Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9971 |
| ensemblid | ENSG00000012504.15 |
| hgncid | 7967 |
| symbol | NR1H4 |
| name | nuclear receptor subfamily 1 group H member 4 |
| refseq_nuc | NM_001206979.2 |
| refseq_prot | NP_001193908.1 |
| ensembl_nuc | ENST00000392986.8 |
| ensembl_prot | ENSP00000376712.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 100473866 |
| end | 100564414 |
| strand | + |
| ver | v1.2 |
| region | chr12:100473866-100564414 |
| region5000 | chr12:100468866-100569414 |
| regionname0 | NR1H4_chr12_100473866_100564414 |
| regionname5000 | NR1H4_chr12_100468866_100569414 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 476 | 300 | 74 | 42 | 138 | 11 | 33 | 104 | NR1H4_chr12_100468866_100569414 | NR1H4 | MGSKM others(471): Show |
chr12 | 100468866 | 100569414 |
| a0002 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | MGSKM others(471): Show |
chr12 | 100468866 | 100569414 |
| a0003 | 0/0 | 476 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | MGSKM others(471): Show |
chr12 | 100468866 | 100569414 |
| a0004 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | MGSKM others(471): Show |
chr12 | 100468866 | 100569414 |
| a0005 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | MGSKM others(471): Show |
chr12 | 100468866 | 100569414 |
| a0006 | 0/0 | 476 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | MGSKM others(471): Show |
chr12 | 100468866 | 100569414 |
| a0007 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | MGSKM others(471): Show |
chr12 | 100468866 | 100569414 |
| a0008 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | MGSKM others(471): Show |
chr12 | 100468866 | 100569414 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1428 | 298 | 74 | 42 | 136 | 11 | 33 | NR1H4_chr12_100468866_100569414 | NR1H4 | ATGGG others(1423): Show |
chr12 | 100468866 | 100569414 | ||
| a0001c0008 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | ATGGG others(1423): Show |
chr12 | 100468866 | 100569414 | ||
| a0001c0010 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | ATGGG others(1423): Show |
chr12 | 100468866 | 100569414 | ||
| a0002c0002 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | ATGGG others(1423): Show |
chr12 | 100468866 | 100569414 | ||
| a0003c0006 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | ATGGG others(1423): Show |
chr12 | 100468866 | 100569414 | ||
| a0004c0005 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | ATGGG others(1423): Show |
chr12 | 100468866 | 100569414 | ||
| a0005c0004 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | ATGGG others(1423): Show |
chr12 | 100468866 | 100569414 | ||
| a0006c0009 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | ATGGG others(1423): Show |
chr12 | 100468866 | 100569414 | ||
| a0007c0007 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | ATGGG others(1423): Show |
chr12 | 100468866 | 100569414 | ||
| a0008c0003 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | ATGGG others(1423): Show |
chr12 | 100468866 | 100569414 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2739 | 241 | 68 | 38 | 95 | 10 | 28 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0001c0001t0002 | 0/0 | 2739 | 47 | 2 | 0 | 41 | 0 | 4 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0001c0001t0003 | 0/0 | 2739 | 6 | 0 | 4 | 0 | 1 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0001c0001t0004 | 0/0 | 2739 | 3 | 3 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0001c0001t0006 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0001c0008t0005 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0001c0010t0001 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0002c0002t0001 | 0/0 | 2739 | 2 | 2 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0003c0006t0001 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0004c0005t0001 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0005c0004t0001 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0006c0009t0001 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0007c0007t0001 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| a0008c0003t0001 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | AGAAG others(2734): Show |
chr12 | 100468866 | 100569414 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0008t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0001c0010t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0002c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0003c0006t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0004c0005t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0005c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0006c0009t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0007c0007t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| a0008c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00099 | hp2 | a0003 | c0006 | t0001 | g0280 | EUR | GBR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | GBR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | FIN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0278 | EUR | FIN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00673 | hp1 | a0001 | c0008 | t0005 | g0271 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | IBS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0260 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02615 | hp1 | a0004 | c0005 | t0001 | g0251 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03453 | hp2 | a0005 | c0004 | t0001 | g0161 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03688 | hp2 | a0006 | c0009 | t0001 | g0247 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | BEB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | YRI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18979 | hp1 | a0007 | c0007 | t0001 | g0012 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18990 | hp1 | a0001 | c0010 | t0001 | g0189 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19081 | hp2 | a0008 | c0003 | t0001 | g0213 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | YRI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ASW | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ASW | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | TSI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0164 | EUR | TSI | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | GIH | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | GIH | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | ACB | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | USA | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | USA | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | USA | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | USA | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0141 | REF | REF | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0166 | REF | REF | NR1H4_chr12_100468866_100569414 | NR1H4 | chr12 | 100468866 | 100569414 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:100510780 | G | A | 1 | a0002 | 2 | HG02257.hp2 HG02965.hp2 |
missense_variant&splice_region_variant | MODERATE | c.82G>A | p.Val28Ile | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/11 | 465/2739 | 82/1431 | 28/476 | chr12 | 100510780 | |||
| chr12:100510798 | G | C | 1 | a0008 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.100G>C | p.Ala34Pro | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/11 | 483/2739 | 100/1431 | 34/476 | chr12 | 100510798 | |||
| chr12:100510799 | C | G | 1 | a0008 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.101C>G | p.Ala34Gly | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/11 | 484/2739 | 101/1431 | 34/476 | chr12 | 100510799 | |||
| chr12:100511044 | G | A | 1 | a0005 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.346G>A | p.Ala116Thr | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/11 | 729/2739 | 346/1431 | 116/476 | chr12 | 100511044 | |||
| chr12:100511090 | G | A | 1 | a0004 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.392G>A | p.Gly131Glu | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/11 | 775/2739 | 392/1431 | 131/476 | chr12 | 100511090 | |||
| chr12:100532530 | T | C | 1 | a0003 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.518T>C | p.Met173Thr | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/11 | 901/2739 | 518/1431 | 173/476 | chr12 | 100532530 | |||
| chr12:100532591 | G | C | 1 | a0007 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.579G>C | p.Leu193Phe | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/11 | 962/2739 | 579/1431 | 193/476 | chr12 | 100532591 | |||
| chr12:100561906 | C | T | 1 | a0006 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.1100C>T | p.Thr367Ile | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 10/11 | 1483/2739 | 1100/1431 | 367/476 | chr12 | 100561906 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:100536574 | C | T | 1 | a0001c0010 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.795C>T | p.Asn265Asn | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 7/11 | 1178/2739 | 795/1431 | 265/476 | chr12 | 100536574 | |||
| chr12:100540781 | G | A | 1 | a0001c0008 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.1041G>A | p.Gly347Gly | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/11 | 1424/2739 | 1041/1431 | 347/476 | chr12 | 100540781 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:100473878 | G | A | 1 | a0001c0001t0004 | 3 | HG02257.hp1 HG02559.hp2 NA20300.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-371G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/11 | chr12 | 100473878 | |||||||
| chr12:100473949 | G | A | 1 | a0001c0008t0005 | 1 | HG00673.hp1 | 5_prime_UTR_variant | MODIFIER | c.-300G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/11 | 19375 | chr12 | 100473949 | ||||||
| chr12:100473966 | A | C | 1 | a0001c0001t0006 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-283A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/11 | 19358 | chr12 | 100473966 | ||||||
| chr12:100493323 | G | T | 1 | a0001c0001t0002 | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-1G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/11 | 1 | chr12 | 100493323 | ||||||
| chr12:100563670 | A | G | 1 | a0001c0001t0003 | 6 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*181A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 11/11 | 181 | chr12 | 100563670 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:100474117 | T | C | 2 | a0002c0002t0001g0015 a0002c0002t0001g0016 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-190+58T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474117 | |||||||
| chr12:100474151 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG00621.hp2 NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-190+92T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474151 | |||||||
| chr12:100474404 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-190+345T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474404 | |||||||
| chr12:100474431 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-190+372G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474431 | |||||||
| chr12:100474657 | G | A | 2 | a0002c0002t0001g0015 a0002c0002t0001g0016 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-190+598G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474657 | |||||||
| chr12:100474730 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(78): Show |
91 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-190+671G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474730 | |||||||
| chr12:100474905 | T | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(78): Show |
91 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-190+846T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474905 | |||||||
| chr12:100474906 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-190+847C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474906 | |||||||
| chr12:100474918 | AT | A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(12): Show |
17 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-190+861delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100474918 | ||||||
| chr12:100474954 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-190+895T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474954 | |||||||
| chr12:100474986 | T | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01261.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-190+927T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100474986 | |||||||
| chr12:100475121 | T | TTACCTAT others(9): Show |
2 | a0001c0001t0001g0074 a0001c0001t0002g0073 |
2 | HG02559.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-190+1065_-190+108 others(20): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475121 | ||||||
| chr12:100475124 | C | CCTAT | 21 | a0001c0001t0001g0093 a0001c0001t0001g0219 a0001c0001t0001g0220 others(18): Show |
21 | HG00597.hp1 HG00609.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.-190+1097_-190+110 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | ||||||
| chr12:100475124 | C | CCTATCTA others(1): Show |
32 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0082 others(29): Show |
34 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.-190+1093_-190+110 others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | ||||||
| chr12:100475124 | C | CCTATCTA others(5): Show |
26 | a0001c0001t0001g0085 a0001c0001t0001g0090 a0001c0001t0001g0091 others(23): Show |
26 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-190+1089_-190+110 others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | ||||||
| chr12:100475124 | C | CCTATCTA others(13): Show |
4 | a0001c0001t0001g0034 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
4 | HG02622.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190+1080_-190+108 others(24): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | ||||||
| chr12:100475124 | C | CCTATCTA others(17): Show |
3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0078 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-190+1080_-190+108 others(28): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | ||||||
| chr12:100475124 | C | CCTATCTA others(9): Show |
1 | a0001c0001t0001g0289 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-190+1085_-190+110 others(20): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | ||||||
| chr12:100475124 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-190+1065C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475124 | |||||||
| chr12:100475124 | CCTAT | C | 4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
4 | HG02886.hp1 HG02922.hp1 NA19090.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190+1097_-190+110 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475124 | ||||||
| chr12:100475128 | T | TCTATCTA others(5): Show |
38 | a0001c0001t0001g0039 a0001c0001t0001g0061 a0001c0001t0001g0062 others(35): Show |
46 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-190+1080_-190+108 others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475128 | ||||||
| chr12:100475132 | T | TCTATCTA others(1): Show |
16 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(13): Show |
18 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-190+1080_-190+108 others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475132 | ||||||
| chr12:100475140 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-190+1081T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475140 | |||||||
| chr12:100475158 | T | TATCTATC others(6): Show |
4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
4 | HG02145.hp1 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190+1100_-190+110 others(17): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475158 | ||||||
| chr12:100475158 | T | TATCTATC others(10): Show |
1 | a0001c0001t0001g0092 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-190+1100_-190+110 others(21): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475158 | ||||||
| chr12:100475159 | A | ATCTATCT others(4): Show |
1 | a0001c0001t0001g0288 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-190+1100_-190+110 others(15): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475159 | |||||||
| chr12:100475161 | A | AT | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(70): Show |
83 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-190+1111dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100475161 | ||||||
| chr12:100475161 | A | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0081 a0001c0001t0001g0086 others(5): Show |
8 | HG02145.hp1 HG02257.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-190+1102A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475161 | |||||||
| chr12:100475328 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-190+1269G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475328 | |||||||
| chr12:100475473 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190+1414C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475473 | |||||||
| chr12:100475665 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0091 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-190+1606C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475665 | |||||||
| chr12:100475712 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-190+1653C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475712 | |||||||
| chr12:100475767 | G | A | 14 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(11): Show |
14 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.-190+1708G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475767 | |||||||
| chr12:100475796 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190+1737C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475796 | |||||||
| chr12:100475805 | G | A | 72 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(69): Show |
76 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.-190+1746G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100475805 | |||||||
| chr12:100476069 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
5 | HG01099.hp1 HG01257.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190+2010A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476069 | |||||||
| chr12:100476198 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
5 | HG00140.hp1 HG00280.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190+2139C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476198 | |||||||
| chr12:100476498 | T | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0091 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-190+2439T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476498 | |||||||
| chr12:100476532 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-190+2473A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476532 | |||||||
| chr12:100476629 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190+2570A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476629 | |||||||
| chr12:100476783 | C | T | 14 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(11): Show |
14 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.-190+2724C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476783 | |||||||
| chr12:100476841 | A | G | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.-190+2782A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476841 | |||||||
| chr12:100476898 | T | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0240 |
2 | HG03139.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-190+2839T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476898 | |||||||
| chr12:100476961 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-190+2902A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476961 | |||||||
| chr12:100476964 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-190+2905A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100476964 | |||||||
| chr12:100477115 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-190+3056G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100477115 | |||||||
| chr12:100477496 | T | A | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.-190+3437T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100477496 | |||||||
| chr12:100478224 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190+4165A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100478224 | |||||||
| chr12:100478448 | G | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0151 a0001c0001t0002g0152 |
4 | NA18961.hp2 NA18979.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190+4389G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100478448 | |||||||
| chr12:100478689 | T | C | 14 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(11): Show |
14 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.-190+4630T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100478689 | |||||||
| chr12:100478825 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-190+4766G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100478825 | |||||||
| chr12:100479192 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-190+5133G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479192 | |||||||
| chr12:100479198 | C | A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(12): Show |
17 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-190+5139C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479198 | |||||||
| chr12:100479222 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-190+5163A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479222 | |||||||
| chr12:100479223 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-190+5164C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479223 | |||||||
| chr12:100479273 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-190+5214T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479273 | |||||||
| chr12:100479345 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-190+5286C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479345 | |||||||
| chr12:100479596 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-190+5537G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479596 | |||||||
| chr12:100479719 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-190+5660G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479719 | |||||||
| chr12:100479746 | C | T | 2 | a0002c0002t0001g0015 a0002c0002t0001g0016 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-190+5687C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479746 | |||||||
| chr12:100479751 | T | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(12): Show |
17 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-190+5692T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479751 | |||||||
| chr12:100479791 | A | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(78): Show |
91 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-190+5732A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479791 | |||||||
| chr12:100479912 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-190+5853C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100479912 | |||||||
| chr12:100480214 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190+6155C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100480214 | |||||||
| chr12:100480286 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-190+6227C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100480286 | |||||||
| chr12:100480292 | T | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(75): Show |
88 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-190+6233T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100480292 | |||||||
| chr12:100480520 | C | A | 1 | a0001c0001t0001g0039 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-190+6461C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100480520 | |||||||
| chr12:100480943 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-190+6884G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100480943 | |||||||
| chr12:100481015 | C | T | 1 | a0001c0001t0002g0072 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-190+6956C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481015 | |||||||
| chr12:100481079 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-190+7020G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481079 | |||||||
| chr12:100481123 | C | T | 31 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0149 others(28): Show |
33 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(30): Show |
intron_variant | MODIFIER | c.-190+7064C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481123 | |||||||
| chr12:100481292 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190+7233C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481292 | |||||||
| chr12:100481491 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-190+7432C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481491 | |||||||
| chr12:100481596 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-190+7537A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481596 | |||||||
| chr12:100481711 | G | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0219 |
2 | HG01074.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-190+7652G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100481711 | |||||||
| chr12:100482045 | C | T | 2 | a0001c0001t0001g0286 a0004c0005t0001g0251 |
2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-190+7986C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482045 | |||||||
| chr12:100482285 | A | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(78): Show |
92 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-190+8226A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482285 | |||||||
| chr12:100482299 | CA | C | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(2): Show |
5 | HG02109.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190+8250delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100482299 | ||||||
| chr12:100482448 | T | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-190+8389T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482448 | |||||||
| chr12:100482670 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-190+8611C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482670 | |||||||
| chr12:100482733 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0091 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-190+8674G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482733 | |||||||
| chr12:100482845 | G | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
8 | HG01346.hp1 HG01358.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.-190+8786G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482845 | |||||||
| chr12:100482854 | G | A | 46 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(43): Show |
55 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-190+8795G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482854 | |||||||
| chr12:100482934 | T | G | 3 | a0001c0001t0001g0262 a0001c0001t0001g0276 a0001c0001t0001g0289 |
3 | HG02602.hp2 HG03017.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-190+8875T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100482934 | |||||||
| chr12:100483091 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0289 |
2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-190+9032A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483091 | |||||||
| chr12:100483204 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-190+9145G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483204 | |||||||
| chr12:100483289 | T | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(78): Show |
92 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-189-9214T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483289 | |||||||
| chr12:100483523 | A | G | 1 | a0001c0001t0002g0068 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-189-8980A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483523 | |||||||
| chr12:100483572 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-189-8931C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483572 | |||||||
| chr12:100483684 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(4): Show |
7 | HG02055.hp2 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-189-8819C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483684 | |||||||
| chr12:100483721 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | HG02647.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189-8782C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483721 | |||||||
| chr12:100483724 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0006g0260 |
2 | HG00099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.-189-8779C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483724 | |||||||
| chr12:100483963 | A | G | 2 | a0002c0002t0001g0015 a0002c0002t0001g0016 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-189-8540A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483963 | |||||||
| chr12:100483976 | T | C | 3 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 |
3 | HG02698.hp1 HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-189-8527T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100483976 | |||||||
| chr12:100483985 | G | GA | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(63): Show |
77 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.-189-8498dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100483985 | ||||||
| chr12:100483985 | GAA | G | 8 | a0001c0001t0001g0081 a0001c0001t0001g0085 a0001c0001t0001g0086 others(5): Show |
8 | HG02145.hp1 HG02257.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-189-8499_-189-849 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100483985 | ||||||
| chr12:100484009 | T | A | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-189-8494T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484009 | |||||||
| chr12:100484091 | T | C | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(2): Show |
5 | HG02559.hp1 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189-8412T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484091 | |||||||
| chr12:100484112 | A | G | 8 | a0001c0001t0001g0081 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
8 | HG02145.hp1 HG02257.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-189-8391A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484112 | |||||||
| chr12:100484354 | G | A | 2 | a0002c0002t0001g0015 a0002c0002t0001g0016 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-189-8149G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484354 | |||||||
| chr12:100484389 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-189-8114A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484389 | |||||||
| chr12:100484609 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-189-7894G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484609 | |||||||
| chr12:100484827 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-189-7676C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484827 | |||||||
| chr12:100484832 | G | A | 2 | a0001c0001t0001g0286 a0004c0005t0001g0251 |
2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-189-7671G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484832 | |||||||
| chr12:100484836 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-189-7667G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484836 | |||||||
| chr12:100484842 | C | T | 3 | a0001c0001t0001g0085 a0002c0002t0001g0015 a0002c0002t0001g0016 |
3 | HG02257.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-189-7661C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484842 | |||||||
| chr12:100484893 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-189-7610T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100484893 | |||||||
| chr12:100485184 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-189-7319G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485184 | |||||||
| chr12:100485335 | C | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG00323.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-189-7168C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485335 | |||||||
| chr12:100485595 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-189-6908C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485595 | |||||||
| chr12:100485727 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-189-6776T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485727 | |||||||
| chr12:100485753 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-189-6750C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485753 | |||||||
| chr12:100485782 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-189-6721C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485782 | |||||||
| chr12:100485824 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-189-6679A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100485824 | |||||||
| chr12:100485835 | CTAGTTCA others(18): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-189-6660_-189-663 others(29): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100485835 | ||||||
| chr12:100486081 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-189-6422C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100486081 | |||||||
| chr12:100486113 | G | A | 9 | a0001c0001t0001g0081 a0001c0001t0001g0085 a0001c0001t0001g0086 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-189-6390G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100486113 | |||||||
| chr12:100486169 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | HG02647.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189-6334C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100486169 | |||||||
| chr12:100486313 | T | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0289 |
2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-189-6190T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100486313 | |||||||
| chr12:100486326 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-189-6177G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100486326 | |||||||
| chr12:100486578 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-189-5925C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100486578 | |||||||
| chr12:100487068 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-189-5435T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487068 | |||||||
| chr12:100487070 | T | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(66): Show |
80 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-189-5433T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487070 | |||||||
| chr12:100487230 | T | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(66): Show |
80 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-189-5273T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487230 | |||||||
| chr12:100487326 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-189-5177C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487326 | |||||||
| chr12:100487395 | G | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(10): Show |
14 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189-5108G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487395 | |||||||
| chr12:100487451 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-189-5052G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487451 | |||||||
| chr12:100487595 | C | CT | 78 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(75): Show |
82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-189-4889dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100487595 | ||||||
| chr12:100487595 | CT | C | 21 | a0001c0001t0001g0035 a0001c0001t0001g0086 a0001c0001t0001g0089 others(18): Show |
21 | HG00597.hp2 HG00673.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.-189-4889delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100487595 | ||||||
| chr12:100487854 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0285 |
2 | HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.-189-4649C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487854 | |||||||
| chr12:100487888 | A | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(66): Show |
80 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-189-4615A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487888 | |||||||
| chr12:100487946 | A | G | 1 | a0001c0001t0002g0063 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-189-4557A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100487946 | |||||||
| chr12:100488001 | CCTTT | C | 3 | a0001c0001t0001g0085 a0002c0002t0001g0015 a0002c0002t0001g0016 |
3 | HG02257.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-189-4493_-189-449 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 100488001 | ||||||
| chr12:100488052 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0091 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-189-4451G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100488052 | |||||||
| chr12:100488819 | A | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(129): Show |
143 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.-189-3684A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100488819 | |||||||
| chr12:100488834 | A | T | 10 | a0001c0001t0001g0081 a0001c0001t0001g0085 a0001c0001t0001g0086 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-189-3669A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100488834 | |||||||
| chr12:100488952 | G | A | 49 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(46): Show |
58 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-189-3551G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100488952 | |||||||
| chr12:100489094 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-189-3409G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489094 | |||||||
| chr12:100489157 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-189-3346A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489157 | |||||||
| chr12:100489225 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-189-3278C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489225 | |||||||
| chr12:100489283 | A | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0078 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-189-3220A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489283 | |||||||
| chr12:100489304 | C | G | 11 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(8): Show |
11 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-189-3199C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489304 | |||||||
| chr12:100489336 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-189-3167G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489336 | |||||||
| chr12:100489461 | A | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(65): Show |
79 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-189-3042A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489461 | |||||||
| chr12:100489565 | A | C | 1 | a0001c0001t0002g0060 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-189-2938A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489565 | |||||||
| chr12:100489607 | C | T | 1 | a0002c0002t0001g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-189-2896C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489607 | |||||||
| chr12:100489720 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-189-2783G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489720 | |||||||
| chr12:100489858 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0078 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-189-2645C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100489858 | |||||||
| chr12:100490337 | T | A | 38 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(35): Show |
47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-189-2166T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100490337 | |||||||
| chr12:100490338 | C | T | 38 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(35): Show |
47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-189-2165C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100490338 | |||||||
| chr12:100490611 | A | G | 60 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(57): Show |
69 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.-189-1892A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100490611 | |||||||
| chr12:100490620 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-189-1883C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100490620 | |||||||
| chr12:100490667 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-189-1836T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100490667 | |||||||
| chr12:100491074 | C | A | 2 | a0002c0002t0001g0015 a0002c0002t0001g0016 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-189-1429C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491074 | |||||||
| chr12:100491084 | T | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
14 | HG02109.hp1 HG02451.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.-189-1419T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491084 | |||||||
| chr12:100491329 | G | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(218): Show |
235 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-189-1174G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491329 | |||||||
| chr12:100491371 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | HG02451.hp2 HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-189-1132G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491371 | |||||||
| chr12:100491487 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-189-1016G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491487 | |||||||
| chr12:100491732 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-189-771C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491732 | |||||||
| chr12:100491738 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-189-765A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491738 | |||||||
| chr12:100491801 | G | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(127): Show |
142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-189-702G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491801 | |||||||
| chr12:100491841 | C | T | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG00609.hp1 HG02040.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-189-662C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491841 | |||||||
| chr12:100491887 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.-189-616C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100491887 | |||||||
| chr12:100492062 | G | A | 56 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(53): Show |
57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.-189-441G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 1/10 | chr12 | 100492062 | |||||||
| chr12:100492839 | T | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0025 |
3 | HG02486.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-55+202T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100492839 | |||||||
| chr12:100493032 | T | G | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-54-238T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100493032 | |||||||
| chr12:100493065 | G | A | 66 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(63): Show |
67 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-54-205G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100493065 | |||||||
| chr12:100493068 | C | T | 13 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-54-202C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100493068 | |||||||
| chr12:100493069 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(3): Show |
6 | HG02109.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54-201G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100493069 | |||||||
| chr12:100493193 | C | T | 5 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0001g0093 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-77C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100493193 | |||||||
| chr12:100493232 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-54-38G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 2/10 | chr12 | 100493232 | |||||||
| chr12:100493518 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79+116C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100493518 | |||||||
| chr12:100493523 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(126): Show |
141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.79+121T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100493523 | |||||||
| chr12:100493826 | C | T | 38 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(35): Show |
47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+424C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100493826 | |||||||
| chr12:100493883 | A | G | 18 | a0001c0001t0001g0212 a0001c0001t0001g0230 a0001c0001t0001g0241 others(15): Show |
18 | HG00597.hp2 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+481A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100493883 | |||||||
| chr12:100494037 | T | C | 3 | a0001c0001t0004g0174 a0001c0001t0004g0175 a0001c0001t0004g0176 |
3 | HG02257.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.79+635T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494037 | |||||||
| chr12:100494106 | G | A | 50 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(47): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.79+704G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494106 | |||||||
| chr12:100494130 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0137 |
3 | HG01258.hp1 HG01358.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.79+728G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494130 | |||||||
| chr12:100494374 | G | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0105 a0001c0001t0001g0147 others(3): Show |
7 | NA18948.hp1 NA18977.hp1 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+972G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494374 | |||||||
| chr12:100494578 | C | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.79+1176C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494578 | |||||||
| chr12:100494638 | C | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0090 |
3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.79+1236C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494638 | |||||||
| chr12:100494680 | C | A | 38 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(35): Show |
47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+1278C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494680 | |||||||
| chr12:100494886 | G | T | 1 | a0001c0001t0001g0284 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.79+1484G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100494886 | |||||||
| chr12:100495126 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.79+1724G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495126 | |||||||
| chr12:100495204 | A | G | 6 | a0001c0001t0001g0173 a0001c0001t0001g0248 a0001c0001t0003g0172 others(3): Show |
6 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1802A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495204 | |||||||
| chr12:100495546 | CATGGTTA | C | 18 | a0001c0001t0001g0212 a0001c0001t0001g0230 a0001c0001t0001g0241 others(15): Show |
18 | HG00597.hp2 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+2146_79+2152del others(7): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100495546 | ||||||
| chr12:100495583 | T | C | 7 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0043 others(4): Show |
9 | NA18966.hp2 NA18968.hp2 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+2181T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495583 | |||||||
| chr12:100495659 | G | GAGT | 274 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(271): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.79+2257_79+2258ins others(3): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495659 | |||||||
| chr12:100495740 | C | CA | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+2348dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100495740 | ||||||
| chr12:100495744 | A | C | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.79+2342A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495744 | |||||||
| chr12:100495822 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.79+2420C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495822 | |||||||
| chr12:100495956 | C | T | 2 | a0002c0002t0001g0015 a0002c0002t0001g0016 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.79+2554C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100495956 | |||||||
| chr12:100496051 | G | C | 3 | a0001c0001t0001g0081 a0002c0002t0001g0015 a0002c0002t0001g0016 |
3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.79+2649G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496051 | |||||||
| chr12:100496138 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79+2736C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496138 | |||||||
| chr12:100496221 | AAT | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(126): Show |
141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.79+2821_79+2822del others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100496221 | ||||||
| chr12:100496449 | C | T | 50 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(47): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.79+3047C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496449 | |||||||
| chr12:100496483 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+3081T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496483 | |||||||
| chr12:100496540 | G | A | 53 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(50): Show |
54 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.79+3138G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496540 | |||||||
| chr12:100496677 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(126): Show |
141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.79+3275T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496677 | |||||||
| chr12:100496689 | G | T | 1 | a0001c0001t0001g0272 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.79+3287G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496689 | |||||||
| chr12:100496967 | A | G | 2 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
2 | NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.79+3565A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100496967 | |||||||
| chr12:100497021 | T | G | 4 | a0001c0001t0002g0006 a0001c0001t0002g0045 a0001c0001t0002g0046 others(1): Show |
5 | NA18951.hp2 NA18962.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+3619T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497021 | |||||||
| chr12:100497073 | C | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(131): Show |
146 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.79+3671C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497073 | |||||||
| chr12:100497202 | C | T | 2 | a0002c0002t0001g0015 a0002c0002t0001g0016 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.79+3800C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497202 | |||||||
| chr12:100497318 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.79+3916G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497318 | |||||||
| chr12:100497729 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.79+4327G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497729 | |||||||
| chr12:100497758 | A | T | 38 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(35): Show |
47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+4356A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497758 | |||||||
| chr12:100497804 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.79+4402T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100497804 | |||||||
| chr12:100498349 | G | A | 18 | a0001c0001t0001g0212 a0001c0001t0001g0230 a0001c0001t0001g0241 others(15): Show |
18 | HG00597.hp2 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+4947G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498349 | |||||||
| chr12:100498365 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.79+4963G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498365 | |||||||
| chr12:100498454 | C | T | 38 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(35): Show |
47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+5052C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498454 | |||||||
| chr12:100498467 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.79+5065C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498467 | |||||||
| chr12:100498498 | C | T | 38 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(35): Show |
47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+5096C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498498 | |||||||
| chr12:100498752 | T | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(131): Show |
146 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.79+5350T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498752 | |||||||
| chr12:100498780 | G | A | 38 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(35): Show |
47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+5378G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498780 | |||||||
| chr12:100498798 | A | C | 17 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(14): Show |
17 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.79+5396A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498798 | |||||||
| chr12:100498800 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.79+5398G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100498800 | |||||||
| chr12:100499303 | C | T | 66 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(63): Show |
67 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.79+5901C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499303 | |||||||
| chr12:100499565 | T | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0090 |
3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.79+6163T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499565 | |||||||
| chr12:100499570 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+6168C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499570 | |||||||
| chr12:100499625 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+6223G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499625 | |||||||
| chr12:100499631 | C | T | 16 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(13): Show |
16 | HG02109.hp1 HG02257.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.79+6229C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499631 | |||||||
| chr12:100499792 | G | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+6390G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499792 | |||||||
| chr12:100499858 | C | T | 66 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(63): Show |
67 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.79+6456C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100499858 | |||||||
| chr12:100500058 | G | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+6656G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500058 | |||||||
| chr12:100500059 | A | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+6657A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500059 | |||||||
| chr12:100500188 | A | G | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 |
3 | HG03831.hp2 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.79+6786A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500188 | |||||||
| chr12:100500250 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+6848A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500250 | |||||||
| chr12:100500313 | C | G | 1 | a0001c0001t0001g0132 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.79+6911C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500313 | |||||||
| chr12:100500353 | A | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(125): Show |
140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.79+6951A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500353 | |||||||
| chr12:100500422 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.79+7020C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500422 | |||||||
| chr12:100500858 | C | T | 38 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(35): Show |
47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+7456C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500858 | |||||||
| chr12:100500864 | T | A | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.79+7462T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500864 | |||||||
| chr12:100500878 | C | T | 1 | a0005c0004t0001g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.79+7476C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100500878 | |||||||
| chr12:100501035 | T | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(126): Show |
141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.79+7633T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501035 | |||||||
| chr12:100501121 | C | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0179 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.79+7719C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501121 | |||||||
| chr12:100501142 | A | G | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 |
3 | HG03831.hp2 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.79+7740A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501142 | |||||||
| chr12:100501236 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.79+7834G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501236 | |||||||
| chr12:100501248 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0090 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.79+7846A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501248 | |||||||
| chr12:100501368 | A | AC | 55 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(52): Show |
64 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.79+7970dupC | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100501368 | ||||||
| chr12:100501372 | C | CT | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(71): Show |
77 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.79+7970_79+7971ins others(1): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501372 | |||||||
| chr12:100501454 | G | T | 1 | a0001c0001t0002g0057 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.79+8052G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501454 | |||||||
| chr12:100501649 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.79+8247C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501649 | |||||||
| chr12:100501757 | A | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0287 |
2 | HG01346.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.79+8355A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100501757 | |||||||
| chr12:100502220 | T | C | 5 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0001g0093 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-8558T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502220 | |||||||
| chr12:100502294 | T | C | 3 | a0001c0001t0001g0081 a0002c0002t0001g0015 a0002c0002t0001g0016 |
3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.80-8484T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502294 | |||||||
| chr12:100502445 | C | T | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-8333C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502445 | |||||||
| chr12:100502446 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.80-8332G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502446 | |||||||
| chr12:100502489 | C | A | 55 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(52): Show |
64 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.80-8289C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502489 | |||||||
| chr12:100502540 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.80-8238A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502540 | |||||||
| chr12:100502574 | C | T | 1 | a0001c0001t0002g0057 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.80-8204C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502574 | |||||||
| chr12:100502972 | G | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0179 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.80-7806G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100502972 | |||||||
| chr12:100503023 | C | A | 3 | a0001c0001t0001g0081 a0002c0002t0001g0015 a0002c0002t0001g0016 |
3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.80-7755C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503023 | |||||||
| chr12:100503042 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80-7736C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503042 | |||||||
| chr12:100503062 | C | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
7 | HG01346.hp1 HG01358.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-7716C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503062 | |||||||
| chr12:100503225 | A | T | 1 | a0001c0001t0001g0208 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.80-7553A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503225 | |||||||
| chr12:100503438 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-7340C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503438 | |||||||
| chr12:100503453 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-7325G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503453 | |||||||
| chr12:100503473 | T | G | 2 | a0002c0002t0001g0015 a0002c0002t0001g0016 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.80-7305T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503473 | |||||||
| chr12:100503631 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(126): Show |
141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.80-7147A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503631 | |||||||
| chr12:100503670 | A | G | 17 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(14): Show |
17 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.80-7108A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503670 | |||||||
| chr12:100503755 | T | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0181 a0001c0001t0001g0182 others(3): Show |
7 | HG00735.hp1 HG01069.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-7023T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503755 | |||||||
| chr12:100503898 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG00735.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.80-6880G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503898 | |||||||
| chr12:100503943 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(131): Show |
146 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.80-6835T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503943 | |||||||
| chr12:100503980 | T | C | 55 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(52): Show |
64 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.80-6798T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100503980 | |||||||
| chr12:100504003 | T | C | 2 | a0001c0001t0002g0048 a0001c0001t0002g0066 |
2 | NA18985.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.80-6775T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504003 | |||||||
| chr12:100504302 | C | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
5 | HG01884.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-6476C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504302 | |||||||
| chr12:100504393 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG00140.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.80-6385G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504393 | |||||||
| chr12:100504439 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0239 |
3 | HG01069.hp1 HG01255.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.80-6339A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504439 | |||||||
| chr12:100504448 | T | C | 71 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(68): Show |
72 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.80-6330T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504448 | |||||||
| chr12:100504557 | G | A | 2 | a0001c0001t0001g0253 a0003c0006t0001g0280 |
2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.80-6221G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504557 | |||||||
| chr12:100504635 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-6143T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504635 | |||||||
| chr12:100504675 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.80-6103C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504675 | |||||||
| chr12:100504783 | G | A | 3 | a0001c0001t0001g0081 a0002c0002t0001g0015 a0002c0002t0001g0016 |
3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.80-5995G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504783 | |||||||
| chr12:100504869 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(76): Show |
82 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.80-5909G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504869 | |||||||
| chr12:100504918 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.80-5860T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100504918 | |||||||
| chr12:100505029 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80-5749G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505029 | |||||||
| chr12:100505101 | CA | C | 53 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(50): Show |
62 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.80-5666delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100505101 | ||||||
| chr12:100505112 | A | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-5666A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505112 | |||||||
| chr12:100505156 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0239 |
3 | HG01069.hp1 HG01255.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.80-5622A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505156 | |||||||
| chr12:100505290 | G | C | 1 | a0001c0001t0002g0102 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.80-5488G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505290 | |||||||
| chr12:100505649 | C | T | 51 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(48): Show |
60 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.80-5129C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505649 | |||||||
| chr12:100505712 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.80-5066A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505712 | |||||||
| chr12:100505812 | C | T | 58 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(55): Show |
59 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.80-4966C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505812 | |||||||
| chr12:100505882 | C | G | 50 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(47): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.80-4896C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100505882 | |||||||
| chr12:100506002 | A | AAC | 78 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(75): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.80-4736_80-4735dup others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506002 | ||||||
| chr12:100506002 | A | AACAC | 13 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(10): Show |
13 | HG00621.hp2 HG02071.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-4738_80-4735dup others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506002 | ||||||
| chr12:100506002 | A | AACACAC | 7 | a0001c0001t0001g0085 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG00408.hp1 HG02129.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-4740_80-4735dup others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506002 | ||||||
| chr12:100506002 | A | AACACACA others(3): Show |
1 | a0002c0002t0001g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.80-4744_80-4735dup others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506002 | ||||||
| chr12:100506002 | AAC | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0130 a0001c0001t0001g0131 others(15): Show |
19 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.80-4736_80-4735del others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506002 | ||||||
| chr12:100506002 | AACAC | A | 5 | a0001c0001t0001g0096 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG03139.hp2 NA18944.hp2 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-4738_80-4735del others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506002 | ||||||
| chr12:100506030 | CACACACA others(9): Show |
C | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-4746_80-4731del others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506030 | ||||||
| chr12:100506032 | CACACACA others(7): Show |
C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0091 a0001c0001t0002g0067 |
3 | HG02109.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.80-4744_80-4731del others(14): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506032 | ||||||
| chr12:100506034 | CACACACA others(5): Show |
C | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
44 | HG00408.hp2 HG00558.hp1 HG02083.hp2 others(41): Show |
intron_variant | MODIFIER | c.80-4742_80-4731del others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506034 | ||||||
| chr12:100506036 | CACACACA others(3): Show |
C | 2 | a0001c0001t0002g0001 a0001c0001t0002g0057 |
2 | HG00423.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.80-4740_80-4731del others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506036 | ||||||
| chr12:100506040 | C | G | 2 | a0001c0001t0001g0097 a0008c0003t0001g0213 |
2 | HG02886.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.80-4738C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506040 | |||||||
| chr12:100506042 | C | CACACACA others(5): Show |
1 | a0001c0001t0001g0002 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.80-4735_80-4734ins others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506042 | ||||||
| chr12:100506042 | C | CACACACA others(3): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.80-4735_80-4734ins others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506042 | ||||||
| chr12:100506042 | C | CACACACA others(1): Show |
7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0025 others(4): Show |
8 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-4735_80-4734ins others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506042 | ||||||
| chr12:100506042 | C | CACACAG | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02647.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-4735_80-4734ins others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100506042 | ||||||
| chr12:100506042 | C | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0097 a0001c0001t0001g0105 others(4): Show |
8 | HG02886.hp1 NA18948.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-4736C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506042 | |||||||
| chr12:100506044 | G | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0265 |
3 | HG02622.hp2 HG03516.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.80-4734G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506044 | |||||||
| chr12:100506232 | G | A | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-4546G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506232 | |||||||
| chr12:100506252 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.80-4526G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506252 | |||||||
| chr12:100506517 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.80-4261G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506517 | |||||||
| chr12:100506518 | T | G | 1 | a0001c0001t0001g0127 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.80-4260T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506518 | |||||||
| chr12:100506665 | G | A | 57 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(54): Show |
58 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.80-4113G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506665 | |||||||
| chr12:100506671 | C | A | 2 | a0001c0001t0001g0149 a0001c0001t0006g0260 |
2 | HG00099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.80-4107C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506671 | |||||||
| chr12:100506729 | AACTCCTT others(3): Show |
A | 5 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(2): Show |
5 | HG02132.hp2 NA18968.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-4048_80-4039del others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506729 | |||||||
| chr12:100506740 | T | C | 5 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(2): Show |
5 | HG02132.hp2 NA18968.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-4038T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506740 | |||||||
| chr12:100506902 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.80-3876A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100506902 | |||||||
| chr12:100507118 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.80-3660G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507118 | |||||||
| chr12:100507456 | GTTTTGT | G | 57 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(54): Show |
58 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.80-3305_80-3300del others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100507456 | ||||||
| chr12:100507473 | G | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA19055.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.80-3305G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507473 | |||||||
| chr12:100507475 | T | G | 55 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(52): Show |
64 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.80-3303T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507475 | |||||||
| chr12:100507616 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.80-3162C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507616 | |||||||
| chr12:100507618 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.80-3160A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507618 | |||||||
| chr12:100507698 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(126): Show |
141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.80-3080T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507698 | |||||||
| chr12:100507699 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.80-3079G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507699 | |||||||
| chr12:100507743 | G | A | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(8): Show |
11 | HG02109.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-3035G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507743 | |||||||
| chr12:100507993 | T | C | 4 | a0001c0001t0001g0230 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02055.hp1 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-2785T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100507993 | |||||||
| chr12:100508040 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.80-2738G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508040 | |||||||
| chr12:100508079 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0264 a0001c0001t0001g0287 |
4 | HG00140.hp1 HG01346.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-2699G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508079 | |||||||
| chr12:100508103 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-2675G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508103 | |||||||
| chr12:100508263 | C | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.80-2515C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508263 | |||||||
| chr12:100508506 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.80-2272C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508506 | |||||||
| chr12:100508512 | C | CTTTGAGA others(10): Show |
1 | a0001c0001t0001g0126 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.80-2265_80-2249dup others(17): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100508512 | ||||||
| chr12:100508566 | A | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(76): Show |
82 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.80-2212A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508566 | |||||||
| chr12:100508642 | T | A | 57 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(54): Show |
58 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.80-2136T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508642 | |||||||
| chr12:100508747 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.80-2031C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508747 | |||||||
| chr12:100508910 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.80-1868C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508910 | |||||||
| chr12:100508913 | T | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.80-1865T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508913 | |||||||
| chr12:100508925 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.80-1853C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508925 | |||||||
| chr12:100508999 | T | G | 1 | a0001c0001t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.80-1779T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100508999 | |||||||
| chr12:100509204 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80-1574G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509204 | |||||||
| chr12:100509264 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.80-1514C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509264 | |||||||
| chr12:100509554 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-1224A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509554 | |||||||
| chr12:100509574 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0252 |
2 | HG00597.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.80-1204A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509574 | |||||||
| chr12:100509596 | C | G | 2 | a0002c0002t0001g0015 a0002c0002t0001g0016 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.80-1182C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509596 | |||||||
| chr12:100509616 | T | A | 2 | a0001c0001t0001g0160 a0005c0004t0001g0161 |
2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.80-1162T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509616 | |||||||
| chr12:100509908 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.80-870C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509908 | |||||||
| chr12:100509910 | TGC | T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0086 others(7): Show |
10 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-863_80-862delGC | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100509910 | ||||||
| chr12:100509913 | GCGCA | G | 63 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(60): Show |
64 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-863_80-860delGC others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100509913 | ||||||
| chr12:100509913 | GCGCACA | G | 3 | a0001c0001t0001g0074 a0002c0002t0001g0015 a0002c0002t0001g0016 |
3 | HG02257.hp2 HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.80-863_80-858delGC others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100509913 | ||||||
| chr12:100509915 | G | A | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0070 others(7): Show |
10 | HG02109.hp1 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-863G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509915 | |||||||
| chr12:100509915 | G | GCA | 36 | a0001c0001t0001g0106 a0001c0001t0002g0001 a0001c0001t0002g0004 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.80-838_80-837dupCA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100509915 | ||||||
| chr12:100509915 | GCACA | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(6): Show |
11 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-840_80-837delCA others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100509915 | ||||||
| chr12:100509917 | A | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0267 |
2 | HG02071.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.80-861A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509917 | |||||||
| chr12:100509921 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-857A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509921 | |||||||
| chr12:100509960 | G | A | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.80-818G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100509960 | |||||||
| chr12:100510203 | A | G | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
5 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-575A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510203 | |||||||
| chr12:100510354 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.80-424C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510354 | |||||||
| chr12:100510399 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.80-379A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510399 | |||||||
| chr12:100510445 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.80-333C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510445 | |||||||
| chr12:100510573 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80-205A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510573 | |||||||
| chr12:100510607 | T | A | 1 | a0001c0010t0001g0189 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.80-171T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510607 | |||||||
| chr12:100510607 | T | TA | 3 | a0001c0001t0001g0107 a0001c0001t0001g0219 a0001c0001t0001g0225 |
3 | HG00323.hp1 HG01169.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.80-171_80-170insA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510607 | |||||||
| chr12:100510607 | T | TATATATA others(8): Show |
1 | a0001c0001t0001g0237 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.80-171_80-170insAT others(13): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510607 | |||||||
| chr12:100510607 | T | TTA | 21 | a0001c0001t0001g0062 a0001c0001t0001g0095 a0001c0001t0001g0097 others(18): Show |
21 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.80-144_80-143dupTA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | T | TTATA | 7 | a0001c0001t0001g0150 a0001c0001t0001g0165 a0001c0001t0001g0167 others(4): Show |
7 | HG00621.hp1 HG01516.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-146_80-143dupTA others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | T | TTATATA | 3 | a0001c0001t0001g0086 a0001c0001t0001g0092 a0001c0001t0001g0214 |
3 | HG02922.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.80-148_80-143dupTA others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0022 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
4 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-150_80-143dupTA others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | T | TTATATAT others(3): Show |
18 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
19 | HG00609.hp2 HG00673.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.80-152_80-143dupTA others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | T | TTATATAT others(5): Show |
18 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(15): Show |
18 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-154_80-143dupTA others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | T | TTATATAT others(7): Show |
13 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0159 others(10): Show |
14 | HG00735.hp1 HG01069.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-156_80-143dupTA others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | T | TTATATAT others(9): Show |
7 | a0001c0001t0001g0080 a0001c0001t0001g0099 a0001c0001t0001g0199 others(4): Show |
7 | HG02132.hp2 HG02922.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-158_80-143dupTA others(14): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | T | TTATATAT others(11): Show |
5 | a0001c0001t0001g0003 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
6 | HG01257.hp2 HG01258.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-160_80-143dupTA others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | T | TTATATAT others(15): Show |
2 | a0001c0001t0001g0027 a0001c0001t0001g0081 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.80-164_80-143dupTA others(20): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | T | TTATATAT others(17): Show |
1 | a0001c0001t0001g0208 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.80-166_80-143dupTA others(22): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | TTA | T | 13 | a0001c0001t0001g0112 a0001c0001t0001g0229 a0001c0001t0001g0230 others(10): Show |
14 | HG00673.hp1 HG02055.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.80-144_80-143delTA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | TTATA | T | 46 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(43): Show |
54 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.80-146_80-143delTA others(2): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510607 | TTATATA | T | 11 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(8): Show |
11 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-148_80-143delTA others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 100510607 | ||||||
| chr12:100510647 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-131T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510647 | |||||||
| chr12:100510669 | AT | A | 58 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(55): Show |
59 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.80-108delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510669 | |||||||
| chr12:100510711 | G | A | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-67G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 3/10 | chr12 | 100510711 | |||||||
| chr12:100511365 | T | G | 50 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(47): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.445+222T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511365 | |||||||
| chr12:100511438 | T | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(76): Show |
90 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.445+295T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511438 | |||||||
| chr12:100511519 | C | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(76): Show |
82 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.445+376C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511519 | |||||||
| chr12:100511633 | AT | A | 12 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.445+491delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511633 | |||||||
| chr12:100511637 | T | A | 1 | a0008c0003t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.445+494T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511637 | |||||||
| chr12:100511750 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.445+607C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511750 | |||||||
| chr12:100511751 | G | A | 71 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(68): Show |
72 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.445+608G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511751 | |||||||
| chr12:100511778 | T | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(150): Show |
165 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.445+635T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100511778 | |||||||
| chr12:100511931 | AT | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(8): Show |
13 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.445+802delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100511931 | ||||||
| chr12:100512012 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.445+869C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512012 | |||||||
| chr12:100512013 | G | A | 12 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.445+870G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512013 | |||||||
| chr12:100512030 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.445+887C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512030 | |||||||
| chr12:100512158 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.445+1015G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512158 | |||||||
| chr12:100512199 | C | T | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.445+1056C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512199 | |||||||
| chr12:100512364 | G | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0281 a0001c0001t0001g0282 |
3 | HG03704.hp2 HG04115.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.445+1221G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512364 | |||||||
| chr12:100512489 | A | C | 9 | a0001c0001t0001g0212 a0001c0001t0001g0241 a0001c0001t0001g0242 others(6): Show |
9 | HG00597.hp2 HG02015.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+1346A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512489 | |||||||
| chr12:100512558 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.445+1415G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512558 | |||||||
| chr12:100512606 | A | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0288 |
2 | HG02083.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.445+1463A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512606 | |||||||
| chr12:100512641 | C | CA | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(69): Show |
83 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.445+1511dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100512641 | ||||||
| chr12:100512716 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.445+1573T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512716 | |||||||
| chr12:100512821 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445+1678G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512821 | |||||||
| chr12:100512898 | C | T | 14 | a0001c0001t0001g0212 a0001c0001t0001g0241 a0001c0001t0001g0242 others(11): Show |
14 | HG00597.hp2 HG00673.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.445+1755C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512898 | |||||||
| chr12:100512987 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.445+1844T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100512987 | |||||||
| chr12:100513431 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.445+2288G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513431 | |||||||
| chr12:100513582 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.445+2439G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513582 | |||||||
| chr12:100513589 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.445+2446G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513589 | |||||||
| chr12:100513798 | CAGAAAGG others(9): Show |
C | 1 | a0001c0001t0001g0145 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.445+2658_445+2673d others(18): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513798 | ||||||
| chr12:100513798 | CAGAAAGG others(12): Show |
C | 1 | a0001c0001t0001g0110 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.445+2657_445+2675d others(21): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513798 | ||||||
| chr12:100513801 | A | AAAGG | 5 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0217 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+2725_445+2728d others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | A | AAAGGAAG others(1): Show |
3 | a0001c0001t0001g0025 a0001c0001t0004g0174 a0001c0001t0004g0175 |
3 | HG02486.hp2 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.445+2721_445+2728d others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | A | AAAGGAAG others(5): Show |
1 | a0001c0001t0001g0038 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445+2717_445+2728d others(14): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | A | AAAGGAAG others(9): Show |
2 | a0001c0001t0001g0037 a0001c0001t0001g0071 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.445+2713_445+2728d others(18): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | AAAGG | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0022 others(20): Show |
25 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(22): Show |
intron_variant | MODIFIER | c.445+2725_445+2728d others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | AAAGGAAG others(1): Show |
A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0021 others(30): Show |
34 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.445+2721_445+2728d others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | AAAGGAAG others(5): Show |
A | 38 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0081 others(35): Show |
38 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.445+2717_445+2728d others(14): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | AAAGGAAG others(9): Show |
A | 68 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(65): Show |
69 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.445+2713_445+2728d others(18): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | AAAGGAAG others(13): Show |
A | 54 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(51): Show |
55 | HG00140.hp2 HG00609.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.445+2709_445+2728d others(22): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | AAAGGAAG others(17): Show |
A | 9 | a0001c0001t0001g0020 a0001c0001t0001g0082 a0001c0001t0001g0091 others(6): Show |
9 | HG02451.hp1 HG02647.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+2705_445+2728d others(26): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | AAAGGAAG others(21): Show |
A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0234 a0001c0001t0001g0238 |
3 | NA18944.hp2 NA18946.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.445+2701_445+2728d others(30): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | AAAGGAAG others(25): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.445+2697_445+2728d others(34): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | AAAGGAAG others(29): Show |
A | 2 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
2 | NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.445+2693_445+2728d others(38): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513801 | AAAGGAAG others(33): Show |
A | 34 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(31): Show |
43 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.445+2689_445+2728d others(42): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513801 | ||||||
| chr12:100513847 | A | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0092 |
3 | HG02145.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.445+2704A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513847 | |||||||
| chr12:100513852 | GGAAGGAA others(12): Show |
G | 1 | a0001c0001t0001g0155 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.445+2710_445+2728d others(21): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513852 | |||||||
| chr12:100513853 | GAAGGAAG others(10): Show |
G | 1 | a0001c0001t0001g0137 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.445+2713_445+2729d others(19): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100513853 | ||||||
| chr12:100513882 | A | G | 58 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(55): Show |
59 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.445+2739A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513882 | |||||||
| chr12:100513937 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.445+2794T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513937 | |||||||
| chr12:100513995 | A | G | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 |
3 | HG03831.hp2 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.445+2852A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100513995 | |||||||
| chr12:100514001 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445+2858G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100514001 | |||||||
| chr12:100514803 | CTATAT | C | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.445+3670_445+3674d others(7): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100514803 | ||||||
| chr12:100515021 | A | T | 1 | a0001c0001t0001g0098 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.445+3878A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515021 | |||||||
| chr12:100515111 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.445+3968C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515111 | |||||||
| chr12:100515144 | G | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(124): Show |
139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.445+4001G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515144 | |||||||
| chr12:100515165 | C | CT | 35 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0034 others(32): Show |
35 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.445+4045dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100515165 | ||||||
| chr12:100515165 | CT | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(53): Show |
67 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.445+4045delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100515165 | ||||||
| chr12:100515228 | T | C | 57 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(54): Show |
58 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.445+4085T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515228 | |||||||
| chr12:100515699 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.445+4556C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515699 | |||||||
| chr12:100515739 | A | G | 8 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0121 others(5): Show |
8 | HG00558.hp2 HG00621.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.445+4596A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515739 | |||||||
| chr12:100515741 | C | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0090 |
3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.445+4598C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100515741 | |||||||
| chr12:100516139 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.445+4996T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516139 | |||||||
| chr12:100516160 | T | C | 3 | a0001c0001t0001g0081 a0002c0002t0001g0015 a0002c0002t0001g0016 |
3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.445+5017T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516160 | |||||||
| chr12:100516341 | C | A | 1 | a0001c0008t0005g0271 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.445+5198C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516341 | |||||||
| chr12:100516515 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.445+5372T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516515 | |||||||
| chr12:100516527 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0078 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.445+5384C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516527 | |||||||
| chr12:100516618 | G | T | 8 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(5): Show |
8 | HG02145.hp1 HG02647.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.445+5475G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516618 | |||||||
| chr12:100516686 | G | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0192 a0001c0001t0001g0196 others(4): Show |
7 | HG02074.hp1 NA18961.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.445+5543G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100516686 | |||||||
| chr12:100517053 | CTT | C | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.445+5911_445+5912d others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100517053 | |||||||
| chr12:100517160 | G | A | 48 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(45): Show |
57 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.445+6017G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100517160 | |||||||
| chr12:100517281 | T | C | 7 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0043 others(4): Show |
9 | NA18966.hp2 NA18968.hp2 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+6138T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100517281 | |||||||
| chr12:100517334 | C | T | 3 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 |
3 | HG02698.hp1 HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.445+6191C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100517334 | |||||||
| chr12:100517426 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.445+6283C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100517426 | |||||||
| chr12:100517432 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.445+6289T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100517432 | |||||||
| chr12:100518038 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.445+6895G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518038 | |||||||
| chr12:100518118 | G | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0078 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.445+6975G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518118 | |||||||
| chr12:100518258 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0078 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.445+7115G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518258 | |||||||
| chr12:100518364 | G | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(16): Show |
20 | HG00609.hp2 HG00621.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.445+7221G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518364 | |||||||
| chr12:100518451 | A | C | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.445+7308A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518451 | |||||||
| chr12:100518478 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.445+7335C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518478 | |||||||
| chr12:100518535 | A | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(129): Show |
144 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.445+7392A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518535 | |||||||
| chr12:100518597 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0090 |
3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.445+7454A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518597 | |||||||
| chr12:100518788 | C | CT | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
80 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.445+7667dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100518788 | ||||||
| chr12:100518788 | CT | C | 12 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(9): Show |
12 | HG00099.hp1 HG02559.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.445+7667delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100518788 | ||||||
| chr12:100518823 | C | T | 1 | a0003c0006t0001g0280 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.445+7680C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518823 | |||||||
| chr12:100518928 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.445+7785C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518928 | |||||||
| chr12:100518953 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.445+7810A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100518953 | |||||||
| chr12:100519034 | C | T | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
5 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+7891C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100519034 | |||||||
| chr12:100519295 | T | C | 2 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
2 | NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.445+8152T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100519295 | |||||||
| chr12:100519684 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.445+8541G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100519684 | |||||||
| chr12:100519698 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445+8555C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100519698 | |||||||
| chr12:100519965 | G | T | 1 | a0001c0001t0001g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.445+8822G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100519965 | |||||||
| chr12:100520092 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.445+8949G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520092 | |||||||
| chr12:100520109 | T | C | 1 | a0001c0001t0002g0151 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.445+8966T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520109 | |||||||
| chr12:100520129 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.445+8986G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520129 | |||||||
| chr12:100520452 | G | A | 12 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.445+9309G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520452 | |||||||
| chr12:100520708 | C | T | 4 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0068 others(1): Show |
4 | HG00558.hp1 NA18944.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+9565C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520708 | |||||||
| chr12:100520722 | A | C | 6 | a0001c0001t0001g0173 a0001c0001t0001g0248 a0001c0001t0003g0172 others(3): Show |
6 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.445+9579A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520722 | |||||||
| chr12:100520747 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445+9604C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520747 | |||||||
| chr12:100520803 | A | G | 3 | a0001c0001t0001g0081 a0002c0002t0001g0015 a0002c0002t0001g0016 |
3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.445+9660A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520803 | |||||||
| chr12:100520934 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(124): Show |
139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.445+9791T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520934 | |||||||
| chr12:100520967 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.445+9824G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100520967 | |||||||
| chr12:100521091 | A | T | 2 | a0002c0002t0001g0015 a0002c0002t0001g0016 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.445+9948A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521091 | |||||||
| chr12:100521105 | C | G | 4 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0002c0002t0001g0015 others(1): Show |
4 | HG02257.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.445+9962C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521105 | |||||||
| chr12:100521127 | A | T | 2 | a0001c0001t0001g0286 a0004c0005t0001g0251 |
2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.445+9984A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521127 | |||||||
| chr12:100521183 | A | T | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.445+10040A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521183 | |||||||
| chr12:100521217 | T | G | 3 | a0001c0001t0004g0174 a0001c0001t0004g0175 a0001c0001t0004g0176 |
3 | HG02257.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.445+10074T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521217 | |||||||
| chr12:100521278 | T | A | 1 | a0001c0001t0001g0285 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.445+10135T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521278 | |||||||
| chr12:100521329 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(124): Show |
139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.445+10186A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521329 | |||||||
| chr12:100521548 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.445+10405G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521548 | |||||||
| chr12:100521631 | A | AT | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.445+10493dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100521631 | ||||||
| chr12:100521734 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.445+10591T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521734 | |||||||
| chr12:100521808 | C | G | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-10650C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521808 | |||||||
| chr12:100521891 | T | A | 14 | a0001c0001t0001g0212 a0001c0001t0001g0241 a0001c0001t0001g0242 others(11): Show |
14 | HG00597.hp2 HG00673.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.446-10567T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521891 | |||||||
| chr12:100521904 | G | C | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-10554G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100521904 | |||||||
| chr12:100522096 | A | AT | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(76): Show |
82 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.446-10362_446-1036 others(5): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522096 | |||||||
| chr12:100522138 | AATGGTG | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
7 | HG01346.hp1 HG01358.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.446-10301_446-1029 others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100522138 | ||||||
| chr12:100522281 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.446-10177T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522281 | |||||||
| chr12:100522484 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.446-9974A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522484 | |||||||
| chr12:100522496 | T | C | 9 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.446-9962T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522496 | |||||||
| chr12:100522544 | GT | G | 7 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.446-9901delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100522544 | ||||||
| chr12:100522553 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.446-9905T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522553 | |||||||
| chr12:100522871 | G | A | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.446-9587G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522871 | |||||||
| chr12:100522948 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.446-9510C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522948 | |||||||
| chr12:100522989 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.446-9469C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100522989 | |||||||
| chr12:100523142 | T | C | 1 | a0001c0001t0002g0079 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.446-9316T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523142 | |||||||
| chr12:100523194 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.446-9264C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523194 | |||||||
| chr12:100523277 | A | C | 57 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(54): Show |
58 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.446-9181A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523277 | |||||||
| chr12:100523346 | A | G | 57 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(54): Show |
58 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.446-9112A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523346 | |||||||
| chr12:100523365 | G | A | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.446-9093G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523365 | |||||||
| chr12:100523499 | G | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.446-8959G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523499 | |||||||
| chr12:100523547 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.446-8911C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523547 | |||||||
| chr12:100523811 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0199 |
2 | NA19043.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.446-8647G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523811 | |||||||
| chr12:100523883 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0155 |
3 | HG01258.hp1 HG01358.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.446-8575T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523883 | |||||||
| chr12:100523944 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.446-8514C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100523944 | |||||||
| chr12:100524077 | G | C | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-8381G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524077 | |||||||
| chr12:100524169 | T | C | 2 | a0002c0002t0001g0015 a0002c0002t0001g0016 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.446-8289T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524169 | |||||||
| chr12:100524179 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0285 |
2 | HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.446-8279C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524179 | |||||||
| chr12:100524221 | T | A | 1 | a0001c0001t0001g0276 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.446-8237T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524221 | |||||||
| chr12:100524240 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.446-8218G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524240 | |||||||
| chr12:100524288 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.446-8170A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524288 | |||||||
| chr12:100524474 | A | G | 58 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(55): Show |
59 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.446-7984A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524474 | |||||||
| chr12:100524702 | T | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(129): Show |
144 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.446-7756T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524702 | |||||||
| chr12:100524826 | T | C | 12 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.446-7632T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524826 | |||||||
| chr12:100524836 | C | T | 3 | a0001c0001t0001g0081 a0002c0002t0001g0015 a0002c0002t0001g0016 |
3 | HG02257.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.446-7622C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524836 | |||||||
| chr12:100524868 | G | T | 48 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(45): Show |
57 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.446-7590G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524868 | |||||||
| chr12:100524917 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0002g0040 |
2 | HG02698.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.446-7541G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524917 | |||||||
| chr12:100524971 | C | A | 12 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.446-7487C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100524971 | |||||||
| chr12:100525073 | T | G | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
13 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.446-7385T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100525073 | |||||||
| chr12:100525222 | T | G | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
14 | HG02145.hp1 HG02647.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.446-7236T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100525222 | |||||||
| chr12:100525484 | A | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(70): Show |
84 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.446-6974A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100525484 | |||||||
| chr12:100525588 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.446-6870A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100525588 | |||||||
| chr12:100525827 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(5): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.446-6631T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100525827 | |||||||
| chr12:100525894 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(4): Show |
9 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.446-6564G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100525894 | |||||||
| chr12:100526028 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.446-6430G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526028 | |||||||
| chr12:100526162 | A | G | 5 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(2): Show |
5 | HG02132.hp2 NA18968.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.446-6296A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526162 | |||||||
| chr12:100526193 | A | AT | 160 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(157): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.446-6253dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100526193 | ||||||
| chr12:100526193 | A | ATT | 58 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0035 others(55): Show |
67 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.446-6254_446-6253d others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100526193 | ||||||
| chr12:100526193 | A | ATTT | 14 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(11): Show |
16 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.446-6255_446-6253d others(5): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100526193 | ||||||
| chr12:100526329 | G | T | 1 | a0001c0001t0001g0246 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.446-6129G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526329 | |||||||
| chr12:100526448 | C | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0085 |
2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.446-6010C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526448 | |||||||
| chr12:100526456 | A | G | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-6002A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526456 | |||||||
| chr12:100526526 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0085 |
2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.446-5932G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526526 | |||||||
| chr12:100526552 | T | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(18): Show |
23 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.446-5906T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526552 | |||||||
| chr12:100526555 | T | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(18): Show |
23 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.446-5903T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526555 | |||||||
| chr12:100526566 | C | T | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-5892C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526566 | |||||||
| chr12:100526657 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.446-5801G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526657 | |||||||
| chr12:100526703 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | NA18959.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.446-5755C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526703 | |||||||
| chr12:100526743 | T | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG00735.hp2 HG01169.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-5715T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526743 | |||||||
| chr12:100526788 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.446-5670C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526788 | |||||||
| chr12:100526905 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0033 |
3 | HG02055.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.446-5553G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100526905 | |||||||
| chr12:100527109 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG00621.hp2 NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.446-5349G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527109 | |||||||
| chr12:100527136 | C | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0081 a0002c0002t0001g0015 others(1): Show |
4 | HG02257.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-5322C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527136 | |||||||
| chr12:100527334 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.446-5124C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527334 | |||||||
| chr12:100527766 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(21): Show |
26 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.446-4692G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527766 | |||||||
| chr12:100527779 | G | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0085 |
2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.446-4679G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527779 | |||||||
| chr12:100527879 | A | T | 1 | a0001c0001t0001g0250 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.446-4579A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527879 | |||||||
| chr12:100527964 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.446-4494T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100527964 | |||||||
| chr12:100528136 | C | T | 2 | a0001c0001t0001g0286 a0004c0005t0001g0251 |
2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.446-4322C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528136 | |||||||
| chr12:100528220 | T | G | 9 | a0001c0001t0001g0212 a0001c0001t0001g0241 a0001c0001t0001g0242 others(6): Show |
9 | HG00597.hp2 HG02015.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.446-4238T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528220 | |||||||
| chr12:100528264 | T | A | 5 | a0001c0001t0001g0248 a0001c0001t0003g0172 a0001c0001t0003g0231 others(2): Show |
5 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-4194T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528264 | |||||||
| chr12:100528372 | G | GA | 11 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0078 others(8): Show |
11 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.446-4074dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 100528372 | ||||||
| chr12:100528401 | G | A | 56 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(53): Show |
57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.446-4057G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528401 | |||||||
| chr12:100528403 | G | A | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-4055G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528403 | |||||||
| chr12:100528650 | A | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0214 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.446-3808A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528650 | |||||||
| chr12:100528875 | T | C | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-3583T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528875 | |||||||
| chr12:100528894 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.446-3564G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528894 | |||||||
| chr12:100528906 | A | G | 7 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0082 others(4): Show |
7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.446-3552A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528906 | |||||||
| chr12:100528940 | G | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0138 a0001c0001t0001g0263 others(3): Show |
7 | HG00140.hp1 HG00280.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.446-3518G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528940 | |||||||
| chr12:100528953 | T | G | 1 | a0001c0001t0001g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.446-3505T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100528953 | |||||||
| chr12:100529184 | C | A | 7 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0082 others(4): Show |
7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.446-3274C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100529184 | |||||||
| chr12:100529358 | T | C | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0069 others(2): Show |
5 | HG02109.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-3100T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100529358 | |||||||
| chr12:100529569 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.446-2889C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100529569 | |||||||
| chr12:100530089 | A | C | 7 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0082 others(4): Show |
7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.446-2369A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530089 | |||||||
| chr12:100530097 | T | C | 1 | a0006c0009t0001g0247 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.446-2361T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530097 | |||||||
| chr12:100530129 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.446-2329A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530129 | |||||||
| chr12:100530316 | T | C | 4 | a0001c0001t0001g0075 a0001c0001t0001g0081 a0002c0002t0001g0015 others(1): Show |
4 | HG02257.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-2142T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530316 | |||||||
| chr12:100530380 | A | G | 1 | a0001c0001t0003g0120 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.446-2078A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530380 | |||||||
| chr12:100530586 | A | G | 1 | a0001c0010t0001g0189 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.446-1872A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530586 | |||||||
| chr12:100530623 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.446-1835T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530623 | |||||||
| chr12:100530788 | C | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0081 a0002c0002t0001g0015 others(1): Show |
4 | HG02257.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-1670C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100530788 | |||||||
| chr12:100531014 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.446-1444C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531014 | |||||||
| chr12:100531226 | C | T | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.446-1232C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531226 | |||||||
| chr12:100531235 | C | G | 1 | a0001c0001t0002g0005 | 2 | NA18968.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.446-1223C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531235 | |||||||
| chr12:100531317 | G | A | 55 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(52): Show |
58 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.446-1141G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531317 | |||||||
| chr12:100531492 | G | A | 1 | a0005c0004t0001g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.446-966G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531492 | |||||||
| chr12:100531524 | A | C | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.446-934A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531524 | |||||||
| chr12:100531540 | C | G | 1 | a0001c0001t0001g0031 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.446-918C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531540 | |||||||
| chr12:100531808 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.446-650G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100531808 | |||||||
| chr12:100532216 | C | A | 1 | a0001c0001t0001g0287 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.446-242C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100532216 | |||||||
| chr12:100532306 | C | T | 9 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.446-152C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100532306 | |||||||
| chr12:100532427 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.446-31C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 4/10 | chr12 | 100532427 | |||||||
| chr12:100532796 | G | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(127): Show |
142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.598+186G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100532796 | |||||||
| chr12:100532941 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.598+331A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100532941 | |||||||
| chr12:100533303 | T | C | 56 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(53): Show |
57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.598+693T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533303 | |||||||
| chr12:100533324 | T | C | 2 | a0001c0001t0001g0286 a0004c0005t0001g0251 |
2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.598+714T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533324 | |||||||
| chr12:100533409 | A | G | 3 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 |
3 | HG02698.hp1 HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.598+799A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533409 | |||||||
| chr12:100533636 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.598+1026A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533636 | |||||||
| chr12:100533668 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.598+1058G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533668 | |||||||
| chr12:100533752 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.599-1138C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533752 | |||||||
| chr12:100533890 | C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0082 others(6): Show |
9 | HG02257.hp2 HG02647.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.599-994_599-986dup others(9): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 100533890 | ||||||
| chr12:100533902 | T | G | 1 | a0001c0001t0001g0031 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.599-988T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533902 | |||||||
| chr12:100533924 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.599-966C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533924 | |||||||
| chr12:100533938 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(21): Show |
26 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.599-952G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533938 | |||||||
| chr12:100533944 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0092 |
3 | HG02145.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.599-946C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100533944 | |||||||
| chr12:100534131 | C | CATG | 13 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0078 others(10): Show |
13 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.599-757_599-756ins others(3): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 100534131 | ||||||
| chr12:100534149 | T | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(57): Show |
71 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.599-741T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100534149 | |||||||
| chr12:100534337 | T | C | 1 | a0006c0009t0001g0247 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.599-553T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100534337 | |||||||
| chr12:100534737 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.599-153G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 5/10 | chr12 | 100534737 | |||||||
| chr12:100535226 | T | G | 7 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0082 others(4): Show |
7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+203T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100535226 | |||||||
| chr12:100535430 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+407C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100535430 | |||||||
| chr12:100536327 | A | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0090 |
3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.733-185A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100536327 | |||||||
| chr12:100536388 | T | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0211 |
2 | NA18961.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.733-124T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100536388 | |||||||
| chr12:100536402 | C | CT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(7): Show |
12 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.733-99dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 100536402 | ||||||
| chr12:100536402 | CT | C | 9 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0084 others(6): Show |
9 | HG02257.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.733-99delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 100536402 | ||||||
| chr12:100536435 | C | G | 55 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(52): Show |
58 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.733-77C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100536435 | |||||||
| chr12:100536440 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.733-72G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100536440 | |||||||
| chr12:100536486 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(24): Show |
29 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.733-26C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 6/10 | chr12 | 100536486 | |||||||
| chr12:100536816 | C | A | 1 | a0001c0001t0001g0205 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.832-132C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 7/10 | chr12 | 100536816 | |||||||
| chr12:100536816 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.832-132C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 7/10 | chr12 | 100536816 | |||||||
| chr12:100536917 | T | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(127): Show |
142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.832-31T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 7/10 | chr12 | 100536917 | |||||||
| chr12:100536932 | T | A | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(34): Show |
39 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(36): Show |
intron_variant | MODIFIER | c.832-16T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 7/10 | chr12 | 100536932 | |||||||
| chr12:100537066 | A | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0169 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.931+19A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537066 | |||||||
| chr12:100537204 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.931+157A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537204 | |||||||
| chr12:100537328 | A | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0090 |
3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.931+281A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537328 | |||||||
| chr12:100537387 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.931+340T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537387 | |||||||
| chr12:100537518 | G | A | 10 | a0001c0001t0001g0037 a0001c0001t0001g0075 a0001c0001t0001g0080 others(7): Show |
10 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.931+471G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537518 | |||||||
| chr12:100537592 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.931+545G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537592 | |||||||
| chr12:100537597 | G | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0092 |
3 | HG02145.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.931+550G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537597 | |||||||
| chr12:100537706 | T | G | 5 | a0001c0001t0001g0108 a0001c0001t0001g0113 a0001c0001t0001g0115 others(2): Show |
5 | HG00423.hp1 NA18747.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+659T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537706 | |||||||
| chr12:100537775 | A | G | 93 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(90): Show |
103 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.931+728A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100537775 | |||||||
| chr12:100538184 | A | G | 56 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(53): Show |
57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.931+1137A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538184 | |||||||
| chr12:100538373 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.931+1326G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538373 | |||||||
| chr12:100538490 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(27): Show |
32 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.931+1443G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538490 | |||||||
| chr12:100538597 | T | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0094 others(11): Show |
15 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.931+1550T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538597 | |||||||
| chr12:100538632 | CT | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0027 |
3 | HG01109.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.931+1586delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538632 | |||||||
| chr12:100538944 | A | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(20): Show |
25 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.932-1728A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538944 | |||||||
| chr12:100538970 | A | C | 1 | a0001c0001t0001g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.932-1702A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100538970 | |||||||
| chr12:100539011 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.932-1661A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100539011 | |||||||
| chr12:100539366 | A | G | 7 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0082 others(4): Show |
7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-1306A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100539366 | |||||||
| chr12:100539535 | C | T | 14 | a0001c0001t0001g0037 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
14 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.932-1137C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100539535 | |||||||
| chr12:100539681 | G | A | 7 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0082 others(4): Show |
7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-991G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100539681 | |||||||
| chr12:100539703 | G | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(131): Show |
146 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.932-969G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100539703 | |||||||
| chr12:100540053 | C | T | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.932-619C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100540053 | |||||||
| chr12:100540114 | T | G | 1 | a0001c0001t0001g0031 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.932-558T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100540114 | |||||||
| chr12:100540468 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.932-204C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100540468 | |||||||
| chr12:100540469 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.932-203C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100540469 | |||||||
| chr12:100540600 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.932-72A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100540600 | |||||||
| chr12:100540635 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.932-37A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 8/10 | chr12 | 100540635 | |||||||
| chr12:100540884 | G | A | 4 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0087 others(1): Show |
4 | HG02922.hp2 HG03098.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078+66G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100540884 | |||||||
| chr12:100541013 | A | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(70): Show |
84 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1078+195A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541013 | |||||||
| chr12:100541067 | C | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(20): Show |
25 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.1078+249C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541067 | |||||||
| chr12:100541139 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1078+321A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541139 | |||||||
| chr12:100541173 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1078+355C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541173 | |||||||
| chr12:100541274 | C | CT | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(70): Show |
84 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1078+462dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100541274 | ||||||
| chr12:100541289 | CT | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0069 a0001c0001t0001g0070 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078+483delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100541289 | ||||||
| chr12:100541351 | G | C | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1078+533G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541351 | |||||||
| chr12:100541453 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1078+635G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541453 | |||||||
| chr12:100541519 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1078+701C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541519 | |||||||
| chr12:100541571 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1078+753C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541571 | |||||||
| chr12:100541605 | CT | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(69): Show |
83 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.1078+800delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100541605 | ||||||
| chr12:100541611 | T | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(25): Show |
30 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1078+793T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541611 | |||||||
| chr12:100541808 | G | A | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1078+990G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541808 | |||||||
| chr12:100541906 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078+1088C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100541906 | |||||||
| chr12:100542102 | T | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(11): Show |
16 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1078+1284T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542102 | |||||||
| chr12:100542116 | G | T | 5 | a0001c0001t0001g0037 a0001c0001t0001g0075 a0001c0001t0001g0081 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078+1298G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542116 | |||||||
| chr12:100542302 | G | A | 36 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1078+1484G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542302 | |||||||
| chr12:100542346 | G | GAA | 7 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0082 others(4): Show |
7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078+1536_1078+153 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100542346 | ||||||
| chr12:100542367 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1078+1549T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542367 | |||||||
| chr12:100542510 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0025 |
3 | HG02486.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1078+1692C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542510 | |||||||
| chr12:100542549 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1078+1731C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542549 | |||||||
| chr12:100542824 | GGTAGATT others(7880): Show |
G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1078+2008_1078+989 others(4): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100542824 | ||||||
| chr12:100542884 | A | G | 7 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0082 others(4): Show |
7 | HG02647.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078+2066A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542884 | |||||||
| chr12:100542923 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1078+2105G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100542923 | |||||||
| chr12:100543040 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1078+2222C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100543040 | |||||||
| chr12:100543058 | G | A | 37 | a0001c0001t0001g0162 a0001c0001t0002g0001 a0001c0001t0002g0004 others(34): Show |
46 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1078+2240G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100543058 | |||||||
| chr12:100543538 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1078+2720T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100543538 | |||||||
| chr12:100543559 | T | TTG | 48 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0037 others(45): Show |
58 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1078+2769_1078+277 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100543559 | ||||||
| chr12:100543559 | T | TTGTG | 3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0090 |
3 | HG02647.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1078+2767_1078+277 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100543559 | ||||||
| chr12:100543663 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1078+2845C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100543663 | |||||||
| chr12:100543975 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1078+3157G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100543975 | |||||||
| chr12:100544106 | G | A | 3 | a0001c0001t0004g0174 a0001c0001t0004g0175 a0001c0001t0004g0176 |
3 | HG02257.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1078+3288G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100544106 | |||||||
| chr12:100544208 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1078+3390C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100544208 | |||||||
| chr12:100544253 | C | CA | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(112): Show |
126 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.1078+3456dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100544253 | ||||||
| chr12:100544253 | C | CAA | 19 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0077 others(16): Show |
19 | HG00423.hp2 HG00673.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.1078+3455_1078+345 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100544253 | ||||||
| chr12:100544253 | CA | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0075 others(5): Show |
9 | HG00140.hp1 HG02257.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1078+3456delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100544253 | ||||||
| chr12:100544452 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1078+3634C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100544452 | |||||||
| chr12:100545006 | G | A | 56 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(53): Show |
57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1078+4188G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545006 | |||||||
| chr12:100545011 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1078+4193A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545011 | |||||||
| chr12:100545048 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1078+4230G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545048 | |||||||
| chr12:100545070 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1078+4252G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545070 | |||||||
| chr12:100545093 | C | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0085 |
2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1078+4275C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545093 | |||||||
| chr12:100545201 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1078+4383G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545201 | |||||||
| chr12:100545242 | CTGAGG | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0264 a0001c0001t0001g0287 |
4 | HG00140.hp1 HG01346.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078+4427_1078+443 others(9): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545242 | ||||||
| chr12:100545286 | G | C | 1 | a0001c0001t0002g0102 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1078+4468G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545286 | |||||||
| chr12:100545616 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(23): Show |
28 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1078+4798T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545616 | |||||||
| chr12:100545641 | C | CA | 61 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(58): Show |
65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1078+4851dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545641 | ||||||
| chr12:100545641 | C | CAA | 12 | a0001c0001t0001g0119 a0001c0001t0001g0124 a0001c0001t0001g0228 others(9): Show |
12 | HG02083.hp2 HG02615.hp2 HG03669.hp1 others(9): Show |
intron_variant | MODIFIER | c.1078+4850_1078+485 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545641 | ||||||
| chr12:100545641 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0087 a0001c0001t0001g0214 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1078+4841_1078+485 others(15): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545641 | ||||||
| chr12:100545641 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1078+4840_1078+485 others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545641 | ||||||
| chr12:100545641 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0082 a0001c0001t0001g0084 |
2 | HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1078+4839_1078+485 others(17): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545641 | ||||||
| chr12:100545660 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1078+4842A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545660 | |||||||
| chr12:100545664 | A | AAAC | 13 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
13 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078+4848_1078+484 others(7): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545664 | ||||||
| chr12:100545664 | A | AAC | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(5): Show |
9 | HG01257.hp2 HG01258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078+4847_1078+484 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545664 | ||||||
| chr12:100545669 | AC | A | 46 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
47 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.1078+4853delC | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100545669 | ||||||
| chr12:100545670 | C | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(230): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1078+4852C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545670 | |||||||
| chr12:100545671 | C | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(21): Show |
26 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1078+4853C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545671 | |||||||
| chr12:100545875 | C | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0025 |
3 | HG02486.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1078+5057C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545875 | |||||||
| chr12:100545899 | A | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | HG02451.hp2 HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1078+5081A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545899 | |||||||
| chr12:100545929 | T | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(35): Show |
40 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(37): Show |
intron_variant | MODIFIER | c.1078+5111T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100545929 | |||||||
| chr12:100546127 | T | TGGAGGCT others(7): Show |
1 | a0001c0001t0001g0125 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1078+5310_1078+532 others(18): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100546127 | ||||||
| chr12:100546438 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1078+5620G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100546438 | |||||||
| chr12:100546450 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1078+5632C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100546450 | |||||||
| chr12:100546481 | G | T | 56 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(53): Show |
57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1078+5663G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100546481 | |||||||
| chr12:100546651 | T | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(70): Show |
84 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1078+5833T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100546651 | |||||||
| chr12:100546709 | C | A | 1 | a0001c0001t0001g0229 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1078+5891C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100546709 | |||||||
| chr12:100546754 | C | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0087 others(1): Show |
4 | HG02922.hp2 HG03098.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078+5936C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100546754 | |||||||
| chr12:100547028 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1078+6210A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547028 | |||||||
| chr12:100547597 | AGGCAGTT others(9): Show |
A | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078+6783_1078+679 others(20): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100547597 | ||||||
| chr12:100547705 | T | TTTTA | 42 | a0001c0001t0001g0020 a0001c0001t0001g0243 a0001c0001t0001g0257 others(39): Show |
50 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1078+6915_1078+691 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100547705 | ||||||
| chr12:100547705 | TTTTA | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(27): Show |
32 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.1078+6915_1078+691 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100547705 | ||||||
| chr12:100547705 | TTTTATTT others(1): Show |
T | 36 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0030 others(33): Show |
36 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1078+6911_1078+691 others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100547705 | ||||||
| chr12:100547705 | TTTTATTT others(5): Show |
T | 1 | a0001c0001t0001g0011 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1078+6907_1078+691 others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100547705 | ||||||
| chr12:100547824 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1078+7006G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547824 | |||||||
| chr12:100547910 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1078+7092C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547910 | |||||||
| chr12:100547918 | T | C | 5 | a0001c0001t0001g0037 a0001c0001t0001g0075 a0001c0001t0001g0081 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078+7100T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547918 | |||||||
| chr12:100547942 | G | C | 1 | a0001c0001t0001g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1078+7124G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547942 | |||||||
| chr12:100547956 | A | G | 1 | a0001c0001t0002g0066 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1078+7138A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547956 | |||||||
| chr12:100547961 | T | C | 1 | a0001c0001t0002g0066 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1078+7143T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547961 | |||||||
| chr12:100547963 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1078+7145G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547963 | |||||||
| chr12:100547971 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1078+7153T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547971 | |||||||
| chr12:100547979 | C | G | 4 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG02647.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078+7161C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100547979 | |||||||
| chr12:100548000 | T | G | 38 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0182 others(35): Show |
47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1078+7182T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548000 | |||||||
| chr12:100548093 | T | C | 106 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(103): Show |
116 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1078+7275T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548093 | |||||||
| chr12:100548095 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1078+7277C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548095 | |||||||
| chr12:100548195 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1078+7377G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548195 | |||||||
| chr12:100548223 | C | T | 36 | a0001c0001t0001g0267 a0001c0001t0002g0001 a0001c0001t0002g0004 others(33): Show |
45 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1078+7405C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548223 | |||||||
| chr12:100548238 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1078+7420G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548238 | |||||||
| chr12:100548299 | G | A | 54 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(51): Show |
55 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1078+7481G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548299 | |||||||
| chr12:100548315 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1078+7497C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548315 | |||||||
| chr12:100548370 | TA | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(86): Show |
93 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1078+7568delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100548370 | ||||||
| chr12:100548370 | TAA | T | 49 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(46): Show |
58 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1078+7567_1078+756 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100548370 | ||||||
| chr12:100548594 | A | C | 1 | a0001c0001t0001g0203 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1078+7776A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548594 | |||||||
| chr12:100548705 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0110 |
2 | HG00323.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1078+7887C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100548705 | |||||||
| chr12:100549430 | T | C | 53 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(50): Show |
54 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.1078+8612T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100549430 | |||||||
| chr12:100549500 | C | A | 1 | a0001c0001t0001g0286 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1078+8682C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100549500 | |||||||
| chr12:100550076 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1078+9258T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550076 | |||||||
| chr12:100550170 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(133): Show |
141 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1078+9352G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550170 | |||||||
| chr12:100550181 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0182 |
2 | HG01361.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1078+9363A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550181 | |||||||
| chr12:100550310 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0182 |
2 | HG01361.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1078+9492A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550310 | |||||||
| chr12:100550526 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0155 |
3 | HG01258.hp1 HG01358.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1078+9708G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550526 | |||||||
| chr12:100550712 | G | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1078+9894G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550712 | |||||||
| chr12:100550939 | A | G | 54 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(51): Show |
55 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1078+10121A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100550939 | |||||||
| chr12:100551093 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1078+10275T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100551093 | |||||||
| chr12:100551302 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1078+10484T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100551302 | |||||||
| chr12:100551385 | GT | G | 6 | a0001c0001t0001g0038 a0001c0001t0001g0069 a0001c0001t0001g0071 others(3): Show |
6 | HG02257.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079-10496delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100551385 | ||||||
| chr12:100551474 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(76): Show |
83 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1079-10411A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100551474 | |||||||
| chr12:100551491 | A | T | 1 | a0001c0001t0001g0078 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1079-10394A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100551491 | |||||||
| chr12:100551914 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1079-9971G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100551914 | |||||||
| chr12:100552029 | G | GATCAAAC others(1): Show |
3 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0214 |
3 | HG02922.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1079-9856_1079-985 others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100552029 | |||||||
| chr12:100552030 | T | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0214 |
3 | HG02922.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1079-9855T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100552030 | |||||||
| chr12:100552251 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1079-9634G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100552251 | |||||||
| chr12:100552500 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1079-9385C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100552500 | |||||||
| chr12:100552720 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1079-9165C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100552720 | |||||||
| chr12:100552919 | A | AT | 74 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0017 others(71): Show |
76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1079-8965dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100552919 | ||||||
| chr12:100552920 | T | TA | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
9 | HG01069.hp1 HG02015.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1079-8952dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100552920 | ||||||
| chr12:100552921 | A | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0144 |
2 | HG01358.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1079-8964A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100552921 | |||||||
| chr12:100553022 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0081 |
2 | HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1079-8863G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553022 | |||||||
| chr12:100553047 | A | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(219): Show |
237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1079-8838A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553047 | |||||||
| chr12:100553072 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1079-8813C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553072 | |||||||
| chr12:100553213 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0269 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1079-8672T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553213 | |||||||
| chr12:100553323 | T | C | 3 | a0001c0001t0001g0187 a0001c0001t0001g0191 a0001c0001t0001g0199 |
3 | NA19063.hp2 NA19074.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1079-8562T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553323 | |||||||
| chr12:100553376 | T | A | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
5 | HG02559.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-8509T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553376 | |||||||
| chr12:100553471 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1079-8414A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553471 | |||||||
| chr12:100553524 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0160 a0005c0004t0001g0161 |
3 | HG02895.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1079-8361G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553524 | |||||||
| chr12:100553568 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1079-8317C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553568 | |||||||
| chr12:100553735 | T | G | 14 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0071 others(11): Show |
14 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1079-8150T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553735 | |||||||
| chr12:100553747 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(173): Show |
190 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1079-8138G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553747 | |||||||
| chr12:100553749 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1079-8136C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553749 | |||||||
| chr12:100553916 | A | T | 12 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0090 others(9): Show |
12 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1079-7969A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100553916 | |||||||
| chr12:100554133 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1079-7752T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554133 | |||||||
| chr12:100554179 | G | A | 15 | a0001c0001t0001g0037 a0001c0001t0001g0081 a0001c0001t0001g0082 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1079-7706G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554179 | |||||||
| chr12:100554336 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1079-7549T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554336 | |||||||
| chr12:100554341 | G | T | 3 | a0001c0001t0001g0093 a0002c0002t0001g0015 a0002c0002t0001g0016 |
3 | HG02257.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1079-7544G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554341 | |||||||
| chr12:100554392 | A | AAC | 24 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0021 others(21): Show |
26 | HG00323.hp1 HG01099.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1079-7462_1079-746 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | ||||||
| chr12:100554392 | A | AACAC | 39 | a0001c0001t0001g0090 a0001c0001t0001g0132 a0001c0001t0001g0192 others(36): Show |
47 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1079-7464_1079-746 others(8): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | ||||||
| chr12:100554392 | A | AACACAC | 11 | a0001c0001t0001g0039 a0001c0001t0001g0082 a0001c0001t0001g0084 others(8): Show |
11 | HG01361.hp1 HG02615.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1079-7466_1079-746 others(10): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | ||||||
| chr12:100554392 | A | AACACACA others(1): Show |
56 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(53): Show |
59 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1079-7468_1079-746 others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | ||||||
| chr12:100554392 | A | AACACACA others(3): Show |
10 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0023 others(7): Show |
10 | HG01884.hp2 HG02451.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079-7470_1079-746 others(14): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | ||||||
| chr12:100554392 | A | AACACACA others(5): Show |
5 | a0001c0001t0001g0150 a0001c0001t0001g0212 a0001c0001t0001g0245 others(2): Show |
5 | HG00597.hp2 HG00621.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-7472_1079-746 others(16): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | ||||||
| chr12:100554392 | AAC | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1079-7462_1079-746 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | ||||||
| chr12:100554392 | AACACACA others(3): Show |
A | 62 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(59): Show |
64 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.1079-7470_1079-746 others(14): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100554392 | ||||||
| chr12:100554621 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1079-7264G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554621 | |||||||
| chr12:100554697 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1079-7188C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554697 | |||||||
| chr12:100554737 | C | T | 35 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0077 others(32): Show |
36 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1079-7148C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554737 | |||||||
| chr12:100554744 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1079-7141G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554744 | |||||||
| chr12:100554938 | T | G | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1079-6947T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554938 | |||||||
| chr12:100554986 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1079-6899T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100554986 | |||||||
| chr12:100555529 | C | A | 1 | a0001c0001t0001g0039 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1079-6356C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100555529 | |||||||
| chr12:100555818 | T | C | 45 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0191 others(42): Show |
54 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1079-6067T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100555818 | |||||||
| chr12:100555840 | G | A | 94 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(91): Show |
96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1079-6045G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100555840 | |||||||
| chr12:100555916 | T | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0288 a0001c0001t0002g0051 |
3 | NA18969.hp2 NA18983.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1079-5969T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100555916 | |||||||
| chr12:100555976 | T | TTGCTCAA others(18): Show |
1 | a0001c0001t0001g0114 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1079-5907_1079-588 others(29): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100555976 | ||||||
| chr12:100556104 | T | G | 4 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079-5781T>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556104 | |||||||
| chr12:100556257 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0228 |
2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1079-5628C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556257 | |||||||
| chr12:100556292 | A | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0160 a0005c0004t0001g0161 |
3 | HG02895.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1079-5593A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556292 | |||||||
| chr12:100556422 | G | A | 4 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079-5463G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556422 | |||||||
| chr12:100556467 | C | CA | 14 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0093 others(11): Show |
14 | HG02145.hp2 HG02257.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1079-5415dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100556467 | ||||||
| chr12:100556471 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(103): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1079-5414G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556471 | |||||||
| chr12:100556482 | C | A | 35 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0077 others(32): Show |
36 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1079-5403C>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556482 | |||||||
| chr12:100556527 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1079-5358C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556527 | |||||||
| chr12:100556593 | G | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(104): Show |
110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1079-5292G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556593 | |||||||
| chr12:100556981 | T | C | 5 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
5 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-4904T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100556981 | |||||||
| chr12:100557084 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1079-4801G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557084 | |||||||
| chr12:100557198 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1079-4687G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557198 | |||||||
| chr12:100557240 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1079-4645G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557240 | |||||||
| chr12:100557245 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(102): Show |
108 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1079-4640G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557245 | |||||||
| chr12:100557269 | AT | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(102): Show |
108 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1079-4615delT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557269 | |||||||
| chr12:100557404 | CA | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0160 a0005c0004t0001g0161 |
3 | HG02895.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1079-4478delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100557404 | ||||||
| chr12:100557492 | C | T | 33 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0094 others(30): Show |
34 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.1079-4393C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557492 | |||||||
| chr12:100557536 | G | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
5 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-4349G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557536 | |||||||
| chr12:100557609 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(156): Show |
171 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1079-4276T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557609 | |||||||
| chr12:100557903 | C | G | 1 | a0001c0001t0001g0132 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1079-3982C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557903 | |||||||
| chr12:100557948 | G | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(233): Show |
251 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.1079-3937G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557948 | |||||||
| chr12:100557988 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1079-3897A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100557988 | |||||||
| chr12:100558032 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1079-3853A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558032 | |||||||
| chr12:100558119 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1079-3766G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558119 | |||||||
| chr12:100558127 | G | A | 4 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079-3758G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558127 | |||||||
| chr12:100558144 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1079-3741A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558144 | |||||||
| chr12:100558157 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1079-3728G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558157 | |||||||
| chr12:100558204 | C | CA | 51 | a0001c0001t0001g0085 a0001c0001t0001g0092 a0001c0001t0001g0093 others(48): Show |
60 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1079-3662dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558204 | ||||||
| chr12:100558204 | C | CAA | 14 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0084 others(11): Show |
14 | HG00558.hp1 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1079-3663_1079-366 others(6): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558204 | ||||||
| chr12:100558204 | CA | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(56): Show |
62 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.1079-3662delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558204 | ||||||
| chr12:100558281 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1079-3604G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558281 | |||||||
| chr12:100558306 | G | A | 5 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0084 others(2): Show |
5 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-3579G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558306 | |||||||
| chr12:100558330 | C | T | 48 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(45): Show |
57 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1079-3555C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558330 | |||||||
| chr12:100558349 | C | CA | 22 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(19): Show |
23 | HG00621.hp1 HG01433.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.1079-3509dupA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558349 | ||||||
| chr12:100558349 | CA | C | 12 | a0001c0001t0001g0074 a0001c0001t0001g0080 a0001c0001t0001g0082 others(9): Show |
12 | HG02451.hp2 HG02559.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1079-3509delA | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558349 | ||||||
| chr12:100558349 | CAAAAAAA | C | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): Show |
12 | HG01884.hp2 HG02809.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1079-3515_1079-350 others(11): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558349 | ||||||
| chr12:100558349 | CAAAAAAA others(1): Show |
C | 87 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(84): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1079-3516_1079-350 others(12): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100558349 | ||||||
| chr12:100558356 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1079-3529A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558356 | |||||||
| chr12:100558369 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1079-3516A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558369 | |||||||
| chr12:100558481 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1079-3404C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558481 | |||||||
| chr12:100558724 | G | C | 2 | a0001c0001t0002g0054 a0001c0001t0002g0057 |
2 | HG00408.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1079-3161G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558724 | |||||||
| chr12:100558759 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1079-3126T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558759 | |||||||
| chr12:100558817 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1079-3068G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558817 | |||||||
| chr12:100558832 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1079-3053G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558832 | |||||||
| chr12:100558943 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1079-2942C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100558943 | |||||||
| chr12:100559022 | A | G | 48 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(45): Show |
57 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1079-2863A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559022 | |||||||
| chr12:100559176 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1079-2709G>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559176 | |||||||
| chr12:100559189 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1079-2696G>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559189 | |||||||
| chr12:100559438 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG00735.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1079-2447C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559438 | |||||||
| chr12:100559499 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1079-2386C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559499 | |||||||
| chr12:100559517 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1079-2368G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559517 | |||||||
| chr12:100559582 | C | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0159 others(2): Show |
5 | HG02040.hp1 NA18967.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-2303C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559582 | |||||||
| chr12:100559737 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
105 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.1079-2148C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559737 | |||||||
| chr12:100559768 | C | T | 93 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(90): Show |
95 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1079-2117C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559768 | |||||||
| chr12:100559789 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(157): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1079-2096A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100559789 | |||||||
| chr12:100560227 | A | C | 99 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(96): Show |
101 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1079-1658A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560227 | |||||||
| chr12:100560322 | A | G | 1 | a0001c0001t0002g0047 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1079-1563A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560322 | |||||||
| chr12:100560336 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1079-1549C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560336 | |||||||
| chr12:100560337 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1079-1548G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560337 | |||||||
| chr12:100560344 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1079-1541G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560344 | |||||||
| chr12:100560363 | C | T | 74 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(71): Show |
77 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1079-1522C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560363 | |||||||
| chr12:100560397 | G | GT | 76 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(73): Show |
79 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1079-1487dupT | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100560397 | ||||||
| chr12:100560450 | G | A | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079-1435G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560450 | |||||||
| chr12:100560543 | G | A | 1 | a0001c0001t0002g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1079-1342G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560543 | |||||||
| chr12:100560633 | A | C | 93 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(90): Show |
95 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1079-1252A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560633 | |||||||
| chr12:100560687 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0071 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1079-1198C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560687 | |||||||
| chr12:100560979 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1079-906G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100560979 | |||||||
| chr12:100561037 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1079-848G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100561037 | |||||||
| chr12:100561343 | A | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(102): Show |
108 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1079-542A>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100561343 | |||||||
| chr12:100561354 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1079-531C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100561354 | |||||||
| chr12:100561401 | AAAAAT | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0037 others(3): Show |
7 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079-475_1079-471d others(7): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 100561401 | ||||||
| chr12:100561526 | C | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
5 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-359C>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100561526 | |||||||
| chr12:100561600 | C | G | 99 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(96): Show |
101 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1079-285C>G | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100561600 | |||||||
| chr12:100561620 | A | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG02451.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079-265A>T | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 9/10 | chr12 | 100561620 | |||||||
| chr12:100562252 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1192+254G>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 10/10 | chr12 | 100562252 | |||||||
| chr12:100562385 | A | C | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1192+387A>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 10/10 | chr12 | 100562385 | |||||||
| chr12:100562419 | C | CAGGAGGC others(1106): Show |
1 | a0001c0001t0001g0094 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1192+435_1192+436i others(1115): Show |
NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 100562419 | ||||||
| chr12:100562922 | T | C | 4 | a0001c0001t0001g0109 a0001c0001t0001g0122 a0001c0001t0001g0127 others(1): Show |
4 | HG02129.hp2 NA18940.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1193-329T>C | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 10/10 | chr12 | 100562922 | |||||||
| chr12:100563004 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1193-247T>A | NR1H4 | ENSG00000012504.15 | transcript | ENST00000392986.8 | protein_coding | 10/10 | chr12 | 100563004 |