Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2908 |
| ensemblid | ENSG00000113580.15 |
| hgncid | 7978 |
| symbol | NR3C1 |
| name | nuclear receptor subfamily 3 group C member 1 |
| refseq_nuc | NM_000176.3 |
| refseq_prot | NP_000167.1 |
| ensembl_nuc | ENST00000394464.7 |
| ensembl_prot | ENSP00000377977.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 143277934 |
| end | 143403686 |
| strand | - |
| ver | v1.2 |
| region | chr5:143277934-143403686 |
| region5000 | chr5:143272934-143408686 |
| regionname0 | NR3C1_chr5_143277934_143403686 |
| regionname5000 | NR3C1_chr5_143272934_143408686 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 777 | 261 | 83 | 44 | 94 | 15 | 23 | 68 | NR3C1_chr5_143272934_143408686 | NR3C1 | MDSKE others(772): Show |
chr5 | 143272934 | 143408686 |
| a0002 | 0/0 | 777 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | MDSKE others(772): Show |
chr5 | 143272934 | 143408686 |
| a0003 | 0/0 | 777 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | MDSKE others(772): Show |
chr5 | 143272934 | 143408686 |
| a0004 | 0/0 | 777 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | MDSKE others(772): Show |
chr5 | 143272934 | 143408686 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2331 | 207 | 60 | 38 | 71 | 13 | 23 | NR3C1_chr5_143272934_143408686 | NR3C1 | ATGGA others(2326): Show |
chr5 | 143272934 | 143408686 | ||
| a0001c0002 | 0/0 | 2331 | 16 | 0 | 0 | 16 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | ATGGA others(2326): Show |
chr5 | 143272934 | 143408686 | ||
| a0001c0003 | 0/0 | 2331 | 13 | 13 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | ATGGA others(2326): Show |
chr5 | 143272934 | 143408686 | ||
| a0001c0004 | 0/0 | 2331 | 12 | 4 | 6 | 0 | 2 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | ATGGA others(2326): Show |
chr5 | 143272934 | 143408686 | ||
| a0001c0005 | 0/0 | 2331 | 7 | 0 | 0 | 7 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | ATGGA others(2326): Show |
chr5 | 143272934 | 143408686 | ||
| a0001c0006 | 0/0 | 2331 | 6 | 6 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | ATGGA others(2326): Show |
chr5 | 143272934 | 143408686 | ||
| a0002c0007 | 0/0 | 2331 | 3 | 3 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | ATGGA others(2326): Show |
chr5 | 143272934 | 143408686 | ||
| a0003c0008 | 0/0 | 2331 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | ATGGA others(2326): Show |
chr5 | 143272934 | 143408686 | ||
| a0004c0009 | 0/0 | 2331 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | ATGGA others(2326): Show |
chr5 | 143272934 | 143408686 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6779 | 99 | 29 | 17 | 41 | 4 | 8 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0002 | 0/1 | 6780 | 41 | 1 | 7 | 23 | 4 | 5 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6775): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0003 | 0/0 | 6782 | 18 | 2 | 9 | 0 | 2 | 5 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6777): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0004 | 0/0 | 6779 | 2 | 1 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0005 | 0/0 | 6781 | 12 | 9 | 2 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6776): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0007 | 0/0 | 6780 | 11 | 11 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6775): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0010 | 0/0 | 6780 | 5 | 0 | 2 | 1 | 0 | 2 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6775): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0012 | 0/0 | 6779 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0013 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0014 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0015 | 1/0 | 6778 | 1 | 0 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6773): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0020 | 0/0 | 6779 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0021 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0022 | 0/0 | 6782 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6777): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0023 | 0/0 | 6781 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6776): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0024 | 0/0 | 6780 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6775): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0025 | 0/0 | 6780 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6775): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0026 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0028 | 0/0 | 6779 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0029 | 0/0 | 6779 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0030 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0031 | 0/0 | 6779 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0032 | 0/0 | 6778 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6773): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0035 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0036 | 0/0 | 6780 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6775): Show |
chr5 | 143272934 | 143408686 |
| a0001c0001t0037 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0002t0004 | 0/0 | 6779 | 3 | 0 | 0 | 3 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0002t0006 | 0/0 | 6780 | 9 | 0 | 0 | 9 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6775): Show |
chr5 | 143272934 | 143408686 |
| a0001c0002t0016 | 0/0 | 6781 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6776): Show |
chr5 | 143272934 | 143408686 |
| a0001c0002t0017 | 0/0 | 6780 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6775): Show |
chr5 | 143272934 | 143408686 |
| a0001c0002t0018 | 0/0 | 6780 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6775): Show |
chr5 | 143272934 | 143408686 |
| a0001c0002t0019 | 0/0 | 6779 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0003t0004 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0003t0006 | 0/0 | 6780 | 3 | 3 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6775): Show |
chr5 | 143272934 | 143408686 |
| a0001c0003t0008 | 0/0 | 6780 | 9 | 9 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6775): Show |
chr5 | 143272934 | 143408686 |
| a0001c0004t0001 | 0/0 | 6779 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0004t0004 | 0/0 | 6779 | 8 | 2 | 5 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0004t0005 | 0/0 | 6781 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6776): Show |
chr5 | 143272934 | 143408686 |
| a0001c0004t0027 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0001c0004t0033 | 0/0 | 6778 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6773): Show |
chr5 | 143272934 | 143408686 |
| a0001c0005t0009 | 0/0 | 6784 | 7 | 0 | 0 | 7 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6779): Show |
chr5 | 143272934 | 143408686 |
| a0001c0006t0001 | 0/0 | 6779 | 6 | 6 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0002c0007t0011 | 0/0 | 6779 | 2 | 2 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0002c0007t0034 | 0/0 | 6779 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| a0003c0008t0003 | 0/0 | 6782 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6777): Show |
chr5 | 143272934 | 143408686 |
| a0004c0009t0001 | 0/0 | 6779 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | GCCGC others(6774): Show |
chr5 | 143272934 | 143408686 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0007g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0010g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0010g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0010g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0010g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0010g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0012g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0014g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0015g0016 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0020g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0021g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0022g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0023g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0024g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0025g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0026g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0028g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0029g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0030g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0031g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0032g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0035g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0036g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0001t0037g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0016g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0017g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0018g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0002t0019g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0003t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0004t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0004t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0004t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0004t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0004t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0004t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0004t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0004t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0004t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0004t0027g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0004t0033g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0005t0009g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0005t0009g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0005t0009g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0005t0009g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0005t0009g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0005t0009g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0006t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0006t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0006t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0006t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0001c0006t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0002c0007t0011g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0002c0007t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0002c0007t0034g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0003c0008t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| a0004c0009t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0022 | g0186 | EUR | GBR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | GBR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0187 | EUR | GBR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00280 | hp1 | a0001 | c0004 | t0004 | g0052 | EUR | FIN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0063 | EUR | FIN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00323 | hp2 | a0003 | c0008 | t0003 | g0179 | EUR | FIN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00408 | hp1 | a0001 | c0001 | t0031 | g0128 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00438 | hp1 | a0001 | c0002 | t0006 | g0037 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00544 | hp2 | a0001 | c0001 | t0029 | g0124 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00639 | hp1 | a0001 | c0001 | t0010 | g0095 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00733 | hp2 | a0001 | c0004 | t0004 | g0057 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00738 | hp1 | a0001 | c0004 | t0004 | g0053 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01070 | hp2 | a0001 | c0004 | t0004 | g0056 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0222 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01256 | hp2 | a0001 | c0004 | t0033 | g0051 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01346 | hp2 | a0001 | c0001 | t0010 | g0061 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0201 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01515 | hp2 | a0001 | c0001 | t0023 | g0208 | EUR | IBS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0219 | EUR | IBS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01516 | hp2 | a0001 | c0004 | t0001 | g0137 | EUR | IBS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0217 | EUR | IBS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01884 | hp1 | a0002 | c0007 | t0011 | g0255 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01884 | hp2 | a0001 | c0004 | t0004 | g0059 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01934 | hp1 | a0001 | c0001 | t0024 | g0206 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG01978 | hp2 | a0001 | c0004 | t0004 | g0050 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02027 | hp1 | a0001 | c0005 | t0009 | g0251 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02055 | hp1 | a0001 | c0003 | t0008 | g0043 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02074 | hp2 | a0001 | c0005 | t0009 | g0249 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02132 | hp2 | a0001 | c0002 | t0006 | g0036 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02135 | hp1 | a0001 | c0005 | t0009 | g0250 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02148 | hp2 | a0001 | c0004 | t0004 | g0055 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02165 | hp1 | a0001 | c0002 | t0004 | g0167 | EAS | CDX | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02258 | hp2 | a0001 | c0003 | t0006 | g0023 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02572 | hp2 | a0001 | c0006 | t0001 | g0102 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02647 | hp2 | a0001 | c0006 | t0001 | g0103 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0253 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02698 | hp2 | a0001 | c0001 | t0010 | g0070 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02717 | hp1 | a0001 | c0006 | t0001 | g0099 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0198 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0211 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02809 | hp1 | a0002 | c0007 | t0034 | g0256 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02886 | hp1 | a0001 | c0003 | t0008 | g0026 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02886 | hp2 | a0001 | c0001 | t0026 | g0115 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02895 | hp2 | a0001 | c0003 | t0008 | g0024 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02896 | hp1 | a0001 | c0003 | t0008 | g0045 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02922 | hp1 | a0001 | c0001 | t0035 | g0117 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02922 | hp2 | a0001 | c0001 | t0013 | g0010 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02965 | hp1 | a0001 | c0006 | t0001 | g0101 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02970 | hp2 | a0001 | c0003 | t0008 | g0027 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03139 | hp1 | a0001 | c0003 | t0008 | g0044 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0019 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03453 | hp1 | a0002 | c0007 | t0011 | g0254 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0098 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | ESN | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03540 | hp2 | a0001 | c0006 | t0001 | g0100 | AFR | GWD | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03579 | hp2 | a0001 | c0003 | t0008 | g0035 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03688 | hp1 | a0001 | c0001 | t0010 | g0064 | SAS | STU | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0185 | SAS | STU | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03704 | hp2 | a0001 | c0001 | t0036 | g0214 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03710 | hp2 | a0001 | c0001 | t0012 | g0009 | SAS | PJL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | BEB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0189 | SAS | STU | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG04204 | hp1 | a0001 | c0001 | t0032 | g0065 | SAS | STU | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | STU | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | YRI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | CHB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18906 | hp1 | a0001 | c0001 | t0037 | g0258 | AFR | YRI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | YRI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18940 | hp1 | a0001 | c0002 | t0004 | g0168 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18942 | hp1 | a0001 | c0001 | t0020 | g0047 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18942 | hp2 | a0001 | c0002 | t0006 | g0032 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18946 | hp2 | a0001 | c0002 | t0006 | g0031 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18959 | hp2 | a0001 | c0001 | t0010 | g0088 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18969 | hp2 | a0001 | c0002 | t0018 | g0040 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18972 | hp1 | a0001 | c0002 | t0019 | g0039 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18974 | hp1 | a0001 | c0002 | t0006 | g0034 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18982 | hp2 | a0001 | c0005 | t0009 | g0252 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18985 | hp2 | a0001 | c0002 | t0016 | g0028 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18988 | hp1 | a0001 | c0002 | t0017 | g0033 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18995 | hp1 | a0001 | c0002 | t0006 | g0030 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19001 | hp2 | a0001 | c0005 | t0009 | g0257 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19003 | hp2 | a0001 | c0002 | t0004 | g0060 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19004 | hp1 | a0001 | c0001 | t0025 | g0224 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19007 | hp1 | a0001 | c0002 | t0006 | g0041 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19057 | hp2 | a0001 | c0005 | t0009 | g0008 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19063 | hp1 | a0001 | c0002 | t0006 | g0029 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19064 | hp1 | a0001 | c0002 | t0006 | g0038 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19070 | hp1 | a0001 | c0005 | t0009 | g0008 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19082 | hp2 | a0001 | c0001 | t0028 | g0159 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0204 | AFR | YRI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA20129 | hp1 | a0001 | c0004 | t0027 | g0058 | AFR | ASW | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA20129 | hp2 | a0001 | c0003 | t0006 | g0046 | AFR | ASW | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0190 | EUR | TSI | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | GIH | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA20905 | hp2 | a0004 | c0009 | t0001 | g0075 | SAS | GIH | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02109 | hp1 | a0001 | c0003 | t0004 | g0054 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02109 | hp2 | a0001 | c0004 | t0004 | g0049 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02486 | hp2 | a0001 | c0003 | t0008 | g0042 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03471 | hp1 | a0001 | c0003 | t0006 | g0022 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG03471 | hp2 | a0001 | c0004 | t0005 | g0048 | AFR | MSL | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG06807 | hp1 | a0001 | c0001 | t0030 | g0194 | AFR | USA | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| HG06807 | hp2 | a0001 | c0001 | t0021 | g0082 | AFR | USA | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA20300 | hp1 | a0001 | c0003 | t0008 | g0025 | AFR | USA | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | USA | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0245 | REF | REF | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0015 | g0016 | REF | REF | NR3C1_chr5_143272934_143408686 | NR3C1 | chr5 | 143272934 | 143408686 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:143300662 | T | C | 1 | a0004 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1570A>G | p.Thr524Ala | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/9 | 2059/6778 | 1570/2334 | 524/777 | chr5 | 143300662 | |||
| chr5:143400647 | A | C | 1 | a0002 | 3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.193T>G | p.Phe65Val | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/9 | 682/6778 | 193/2334 | 65/777 | chr5 | 143400647 | |||
| chr5:143400772 | C | T | 1 | a0003 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.68G>A | p.Arg23Lys | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/9 | 557/6778 | 68/2334 | 23/777 | chr5 | 143400772 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:143281925 | A | G | 3 | a0001c0002 a0001c0003 a0001c0004 |
41 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(38): Show |
synonymous_variant | LOW | c.2298T>C | p.Asn766Asn | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2787/6778 | 2298/2334 | 766/777 | chr5 | 143281925 | |||
| chr5:143281973 | G | A | 1 | a0001c0005 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
synonymous_variant | LOW | c.2250C>T | p.Pro750Pro | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2739/6778 | 2250/2334 | 750/777 | chr5 | 143281973 | |||
| chr5:143282715 | G | A | 2 | a0001c0002 a0001c0003 |
29 | HG00438.hp1 HG02055.hp1 HG02109.hp1 others(26): Show |
synonymous_variant | LOW | c.2034C>T | p.Asp678Asp | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/9 | 2523/6778 | 2034/2334 | 678/777 | chr5 | 143282715 | |||
| chr5:143298796 | G | A | 1 | a0001c0002 | 16 | HG00438.hp1 HG02132.hp2 HG02165.hp1 others(13): Show |
synonymous_variant | LOW | c.1764C>T | p.His588His | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/9 | 2253/6778 | 1764/2334 | 588/777 | chr5 | 143298796 | |||
| chr5:143314111 | T | C | 1 | a0001c0005 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
synonymous_variant | LOW | c.1242A>G | p.Thr414Thr | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/9 | 1731/6778 | 1242/2334 | 414/777 | chr5 | 143314111 | |||
| chr5:143399943 | T | C | 1 | a0001c0005 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
synonymous_variant | LOW | c.897A>G | p.Thr299Thr | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/9 | 1386/6778 | 897/2334 | 299/777 | chr5 | 143399943 | |||
| chr5:143399961 | C | T | 1 | a0001c0006 | 6 | HG02572.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
synonymous_variant | LOW | c.879G>A | p.Lys293Lys | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/9 | 1368/6778 | 879/2334 | 293/777 | chr5 | 143399961 | |||
| chr5:143400774 | C | T | 1 | a0003c0008 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.66G>A | p.Glu22Glu | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/9 | 555/6778 | 66/2334 | 22/777 | chr5 | 143400774 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:143278056 | T | C | 5 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0023 others(2): Show |
22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3833A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3833 | chr5 | 143278056 | ||||||
| chr5:143278113 | C | T | 1 | a0001c0001t0028 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3776G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3776 | chr5 | 143278113 | ||||||
| chr5:143278138 | T | A | 1 | a0001c0001t0029 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3751A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3751 | chr5 | 143278138 | ||||||
| chr5:143278172 | C | T | 1 | a0001c0002t0017 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3717G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3717 | chr5 | 143278172 | ||||||
| chr5:143278589 | C | A | 1 | a0001c0001t0025 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3300G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3300 | chr5 | 143278589 | ||||||
| chr5:143278591 | C | A | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(27): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*3298G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3298 | chr5 | 143278591 | ||||||
| chr5:143278736 | G | A | 1 | a0001c0005t0009 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3153C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3153 | chr5 | 143278736 | ||||||
| chr5:143278813 | G | A | 1 | a0001c0005t0009 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3076C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 3076 | chr5 | 143278813 | ||||||
| chr5:143278927 | T | C | 1 | a0001c0001t0031 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2962A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2962 | chr5 | 143278927 | ||||||
| chr5:143279050 | A | G | 1 | a0001c0001t0022 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2839T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2839 | chr5 | 143279050 | ||||||
| chr5:143279450 | T | A | 1 | a0001c0001t0014 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2439A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2439 | chr5 | 143279450 | ||||||
| chr5:143279522 | G | A | 1 | a0001c0002t0018 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2367C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2367 | chr5 | 143279522 | ||||||
| chr5:143279543 | T | C | 1 | a0001c0001t0014 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2346A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2346 | chr5 | 143279543 | ||||||
| chr5:143279701 | T | C | 1 | a0001c0003t0008 | 9 | HG02055.hp1 HG02486.hp2 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2188A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2188 | chr5 | 143279701 | ||||||
| chr5:143279845 | C | G | 1 | a0001c0004t0027 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2044G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2044 | chr5 | 143279845 | ||||||
| chr5:143279847 | G | A | 1 | a0001c0005t0009 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2042C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 2042 | chr5 | 143279847 | ||||||
| chr5:143280009 | T | C | 1 | a0002c0007t0011 | 2 | HG01884.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1880A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 1880 | chr5 | 143280009 | ||||||
| chr5:143280663 | A | AATCAGT | 1 | a0001c0005t0009 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1220_*1225dupACTG others(2): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 1225 | chr5 | 143280663 | ||||||
| chr5:143280820 | C | G | 1 | a0001c0001t0026 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1069G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 1069 | chr5 | 143280820 | ||||||
| chr5:143280952 | G | T | 1 | a0002c0007t0034 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*937C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 937 | chr5 | 143280952 | ||||||
| chr5:143281053 | G | T | 1 | a0001c0001t0024 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 836 | chr5 | 143281053 | ||||||
| chr5:143281119 | C | CT | 8 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0013 others(5): Show |
51 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*769dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 769 | chr5 | 143281119 | ||||||
| chr5:143281119 | C | CTT | 4 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0023 others(1): Show |
25 | HG00323.hp1 HG01074.hp1 HG01496.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*768_*769dupAA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 769 | chr5 | 143281119 | ||||||
| chr5:143281119 | C | CTTT | 3 | a0001c0001t0003 a0001c0001t0022 a0003c0008t0003 |
20 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*767_*769dupAAA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 769 | chr5 | 143281119 | ||||||
| chr5:143281119 | CT | C | 4 | a0001c0001t0032 a0001c0002t0019 a0001c0004t0033 others(1): Show |
10 | HG01256.hp2 HG02027.hp1 HG02074.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*769delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 769 | chr5 | 143281119 | ||||||
| chr5:143281237 | T | A | 1 | a0002c0007t0034 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*652A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 652 | chr5 | 143281237 | ||||||
| chr5:143281446 | A | G | 1 | a0001c0001t0021 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*443T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 443 | chr5 | 143281446 | ||||||
| chr5:143281599 | T | G | 1 | a0001c0005t0009 | 7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*290A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 290 | chr5 | 143281599 | ||||||
| chr5:143281630 | G | A | 1 | a0001c0001t0035 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*259C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 259 | chr5 | 143281630 | ||||||
| chr5:143281874 | T | C | 1 | a0001c0001t0036 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 9/9 | 15 | chr5 | 143281874 | ||||||
| chr5:143403227 | G | T | 1 | a0001c0001t0020 | 1 | NA18942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2388 | chr5 | 143403227 | ||||||
| chr5:143403255 | C | A | 1 | a0001c0001t0037 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2416 | chr5 | 143403255 | ||||||
| chr5:143403312 | A | AT | 7 | a0001c0002t0006 a0001c0002t0016 a0001c0002t0017 others(4): Show |
25 | HG00438.hp1 HG02055.hp1 HG02132.hp2 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-116dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2474 | chr5 | 143403312 | ||||||
| chr5:143403334 | A | T | 1 | a0001c0001t0013 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2495 | chr5 | 143403334 | ||||||
| chr5:143403448 | A | G | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(39): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
5_prime_UTR_variant | MODIFIER | c.-251T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2609 | chr5 | 143403448 | ||||||
| chr5:143403450 | G | GC | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(39): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
5_prime_UTR_variant | MODIFIER | c.-254_-253insG | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2612 | chr5 | 143403450 | ||||||
| chr5:143403522 | A | C | 1 | a0001c0001t0012 | 1 | HG03710.hp2 | 5_prime_UTR_variant | MODIFIER | c.-325T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/9 | 2683 | chr5 | 143403522 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:143282050 | G | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2182-9C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282050 | |||||||
| chr5:143282187 | C | T | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2182-146G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282187 | |||||||
| chr5:143282199 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2182-158T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282199 | |||||||
| chr5:143282222 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2182-181C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282222 | |||||||
| chr5:143282277 | G | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2182-236C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282277 | |||||||
| chr5:143282324 | A | G | 79 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(76): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.2181+244T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282324 | |||||||
| chr5:143282365 | T | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2181+203A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282365 | |||||||
| chr5:143282487 | C | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2181+81G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 8/8 | chr5 | 143282487 | |||||||
| chr5:143282772 | CTTTTCT | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-53_2024-48del others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143282772 | |||||||
| chr5:143282777 | C | CT | 9 | a0001c0001t0007g0001 a0001c0001t0007g0011 a0001c0001t0007g0012 others(6): Show |
10 | HG00099.hp1 HG01884.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2024-53dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143282777 | |||||||
| chr5:143282834 | CAGTGGCA others(100): Show |
C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-216_2024-110d others(2): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143282834 | |||||||
| chr5:143283048 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-323A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283048 | |||||||
| chr5:143283321 | G | A | 2 | a0001c0002t0006g0030 a0001c0002t0006g0034 |
2 | NA18974.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2024-596C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283321 | |||||||
| chr5:143283358 | A | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2024-633T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283358 | |||||||
| chr5:143283590 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2024-865G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283590 | |||||||
| chr5:143283593 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-868A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283593 | |||||||
| chr5:143283851 | A | G | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2024-1126T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283851 | |||||||
| chr5:143283975 | G | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-1250C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143283975 | |||||||
| chr5:143284236 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2024-1511G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284236 | |||||||
| chr5:143284329 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-1604C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284329 | |||||||
| chr5:143284374 | T | G | 29 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(26): Show |
29 | HG00438.hp1 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2024-1649A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284374 | |||||||
| chr5:143284470 | C | CATTACTA others(16): Show |
28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.2024-1768_2024-174 others(27): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284470 | |||||||
| chr5:143284524 | TTATAGTT others(13): Show |
T | 7 | a0001c0001t0012g0009 a0001c0005t0009g0008 a0001c0005t0009g0249 others(4): Show |
8 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.2024-1819_2024-180 others(24): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284524 | |||||||
| chr5:143284564 | G | A | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2024-1839C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284564 | |||||||
| chr5:143284777 | A | G | 12 | a0001c0001t0007g0001 a0001c0001t0007g0011 a0001c0001t0007g0012 others(9): Show |
13 | HG02572.hp1 HG02615.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.2024-2052T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284777 | |||||||
| chr5:143284883 | C | T | 2 | a0001c0001t0005g0210 a0001c0001t0005g0211 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2024-2158G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284883 | |||||||
| chr5:143284951 | T | TAATTTAT others(58): Show |
1 | a0001c0001t0001g0148 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2024-2291_2024-222 others(69): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284951 | |||||||
| chr5:143284951 | T | TAATTTAT others(123): Show |
1 | a0001c0001t0001g0106 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2024-2356_2024-222 others(134): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284951 | |||||||
| chr5:143284951 | TAATTTAT others(58): Show |
T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0067 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2024-2291_2024-222 others(69): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284951 | |||||||
| chr5:143284951 | TAATTTAT others(123): Show |
T | 8 | a0001c0001t0001g0066 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG00741.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2024-2356_2024-222 others(4): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143284951 | |||||||
| chr5:143285042 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2024-2317G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285042 | |||||||
| chr5:143285389 | A | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-2664T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285389 | |||||||
| chr5:143285456 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2024-2731C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285456 | |||||||
| chr5:143285461 | A | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-2736T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285461 | |||||||
| chr5:143285965 | CTGAT | C | 27 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(24): Show |
27 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.2024-3244_2024-324 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285965 | |||||||
| chr5:143285970 | T | A | 1 | a0001c0001t0003g0253 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2024-3245A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285970 | |||||||
| chr5:143285970 | TA | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0069 others(20): Show |
25 | HG00423.hp2 HG01070.hp1 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.2024-3246delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143285970 | |||||||
| chr5:143286247 | C | G | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.2024-3522G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286247 | |||||||
| chr5:143286467 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2024-3742T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286467 | |||||||
| chr5:143286512 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-3787T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286512 | |||||||
| chr5:143286540 | A | G | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2024-3815T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286540 | |||||||
| chr5:143286641 | G | A | 2 | a0001c0001t0003g0180 a0001c0001t0003g0181 |
2 | HG01256.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2024-3916C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286641 | |||||||
| chr5:143286642 | A | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2024-3917T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286642 | |||||||
| chr5:143286789 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2024-4064A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286789 | |||||||
| chr5:143286930 | G | C | 1 | a0001c0001t0002g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2024-4205C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143286930 | |||||||
| chr5:143287364 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2024-4639A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143287364 | |||||||
| chr5:143287365 | C | A | 1 | a0001c0004t0033g0051 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2024-4640G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143287365 | |||||||
| chr5:143287691 | T | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-4966A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143287691 | |||||||
| chr5:143287806 | T | G | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2024-5081A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143287806 | |||||||
| chr5:143287990 | C | G | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2024-5265G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143287990 | |||||||
| chr5:143288118 | A | AT | 12 | a0001c0001t0001g0086 a0001c0001t0001g0157 a0001c0001t0010g0088 others(9): Show |
13 | HG00099.hp2 HG01884.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.2024-5394dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288118 | |||||||
| chr5:143288222 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-5497C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288222 | |||||||
| chr5:143288276 | G | A | 2 | a0001c0001t0003g0185 a0003c0008t0003g0179 |
2 | HG00323.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2024-5551C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288276 | |||||||
| chr5:143288411 | G | A | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2024-5686C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288411 | |||||||
| chr5:143288419 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-5694T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288419 | |||||||
| chr5:143288606 | G | A | 2 | a0001c0001t0005g0210 a0001c0001t0005g0211 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2024-5881C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288606 | |||||||
| chr5:143288662 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-5937T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288662 | |||||||
| chr5:143288698 | C | G | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2024-5973G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288698 | |||||||
| chr5:143288899 | G | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2024-6174C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288899 | |||||||
| chr5:143288933 | C | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2024-6208G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143288933 | |||||||
| chr5:143289072 | C | CA | 55 | a0001c0001t0001g0094 a0001c0001t0001g0107 a0001c0001t0002g0004 others(52): Show |
60 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.2024-6348dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289072 | |||||||
| chr5:143289072 | CA | C | 12 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(9): Show |
13 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.2024-6348delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289072 | |||||||
| chr5:143289306 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+6154T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289306 | |||||||
| chr5:143289366 | G | A | 1 | a0001c0003t0004g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2023+6094C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289366 | |||||||
| chr5:143289385 | T | C | 1 | a0001c0006t0001g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2023+6075A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289385 | |||||||
| chr5:143289420 | C | T | 8 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
8 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2023+6040G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289420 | |||||||
| chr5:143289471 | G | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2023+5989C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289471 | |||||||
| chr5:143289583 | T | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+5877A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289583 | |||||||
| chr5:143289601 | G | A | 1 | a0001c0002t0018g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2023+5859C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289601 | |||||||
| chr5:143289658 | A | G | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.2023+5802T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289658 | |||||||
| chr5:143289886 | A | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2023+5574T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289886 | |||||||
| chr5:143289922 | C | T | 1 | a0003c0008t0003g0179 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2023+5538G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143289922 | |||||||
| chr5:143290504 | A | T | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2023+4956T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290504 | |||||||
| chr5:143290686 | G | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+4774C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290686 | |||||||
| chr5:143290743 | T | G | 68 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(65): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.2023+4717A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290743 | |||||||
| chr5:143290753 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2023+4707G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290753 | |||||||
| chr5:143290762 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+4698C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290762 | |||||||
| chr5:143290813 | CAGCCTCC others(24): Show |
C | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2023+4616_2023+464 others(35): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290813 | |||||||
| chr5:143290983 | A | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2023+4477T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143290983 | |||||||
| chr5:143291174 | T | C | 1 | a0001c0001t0013g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2023+4286A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291174 | |||||||
| chr5:143291273 | T | G | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2023+4187A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291273 | |||||||
| chr5:143291504 | G | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2023+3956C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291504 | |||||||
| chr5:143291527 | A | ATTACTTT others(13): Show |
117 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(114): Show |
122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.2023+3932_2023+393 others(24): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291527 | |||||||
| chr5:143291566 | A | C | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2023+3894T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291566 | |||||||
| chr5:143291644 | T | C | 3 | a0001c0001t0001g0116 a0001c0001t0026g0115 a0001c0001t0035g0117 |
3 | HG02559.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2023+3816A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291644 | |||||||
| chr5:143291692 | G | A | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2023+3768C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291692 | |||||||
| chr5:143291835 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2023+3625C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291835 | |||||||
| chr5:143291954 | T | G | 1 | a0001c0001t0005g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2023+3506A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143291954 | |||||||
| chr5:143292093 | A | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+3367T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292093 | |||||||
| chr5:143292096 | C | G | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.2023+3364G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292096 | |||||||
| chr5:143292217 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+3243C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292217 | |||||||
| chr5:143292220 | C | T | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2023+3240G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292220 | |||||||
| chr5:143292316 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+3144C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292316 | |||||||
| chr5:143292323 | A | G | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2023+3137T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292323 | |||||||
| chr5:143292348 | A | G | 3 | a0001c0001t0001g0110 a0001c0001t0001g0126 a0001c0001t0001g0130 |
3 | HG01169.hp1 HG01934.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2023+3112T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292348 | |||||||
| chr5:143292468 | G | A | 12 | a0001c0001t0007g0001 a0001c0001t0007g0011 a0001c0001t0007g0012 others(9): Show |
13 | HG02572.hp1 HG02615.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.2023+2992C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292468 | |||||||
| chr5:143292470 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2023+2990A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292470 | |||||||
| chr5:143292520 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2023+2940G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292520 | |||||||
| chr5:143292589 | C | T | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2023+2871G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292589 | |||||||
| chr5:143292751 | G | A | 38 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(35): Show |
38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.2023+2709C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143292751 | |||||||
| chr5:143293143 | C | G | 1 | a0001c0002t0006g0034 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2023+2317G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293143 | |||||||
| chr5:143293178 | C | A | 1 | a0001c0003t0004g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2023+2282G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293178 | |||||||
| chr5:143293297 | A | C | 6 | a0001c0006t0001g0098 a0001c0006t0001g0099 a0001c0006t0001g0100 others(3): Show |
6 | HG02572.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2023+2163T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293297 | |||||||
| chr5:143293397 | G | GAAAGACT others(43): Show |
1 | a0001c0001t0001g0177 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2023+2013_2023+206 others(54): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293397 | |||||||
| chr5:143293524 | C | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0126 a0001c0001t0001g0130 |
3 | HG01169.hp1 HG01934.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2023+1936G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293524 | |||||||
| chr5:143293613 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2023+1847A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293613 | |||||||
| chr5:143293832 | A | G | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.2023+1628T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293832 | |||||||
| chr5:143293864 | CT | C | 9 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0003g0197 others(6): Show |
9 | HG00323.hp2 HG01257.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2023+1595delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293864 | |||||||
| chr5:143293864 | CTT | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+1594_2023+159 others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293864 | |||||||
| chr5:143293868 | T | C | 2 | a0001c0001t0005g0210 a0001c0001t0005g0211 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2023+1592A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293868 | |||||||
| chr5:143293992 | C | T | 1 | a0001c0001t0004g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2023+1468G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143293992 | |||||||
| chr5:143294002 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+1458T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294002 | |||||||
| chr5:143294322 | A | G | 3 | a0001c0001t0007g0013 a0001c0001t0007g0017 a0001c0001t0007g0018 |
3 | HG03098.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2023+1138T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294322 | |||||||
| chr5:143294355 | A | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2023+1105T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294355 | |||||||
| chr5:143294374 | AT | A | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(37): Show |
44 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.2023+1085delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294374 | |||||||
| chr5:143294377 | C | G | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(37): Show |
44 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.2023+1083G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294377 | |||||||
| chr5:143294391 | G | A | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2023+1069C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294391 | |||||||
| chr5:143294394 | C | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+1066G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294394 | |||||||
| chr5:143294580 | T | C | 1 | a0001c0001t0002g0004 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2023+880A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294580 | |||||||
| chr5:143294582 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+878C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294582 | |||||||
| chr5:143294791 | C | T | 2 | a0001c0001t0005g0210 a0001c0001t0005g0211 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2023+669G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294791 | |||||||
| chr5:143294876 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2023+584G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143294876 | |||||||
| chr5:143295011 | C | A | 1 | a0001c0001t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2023+449G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143295011 | |||||||
| chr5:143295113 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023+347A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143295113 | |||||||
| chr5:143295125 | G | A | 78 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2023+335C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 7/8 | chr5 | 143295125 | |||||||
| chr5:143296201 | A | C | 3 | a0001c0002t0006g0030 a0001c0002t0006g0034 a0001c0002t0017g0033 |
3 | NA18974.hp1 NA18988.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1893-611T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296201 | |||||||
| chr5:143296258 | C | T | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1893-668G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296258 | |||||||
| chr5:143296276 | A | AT | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1893-687dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296276 | |||||||
| chr5:143296276 | AT | A | 11 | a0001c0001t0020g0047 a0001c0005t0009g0008 a0001c0005t0009g0249 others(8): Show |
12 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1893-687delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296276 | |||||||
| chr5:143296369 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1893-779G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296369 | |||||||
| chr5:143296381 | ATAAAT | A | 9 | a0001c0004t0004g0049 a0001c0004t0004g0050 a0001c0004t0004g0052 others(6): Show |
9 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1893-796_1893-792d others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296381 | |||||||
| chr5:143296616 | AAAC | A | 39 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(36): Show |
39 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1893-1029_1893-102 others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296616 | |||||||
| chr5:143296627 | AT | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1893-1038delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296627 | |||||||
| chr5:143296763 | G | A | 1 | a0001c0001t0028g0159 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1893-1173C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296763 | |||||||
| chr5:143296839 | G | T | 67 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(64): Show |
67 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.1893-1249C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296839 | |||||||
| chr5:143296905 | C | T | 12 | a0001c0001t0007g0001 a0001c0001t0007g0011 a0001c0001t0007g0012 others(9): Show |
13 | HG02572.hp1 HG02615.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1893-1315G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296905 | |||||||
| chr5:143296906 | G | A | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1893-1316C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143296906 | |||||||
| chr5:143297075 | C | CA | 50 | a0001c0001t0001g0105 a0001c0001t0001g0171 a0001c0001t0001g0174 others(47): Show |
52 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1893-1486dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143297075 | |||||||
| chr5:143297075 | CA | C | 17 | a0001c0001t0001g0069 a0001c0001t0001g0123 a0001c0001t0001g0134 others(14): Show |
18 | HG01099.hp1 HG01109.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1893-1486delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143297075 | |||||||
| chr5:143297443 | T | A | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02055.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1892+1225A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143297443 | |||||||
| chr5:143297639 | C | G | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1892+1029G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143297639 | |||||||
| chr5:143297656 | C | T | 1 | a0001c0003t0008g0045 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1892+1012G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143297656 | |||||||
| chr5:143297780 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1892+888A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143297780 | |||||||
| chr5:143298102 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1892+566G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298102 | |||||||
| chr5:143298137 | T | C | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1892+531A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298137 | |||||||
| chr5:143298170 | TCTC | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1892+495_1892+497d others(5): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298170 | |||||||
| chr5:143298175 | C | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1892+493G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298175 | |||||||
| chr5:143298215 | C | T | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1892+453G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298215 | |||||||
| chr5:143298299 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1892+369G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298299 | |||||||
| chr5:143298338 | C | T | 2 | a0001c0001t0001g0074 a0004c0009t0001g0075 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1892+330G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298338 | |||||||
| chr5:143298405 | C | T | 1 | a0004c0009t0001g0075 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1892+263G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298405 | |||||||
| chr5:143298539 | T | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0169 |
2 | NA19081.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1892+129A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 6/8 | chr5 | 143298539 | |||||||
| chr5:143299001 | T | G | 1 | a0001c0001t0002g0246 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1748-189A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299001 | |||||||
| chr5:143299005 | G | GT | 82 | a0001c0001t0001g0113 a0001c0001t0001g0126 a0001c0001t0001g0133 others(79): Show |
86 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1748-194dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299005 | |||||||
| chr5:143299005 | G | GTT | 32 | a0001c0001t0002g0213 a0001c0001t0002g0221 a0001c0001t0002g0229 others(29): Show |
32 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.1748-195_1748-194d others(4): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299005 | |||||||
| chr5:143299005 | G | GTTTT | 5 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(2): Show |
6 | HG02074.hp2 HG02135.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1748-197_1748-194d others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299005 | |||||||
| chr5:143299010 | T | G | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1748-198A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299010 | |||||||
| chr5:143299084 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1748-272C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299084 | |||||||
| chr5:143299343 | T | TA | 6 | a0001c0001t0001g0123 a0001c0001t0001g0146 a0001c0001t0001g0171 others(3): Show |
6 | HG01175.hp1 HG02027.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1748-532dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299343 | |||||||
| chr5:143299343 | T | TAA | 6 | a0001c0001t0002g0223 a0001c0001t0010g0061 a0001c0001t0024g0206 others(3): Show |
6 | HG01346.hp2 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1748-533_1748-532d others(4): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299343 | |||||||
| chr5:143299343 | TAAAA | T | 37 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(34): Show |
37 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1748-535_1748-532d others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299343 | |||||||
| chr5:143299434 | C | T | 3 | a0001c0001t0007g0014 a0001c0001t0007g0015 a0001c0001t0013g0010 |
3 | HG02572.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1748-622G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299434 | |||||||
| chr5:143299490 | C | T | 1 | a0001c0001t0007g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1748-678G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299490 | |||||||
| chr5:143299587 | G | C | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1748-775C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299587 | |||||||
| chr5:143299642 | C | T | 1 | a0001c0006t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1748-830G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299642 | |||||||
| chr5:143299670 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1747+815C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299670 | |||||||
| chr5:143299783 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1747+702C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299783 | |||||||
| chr5:143299832 | C | T | 68 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.1747+653G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299832 | |||||||
| chr5:143299850 | C | G | 1 | a0001c0006t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1747+635G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299850 | |||||||
| chr5:143299858 | A | C | 4 | a0001c0001t0003g0183 a0001c0001t0003g0187 a0001c0001t0003g0207 others(1): Show |
4 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747+627T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299858 | |||||||
| chr5:143299997 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1747+488A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143299997 | |||||||
| chr5:143300067 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1747+418A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143300067 | |||||||
| chr5:143300394 | C | G | 2 | a0001c0006t0001g0098 a0001c0006t0001g0100 |
2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1747+91G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 5/8 | chr5 | 143300394 | |||||||
| chr5:143300779 | C | A | 78 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1469-16G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143300779 | |||||||
| chr5:143300892 | T | C | 1 | a0001c0005t0009g0257 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1469-129A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143300892 | |||||||
| chr5:143301033 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469-270C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301033 | |||||||
| chr5:143301037 | T | C | 1 | a0001c0006t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1469-274A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301037 | |||||||
| chr5:143301402 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469-639A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301402 | |||||||
| chr5:143301441 | A | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0248 a0001c0001t0026g0115 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-678T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301441 | |||||||
| chr5:143301522 | A | ATAAAT | 32 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0108 others(29): Show |
32 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1469-764_1469-760d others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301522 | |||||||
| chr5:143301594 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469-831A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301594 | |||||||
| chr5:143301715 | C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1469-952G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301715 | |||||||
| chr5:143301946 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1469-1183C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143301946 | |||||||
| chr5:143302204 | T | A | 1 | a0001c0006t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1469-1441A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143302204 | |||||||
| chr5:143302211 | T | C | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1469-1448A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143302211 | |||||||
| chr5:143303008 | A | G | 2 | a0001c0001t0005g0210 a0001c0001t0005g0211 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1469-2245T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303008 | |||||||
| chr5:143303046 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1469-2283T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303046 | |||||||
| chr5:143303133 | CT | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469-2371delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303133 | |||||||
| chr5:143303247 | G | A | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1469-2484C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303247 | |||||||
| chr5:143303272 | A | G | 1 | a0001c0001t0030g0194 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1469-2509T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303272 | |||||||
| chr5:143303809 | A | G | 1 | a0001c0003t0004g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1469-3046T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303809 | |||||||
| chr5:143303856 | G | A | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1469-3093C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303856 | |||||||
| chr5:143303904 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469-3141T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143303904 | |||||||
| chr5:143304158 | A | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1469-3395T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143304158 | |||||||
| chr5:143304176 | T | C | 79 | a0001c0001t0001g0146 a0001c0001t0003g0180 a0001c0001t0003g0181 others(76): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1469-3413A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143304176 | |||||||
| chr5:143304215 | G | A | 1 | a0001c0004t0004g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1469-3452C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143304215 | |||||||
| chr5:143304375 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1469-3612C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143304375 | |||||||
| chr5:143304491 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1469-3728T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143304491 | |||||||
| chr5:143304829 | G | A | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1469-4066C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143304829 | |||||||
| chr5:143305117 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1469-4354T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305117 | |||||||
| chr5:143305345 | A | G | 2 | a0001c0003t0006g0023 a0001c0003t0006g0046 |
2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1469-4582T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305345 | |||||||
| chr5:143305349 | AATTAAGA others(8): Show |
A | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1469-4601_1469-458 others(19): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305349 | |||||||
| chr5:143305367 | C | A | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1469-4604G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305367 | |||||||
| chr5:143305547 | T | A | 1 | a0001c0002t0018g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1468+4550A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305547 | |||||||
| chr5:143305592 | A | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0069 others(6): Show |
10 | HG02451.hp2 HG02615.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1468+4505T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305592 | |||||||
| chr5:143305695 | T | C | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1468+4402A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305695 | |||||||
| chr5:143305873 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1468+4224A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305873 | |||||||
| chr5:143305916 | A | G | 2 | a0001c0001t0003g0184 a0001c0001t0003g0188 |
2 | HG01175.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1468+4181T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305916 | |||||||
| chr5:143305980 | C | T | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1468+4117G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305980 | |||||||
| chr5:143305990 | C | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+4107G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143305990 | |||||||
| chr5:143306040 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0010g0064 |
2 | HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1468+4057G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306040 | |||||||
| chr5:143306104 | T | TA | 7 | a0001c0001t0001g0093 a0001c0005t0009g0008 a0001c0005t0009g0249 others(4): Show |
8 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1468+3992dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306104 | |||||||
| chr5:143306105 | A | T | 8 | a0001c0004t0004g0049 a0001c0004t0004g0050 a0001c0004t0004g0052 others(5): Show |
8 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1468+3992T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306105 | |||||||
| chr5:143306138 | T | C | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1468+3959A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306138 | |||||||
| chr5:143306161 | C | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+3936G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306161 | |||||||
| chr5:143306314 | C | T | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1468+3783G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306314 | |||||||
| chr5:143306361 | T | TA | 52 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0069 others(49): Show |
57 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1468+3735dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306361 | |||||||
| chr5:143306646 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1468+3451T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306646 | |||||||
| chr5:143306746 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0151 |
2 | HG00544.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1468+3351G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306746 | |||||||
| chr5:143306793 | G | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+3304C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306793 | |||||||
| chr5:143306874 | A | ATTT | 5 | a0001c0001t0002g0238 a0001c0001t0007g0001 a0001c0001t0007g0011 others(2): Show |
6 | HG02258.hp2 HG02683.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1468+3220_1468+322 others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0007g0013 a0001c0001t0007g0017 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1468+3212_1468+322 others(15): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | A | ATTTTTTT others(9): Show |
1 | a0001c0001t0007g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1468+3207_1468+322 others(20): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | AT | A | 11 | a0001c0001t0005g0063 a0001c0001t0005g0211 a0001c0002t0006g0030 others(8): Show |
11 | HG00323.hp1 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1468+3222delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATT | A | 11 | a0001c0001t0002g0243 a0001c0001t0005g0222 a0001c0002t0004g0168 others(8): Show |
11 | HG00438.hp1 HG01074.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1468+3221_1468+322 others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTT | A | 12 | a0001c0001t0002g0006 a0001c0001t0002g0062 a0001c0001t0002g0242 others(9): Show |
13 | HG00597.hp2 HG01934.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1468+3220_1468+322 others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTTT | A | 20 | a0001c0001t0002g0007 a0001c0001t0002g0212 a0001c0001t0002g0215 others(17): Show |
21 | HG01109.hp1 HG01891.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1468+3219_1468+322 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTTTT | A | 30 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0213 others(27): Show |
32 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(29): Show |
intron_variant | MODIFIER | c.1468+3218_1468+322 others(9): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTTTTTT others(3): Show |
A | 1 | a0001c0005t0009g0252 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1468+3213_1468+322 others(14): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTTTTTT others(4): Show |
A | 1 | a0001c0003t0008g0045 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1468+3212_1468+322 others(15): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0003g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1468+3211_1468+322 others(16): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTTTTTT others(6): Show |
A | 10 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0001t0003g0190 others(7): Show |
10 | HG01099.hp1 HG01169.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1468+3210_1468+322 others(17): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTTTTTT others(7): Show |
A | 1 | a0001c0004t0004g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1468+3209_1468+322 others(18): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTTTTTT others(8): Show |
A | 7 | a0001c0004t0004g0049 a0001c0004t0004g0050 a0001c0004t0004g0052 others(4): Show |
7 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468+3208_1468+322 others(19): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTTTTTT others(9): Show |
A | 13 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0133 others(10): Show |
13 | HG00544.hp2 HG00733.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1468+3207_1468+322 others(20): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTTTTTT others(10): Show |
A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(103): Show |
108 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1468+3206_1468+322 others(21): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTTTTTT others(11): Show |
A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0113 a0001c0001t0001g0164 |
3 | HG03041.hp2 NA18950.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1468+3205_1468+322 others(22): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306874 | ATTTTTTT others(16): Show |
A | 1 | a0001c0001t0002g0221 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1468+3200_1468+322 others(27): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306874 | |||||||
| chr5:143306927 | C | T | 7 | a0001c0001t0032g0065 a0001c0005t0009g0008 a0001c0005t0009g0249 others(4): Show |
8 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1468+3170G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143306927 | |||||||
| chr5:143307045 | C | T | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1468+3052G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307045 | |||||||
| chr5:143307118 | G | A | 1 | a0001c0001t0032g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1468+2979C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307118 | |||||||
| chr5:143307216 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+2881A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307216 | |||||||
| chr5:143307239 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1468+2858T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307239 | |||||||
| chr5:143307371 | G | A | 26 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0062 others(23): Show |
28 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1468+2726C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307371 | |||||||
| chr5:143307426 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1468+2671A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307426 | |||||||
| chr5:143307710 | A | T | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1468+2387T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307710 | |||||||
| chr5:143307916 | T | G | 4 | a0001c0002t0006g0029 a0001c0002t0006g0032 a0001c0002t0006g0041 others(1): Show |
4 | NA18942.hp2 NA18985.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+2181A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307916 | |||||||
| chr5:143307929 | A | G | 78 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1468+2168T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143307929 | |||||||
| chr5:143308134 | T | C | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1468+1963A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143308134 | |||||||
| chr5:143308177 | T | C | 9 | a0001c0004t0004g0049 a0001c0004t0004g0050 a0001c0004t0004g0052 others(6): Show |
9 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1468+1920A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143308177 | |||||||
| chr5:143308505 | T | C | 3 | a0001c0001t0002g0244 a0001c0001t0002g0246 a0001c0001t0002g0247 |
3 | HG02148.hp1 HG02273.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1468+1592A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143308505 | |||||||
| chr5:143308664 | T | G | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1468+1433A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143308664 | |||||||
| chr5:143308758 | T | C | 68 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(65): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1468+1339A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143308758 | |||||||
| chr5:143308914 | G | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+1183C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143308914 | |||||||
| chr5:143309073 | C | CT | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0067 others(83): Show |
88 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1468+1023dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309073 | |||||||
| chr5:143309127 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+970T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309127 | |||||||
| chr5:143309234 | C | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+863G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309234 | |||||||
| chr5:143309306 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(17): Show |
21 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1468+791G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309306 | |||||||
| chr5:143309313 | C | T | 1 | a0001c0002t0006g0032 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1468+784G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309313 | |||||||
| chr5:143309372 | C | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+725G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309372 | |||||||
| chr5:143309469 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1468+628G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309469 | |||||||
| chr5:143309486 | T | C | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1468+611A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309486 | |||||||
| chr5:143309540 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1468+557G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309540 | |||||||
| chr5:143309629 | GT | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+467delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309629 | |||||||
| chr5:143309652 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1468+445G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309652 | |||||||
| chr5:143309678 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+419C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 4/8 | chr5 | 143309678 | |||||||
| chr5:143310270 | A | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1352-57T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310270 | |||||||
| chr5:143310420 | A | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1352-207T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310420 | |||||||
| chr5:143310466 | A | G | 3 | a0001c0001t0007g0013 a0001c0001t0007g0017 a0001c0001t0007g0018 |
3 | HG03098.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1352-253T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310466 | |||||||
| chr5:143310830 | A | C | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1352-617T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310830 | |||||||
| chr5:143310877 | C | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02080.hp1 HG02129.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1352-664G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310877 | |||||||
| chr5:143310934 | G | A | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1352-721C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310934 | |||||||
| chr5:143310958 | T | C | 6 | a0001c0001t0001g0114 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1352-745A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143310958 | |||||||
| chr5:143311031 | T | C | 40 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(37): Show |
40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1352-818A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311031 | |||||||
| chr5:143311162 | G | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1352-949C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311162 | |||||||
| chr5:143311407 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1352-1194A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311407 | |||||||
| chr5:143311783 | A | G | 6 | a0001c0001t0001g0114 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1352-1570T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311783 | |||||||
| chr5:143311788 | G | GT | 38 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0069 others(35): Show |
39 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1352-1576dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311788 | |||||||
| chr5:143311788 | GT | G | 61 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.1352-1576delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311788 | |||||||
| chr5:143311788 | GTT | G | 6 | a0001c0001t0001g0094 a0001c0005t0009g0008 a0001c0005t0009g0249 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1352-1577_1352-157 others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311788 | |||||||
| chr5:143311808 | T | C | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1352-1595A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311808 | |||||||
| chr5:143311828 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1352-1615C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311828 | |||||||
| chr5:143311925 | ACAGCCCA others(21): Show |
A | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1352-1740_1352-171 others(32): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143311925 | |||||||
| chr5:143312188 | C | A | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1351+1814G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143312188 | |||||||
| chr5:143312249 | C | T | 7 | a0001c0001t0012g0009 a0001c0005t0009g0008 a0001c0005t0009g0249 others(4): Show |
8 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1351+1753G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143312249 | |||||||
| chr5:143312722 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1351+1280G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143312722 | |||||||
| chr5:143312824 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1351+1178C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143312824 | |||||||
| chr5:143312845 | G | A | 1 | a0001c0001t0005g0203 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1351+1157C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143312845 | |||||||
| chr5:143312968 | G | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(32): Show |
37 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.1351+1034C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143312968 | |||||||
| chr5:143313467 | T | G | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0083 others(2): Show |
5 | HG01255.hp1 HG06807.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.1351+535A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143313467 | |||||||
| chr5:143313833 | T | C | 68 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(65): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1351+169A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143313833 | |||||||
| chr5:143313922 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0156 |
2 | NA19000.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1351+80T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 3/8 | chr5 | 143313922 | |||||||
| chr5:143314260 | TCA | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-94_1185-93del others(2): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314260 | |||||||
| chr5:143314281 | A | G | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1185-113T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314281 | |||||||
| chr5:143314386 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-218T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314386 | |||||||
| chr5:143314421 | CT | C | 9 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0108 others(6): Show |
9 | HG00597.hp1 HG01256.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1185-254delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314421 | |||||||
| chr5:143314421 | CTT | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-255_1185-254d others(4): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314421 | |||||||
| chr5:143314424 | T | C | 3 | a0001c0001t0001g0139 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG02647.hp1 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1185-256A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314424 | |||||||
| chr5:143314736 | A | G | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-568T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143314736 | |||||||
| chr5:143315000 | C | T | 2 | a0001c0001t0003g0185 a0001c0001t0003g0253 |
2 | HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1185-832G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143315000 | |||||||
| chr5:143315248 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-1080C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143315248 | |||||||
| chr5:143315677 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1185-1509A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143315677 | |||||||
| chr5:143315736 | T | C | 2 | a0001c0001t0003g0180 a0001c0001t0003g0181 |
2 | HG01256.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1185-1568A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143315736 | |||||||
| chr5:143315765 | T | C | 6 | a0001c0001t0001g0114 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-1597A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143315765 | |||||||
| chr5:143315877 | C | T | 1 | a0001c0003t0008g0045 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1185-1709G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143315877 | |||||||
| chr5:143316030 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1185-1862G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143316030 | |||||||
| chr5:143316471 | G | A | 38 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0006g0029 others(35): Show |
38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1185-2303C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143316471 | |||||||
| chr5:143316541 | C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-2373G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143316541 | |||||||
| chr5:143316882 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-2714C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143316882 | |||||||
| chr5:143316941 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1185-2773C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143316941 | |||||||
| chr5:143316947 | G | C | 6 | a0001c0006t0001g0098 a0001c0006t0001g0099 a0001c0006t0001g0100 others(3): Show |
6 | HG02572.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-2779C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143316947 | |||||||
| chr5:143317004 | G | C | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1185-2836C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143317004 | |||||||
| chr5:143317093 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1185-2925C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143317093 | |||||||
| chr5:143317484 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1185-3316A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143317484 | |||||||
| chr5:143317709 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1185-3541A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143317709 | |||||||
| chr5:143317730 | A | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(123): Show |
128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1185-3562T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143317730 | |||||||
| chr5:143317994 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-3826T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143317994 | |||||||
| chr5:143318065 | G | A | 1 | a0001c0001t0005g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1185-3897C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318065 | |||||||
| chr5:143318209 | A | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-4041T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318209 | |||||||
| chr5:143318364 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0004g0087 |
2 | HG00099.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1185-4196T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318364 | |||||||
| chr5:143318435 | T | G | 2 | a0001c0001t0003g0184 a0001c0001t0003g0188 |
2 | HG01175.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1185-4267A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318435 | |||||||
| chr5:143318660 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1185-4492A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318660 | |||||||
| chr5:143318675 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1185-4507C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318675 | |||||||
| chr5:143318791 | A | G | 1 | a0001c0001t0010g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1185-4623T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143318791 | |||||||
| chr5:143319029 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1185-4861G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319029 | |||||||
| chr5:143319180 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-5012A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319180 | |||||||
| chr5:143319342 | A | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-5174T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319342 | |||||||
| chr5:143319347 | T | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-5179A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319347 | |||||||
| chr5:143319378 | A | C | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-5210T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319378 | |||||||
| chr5:143319448 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-5280A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319448 | |||||||
| chr5:143319479 | A | G | 1 | a0001c0001t0029g0124 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1185-5311T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319479 | |||||||
| chr5:143319632 | G | A | 3 | a0001c0001t0003g0185 a0001c0001t0003g0253 a0003c0008t0003g0179 |
3 | HG00323.hp2 HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1185-5464C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319632 | |||||||
| chr5:143319634 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-5466A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319634 | |||||||
| chr5:143319943 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1185-5775A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143319943 | |||||||
| chr5:143320023 | G | A | 6 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(3): Show |
6 | NA18946.hp1 NA18974.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-5855C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320023 | |||||||
| chr5:143320154 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(250): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1185-5986T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320154 | |||||||
| chr5:143320203 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1185-6035A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320203 | |||||||
| chr5:143320206 | A | G | 1 | a0001c0004t0004g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1185-6038T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320206 | |||||||
| chr5:143320236 | A | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-6068T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320236 | |||||||
| chr5:143320237 | T | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-6069A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320237 | |||||||
| chr5:143320239 | T | TTTAGCAG others(3): Show |
1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-6072_1185-607 others(14): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320239 | |||||||
| chr5:143320472 | T | C | 3 | a0001c0001t0005g0199 a0001c0001t0005g0200 a0001c0001t0005g0201 |
3 | HG01496.hp1 HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1185-6304A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320472 | |||||||
| chr5:143320934 | C | T | 38 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(35): Show |
38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1185-6766G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143320934 | |||||||
| chr5:143321028 | G | A | 2 | a0001c0001t0005g0210 a0001c0001t0005g0211 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1185-6860C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321028 | |||||||
| chr5:143321106 | T | C | 1 | a0001c0002t0017g0033 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1185-6938A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321106 | |||||||
| chr5:143321238 | A | G | 2 | a0001c0001t0002g0212 a0001c0001t0002g0227 |
2 | NA19009.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1185-7070T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321238 | |||||||
| chr5:143321291 | G | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1185-7123C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321291 | |||||||
| chr5:143321438 | A | G | 1 | a0001c0006t0001g0098 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1185-7270T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321438 | |||||||
| chr5:143321457 | C | T | 1 | a0001c0001t0026g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1185-7289G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321457 | |||||||
| chr5:143321985 | T | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-7817A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143321985 | |||||||
| chr5:143322010 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1185-7842A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143322010 | |||||||
| chr5:143322115 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1185-7947T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143322115 | |||||||
| chr5:143322315 | A | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-8147T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143322315 | |||||||
| chr5:143322336 | T | C | 1 | a0001c0005t0009g0257 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1185-8168A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143322336 | |||||||
| chr5:143322402 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-8234C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143322402 | |||||||
| chr5:143322496 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-8328C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143322496 | |||||||
| chr5:143323374 | T | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-9206A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323374 | |||||||
| chr5:143323405 | C | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-9237G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323405 | |||||||
| chr5:143323424 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1185-9256G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323424 | |||||||
| chr5:143323437 | C | T | 1 | a0001c0001t0014g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1185-9269G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323437 | |||||||
| chr5:143323757 | C | T | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-9589G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323757 | |||||||
| chr5:143323769 | G | A | 1 | a0001c0006t0001g0103 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1185-9601C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323769 | |||||||
| chr5:143323875 | T | C | 2 | a0001c0001t0002g0246 a0001c0001t0002g0247 |
2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1185-9707A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143323875 | |||||||
| chr5:143324008 | G | GCAGGGTA | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-9841_1185-984 others(11): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143324008 | |||||||
| chr5:143324082 | G | A | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-9914C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143324082 | |||||||
| chr5:143324441 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1185-10273C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143324441 | |||||||
| chr5:143324485 | C | T | 1 | a0001c0002t0016g0028 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1185-10317G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143324485 | |||||||
| chr5:143325168 | A | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-11000T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325168 | |||||||
| chr5:143325247 | C | T | 1 | a0001c0001t0014g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1185-11079G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325247 | |||||||
| chr5:143325297 | A | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-11129T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325297 | |||||||
| chr5:143325463 | C | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-11295G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325463 | |||||||
| chr5:143325484 | C | T | 2 | a0001c0001t0001g0074 a0004c0009t0001g0075 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1185-11316G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325484 | |||||||
| chr5:143325559 | T | C | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-11391A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325559 | |||||||
| chr5:143325769 | C | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG00597.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1185-11601G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325769 | |||||||
| chr5:143325856 | G | A | 67 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(64): Show |
67 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.1185-11688C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143325856 | |||||||
| chr5:143326034 | C | A | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-11866G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143326034 | |||||||
| chr5:143326330 | T | G | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1185-12162A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143326330 | |||||||
| chr5:143326580 | C | T | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1185-12412G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143326580 | |||||||
| chr5:143326833 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1185-12665C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143326833 | |||||||
| chr5:143327047 | T | C | 1 | a0001c0001t0003g0191 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1185-12879A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327047 | |||||||
| chr5:143327361 | C | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-13193G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327361 | |||||||
| chr5:143327584 | A | T | 7 | a0001c0004t0004g0049 a0001c0004t0004g0050 a0001c0004t0004g0052 others(4): Show |
7 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-13416T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327584 | |||||||
| chr5:143327658 | C | T | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-13490G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327658 | |||||||
| chr5:143327768 | C | T | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-13600G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327768 | |||||||
| chr5:143327829 | G | A | 1 | a0001c0001t0032g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1185-13661C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327829 | |||||||
| chr5:143327910 | G | C | 1 | a0001c0001t0002g0231 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1185-13742C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143327910 | |||||||
| chr5:143328087 | T | A | 1 | a0001c0004t0004g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1185-13919A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328087 | |||||||
| chr5:143328136 | C | T | 6 | a0001c0003t0008g0024 a0001c0003t0008g0025 a0001c0003t0008g0026 others(3): Show |
6 | HG00738.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-13968G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328136 | |||||||
| chr5:143328137 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-13969C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328137 | |||||||
| chr5:143328169 | C | T | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1185-14001G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328169 | |||||||
| chr5:143328416 | T | C | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-14248A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328416 | |||||||
| chr5:143328765 | C | T | 4 | a0001c0002t0006g0029 a0001c0002t0006g0032 a0001c0002t0006g0041 others(1): Show |
4 | NA18942.hp2 NA18985.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1185-14597G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328765 | |||||||
| chr5:143328780 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1185-14612A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328780 | |||||||
| chr5:143328815 | T | C | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1185-14647A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328815 | |||||||
| chr5:143328841 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1185-14673G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328841 | |||||||
| chr5:143328862 | A | G | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-14694T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328862 | |||||||
| chr5:143328904 | G | C | 68 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(65): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1185-14736C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328904 | |||||||
| chr5:143328994 | T | G | 2 | a0001c0001t0005g0210 a0001c0001t0005g0211 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1185-14826A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143328994 | |||||||
| chr5:143329169 | T | C | 40 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(37): Show |
40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1185-15001A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329169 | |||||||
| chr5:143329287 | G | A | 40 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(37): Show |
40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1185-15119C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329287 | |||||||
| chr5:143329310 | T | C | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-15142A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329310 | |||||||
| chr5:143329404 | A | G | 1 | a0001c0001t0003g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1185-15236T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329404 | |||||||
| chr5:143329422 | A | G | 2 | a0001c0003t0008g0024 a0001c0003t0008g0025 |
2 | HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1185-15254T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329422 | |||||||
| chr5:143329547 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-15379T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329547 | |||||||
| chr5:143329823 | T | A | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1185-15655A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329823 | |||||||
| chr5:143329889 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-15721T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143329889 | |||||||
| chr5:143330158 | T | C | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1185-15990A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330158 | |||||||
| chr5:143330344 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-16176T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330344 | |||||||
| chr5:143330421 | C | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1185-16253G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330421 | |||||||
| chr5:143330745 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1185-16577G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330745 | |||||||
| chr5:143330766 | C | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-16598G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330766 | |||||||
| chr5:143330775 | C | G | 2 | a0001c0001t0002g0217 a0001c0001t0002g0219 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1185-16607G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330775 | |||||||
| chr5:143330892 | C | T | 6 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(3): Show |
6 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-16724G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330892 | |||||||
| chr5:143330976 | A | C | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02055.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-16808T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143330976 | |||||||
| chr5:143331046 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1185-16878G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331046 | |||||||
| chr5:143331079 | C | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-16911G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331079 | |||||||
| chr5:143331131 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1185-16963G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331131 | |||||||
| chr5:143331324 | A | C | 1 | a0001c0001t0037g0258 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1185-17156T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331324 | |||||||
| chr5:143331446 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1185-17278C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331446 | |||||||
| chr5:143331475 | A | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-17307T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331475 | |||||||
| chr5:143331480 | T | C | 1 | a0001c0001t0004g0239 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1185-17312A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331480 | |||||||
| chr5:143331523 | G | A | 2 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1185-17355C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331523 | |||||||
| chr5:143331863 | C | G | 6 | a0001c0001t0001g0114 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-17695G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331863 | |||||||
| chr5:143331866 | C | G | 2 | a0001c0001t0005g0063 a0001c0001t0005g0222 |
2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1185-17698G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331866 | |||||||
| chr5:143331938 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-17770A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143331938 | |||||||
| chr5:143332312 | G | GTT | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-18146_1185-18 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332312 | |||||||
| chr5:143332393 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-18225C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332393 | |||||||
| chr5:143332406 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1185-18238C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332406 | |||||||
| chr5:143332413 | G | C | 5 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
5 | HG02080.hp1 HG02129.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1185-18245C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332413 | |||||||
| chr5:143332471 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1185-18303C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332471 | |||||||
| chr5:143332499 | G | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1185-18331C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332499 | |||||||
| chr5:143332526 | C | A | 38 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(35): Show |
38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1185-18358G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332526 | |||||||
| chr5:143332610 | GT | G | 78 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1185-18443delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332610 | |||||||
| chr5:143332767 | T | C | 1 | a0001c0005t0009g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-18599A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332767 | |||||||
| chr5:143332793 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1185-18625C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143332793 | |||||||
| chr5:143333032 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1185-18864C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333032 | |||||||
| chr5:143333158 | T | TA | 68 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(65): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1185-18991dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333158 | |||||||
| chr5:143333314 | C | A | 3 | a0001c0001t0003g0185 a0001c0001t0003g0253 a0003c0008t0003g0179 |
3 | HG00323.hp2 HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1185-19146G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333314 | |||||||
| chr5:143333745 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1185-19577G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333745 | |||||||
| chr5:143333760 | C | G | 6 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(3): Show |
6 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-19592G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333760 | |||||||
| chr5:143333767 | A | G | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-19599T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333767 | |||||||
| chr5:143333769 | A | AAAAC | 3 | a0001c0001t0001g0081 a0001c0003t0008g0042 a0001c0003t0008g0043 |
3 | HG02055.hp1 HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1185-19605_1185-19 others(10): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333769 | |||||||
| chr5:143333769 | AAAAC | A | 15 | a0001c0001t0001g0106 a0001c0003t0008g0024 a0001c0003t0008g0025 others(12): Show |
16 | HG00408.hp2 HG01884.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.1185-19605_1185-19 others(10): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333769 | |||||||
| chr5:143333807 | T | C | 1 | a0001c0003t0006g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1185-19639A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333807 | |||||||
| chr5:143333963 | C | T | 5 | a0001c0001t0002g0216 a0001c0001t0002g0233 a0001c0001t0002g0234 others(2): Show |
5 | HG00438.hp2 NA18747.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-19795G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143333963 | |||||||
| chr5:143334001 | T | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-19833A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334001 | |||||||
| chr5:143334008 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1185-19840A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334008 | |||||||
| chr5:143334107 | C | T | 1 | a0001c0001t0013g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1185-19939G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334107 | |||||||
| chr5:143334215 | C | G | 1 | a0001c0004t0033g0051 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1185-20047G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334215 | |||||||
| chr5:143334413 | T | C | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1185-20245A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334413 | |||||||
| chr5:143334521 | G | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-20353C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334521 | |||||||
| chr5:143334600 | A | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-20432T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334600 | |||||||
| chr5:143334725 | G | GA | 42 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(39): Show |
46 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1185-20558dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334725 | |||||||
| chr5:143334725 | G | GAA | 6 | a0001c0001t0002g0237 a0001c0005t0009g0008 a0001c0005t0009g0249 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-20559_1185-20 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334725 | |||||||
| chr5:143334924 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-20756T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334924 | |||||||
| chr5:143334972 | T | G | 1 | a0001c0004t0004g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1185-20804A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143334972 | |||||||
| chr5:143335046 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1185-20878C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335046 | |||||||
| chr5:143335077 | C | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0127 others(5): Show |
8 | HG00408.hp1 HG02165.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.1185-20909G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335077 | |||||||
| chr5:143335193 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1185-21025C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335193 | |||||||
| chr5:143335624 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
7 | HG02451.hp2 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185-21456T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335624 | |||||||
| chr5:143335694 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1185-21526T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335694 | |||||||
| chr5:143335879 | G | A | 1 | a0001c0002t0016g0028 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1185-21711C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335879 | |||||||
| chr5:143335918 | T | C | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-21750A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143335918 | |||||||
| chr5:143336121 | G | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-21953C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336121 | |||||||
| chr5:143336214 | A | G | 2 | a0001c0006t0001g0098 a0001c0006t0001g0100 |
2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1185-22046T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336214 | |||||||
| chr5:143336232 | T | C | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1185-22064A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336232 | |||||||
| chr5:143336714 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1185-22546C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336714 | |||||||
| chr5:143336737 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22569A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336737 | |||||||
| chr5:143336738 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22570T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336738 | |||||||
| chr5:143336740 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22572T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336740 | |||||||
| chr5:143336743 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22575T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336743 | |||||||
| chr5:143336747 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22579T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336747 | |||||||
| chr5:143336753 | CTTGACGT others(3): Show |
C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22595_1185-22 others(16): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336753 | |||||||
| chr5:143336774 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22606C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336774 | |||||||
| chr5:143336780 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22612A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336780 | |||||||
| chr5:143336783 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22615T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336783 | |||||||
| chr5:143336786 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22618A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336786 | |||||||
| chr5:143336790 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22622C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336790 | |||||||
| chr5:143336792 | C | T | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1185-22624G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336792 | |||||||
| chr5:143336793 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22625A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336793 | |||||||
| chr5:143336795 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22627A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336795 | |||||||
| chr5:143336799 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22631G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336799 | |||||||
| chr5:143336801 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22633A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336801 | |||||||
| chr5:143336804 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22636G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336804 | |||||||
| chr5:143336812 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22644A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336812 | |||||||
| chr5:143336815 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22647A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336815 | |||||||
| chr5:143336820 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22652A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336820 | |||||||
| chr5:143336841 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22673A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336841 | |||||||
| chr5:143336842 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22674T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336842 | |||||||
| chr5:143336844 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22676C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336844 | |||||||
| chr5:143336850 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22682T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336850 | |||||||
| chr5:143336851 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22683A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336851 | |||||||
| chr5:143336852 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22684T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336852 | |||||||
| chr5:143336859 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22691T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336859 | |||||||
| chr5:143336863 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22695A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336863 | |||||||
| chr5:143336871 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22703G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336871 | |||||||
| chr5:143336875 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22707A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336875 | |||||||
| chr5:143336876 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22708A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336876 | |||||||
| chr5:143336883 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22715T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336883 | |||||||
| chr5:143336891 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22723T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336891 | |||||||
| chr5:143336892 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22724T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336892 | |||||||
| chr5:143336895 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22727A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336895 | |||||||
| chr5:143336903 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22735T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336903 | |||||||
| chr5:143336909 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22741A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336909 | |||||||
| chr5:143336914 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22746C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336914 | |||||||
| chr5:143336915 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22747G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336915 | |||||||
| chr5:143336927 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22759T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336927 | |||||||
| chr5:143336931 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22763G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336931 | |||||||
| chr5:143336932 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22764A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336932 | |||||||
| chr5:143336933 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22765C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336933 | |||||||
| chr5:143336934 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22766A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336934 | |||||||
| chr5:143336937 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1185-22769G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336937 | |||||||
| chr5:143336938 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22770C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336938 | |||||||
| chr5:143336956 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22788A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336956 | |||||||
| chr5:143336964 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22796A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336964 | |||||||
| chr5:143336970 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22802G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336970 | |||||||
| chr5:143336972 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22804A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336972 | |||||||
| chr5:143336982 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22815_1185-22 others(36): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143336982 | |||||||
| chr5:143337036 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-22868G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337036 | |||||||
| chr5:143337237 | G | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-23069C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337237 | |||||||
| chr5:143337463 | T | C | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-23295A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337463 | |||||||
| chr5:143337671 | C | T | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-23503G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337671 | |||||||
| chr5:143337691 | C | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-23523G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337691 | |||||||
| chr5:143337718 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-23550A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337718 | |||||||
| chr5:143337759 | T | C | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-23591A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337759 | |||||||
| chr5:143337804 | T | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-23636A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337804 | |||||||
| chr5:143337856 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-23688G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337856 | |||||||
| chr5:143337966 | A | G | 1 | a0001c0001t0025g0224 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1185-23798T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143337966 | |||||||
| chr5:143338160 | C | A | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-23992G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338160 | |||||||
| chr5:143338161 | A | C | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-23993T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338161 | |||||||
| chr5:143338162 | T | A | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-23994A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338162 | |||||||
| chr5:143338234 | CA | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-24067delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338234 | |||||||
| chr5:143338344 | C | CT | 39 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(36): Show |
39 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1185-24177dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338344 | |||||||
| chr5:143338467 | C | T | 1 | a0001c0002t0019g0039 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1185-24299G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338467 | |||||||
| chr5:143338488 | T | C | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-24320A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338488 | |||||||
| chr5:143338696 | A | G | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-24528T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338696 | |||||||
| chr5:143338725 | G | C | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1185-24557C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338725 | |||||||
| chr5:143338985 | G | A | 2 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1185-24817C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143338985 | |||||||
| chr5:143339068 | C | T | 1 | a0001c0001t0004g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1185-24900G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339068 | |||||||
| chr5:143339240 | TA | T | 38 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(35): Show |
38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1185-25073delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339240 | |||||||
| chr5:143339373 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-25205G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339373 | |||||||
| chr5:143339549 | T | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-25381A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339549 | |||||||
| chr5:143339551 | A | C | 1 | a0001c0001t0036g0214 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1185-25383T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339551 | |||||||
| chr5:143339654 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0161 |
2 | NA18974.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1185-25486A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339654 | |||||||
| chr5:143339853 | G | A | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-25685C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339853 | |||||||
| chr5:143339940 | A | AG | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-25773dupC | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143339940 | |||||||
| chr5:143340135 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-25967A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340135 | |||||||
| chr5:143340277 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1185-26109T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340277 | |||||||
| chr5:143340349 | C | CT | 41 | a0001c0001t0002g0237 a0001c0002t0004g0060 a0001c0002t0004g0167 others(38): Show |
41 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1185-26182dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340349 | |||||||
| chr5:143340364 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1185-26196A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340364 | |||||||
| chr5:143340411 | A | T | 3 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0252 |
4 | HG02074.hp2 NA18982.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-26243T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340411 | |||||||
| chr5:143340476 | A | AT | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(97): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1185-26309dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340476 | |||||||
| chr5:143340476 | A | ATT | 43 | a0001c0001t0001g0071 a0001c0001t0001g0077 a0001c0001t0001g0078 others(40): Show |
44 | HG00408.hp2 HG00423.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1185-26310_1185-26 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340476 | |||||||
| chr5:143340476 | A | ATTT | 7 | a0001c0001t0002g0007 a0001c0001t0002g0223 a0001c0001t0002g0227 others(4): Show |
8 | HG02027.hp1 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-26311_1185-26 others(9): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340476 | |||||||
| chr5:143340476 | AT | A | 37 | a0001c0001t0002g0237 a0001c0001t0003g0181 a0001c0001t0005g0204 others(34): Show |
37 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1185-26309delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340476 | |||||||
| chr5:143340513 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1185-26345G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340513 | |||||||
| chr5:143340556 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1185-26388G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340556 | |||||||
| chr5:143340628 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1185-26460C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340628 | |||||||
| chr5:143340631 | C | T | 7 | a0001c0004t0004g0053 a0001c0005t0009g0008 a0001c0005t0009g0249 others(4): Show |
8 | HG00738.hp1 HG02027.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1185-26463G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340631 | |||||||
| chr5:143340717 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1185-26549C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340717 | |||||||
| chr5:143340786 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-26618C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143340786 | |||||||
| chr5:143341025 | C | A | 3 | a0001c0001t0007g0001 a0001c0001t0007g0020 a0001c0001t0007g0021 |
4 | HG02896.hp2 HG02897.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-26857G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341025 | |||||||
| chr5:143341028 | A | G | 1 | a0001c0004t0004g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1185-26860T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341028 | |||||||
| chr5:143341056 | G | T | 1 | a0001c0001t0002g0237 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1185-26888C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341056 | |||||||
| chr5:143341059 | C | G | 1 | a0001c0001t0002g0237 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1185-26891G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341059 | |||||||
| chr5:143341060 | A | C | 1 | a0001c0001t0002g0237 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1185-26892T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341060 | |||||||
| chr5:143341161 | T | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(53): Show |
58 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1185-26993A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341161 | |||||||
| chr5:143341185 | G | T | 1 | a0001c0001t0002g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1185-27017C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341185 | |||||||
| chr5:143341375 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1185-27207G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341375 | |||||||
| chr5:143341500 | T | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0001g0135 others(2): Show |
5 | HG00408.hp1 NA18747.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-27332A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341500 | |||||||
| chr5:143341526 | T | C | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-27358A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341526 | |||||||
| chr5:143341965 | C | A | 1 | a0001c0001t0002g0238 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1185-27797G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143341965 | |||||||
| chr5:143342015 | G | A | 1 | a0001c0001t0002g0243 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1185-27847C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143342015 | |||||||
| chr5:143342192 | C | T | 2 | a0001c0001t0005g0210 a0001c0001t0005g0211 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1185-28024G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143342192 | |||||||
| chr5:143342193 | G | A | 6 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(3): Show |
6 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-28025C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143342193 | |||||||
| chr5:143342788 | T | C | 40 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(37): Show |
40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1185-28620A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143342788 | |||||||
| chr5:143342828 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-28660G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143342828 | |||||||
| chr5:143343095 | G | C | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1185-28927C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343095 | |||||||
| chr5:143343146 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1185-28978G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343146 | |||||||
| chr5:143343297 | C | T | 11 | a0001c0001t0003g0184 a0001c0001t0003g0188 a0001c0001t0003g0189 others(8): Show |
11 | HG01099.hp1 HG01169.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1185-29129G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343297 | |||||||
| chr5:143343316 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1185-29148A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343316 | |||||||
| chr5:143343351 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1185-29183A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343351 | |||||||
| chr5:143343450 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
6 | HG02451.hp2 HG03098.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-29282A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343450 | |||||||
| chr5:143343657 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0031g0128 |
2 | HG00408.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1185-29489G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343657 | |||||||
| chr5:143343719 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1185-29551C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343719 | |||||||
| chr5:143343772 | T | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
7 | HG02451.hp2 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185-29604A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343772 | |||||||
| chr5:143343808 | G | C | 40 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(37): Show |
40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1185-29640C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343808 | |||||||
| chr5:143343851 | T | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-29683A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343851 | |||||||
| chr5:143343868 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-29700G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143343868 | |||||||
| chr5:143344030 | T | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-29862A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344030 | |||||||
| chr5:143344067 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1185-29899T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344067 | |||||||
| chr5:143344156 | T | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-29988A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344156 | |||||||
| chr5:143344372 | T | G | 34 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0108 others(31): Show |
34 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.1185-30204A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344372 | |||||||
| chr5:143344599 | G | A | 1 | a0001c0001t0003g0191 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1185-30431C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344599 | |||||||
| chr5:143344643 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-30475G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344643 | |||||||
| chr5:143344865 | G | A | 39 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(36): Show |
39 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1185-30697C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344865 | |||||||
| chr5:143344892 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1185-30724G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143344892 | |||||||
| chr5:143345025 | TGTGTGTG others(31): Show |
T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30895_1185-30 others(44): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345025 | |||||||
| chr5:143345090 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30922C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345090 | |||||||
| chr5:143345102 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30934C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345102 | |||||||
| chr5:143345146 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30978A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345146 | |||||||
| chr5:143345148 | T | A | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30980A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345148 | |||||||
| chr5:143345149 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30981T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345149 | |||||||
| chr5:143345151 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-30983C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345151 | |||||||
| chr5:143345186 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31018T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345186 | |||||||
| chr5:143345227 | T | TGTGGGGG others(3): Show |
1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31060_1185-31 others(16): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345227 | |||||||
| chr5:143345228 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31060A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345228 | |||||||
| chr5:143345230 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31062T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345230 | |||||||
| chr5:143345241 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31073T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345241 | |||||||
| chr5:143345242 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31074C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345242 | |||||||
| chr5:143345256 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31088G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345256 | |||||||
| chr5:143345258 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31090C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345258 | |||||||
| chr5:143345267 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31099C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345267 | |||||||
| chr5:143345272 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31104G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345272 | |||||||
| chr5:143345273 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31105T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345273 | |||||||
| chr5:143345314 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-31146T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345314 | |||||||
| chr5:143345519 | A | T | 78 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1185-31351T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345519 | |||||||
| chr5:143345748 | A | G | 2 | a0001c0001t0002g0006 a0001c0001t0002g0241 |
3 | HG00597.hp2 NA19007.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1185-31580T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345748 | |||||||
| chr5:143345907 | T | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0135 a0001c0001t0001g0138 |
3 | NA18747.hp2 NA18940.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1185-31739A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345907 | |||||||
| chr5:143345995 | T | C | 1 | a0001c0001t0025g0224 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1185-31827A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143345995 | |||||||
| chr5:143346270 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-32102C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143346270 | |||||||
| chr5:143346300 | C | A | 1 | a0001c0001t0010g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-32132G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143346300 | |||||||
| chr5:143346605 | C | T | 76 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(73): Show |
77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1185-32437G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143346605 | |||||||
| chr5:143346630 | C | A | 1 | a0001c0001t0002g0226 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1185-32462G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143346630 | |||||||
| chr5:143346960 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-32792C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143346960 | |||||||
| chr5:143347329 | C | CACACACA others(1): Show |
6 | a0001c0001t0001g0114 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-33169_1185-33 others(14): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143347329 | |||||||
| chr5:143347564 | C | T | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-33396G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143347564 | |||||||
| chr5:143347628 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(117): Show |
122 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1185-33460C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143347628 | |||||||
| chr5:143347680 | A | G | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-33512T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143347680 | |||||||
| chr5:143347845 | A | C | 1 | a0001c0001t0002g0213 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1185-33677T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143347845 | |||||||
| chr5:143347977 | GT | G | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-33810delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143347977 | |||||||
| chr5:143348165 | C | T | 2 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1185-33997G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348165 | |||||||
| chr5:143348197 | T | C | 1 | a0001c0001t0032g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1185-34029A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348197 | |||||||
| chr5:143348381 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1185-34213G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348381 | |||||||
| chr5:143348466 | T | C | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1185-34298A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348466 | |||||||
| chr5:143348494 | C | T | 1 | a0001c0001t0035g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1185-34326G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348494 | |||||||
| chr5:143348764 | A | G | 4 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0005g0210 others(1): Show |
4 | HG02723.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1185-34596T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348764 | |||||||
| chr5:143348781 | A | G | 22 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.1185-34613T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348781 | |||||||
| chr5:143348854 | A | G | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1185-34686T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348854 | |||||||
| chr5:143348859 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-34691C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348859 | |||||||
| chr5:143348900 | T | C | 2 | a0001c0001t0001g0074 a0004c0009t0001g0075 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1185-34732A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143348900 | |||||||
| chr5:143349121 | T | C | 1 | a0001c0004t0004g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1185-34953A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349121 | |||||||
| chr5:143349141 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1185-34973C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349141 | |||||||
| chr5:143349143 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-34975A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349143 | |||||||
| chr5:143349194 | T | C | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-35026A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349194 | |||||||
| chr5:143349539 | G | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-35371C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349539 | |||||||
| chr5:143349638 | T | G | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1185-35470A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349638 | |||||||
| chr5:143349874 | G | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-35706C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143349874 | |||||||
| chr5:143350251 | G | A | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1185-36083C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350251 | |||||||
| chr5:143350358 | A | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-36190T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350358 | |||||||
| chr5:143350640 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-36472A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350640 | |||||||
| chr5:143350811 | G | C | 34 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0108 others(31): Show |
34 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.1185-36643C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350811 | |||||||
| chr5:143350867 | G | T | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1185-36699C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350867 | |||||||
| chr5:143350904 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-36736C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350904 | |||||||
| chr5:143350915 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1185-36747T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143350915 | |||||||
| chr5:143351120 | C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-36952G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143351120 | |||||||
| chr5:143351291 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1185-37123C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143351291 | |||||||
| chr5:143351392 | TA | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-37225delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143351392 | |||||||
| chr5:143351444 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1185-37276A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143351444 | |||||||
| chr5:143352016 | A | C | 1 | a0001c0001t0001g0127 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1185-37848T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143352016 | |||||||
| chr5:143352821 | A | G | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-38653T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143352821 | |||||||
| chr5:143352941 | A | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-38773T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143352941 | |||||||
| chr5:143353042 | C | T | 29 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(26): Show |
29 | HG00438.hp1 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1185-38874G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353042 | |||||||
| chr5:143353356 | G | A | 1 | a0001c0002t0017g0033 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1185-39188C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353356 | |||||||
| chr5:143353498 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1185-39330G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353498 | |||||||
| chr5:143353502 | C | T | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-39334G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353502 | |||||||
| chr5:143353522 | G | C | 1 | a0001c0001t0003g0187 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1185-39354C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353522 | |||||||
| chr5:143353576 | T | G | 1 | a0001c0006t0001g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1185-39408A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353576 | |||||||
| chr5:143353608 | A | G | 6 | a0001c0001t0001g0114 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-39440T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353608 | |||||||
| chr5:143353626 | G | C | 4 | a0001c0001t0001g0116 a0001c0001t0001g0248 a0001c0001t0026g0115 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1185-39458C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353626 | |||||||
| chr5:143353636 | A | T | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1185-39468T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353636 | |||||||
| chr5:143353724 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-39556G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353724 | |||||||
| chr5:143353814 | G | A | 1 | a0001c0001t0003g0207 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1185-39646C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143353814 | |||||||
| chr5:143354043 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1185-39875A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354043 | |||||||
| chr5:143354054 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1185-39886G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354054 | |||||||
| chr5:143354220 | T | C | 1 | a0001c0004t0004g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1185-40052A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354220 | |||||||
| chr5:143354510 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-40342A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354510 | |||||||
| chr5:143354537 | G | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1185-40369C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354537 | |||||||
| chr5:143354576 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-40408C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354576 | |||||||
| chr5:143354586 | T | C | 40 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(37): Show |
40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1185-40418A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354586 | |||||||
| chr5:143354674 | G | C | 1 | a0001c0001t0001g0175 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1185-40506C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354674 | |||||||
| chr5:143354675 | C | A | 1 | a0001c0001t0001g0175 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1185-40507G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354675 | |||||||
| chr5:143354768 | C | T | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-40600G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354768 | |||||||
| chr5:143354827 | G | A | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1185-40659C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354827 | |||||||
| chr5:143354922 | C | CAA | 4 | a0001c0005t0009g0008 a0001c0005t0009g0251 a0001c0005t0009g0252 others(1): Show |
5 | HG02027.hp1 NA18982.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-40756_1185-40 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354922 | |||||||
| chr5:143354922 | CA | C | 5 | a0001c0001t0001g0085 a0001c0001t0001g0165 a0001c0001t0005g0204 others(2): Show |
5 | HG01070.hp1 HG01243.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-40755delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354922 | |||||||
| chr5:143354940 | G | A | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-40772C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354940 | |||||||
| chr5:143354970 | G | A | 10 | a0001c0001t0003g0184 a0001c0001t0003g0188 a0001c0001t0003g0189 others(7): Show |
10 | HG01175.hp2 HG01192.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1185-40802C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143354970 | |||||||
| chr5:143355141 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-40973G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143355141 | |||||||
| chr5:143355177 | T | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(250): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1185-41009A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143355177 | |||||||
| chr5:143355482 | A | AATAATAA others(6): Show |
6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-41315_1185-41 others(19): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143355482 | |||||||
| chr5:143355483 | T | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-41315A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143355483 | |||||||
| chr5:143355483 | T | TAATAAAT others(5): Show |
3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-41327_1185-41 others(18): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143355483 | |||||||
| chr5:143355974 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1185-41806G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143355974 | |||||||
| chr5:143356000 | CAT | C | 5 | a0001c0003t0008g0024 a0001c0003t0008g0025 a0001c0003t0008g0026 others(2): Show |
5 | HG02886.hp1 HG02895.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-41834_1185-41 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356000 | |||||||
| chr5:143356002 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0097 |
3 | HG02451.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1185-41834A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356002 | |||||||
| chr5:143356273 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-42105C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356273 | |||||||
| chr5:143356417 | G | A | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-42249C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356417 | |||||||
| chr5:143356423 | T | C | 1 | a0001c0001t0003g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1185-42255A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356423 | |||||||
| chr5:143356445 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1185-42277A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356445 | |||||||
| chr5:143356688 | C | CA | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(117): Show |
122 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1185-42521dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356688 | |||||||
| chr5:143356688 | CA | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-42521delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356688 | |||||||
| chr5:143356699 | A | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-42531T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356699 | |||||||
| chr5:143356822 | A | C | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1185-42654T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143356822 | |||||||
| chr5:143357059 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1184+42597C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357059 | |||||||
| chr5:143357084 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1184+42572A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357084 | |||||||
| chr5:143357217 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+42439C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357217 | |||||||
| chr5:143357253 | A | AT | 29 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(26): Show |
29 | HG00438.hp1 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1184+42402dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357253 | |||||||
| chr5:143357275 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+42381C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357275 | |||||||
| chr5:143357317 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+42339A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357317 | |||||||
| chr5:143357347 | G | A | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+42309C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357347 | |||||||
| chr5:143357401 | T | G | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02055.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+42255A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357401 | |||||||
| chr5:143357499 | T | C | 1 | a0001c0002t0018g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1184+42157A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357499 | |||||||
| chr5:143357549 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+42107T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357549 | |||||||
| chr5:143357651 | T | G | 1 | a0001c0003t0006g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1184+42005A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357651 | |||||||
| chr5:143357700 | T | C | 1 | a0001c0001t0007g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1184+41956A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143357700 | |||||||
| chr5:143358006 | A | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+41650T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358006 | |||||||
| chr5:143358163 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1184+41493C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358163 | |||||||
| chr5:143358194 | A | G | 2 | a0001c0001t0003g0195 a0001c0001t0003g0196 |
2 | HG01099.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1184+41462T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358194 | |||||||
| chr5:143358215 | A | C | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0083 others(2): Show |
5 | HG01255.hp1 HG06807.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+41441T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358215 | |||||||
| chr5:143358231 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1184+41425A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358231 | |||||||
| chr5:143358624 | G | A | 1 | a0001c0001t0002g0237 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1184+41032C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358624 | |||||||
| chr5:143358699 | C | T | 8 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
8 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+40957G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358699 | |||||||
| chr5:143358768 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1184+40888G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358768 | |||||||
| chr5:143358800 | T | C | 1 | a0001c0004t0027g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1184+40856A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358800 | |||||||
| chr5:143358894 | C | T | 2 | a0001c0001t0007g0014 a0001c0001t0013g0010 |
2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1184+40762G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358894 | |||||||
| chr5:143358898 | T | C | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+40758A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358898 | |||||||
| chr5:143358900 | C | CA | 5 | a0001c0001t0005g0063 a0001c0001t0005g0222 a0002c0007t0011g0254 others(2): Show |
5 | HG00323.hp1 HG01074.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+40755dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358900 | |||||||
| chr5:143358900 | CA | C | 9 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0127 others(6): Show |
9 | HG00408.hp1 HG02165.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.1184+40755delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143358900 | |||||||
| chr5:143359062 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1184+40594A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359062 | |||||||
| chr5:143359124 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1184+40532T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359124 | |||||||
| chr5:143359181 | G | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+40475C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359181 | |||||||
| chr5:143359215 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1184+40441G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359215 | |||||||
| chr5:143359424 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1184+40232C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359424 | |||||||
| chr5:143359606 | C | T | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+40050G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359606 | |||||||
| chr5:143359681 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+39975C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143359681 | |||||||
| chr5:143360167 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1184+39489G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143360167 | |||||||
| chr5:143360327 | T | C | 1 | a0001c0001t0007g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1184+39329A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143360327 | |||||||
| chr5:143360601 | G | A | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+39055C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143360601 | |||||||
| chr5:143360950 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1184+38706T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143360950 | |||||||
| chr5:143361005 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1184+38651G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361005 | |||||||
| chr5:143361175 | T | C | 1 | a0001c0001t0002g0238 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1184+38481A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361175 | |||||||
| chr5:143361181 | G | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+38475C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361181 | |||||||
| chr5:143361190 | G | T | 1 | a0001c0001t0007g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1184+38466C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361190 | |||||||
| chr5:143361228 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+38428C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361228 | |||||||
| chr5:143361381 | T | C | 1 | a0001c0001t0002g0220 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1184+38275A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361381 | |||||||
| chr5:143361390 | T | C | 3 | a0001c0001t0007g0013 a0001c0001t0007g0017 a0001c0001t0007g0018 |
3 | HG03098.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1184+38266A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361390 | |||||||
| chr5:143361462 | C | T | 78 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1184+38194G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361462 | |||||||
| chr5:143361464 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1184+38192A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361464 | |||||||
| chr5:143361680 | G | A | 3 | a0001c0001t0007g0001 a0001c0001t0007g0020 a0001c0001t0007g0021 |
4 | HG02896.hp2 HG02897.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+37976C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361680 | |||||||
| chr5:143361874 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+37782T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143361874 | |||||||
| chr5:143362176 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+37480G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362176 | |||||||
| chr5:143362341 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1184+37315T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362341 | |||||||
| chr5:143362360 | G | GT | 19 | a0001c0001t0001g0066 a0001c0001t0001g0089 a0001c0001t0001g0114 others(16): Show |
19 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184+37295dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362360 | |||||||
| chr5:143362453 | T | C | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+37203A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362453 | |||||||
| chr5:143362508 | C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+37148G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362508 | |||||||
| chr5:143362525 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+37131A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362525 | |||||||
| chr5:143362552 | A | G | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+37104T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362552 | |||||||
| chr5:143362583 | AATCTCCT others(9): Show |
A | 1 | a0001c0001t0001g0138 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1184+37057_1184+37 others(22): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362583 | |||||||
| chr5:143362629 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+37027C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362629 | |||||||
| chr5:143362878 | A | G | 1 | a0001c0001t0014g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1184+36778T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362878 | |||||||
| chr5:143362926 | C | T | 78 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1184+36730G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362926 | |||||||
| chr5:143362972 | T | C | 40 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(37): Show |
40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1184+36684A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362972 | |||||||
| chr5:143362995 | T | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+36661A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143362995 | |||||||
| chr5:143363040 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+36616C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363040 | |||||||
| chr5:143363134 | A | G | 4 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0005g0210 others(1): Show |
4 | HG02723.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+36522T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363134 | |||||||
| chr5:143363397 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1184+36259G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363397 | |||||||
| chr5:143363490 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1184+36166C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363490 | |||||||
| chr5:143363503 | G | T | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+36153C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363503 | |||||||
| chr5:143363538 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+36118T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363538 | |||||||
| chr5:143363581 | TA | T | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1184+36074delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363581 | |||||||
| chr5:143363760 | C | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+35896G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363760 | |||||||
| chr5:143363905 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+35751A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143363905 | |||||||
| chr5:143364028 | A | G | 1 | a0001c0002t0004g0060 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1184+35628T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364028 | |||||||
| chr5:143364054 | A | G | 1 | a0001c0001t0007g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+35602T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364054 | |||||||
| chr5:143364292 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1184+35364G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364292 | |||||||
| chr5:143364295 | T | C | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+35361A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364295 | |||||||
| chr5:143364527 | G | C | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+35129C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364527 | |||||||
| chr5:143364614 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1184+35042T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364614 | |||||||
| chr5:143364712 | T | C | 6 | a0001c0006t0001g0098 a0001c0006t0001g0099 a0001c0006t0001g0100 others(3): Show |
6 | HG02572.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+34944A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364712 | |||||||
| chr5:143364732 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1184+34924C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143364732 | |||||||
| chr5:143365249 | C | A | 1 | a0001c0001t0036g0214 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1184+34407G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365249 | |||||||
| chr5:143365284 | G | T | 1 | a0001c0001t0025g0224 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1184+34372C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365284 | |||||||
| chr5:143365398 | A | C | 40 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(37): Show |
40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1184+34258T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365398 | |||||||
| chr5:143365420 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+34236C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365420 | |||||||
| chr5:143365480 | A | G | 1 | a0001c0001t0014g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1184+34176T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365480 | |||||||
| chr5:143365495 | C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+34161G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365495 | |||||||
| chr5:143365610 | C | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+34046G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365610 | |||||||
| chr5:143365750 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1184+33906A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365750 | |||||||
| chr5:143365809 | C | T | 1 | a0001c0005t0009g0257 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1184+33847G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365809 | |||||||
| chr5:143365902 | C | T | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1184+33754G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365902 | |||||||
| chr5:143365937 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1184+33719C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143365937 | |||||||
| chr5:143366390 | A | G | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1184+33266T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366390 | |||||||
| chr5:143366458 | C | T | 38 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(35): Show |
38 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1184+33198G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366458 | |||||||
| chr5:143366463 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+33193A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366463 | |||||||
| chr5:143366477 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1184+33179A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366477 | |||||||
| chr5:143366510 | C | CA | 5 | a0001c0001t0001g0135 a0001c0001t0001g0155 a0001c0001t0001g0161 others(2): Show |
5 | HG01346.hp2 NA18961.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+33145dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366510 | |||||||
| chr5:143366510 | CA | C | 46 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(43): Show |
47 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.1184+33145delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366510 | |||||||
| chr5:143366528 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1184+33128A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366528 | |||||||
| chr5:143366614 | G | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+33042C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366614 | |||||||
| chr5:143366798 | A | C | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1184+32858T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143366798 | |||||||
| chr5:143367036 | C | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+32620G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367036 | |||||||
| chr5:143367070 | C | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+32586G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367070 | |||||||
| chr5:143367088 | A | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+32568T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367088 | |||||||
| chr5:143367282 | G | A | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1184+32374C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367282 | |||||||
| chr5:143367700 | A | G | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+31956T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367700 | |||||||
| chr5:143367723 | A | G | 1 | a0001c0001t0030g0194 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1184+31933T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367723 | |||||||
| chr5:143367755 | A | G | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+31901T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143367755 | |||||||
| chr5:143368168 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1184+31488C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368168 | |||||||
| chr5:143368534 | T | TAC | 46 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(43): Show |
47 | HG00438.hp2 HG00639.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1184+31120_1184+31 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368534 | |||||||
| chr5:143368534 | T | TACAC | 5 | a0001c0001t0003g0193 a0001c0001t0003g0197 a0001c0001t0004g0239 others(2): Show |
5 | HG01243.hp2 HG01257.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+31118_1184+31 others(10): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368534 | |||||||
| chr5:143368534 | TAC | T | 35 | a0001c0001t0001g0086 a0001c0001t0004g0087 a0001c0002t0004g0060 others(32): Show |
36 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.1184+31120_1184+31 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368534 | |||||||
| chr5:143368534 | TACAC | T | 4 | a0001c0001t0024g0206 a0002c0007t0011g0254 a0002c0007t0011g0255 others(1): Show |
4 | HG01884.hp1 HG01934.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+31118_1184+31 others(10): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368534 | |||||||
| chr5:143368534 | TACACACA others(7): Show |
T | 1 | a0001c0001t0002g0004 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1184+31108_1184+31 others(20): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368534 | |||||||
| chr5:143368686 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+30970C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368686 | |||||||
| chr5:143368700 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1184+30956T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368700 | |||||||
| chr5:143368786 | A | G | 1 | a0001c0001t0002g0223 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1184+30870T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143368786 | |||||||
| chr5:143369009 | T | C | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1184+30647A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369009 | |||||||
| chr5:143369114 | T | C | 1 | a0001c0003t0006g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1184+30542A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369114 | |||||||
| chr5:143369391 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+30265A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369391 | |||||||
| chr5:143369489 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1184+30167T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369489 | |||||||
| chr5:143369743 | A | G | 1 | a0001c0001t0029g0124 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1184+29913T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369743 | |||||||
| chr5:143369784 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+29872G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369784 | |||||||
| chr5:143369847 | T | C | 2 | a0001c0001t0003g0182 a0001c0001t0030g0194 |
2 | HG02602.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1184+29809A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143369847 | |||||||
| chr5:143370222 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1184+29434A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370222 | |||||||
| chr5:143370302 | G | A | 1 | a0001c0006t0001g0098 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1184+29354C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370302 | |||||||
| chr5:143370639 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1184+29017G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370639 | |||||||
| chr5:143370657 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG01496.hp2 NA18971.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+28999C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370657 | |||||||
| chr5:143370736 | A | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(212): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1184+28920T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370736 | |||||||
| chr5:143370881 | C | T | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+28775G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370881 | |||||||
| chr5:143370884 | A | G | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1184+28772T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370884 | |||||||
| chr5:143370968 | T | G | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+28688A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143370968 | |||||||
| chr5:143371147 | T | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+28509A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143371147 | |||||||
| chr5:143371178 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1184+28478A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143371178 | |||||||
| chr5:143371257 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+28399A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143371257 | |||||||
| chr5:143371605 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+28051C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143371605 | |||||||
| chr5:143371654 | G | A | 6 | a0001c0001t0001g0114 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+28002C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143371654 | |||||||
| chr5:143371863 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+27793G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143371863 | |||||||
| chr5:143372259 | C | T | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+27397G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372259 | |||||||
| chr5:143372425 | T | C | 9 | a0001c0004t0004g0049 a0001c0004t0004g0050 a0001c0004t0004g0052 others(6): Show |
9 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+27231A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372425 | |||||||
| chr5:143372534 | C | T | 2 | a0001c0001t0005g0063 a0001c0001t0005g0222 |
2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1184+27122G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372534 | |||||||
| chr5:143372617 | C | T | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1184+27039G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372617 | |||||||
| chr5:143372627 | G | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+27029C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372627 | |||||||
| chr5:143372754 | A | G | 1 | a0001c0001t0010g0088 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1184+26902T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372754 | |||||||
| chr5:143372762 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1184+26894G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372762 | |||||||
| chr5:143372801 | C | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+26855G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372801 | |||||||
| chr5:143372915 | C | T | 8 | a0001c0004t0004g0049 a0001c0004t0004g0050 a0001c0004t0004g0052 others(5): Show |
8 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+26741G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372915 | |||||||
| chr5:143372990 | A | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+26666T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143372990 | |||||||
| chr5:143373300 | G | C | 1 | a0001c0001t0007g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1184+26356C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373300 | |||||||
| chr5:143373466 | G | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+26190C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373466 | |||||||
| chr5:143373606 | T | C | 1 | a0001c0004t0001g0137 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1184+26050A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373606 | |||||||
| chr5:143373688 | TAG | T | 9 | a0001c0003t0008g0024 a0001c0003t0008g0025 a0001c0003t0008g0026 others(6): Show |
9 | HG02055.hp1 HG02486.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+25966_1184+25 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373688 | |||||||
| chr5:143373691 | G | C | 9 | a0001c0003t0008g0024 a0001c0003t0008g0025 a0001c0003t0008g0026 others(6): Show |
9 | HG02055.hp1 HG02486.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+25965C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373691 | |||||||
| chr5:143373739 | A | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+25917T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373739 | |||||||
| chr5:143373774 | G | A | 1 | a0001c0001t0030g0194 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1184+25882C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373774 | |||||||
| chr5:143373900 | T | C | 1 | a0001c0006t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1184+25756A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373900 | |||||||
| chr5:143373908 | TG | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+25747delC | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373908 | |||||||
| chr5:143373971 | G | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+25685C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143373971 | |||||||
| chr5:143374054 | C | T | 7 | a0001c0001t0001g0123 a0001c0005t0009g0008 a0001c0005t0009g0249 others(4): Show |
8 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+25602G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374054 | |||||||
| chr5:143374104 | C | A | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+25552G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374104 | |||||||
| chr5:143374148 | G | C | 1 | a0001c0001t0012g0009 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1184+25508C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374148 | |||||||
| chr5:143374218 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+25438A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374218 | |||||||
| chr5:143374220 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+25436A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374220 | |||||||
| chr5:143374221 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+25435C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374221 | |||||||
| chr5:143374231 | G | A | 37 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(34): Show |
38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1184+25425C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374231 | |||||||
| chr5:143374258 | C | T | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+25398G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374258 | |||||||
| chr5:143374264 | G | T | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1184+25392C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374264 | |||||||
| chr5:143374306 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1184+25350G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374306 | |||||||
| chr5:143374308 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1184+25348G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374308 | |||||||
| chr5:143374342 | A | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+25314T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374342 | |||||||
| chr5:143374422 | C | T | 1 | a0001c0006t0001g0098 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1184+25234G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374422 | |||||||
| chr5:143374423 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1184+25233C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374423 | |||||||
| chr5:143374490 | C | CA | 36 | a0001c0001t0002g0240 a0001c0001t0003g0180 a0001c0001t0003g0181 others(33): Show |
36 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.1184+25165dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374490 | |||||||
| chr5:143374490 | CA | C | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+25165delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374490 | |||||||
| chr5:143374699 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1184+24957G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374699 | |||||||
| chr5:143374705 | G | A | 1 | a0001c0003t0008g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1184+24951C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374705 | |||||||
| chr5:143374943 | G | A | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1184+24713C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143374943 | |||||||
| chr5:143375125 | T | C | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1184+24531A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375125 | |||||||
| chr5:143375238 | C | T | 1 | a0001c0001t0004g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1184+24418G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375238 | |||||||
| chr5:143375268 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
6 | HG02451.hp2 HG02615.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+24388C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375268 | |||||||
| chr5:143375339 | T | C | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+24317A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375339 | |||||||
| chr5:143375432 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+24224C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375432 | |||||||
| chr5:143375566 | T | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+24090A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375566 | |||||||
| chr5:143375889 | A | G | 1 | a0001c0002t0006g0036 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1184+23767T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375889 | |||||||
| chr5:143375978 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+23678G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143375978 | |||||||
| chr5:143376008 | G | T | 1 | a0001c0001t0001g0169 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1184+23648C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376008 | |||||||
| chr5:143376069 | GA | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+23586delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376069 | |||||||
| chr5:143376129 | GA | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+23526delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376129 | |||||||
| chr5:143376182 | T | C | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+23474A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376182 | |||||||
| chr5:143376397 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1184+23259A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376397 | |||||||
| chr5:143376439 | A | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(64): Show |
69 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1184+23217T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376439 | |||||||
| chr5:143376640 | T | G | 1 | a0001c0003t0006g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1184+23016A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376640 | |||||||
| chr5:143376701 | G | C | 39 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(36): Show |
39 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1184+22955C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376701 | |||||||
| chr5:143376875 | A | G | 1 | a0001c0004t0004g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1184+22781T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143376875 | |||||||
| chr5:143377446 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1184+22210G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143377446 | |||||||
| chr5:143377547 | C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+22109G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143377547 | |||||||
| chr5:143377901 | G | A | 1 | a0001c0001t0035g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1184+21755C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143377901 | |||||||
| chr5:143377923 | G | A | 8 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
8 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+21733C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143377923 | |||||||
| chr5:143377941 | G | A | 6 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(3): Show |
6 | NA18946.hp1 NA18974.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+21715C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143377941 | |||||||
| chr5:143378076 | CCT | C | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+21578_1184+21 others(8): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378076 | |||||||
| chr5:143378302 | G | A | 1 | a0001c0003t0008g0045 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1184+21354C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378302 | |||||||
| chr5:143378327 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+21329G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378327 | |||||||
| chr5:143378510 | T | C | 16 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(13): Show |
16 | HG00438.hp1 HG02132.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.1184+21146A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378510 | |||||||
| chr5:143378536 | A | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0106 |
2 | HG00408.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1184+21120T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378536 | |||||||
| chr5:143378623 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+21033C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378623 | |||||||
| chr5:143378829 | T | C | 9 | a0001c0004t0004g0049 a0001c0004t0004g0050 a0001c0004t0004g0052 others(6): Show |
9 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+20827A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378829 | |||||||
| chr5:143378931 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(200): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1184+20725A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143378931 | |||||||
| chr5:143379035 | T | C | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+20621A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379035 | |||||||
| chr5:143379036 | A | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+20620T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379036 | |||||||
| chr5:143379320 | A | T | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02055.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+20336T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379320 | |||||||
| chr5:143379646 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+20010T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379646 | |||||||
| chr5:143379775 | A | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+19881T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379775 | |||||||
| chr5:143379789 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184+19867G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379789 | |||||||
| chr5:143379927 | A | G | 3 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0252 |
4 | HG02074.hp2 NA18982.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+19729T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143379927 | |||||||
| chr5:143380073 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1184+19583A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380073 | |||||||
| chr5:143380103 | T | C | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1184+19553A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380103 | |||||||
| chr5:143380118 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1184+19538T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380118 | |||||||
| chr5:143380220 | A | G | 68 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(65): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1184+19436T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380220 | |||||||
| chr5:143380235 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+19421C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380235 | |||||||
| chr5:143380359 | A | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+19297T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380359 | |||||||
| chr5:143380399 | AT | A | 4 | a0001c0006t0001g0103 a0002c0007t0011g0254 a0002c0007t0011g0255 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+19256delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380399 | |||||||
| chr5:143380431 | G | T | 1 | a0001c0001t0005g0204 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1184+19225C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380431 | |||||||
| chr5:143380561 | T | G | 1 | a0001c0005t0009g0251 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1184+19095A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380561 | |||||||
| chr5:143380694 | C | T | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+18962G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380694 | |||||||
| chr5:143380761 | G | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+18895C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380761 | |||||||
| chr5:143380769 | A | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+18887T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380769 | |||||||
| chr5:143380975 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+18681C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143380975 | |||||||
| chr5:143381007 | T | A | 1 | a0001c0002t0018g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1184+18649A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381007 | |||||||
| chr5:143381018 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1184+18638C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381018 | |||||||
| chr5:143381186 | T | C | 2 | a0001c0001t0003g0195 a0001c0001t0003g0196 |
2 | HG01099.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1184+18470A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381186 | |||||||
| chr5:143381240 | G | GA | 7 | a0001c0001t0001g0209 a0001c0001t0007g0001 a0001c0001t0007g0011 others(4): Show |
8 | HG02723.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+18415dupT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381240 | |||||||
| chr5:143381474 | C | T | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+18182G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381474 | |||||||
| chr5:143381475 | G | A | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+18181C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381475 | |||||||
| chr5:143381550 | A | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+18106T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381550 | |||||||
| chr5:143381962 | C | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(181): Show |
192 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1184+17694G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143381962 | |||||||
| chr5:143382060 | C | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0248 a0001c0001t0026g0115 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+17596G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143382060 | |||||||
| chr5:143382248 | T | C | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+17408A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143382248 | |||||||
| chr5:143382302 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1184+17354A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143382302 | |||||||
| chr5:143382445 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+17211T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143382445 | |||||||
| chr5:143382707 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1184+16949C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143382707 | |||||||
| chr5:143382769 | G | A | 6 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(3): Show |
6 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+16887C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143382769 | |||||||
| chr5:143383212 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1184+16444C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383212 | |||||||
| chr5:143383413 | G | A | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+16243C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383413 | |||||||
| chr5:143383465 | TA | T | 7 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0217 others(4): Show |
9 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+16190delT | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383465 | |||||||
| chr5:143383485 | A | C | 1 | a0001c0004t0004g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1184+16171T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383485 | |||||||
| chr5:143383492 | A | T | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1184+16164T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383492 | |||||||
| chr5:143383608 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+16048T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383608 | |||||||
| chr5:143383704 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+15952G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143383704 | |||||||
| chr5:143384241 | C | A | 1 | a0001c0005t0009g0252 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1184+15415G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384241 | |||||||
| chr5:143384315 | G | A | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+15341C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384315 | |||||||
| chr5:143384544 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+15112G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384544 | |||||||
| chr5:143384552 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1184+15104T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384552 | |||||||
| chr5:143384885 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1184+14771G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384885 | |||||||
| chr5:143384895 | G | A | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+14761C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384895 | |||||||
| chr5:143384911 | T | A | 1 | a0001c0001t0002g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1184+14745A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384911 | |||||||
| chr5:143384938 | T | A | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+14718A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143384938 | |||||||
| chr5:143385007 | G | A | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1184+14649C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385007 | |||||||
| chr5:143385124 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1184+14532A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385124 | |||||||
| chr5:143385134 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+14522A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385134 | |||||||
| chr5:143385176 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1184+14480A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385176 | |||||||
| chr5:143385220 | C | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+14436G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385220 | |||||||
| chr5:143385247 | C | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+14409G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385247 | |||||||
| chr5:143385304 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1184+14352A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385304 | |||||||
| chr5:143385343 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+14313A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385343 | |||||||
| chr5:143385534 | T | C | 8 | a0001c0004t0004g0049 a0001c0004t0004g0050 a0001c0004t0004g0052 others(5): Show |
8 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+14122A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385534 | |||||||
| chr5:143385556 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1184+14100T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385556 | |||||||
| chr5:143385570 | G | A | 78 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1184+14086C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385570 | |||||||
| chr5:143385571 | A | T | 77 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(74): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1184+14085T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385571 | |||||||
| chr5:143385608 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+14048C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385608 | |||||||
| chr5:143385848 | C | T | 1 | a0001c0001t0010g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+13808G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385848 | |||||||
| chr5:143385854 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+13802A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385854 | |||||||
| chr5:143385868 | T | C | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+13788A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385868 | |||||||
| chr5:143385874 | C | T | 1 | a0001c0004t0004g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1184+13782G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385874 | |||||||
| chr5:143385875 | G | A | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+13781C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143385875 | |||||||
| chr5:143386038 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+13618A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143386038 | |||||||
| chr5:143386168 | C | T | 8 | a0001c0004t0004g0049 a0001c0004t0004g0050 a0001c0004t0004g0052 others(5): Show |
8 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+13488G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143386168 | |||||||
| chr5:143386224 | C | T | 4 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(1): Show |
4 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+13432G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143386224 | |||||||
| chr5:143386256 | T | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(252): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1184+13400A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143386256 | |||||||
| chr5:143386571 | A | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+13085T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143386571 | |||||||
| chr5:143386876 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0020g0047 a0001c0001t0024g0206 |
3 | HG01934.hp1 HG03486.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.1184+12780A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143386876 | |||||||
| chr5:143387029 | A | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+12627T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387029 | |||||||
| chr5:143387081 | T | C | 1 | a0001c0004t0004g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1184+12575A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387081 | |||||||
| chr5:143387091 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184+12565A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387091 | |||||||
| chr5:143387170 | C | T | 1 | a0001c0001t0003g0183 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1184+12486G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387170 | |||||||
| chr5:143387358 | G | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+12298C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387358 | |||||||
| chr5:143387428 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184+12228A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387428 | |||||||
| chr5:143387524 | A | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+12132T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387524 | |||||||
| chr5:143387536 | C | T | 1 | a0001c0001t0007g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1184+12120G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387536 | |||||||
| chr5:143387595 | T | C | 40 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(37): Show |
40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1184+12061A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387595 | |||||||
| chr5:143387690 | C | T | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+11966G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387690 | |||||||
| chr5:143387722 | G | A | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+11934C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387722 | |||||||
| chr5:143387761 | T | C | 2 | a0002c0007t0011g0254 a0002c0007t0011g0255 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+11895A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387761 | |||||||
| chr5:143387851 | C | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0164 |
2 | NA18950.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1184+11805G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387851 | |||||||
| chr5:143387852 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0164 |
2 | NA18950.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1184+11804G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143387852 | |||||||
| chr5:143388123 | C | T | 1 | a0001c0001t0005g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1184+11533G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388123 | |||||||
| chr5:143388175 | C | A | 30 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0109 others(27): Show |
30 | HG00408.hp2 HG00544.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1184+11481G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388175 | |||||||
| chr5:143388213 | T | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(240): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1184+11443A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388213 | |||||||
| chr5:143388273 | T | C | 4 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0005g0210 others(1): Show |
4 | HG02723.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+11383A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388273 | |||||||
| chr5:143388400 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+11256A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388400 | |||||||
| chr5:143388887 | G | C | 1 | a0001c0003t0008g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1184+10769C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388887 | |||||||
| chr5:143388895 | G | A | 2 | a0001c0001t0002g0242 a0001c0001t0002g0243 |
2 | HG02080.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1184+10761C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143388895 | |||||||
| chr5:143389075 | T | C | 1 | a0001c0001t0004g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1184+10581A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143389075 | |||||||
| chr5:143389109 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184+10547G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143389109 | |||||||
| chr5:143389216 | A | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+10440T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143389216 | |||||||
| chr5:143389386 | G | A | 1 | a0001c0002t0006g0041 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1184+10270C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143389386 | |||||||
| chr5:143389416 | G | C | 3 | a0001c0005t0009g0250 a0001c0005t0009g0251 a0001c0005t0009g0257 |
3 | HG02027.hp1 HG02135.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1184+10240C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143389416 | |||||||
| chr5:143389476 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1184+10180G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143389476 | |||||||
| chr5:143390183 | T | C | 3 | a0001c0001t0002g0244 a0001c0001t0002g0246 a0001c0001t0002g0247 |
3 | HG02148.hp1 HG02273.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1184+9473A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143390183 | |||||||
| chr5:143390570 | T | C | 6 | a0001c0002t0004g0060 a0001c0002t0006g0036 a0001c0002t0006g0037 others(3): Show |
6 | HG00438.hp1 HG02132.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+9086A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143390570 | |||||||
| chr5:143390660 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184+8996G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143390660 | |||||||
| chr5:143390967 | G | A | 1 | a0001c0001t0003g0197 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1184+8689C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143390967 | |||||||
| chr5:143391218 | G | A | 1 | a0001c0001t0024g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1184+8438C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391218 | |||||||
| chr5:143391283 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1184+8373A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391283 | |||||||
| chr5:143391588 | A | G | 2 | a0001c0001t0003g0180 a0001c0001t0003g0181 |
2 | HG01256.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1184+8068T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391588 | |||||||
| chr5:143391632 | T | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+8024A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391632 | |||||||
| chr5:143391929 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1184+7727G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391929 | |||||||
| chr5:143391954 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1184+7702T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391954 | |||||||
| chr5:143391964 | C | CTTT | 5 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(2): Show |
6 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+7689_1184+769 others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143391964 | |||||||
| chr5:143392005 | G | A | 1 | a0001c0001t0004g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1184+7651C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392005 | |||||||
| chr5:143392034 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0012g0009 |
2 | HG03710.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1184+7622G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392034 | |||||||
| chr5:143392122 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+7534A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392122 | |||||||
| chr5:143392339 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1184+7317C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392339 | |||||||
| chr5:143392519 | G | GT | 7 | a0001c0001t0001g0109 a0001c0005t0009g0008 a0001c0005t0009g0249 others(4): Show |
8 | HG01891.hp1 HG02027.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1184+7136dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392519 | |||||||
| chr5:143392749 | A | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+6907T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392749 | |||||||
| chr5:143392937 | T | C | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1184+6719A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392937 | |||||||
| chr5:143392971 | T | C | 6 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(3): Show |
6 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+6685A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143392971 | |||||||
| chr5:143393025 | T | C | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+6631A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393025 | |||||||
| chr5:143393056 | C | A | 1 | a0001c0003t0006g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1184+6600G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393056 | |||||||
| chr5:143393087 | G | C | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+6569C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393087 | |||||||
| chr5:143393242 | G | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
5 | HG02080.hp1 HG02129.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+6414C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393242 | |||||||
| chr5:143393351 | C | A | 1 | a0001c0002t0006g0041 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1184+6305G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393351 | |||||||
| chr5:143393376 | A | C | 1 | a0001c0001t0001g0169 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1184+6280T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393376 | |||||||
| chr5:143393791 | T | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+5865A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393791 | |||||||
| chr5:143393865 | G | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG00597.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1184+5791C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143393865 | |||||||
| chr5:143394186 | C | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+5470G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143394186 | |||||||
| chr5:143394761 | A | G | 1 | a0001c0002t0004g0167 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1184+4895T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143394761 | |||||||
| chr5:143394840 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1184+4816T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143394840 | |||||||
| chr5:143395127 | C | T | 40 | a0001c0002t0004g0060 a0001c0002t0004g0167 a0001c0002t0004g0168 others(37): Show |
40 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1184+4529G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143395127 | |||||||
| chr5:143395352 | C | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+4304G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143395352 | |||||||
| chr5:143395392 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0097 |
3 | HG02451.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1184+4264C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143395392 | |||||||
| chr5:143395535 | T | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+4121A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143395535 | |||||||
| chr5:143395771 | C | G | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1184+3885G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143395771 | |||||||
| chr5:143395969 | A | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+3687T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143395969 | |||||||
| chr5:143396132 | T | C | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+3524A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396132 | |||||||
| chr5:143396394 | C | G | 3 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 |
3 | HG01256.hp1 HG02602.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1184+3262G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396394 | |||||||
| chr5:143396400 | C | T | 3 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 |
3 | HG01256.hp1 HG02602.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1184+3256G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396400 | |||||||
| chr5:143396691 | CTTAATT | C | 28 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+2959_1184+296 others(10): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396691 | |||||||
| chr5:143396732 | T | C | 4 | a0001c0003t0008g0042 a0001c0003t0008g0043 a0001c0003t0008g0044 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+2924A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396732 | |||||||
| chr5:143396787 | T | G | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2869A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396787 | |||||||
| chr5:143396868 | A | G | 2 | a0001c0004t0004g0049 a0001c0004t0004g0050 |
2 | HG01978.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1184+2788T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143396868 | |||||||
| chr5:143397119 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1184+2537A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143397119 | |||||||
| chr5:143397346 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1184+2310A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143397346 | |||||||
| chr5:143397550 | G | A | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2106C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143397550 | |||||||
| chr5:143397883 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+1773C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143397883 | |||||||
| chr5:143397885 | T | G | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+1771A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143397885 | |||||||
| chr5:143397938 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1184+1718A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143397938 | |||||||
| chr5:143398355 | G | GGT | 68 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.1184+1299_1184+130 others(6): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398355 | |||||||
| chr5:143398356 | G | GT | 9 | a0001c0001t0001g0066 a0001c0001t0001g0104 a0001c0001t0001g0105 others(6): Show |
9 | HG00741.hp1 HG01192.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1184+1299dupA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398356 | |||||||
| chr5:143398356 | G | GTGT | 39 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0001c0001t0002g0215 others(36): Show |
39 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.1184+1299_1184+130 others(7): Show |
NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398356 | |||||||
| chr5:143398356 | GT | G | 14 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0096 others(11): Show |
15 | HG00639.hp1 HG01070.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1184+1299delA | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398356 | |||||||
| chr5:143398512 | G | T | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+1144C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398512 | |||||||
| chr5:143398611 | C | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+1045G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398611 | |||||||
| chr5:143398879 | T | G | 2 | a0001c0001t0005g0210 a0001c0001t0005g0211 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1184+777A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143398879 | |||||||
| chr5:143399010 | G | C | 82 | a0001c0001t0001g0169 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
86 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1184+646C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143399010 | |||||||
| chr5:143399038 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1184+618A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143399038 | |||||||
| chr5:143399435 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184+221A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143399435 | |||||||
| chr5:143399509 | T | C | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG00423.hp1 HG01496.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+147A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143399509 | |||||||
| chr5:143399587 | T | C | 6 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(3): Show |
7 | HG02027.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+69A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 2/8 | chr5 | 143399587 | |||||||
| chr5:143400982 | T | C | 1 | a0001c0003t0006g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-13-130A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143400982 | |||||||
| chr5:143401092 | A | G | 1 | a0001c0001t0002g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-13-240T>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401092 | |||||||
| chr5:143401130 | C | A | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(119): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-13-278G>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401130 | |||||||
| chr5:143401132 | C | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(119): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-13-280G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401132 | |||||||
| chr5:143401140 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-13-288C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401140 | |||||||
| chr5:143401390 | T | G | 1 | a0001c0003t0006g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-13-538A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401390 | |||||||
| chr5:143401483 | T | A | 1 | a0001c0002t0004g0060 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-13-631A>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401483 | |||||||
| chr5:143401603 | T | C | 9 | a0001c0005t0009g0008 a0001c0005t0009g0249 a0001c0005t0009g0250 others(6): Show |
10 | HG01884.hp1 HG02027.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13-751A>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401603 | |||||||
| chr5:143401756 | A | C | 1 | a0001c0001t0010g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-13-904T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401756 | |||||||
| chr5:143401976 | G | C | 1 | a0001c0001t0003g0253 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-13-1124C>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143401976 | |||||||
| chr5:143402002 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(35): Show |
40 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.-13-1150G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402002 | |||||||
| chr5:143402147 | C | T | 1 | a0001c0001t0007g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-14+1064G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402147 | |||||||
| chr5:143402285 | G | T | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-14+926C>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402285 | |||||||
| chr5:143402467 | G | A | 3 | a0002c0007t0011g0254 a0002c0007t0011g0255 a0002c0007t0034g0256 |
3 | HG01884.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-14+744C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402467 | |||||||
| chr5:143402573 | G | A | 1 | a0002c0007t0034g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14+638C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402573 | |||||||
| chr5:143402635 | A | C | 1 | a0001c0001t0005g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-14+576T>G | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402635 | |||||||
| chr5:143402746 | C | G | 1 | a0001c0001t0002g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-14+465G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402746 | |||||||
| chr5:143402749 | C | G | 1 | a0001c0001t0010g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-14+462G>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402749 | |||||||
| chr5:143402790 | G | A | 1 | a0001c0005t0009g0257 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-14+421C>T | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402790 | |||||||
| chr5:143402836 | A | T | 1 | a0001c0004t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-14+375T>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402836 | |||||||
| chr5:143402837 | C | T | 38 | a0001c0002t0004g0060 a0001c0002t0006g0029 a0001c0002t0006g0030 others(35): Show |
38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-14+374G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143402837 | |||||||
| chr5:143403006 | T | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0066 others(241): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-14+205A>C | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143403006 | |||||||
| chr5:143403131 | C | T | 2 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-14+80G>A | NR3C1 | ENSG00000113580.15 | transcript | ENST00000394464.7 | protein_coding | 1/8 | chr5 | 143403131 |