 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(58): Show | 61 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.100+12570A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124758450 | ||||||
| chr9:124758947
|
C | A | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.100+12073G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124758947 | ||||||
| chr9:124759001
|
T | C | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.100+12019A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124759001 | ||||||
| chr9:124759085
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100+11935A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124759085 | ||||||
| chr9:124759099
|
A | C | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.100+11921T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124759099 | ||||||
| chr9:124759483
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.100+11537T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124759483 | ||||||
| chr9:124759649
|
T | C | 1 | a0001c0001t0002g0149 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.100+11371A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124759649 | ||||||
| chr9:124759697
|
G | A | 23 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 23 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.100+11323C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124759697 | ||||||
| chr9:124759827
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+11193T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124759827 | ||||||
| chr9:124760039
|
C | CA | 6 | a0001c0001t0001g0065a0001c0001t0002g0149a0001c0001t0021g0148others(3): Show | 6 | HG00438.hp2 HG00639.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+10980dupT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760039 | ||||||
| chr9:124760110
|
G | A | 7 | a0001c0001t0014g0069a0001c0001t0014g0071a0001c0001t0014g0072others(4): Show | 7 | HG01167.hp2 HG02647.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+10910C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760110 | ||||||
| chr9:124760118
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0050g0024 | 2 | HG00558.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.100+10902G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760118 | ||||||
| chr9:124760269
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+10751C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760269 | ||||||
| chr9:124760311
|
A | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+10709T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760311 | ||||||
| chr9:124760394
|
T | C | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100+10626A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760394 | ||||||
| chr9:124760420
|
A | G | 2 | a0001c0001t0030g0004a0001c0001t0031g0005 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.100+10600T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760420 | ||||||
| chr9:124760634
|
G | C | 1 | a0001c0001t0001g0009 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.100+10386C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760634 | ||||||
| chr9:124760692
|
T | G | 1 | a0001c0001t0009g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.100+10328A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760692 | ||||||
| chr9:124760717
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.100+10303A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760717 | ||||||
| chr9:124760838
|
A | G | 2 | a0001c0001t0008g0094a0001c0001t0008g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.100+10182T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760838 | ||||||
| chr9:124760841
|
C | A | 1 | a0001c0001t0006g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100+10179G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760841 | ||||||
| chr9:124760997
|
G | C | 1 | a0001c0001t0002g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.100+10023C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124760997 | ||||||
| chr9:124761020
|
A | G | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+10000T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124761020 | ||||||
| chr9:124761202
|
T | A | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100+9818A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124761202 | ||||||
| chr9:124761263
|
A | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100+9757T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124761263 | ||||||
| chr9:124761275
|
G | C | 1 | a0001c0001t0002g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.100+9745C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124761275 | ||||||
| chr9:124761332
|
C | T | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.100+9688G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124761332 | ||||||
| chr9:124761394
|
A | G | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100+9626T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124761394 | ||||||
| chr9:124761619
|
A | G | 1 | a0001c0001t0001g0022 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.100+9401T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124761619 | ||||||
| chr9:124761667
|
C | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0002g0018others(2): Show | 5 | HG00621.hp2 NA18983.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+9353G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124761667 | ||||||
| chr9:124761730
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.100+9290A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124761730 | ||||||
| chr9:124761772
|
A | G | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.100+9248T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124761772 | ||||||
| chr9:124761921
|
C | G | 1 | a0001c0001t0003g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.100+9099G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124761921 | ||||||
| chr9:124762097
|
C | A | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.100+8923G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124762097 | ||||||
| chr9:124762135
|
T | C | 3 | a0001c0001t0007g0088a0001c0001t0007g0089a0001c0001t0007g0090 | 3 | HG02723.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.100+8885A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124762135 | ||||||
| chr9:124762229
|
A | G | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+8791T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124762229 | ||||||
| chr9:124762615
|
T | A | 4 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+8405A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124762615 | ||||||
| chr9:124762797
|
C | T | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.100+8223G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124762797 | ||||||
| chr9:124762854
|
T | C | 2 | a0001c0003t0048g0102a0001c0003t0055g0181 | 2 | HG00423.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.100+8166A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124762854 | ||||||
| chr9:124762865
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+8155A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124762865 | ||||||
| chr9:124762880
|
C | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+8140G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124762880 | ||||||
| chr9:124763015
|
G | A | 1 | a0001c0001t0019g0074 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.100+8005C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124763015 | ||||||
| chr9:124763091
|
C | T | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.100+7929G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124763091 | ||||||
| chr9:124763253
|
G | C | 1 | a0001c0001t0002g0216 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.100+7767C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124763253 | ||||||
| chr9:124763261
|
G | A | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+7759C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124763261 | ||||||
| chr9:124763630
|
T | C | 24 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(21): Show | 24 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.100+7390A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124763630 | ||||||
| chr9:124763654
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.100+7366C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124763654 | ||||||
| chr9:124763911
|
C | T | 1 | a0001c0001t0033g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100+7109G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124763911 | ||||||
| chr9:124764044
|
C | T | 4 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(1): Show | 4 | HG02723.hp1 NA18522.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+6976G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124764044 | ||||||
| chr9:124764050
|
G | T | 1 | a0001c0001t0008g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100+6970C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124764050 | ||||||
| chr9:124764121
|
T | G | 1 | a0001c0001t0002g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.100+6899A>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124764121 | ||||||
| chr9:124764166
|
A | G | 182 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(179): Show | 182 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.100+6854T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124764166 | ||||||
| chr9:124764183
|
CA | C | 38 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(35): Show | 38 | HG00544.hp2 HG00639.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.100+6836delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124764183 | ||||||
| chr9:124764216
|
G | A | 11 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(8): Show | 11 | HG02258.hp2 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+6804C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124764216 | ||||||
| chr9:124764479
|
CAG | C | 12 | a0001c0001t0016g0075a0001c0001t0016g0077a0001c0001t0016g0078others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.100+6539_100+6540d others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124764479 | ||||||
| chr9:124764621
|
G | A | 3 | a0001c0001t0008g0094a0001c0001t0008g0095a0001c0001t0008g0096 | 3 | HG02717.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.100+6399C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124764621 | ||||||
| chr9:124764740
|
A | C | 1 | a0001c0001t0035g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.100+6280T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124764740 | ||||||
| chr9:124765049
|
G | A | 33 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(30): Show | 33 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.100+5971C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124765049 | ||||||
| chr9:124765126
|
G | A | 85 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(82): Show | 85 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.100+5894C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124765126 | ||||||
| chr9:124765185
|
T | C | 8 | a0001c0001t0024g0012a0001c0001t0024g0013a0001c0001t0025g0014others(5): Show | 8 | HG00639.hp1 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+5835A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124765185 | ||||||
| chr9:124765398
|
C | G | 3 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195 | 3 | HG02027.hp1 NA18969.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.100+5622G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124765398 | ||||||
| chr9:124765756
|
C | A | 171 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(168): Show | 171 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.100+5264G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124765756 | ||||||
| chr9:124765842
|
T | C | 7 | a0001c0001t0001g0079a0001c0001t0002g0011a0001c0001t0002g0080others(4): Show | 7 | NA18943.hp2 NA19010.hp2 NA19011.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+5178A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124765842 | ||||||
| chr9:124765910
|
G | T | 1 | a0001c0001t0003g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.100+5110C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124765910 | ||||||
| chr9:124765996
|
G | A | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.100+5024C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124765996 | ||||||
| chr9:124766015
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.100+5005G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124766015 | ||||||
| chr9:124766080
|
C | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+4940G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124766080 | ||||||
| chr9:124766080
|
CG | C | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+4939delC | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124766080 | ||||||
| chr9:124766137
|
C | A | 2 | a0001c0001t0022g0217a0001c0001t0022g0220 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.100+4883G>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124766137 | ||||||
| chr9:124766156
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.100+4864G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124766156 | ||||||
| chr9:124766563
|
C | T | 170 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(167): Show | 170 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.100+4457G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124766563 | ||||||
| chr9:124766588
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.100+4432C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124766588 | ||||||
| chr9:124766598
|
T | C | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100+4422A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124766598 | ||||||
| chr9:124766621
|
T | A | 2 | a0001c0001t0001g0085a0001c0001t0002g0084 | 2 | HG01361.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.100+4399A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124766621 | ||||||
| chr9:124766726
|
G | A | 48 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(45): Show | 48 | HG00544.hp2 HG00639.hp1 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.100+4294C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124766726 | ||||||
| chr9:124766822
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0002g0183 | 2 | HG02523.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.100+4198C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124766822 | ||||||
| chr9:124767184
|
G | T | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+3836C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124767184 | ||||||
| chr9:124767513
|
GA | G | 10 | a0001c0001t0004g0209a0001c0001t0024g0012a0001c0001t0024g0013others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+3506delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124767513 | ||||||
| chr9:124767522
|
A | G | 19 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(16): Show | 19 | HG00544.hp2 HG02015.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.100+3498T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124767522 | ||||||
| chr9:124767552
|
A | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100+3468T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124767552 | ||||||
| chr9:124767736
|
A | C | 1 | a0001c0001t0002g0011 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.100+3284T>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124767736 | ||||||
| chr9:124767774
|
T | C | 1 | a0001c0001t0003g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.100+3246A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124767774 | ||||||
| chr9:124767794
|
T | C | 1 | a0001c0001t0042g0099 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.100+3226A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124767794 | ||||||
| chr9:124767843
|
C | T | 1 | a0001c0001t0057g0192 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.100+3177G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124767843 | ||||||
| chr9:124767882
|
C | T | 32 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.100+3138G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124767882 | ||||||
| chr9:124767941
|
T | C | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.100+3079A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124767941 | ||||||
| chr9:124768099
|
TTCTGACA others(3): Show |
T | 5 | a0001c0002t0010g0222a0001c0002t0010g0223a0001c0002t0010g0224others(2): Show | 5 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2911_100+2920d others(12): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124768099 | ||||||
| chr9:124768231
|
T | C | 2 | a0001c0001t0015g0155a0001c0001t0015g0156 | 2 | NA18955.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.100+2789A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124768231 | ||||||
| chr9:124768293
|
T | C | 33 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(30): Show | 33 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.100+2727A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124768293 | ||||||
| chr9:124768341
|
A | T | 1 | a0004c0004t0036g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100+2679T>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124768341 | ||||||
| chr9:124768392
|
T | C | 12 | a0001c0001t0028g0002a0001c0001t0029g0003a0001c0002t0005g0226others(9): Show | 12 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.100+2628A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124768392 | ||||||
| chr9:124768410
|
T | A | 1 | a0001c0001t0002g0187 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.100+2610A>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124768410 | ||||||
| chr9:124769103
|
C | T | 1 | a0001c0001t0066g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.100+1917G>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124769103 | ||||||
| chr9:124769160
|
T | C | 7 | a0001c0001t0002g0162a0001c0001t0002g0185a0001c0001t0002g0186others(4): Show | 7 | HG00438.hp1 HG02056.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+1860A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124769160 | ||||||
| chr9:124769252
|
TA | T | 135 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0022others(132): Show | 135 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.100+1767delT | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124769252 | ||||||
| chr9:124769252
|
TAA | T | 7 | a0001c0001t0001g0009a0001c0001t0006g0191a0001c0001t0013g0190others(4): Show | 7 | HG00639.hp1 HG01884.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+1766_100+1767d others(4): Show |
NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124769252 | ||||||
| chr9:124769638
|
T | C | 2 | a0001c0001t0047g0105a0001c0001t0062g0104 | 2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.100+1382A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124769638 | ||||||
| chr9:124769689
|
T | C | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+1331A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124769689 | ||||||
| chr9:124770073
|
G | A | 2 | a0001c0001t0002g0189a0001c0001t0023g0188 | 2 | NA18959.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.100+947C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770073 | ||||||
| chr9:124770280
|
G | A | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100+740C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770280 | ||||||
| chr9:124770293
|
G | A | 1 | a0001c0001t0027g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.100+727C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770293 | ||||||
| chr9:124770306
|
G | C | 3 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159 | 3 | HG02602.hp1 HG02683.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.100+714C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770306 | ||||||
| chr9:124770379
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0043g0107 | 2 | HG00609.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.100+641C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770379 | ||||||
| chr9:124770419
|
G | A | 2 | a0001c0001t0028g0002a0001c0001t0029g0003 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100+601C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770419 | ||||||
| chr9:124770591
|
C | G | 1 | a0001c0001t0068g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100+429G>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770591 | ||||||
| chr9:124770625
|
A | G | 179 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(176): Show | 179 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.100+395T>C | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770625 | ||||||
| chr9:124770632
|
G | C | 1 | a0001c0001t0022g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.100+388C>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770632 | ||||||
| chr9:124770638
|
G | A | 30 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(27): Show | 30 | HG00423.hp2 HG00438.hp1 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+382C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770638 | ||||||
| chr9:124770694
|
T | C | 32 | a0001c0001t0001g0219a0001c0001t0002g0211a0001c0001t0002g0216others(29): Show | 32 | HG00544.hp2 HG00609.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.100+326A>G | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770694 | ||||||
| chr9:124770737
|
G | A | 10 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+283C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770737 | ||||||
| chr9:124770845
|
G | A | 1 | a0001c0001t0049g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+175C>T | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770845 | ||||||
| chr9:124770910
|
G | T | 1 | a0002c0006t0069g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+110C>A | NR6A1 | ENSG00000148200.17 | transcript | ENST00000487099.7 | protein_coding | 1/9 | chr9 | 124770910 |