Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9975 |
| ensemblid | ENSG00000174738.13 |
| hgncid | 7963 |
| symbol | NR1D2 |
| name | nuclear receptor subfamily 1 group D member 2 |
| refseq_nuc | NM_005126.5 |
| refseq_prot | NP_005117.3 |
| ensembl_nuc | ENST00000312521.9 |
| ensembl_prot | ENSP00000310006.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 23945286 |
| end | 23980617 |
| strand | + |
| ver | v1.2 |
| region | chr3:23945286-23980617 |
| region5000 | chr3:23940286-23985617 |
| regionname0 | NR1D2_chr3_23945286_23980617 |
| regionname5000 | NR1D2_chr3_23940286_23985617 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 579 | 368 | 78 | 79 | 153 | 12 | 44 | 121 | NR1D2_chr3_23940286_23985617 | NR1D2 | MEVNA others(574): Show |
chr3 | 23940286 | 23985617 |
| a0002 | 0/0 | 579 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NR1D2_chr3_23940286_23985617 | NR1D2 | MEVNA others(574): Show |
chr3 | 23940286 | 23985617 |
| a0003 | 0/0 | 579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | MEVNA others(574): Show |
chr3 | 23940286 | 23985617 |
| a0004 | 0/0 | 579 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | MEVNA others(574): Show |
chr3 | 23940286 | 23985617 |
| a0005 | 0/0 | 579 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | MEVNA others(574): Show |
chr3 | 23940286 | 23985617 |
| a0006 | 0/0 | 579 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | MEVNA others(574): Show |
chr3 | 23940286 | 23985617 |
| a0007 | 0/0 | 579 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | MEVNA others(574): Show |
chr3 | 23940286 | 23985617 |
| a0008 | 0/0 | 579 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | MEVNA others(574): Show |
chr3 | 23940286 | 23985617 |
| a0009 | 0/0 | 579 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | MEVNA others(574): Show |
chr3 | 23940286 | 23985617 |
| a0010 | 0/0 | 579 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | MEVNA others(574): Show |
chr3 | 23940286 | 23985617 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1737 | 344 | 70 | 73 | 149 | 12 | 38 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0001c0002 | 0/0 | 1737 | 10 | 0 | 0 | 4 | 0 | 6 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0001c0003 | 0/0 | 1737 | 9 | 8 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0001c0005 | 0/0 | 1737 | 3 | 0 | 3 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0001c0007 | 0/0 | 1737 | 2 | 0 | 2 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0002c0004 | 0/0 | 1737 | 3 | 0 | 0 | 3 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0003c0006 | 0/0 | 1737 | 2 | 2 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0004c0009 | 0/0 | 1737 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0005c0013 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0006c0014 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0007c0008 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0008c0010 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0009c0012 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 | ||
| a0010c0011 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | ATGGA others(1732): Show |
chr3 | 23940286 | 23985617 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5231 | 84 | 7 | 15 | 50 | 5 | 5 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0002 | 0/0 | 5234 | 74 | 8 | 16 | 33 | 4 | 13 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5229): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0003 | 0/0 | 5230 | 52 | 13 | 17 | 15 | 2 | 5 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5225): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0004 | 0/0 | 5231 | 48 | 3 | 1 | 40 | 0 | 4 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0005 | 0/0 | 5233 | 30 | 16 | 7 | 0 | 0 | 7 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5228): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0007 | 0/0 | 5231 | 8 | 5 | 2 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0008 | 0/0 | 5234 | 9 | 0 | 8 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5229): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0009 | 0/0 | 5231 | 6 | 5 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0011 | 0/0 | 5231 | 4 | 0 | 0 | 4 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0012 | 0/0 | 5233 | 4 | 0 | 3 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5228): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0013 | 0/0 | 5236 | 3 | 3 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5231): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0015 | 0/0 | 5234 | 2 | 2 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5229): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0016 | 0/0 | 5234 | 2 | 0 | 2 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5229): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0018 | 0/0 | 5225 | 2 | 2 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5220): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0019 | 0/0 | 5230 | 2 | 2 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5225): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0020 | 0/0 | 5230 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5225): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0021 | 0/0 | 5231 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0022 | 0/0 | 5225 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5220): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0023 | 0/0 | 5182 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5177): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0024 | 0/0 | 5234 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5229): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0025 | 0/0 | 5234 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5229): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0026 | 0/0 | 5233 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5228): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0027 | 0/0 | 5236 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5231): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0028 | 0/0 | 5230 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5225): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0029 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5224): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0030 | 0/0 | 5230 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5225): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0031 | 0/0 | 5231 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0032 | 0/0 | 5231 | 1 | 0 | 0 | 0 | 1 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0001c0001t0033 | 0/0 | 5231 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0001c0002t0010 | 0/0 | 5229 | 6 | 0 | 0 | 0 | 0 | 6 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5224): Show |
chr3 | 23940286 | 23985617 |
| a0001c0002t0014 | 0/0 | 5229 | 3 | 0 | 0 | 3 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5224): Show |
chr3 | 23940286 | 23985617 |
| a0001c0002t0034 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5224): Show |
chr3 | 23940286 | 23985617 |
| a0001c0003t0006 | 0/0 | 5229 | 9 | 8 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5224): Show |
chr3 | 23940286 | 23985617 |
| a0001c0005t0002 | 0/0 | 5234 | 3 | 0 | 3 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5229): Show |
chr3 | 23940286 | 23985617 |
| a0001c0007t0003 | 0/0 | 5230 | 2 | 0 | 2 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5225): Show |
chr3 | 23940286 | 23985617 |
| a0002c0004t0002 | 0/0 | 5234 | 2 | 0 | 0 | 2 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5229): Show |
chr3 | 23940286 | 23985617 |
| a0002c0004t0009 | 0/0 | 5231 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0003c0006t0017 | 0/0 | 5230 | 2 | 2 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5225): Show |
chr3 | 23940286 | 23985617 |
| a0004c0009t0001 | 0/0 | 5231 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0005c0013t0006 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5224): Show |
chr3 | 23940286 | 23985617 |
| a0006c0014t0006 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5224): Show |
chr3 | 23940286 | 23985617 |
| a0007c0008t0007 | 0/0 | 5231 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0008c0010t0002 | 0/0 | 5234 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5229): Show |
chr3 | 23940286 | 23985617 |
| a0009c0012t0004 | 0/0 | 5231 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| a0010c0011t0007 | 0/0 | 5231 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | GTCAG others(5226): Show |
chr3 | 23940286 | 23985617 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 4 | 1 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0017 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0002 | 0/0 | 10 | 0 | 5 | 3 | 0 | 2 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0003 | 0/0 | 7 | 1 | 0 | 4 | 0 | 2 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0007g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0008g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0008g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0008g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0008g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0008g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0008g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0008g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0009g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0009g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0011g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0011g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0011g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0012g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0012g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0012g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0013g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0013g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0013g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0015g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0015g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0016g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0016g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0018g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0018g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0019g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0019g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0020g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0021g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0022g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0023g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0024g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0025g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0026g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0027g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0028g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0029g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0030g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0031g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0032g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0001t0033g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0002t0010g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0002t0010g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0002t0010g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0002t0010g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0002t0010g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0002t0010g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0002t0014g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0002t0014g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0002t0034g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0003t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0003t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0003t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0003t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0003t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0003t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0003t0006g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0003t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0003t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0005t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0005t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0005t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0007t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0001c0007t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0002c0004t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0002c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0002c0004t0009g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0003c0006t0017g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0003c0006t0017g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0004c0009t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0005c0013t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0006c0014t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0007c0008t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0008c0010t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0009c0012t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| a0010c0011t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0243 | EUR | GBR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0199 | EUR | GBR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0234 | EUR | GBR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00408 | hp1 | a0001 | c0001 | t0011 | g0057 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00558 | hp2 | a0001 | c0002 | t0034 | g0311 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00609 | hp1 | a0002 | c0004 | t0002 | g0074 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0219 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00639 | hp2 | a0001 | c0005 | t0002 | g0155 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00642 | hp2 | a0001 | c0007 | t0003 | g0233 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | CHS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00738 | hp1 | a0001 | c0005 | t0002 | g0075 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00738 | hp2 | a0001 | c0001 | t0007 | g0222 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0036 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01070 | hp1 | a0001 | c0001 | t0012 | g0032 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01070 | hp2 | a0001 | c0005 | t0002 | g0176 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01071 | hp2 | a0001 | c0001 | t0012 | g0032 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01074 | hp1 | a0001 | c0001 | t0008 | g0188 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01081 | hp2 | a0001 | c0001 | t0016 | g0132 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01106 | hp2 | a0004 | c0009 | t0001 | g0017 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0269 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0196 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01175 | hp2 | a0001 | c0001 | t0008 | g0048 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0030 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01243 | hp1 | a0001 | c0003 | t0006 | g0256 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01261 | hp1 | a0001 | c0001 | t0016 | g0266 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0316 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01346 | hp2 | a0001 | c0001 | t0021 | g0200 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0295 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01361 | hp1 | a0001 | c0001 | t0008 | g0194 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0045 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01496 | hp1 | a0001 | c0001 | t0024 | g0195 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0198 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0161 | EUR | IBS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0134 | EUR | IBS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0297 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0293 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0201 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0292 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01993 | hp1 | a0001 | c0007 | t0003 | g0240 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | KHV | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02055 | hp1 | a0001 | c0003 | t0006 | g0252 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | KHV | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02083 | hp1 | a0001 | c0001 | t0025 | g0180 | EAS | KHV | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | KHV | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02132 | hp1 | a0001 | c0001 | t0028 | g0246 | EAS | KHV | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CDX | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | CDX | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CDX | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02258 | hp2 | a0001 | c0003 | t0006 | g0254 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0030 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0141 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0232 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02300 | hp2 | a0001 | c0001 | t0012 | g0279 | AMR | PEL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02602 | hp1 | a0001 | c0002 | t0010 | g0012 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02615 | hp1 | a0001 | c0001 | t0019 | g0213 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0303 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0315 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02717 | hp1 | a0001 | c0001 | t0013 | g0309 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0299 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02735 | hp1 | a0001 | c0001 | t0012 | g0280 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02738 | hp1 | a0001 | c0002 | t0010 | g0277 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02809 | hp1 | a0001 | c0001 | t0013 | g0308 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0226 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0310 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02818 | hp2 | a0001 | c0003 | t0006 | g0061 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0185 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02886 | hp2 | a0001 | c0001 | t0022 | g0216 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02895 | hp1 | a0001 | c0001 | t0015 | g0290 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02895 | hp2 | a0001 | c0001 | t0033 | g0135 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0304 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02897 | hp2 | a0001 | c0001 | t0015 | g0283 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02922 | hp1 | a0003 | c0006 | t0017 | g0214 | AFR | ESN | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02922 | hp2 | a0001 | c0001 | t0020 | g0218 | AFR | ESN | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0305 | AFR | ESN | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0289 | AFR | ESN | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02976 | hp1 | a0001 | c0001 | t0018 | g0217 | AFR | ESN | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0225 | AFR | ESN | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03017 | hp2 | a0001 | c0001 | t0027 | g0288 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0306 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03041 | hp2 | a0001 | c0003 | t0006 | g0253 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0300 | AFR | MSL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03098 | hp2 | a0001 | c0001 | t0018 | g0271 | AFR | MSL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0274 | AFR | ESN | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03195 | hp1 | a0001 | c0003 | t0006 | g0258 | AFR | ESN | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03195 | hp2 | a0001 | c0003 | t0006 | g0062 | AFR | ESN | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0184 | AFR | MSL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | MSL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | MSL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | MSL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0296 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03516 | hp1 | a0001 | c0001 | t0029 | g0228 | AFR | ESN | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03516 | hp2 | a0006 | c0014 | t0006 | g0052 | AFR | ESN | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0136 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0301 | AFR | MSL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03579 | hp2 | a0001 | c0003 | t0006 | g0257 | AFR | MSL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0223 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | STU | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03688 | hp2 | a0001 | c0002 | t0010 | g0313 | SAS | STU | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0291 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0079 | SAS | BEB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | BEB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0024 | SAS | BEB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | BEB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03927 | hp2 | a0001 | c0002 | t0010 | g0276 | SAS | BEB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0285 | SAS | BEB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | BEB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0302 | SAS | BEB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG04184 | hp2 | a0001 | c0002 | t0010 | g0312 | SAS | BEB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG04199 | hp1 | a0001 | c0001 | t0009 | g0267 | SAS | STU | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0275 | SAS | STU | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0286 | SAS | STU | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG04204 | hp2 | a0001 | c0002 | t0010 | g0278 | SAS | STU | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18522 | hp1 | a0007 | c0008 | t0007 | g0260 | AFR | YRI | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0298 | AFR | YRI | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | CHB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | CHB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18747 | hp2 | a0008 | c0010 | t0002 | g0098 | EAS | CHB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | YRI | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | YRI | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0076 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18946 | hp2 | a0002 | c0004 | t0009 | g0154 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18950 | hp2 | a0001 | c0002 | t0014 | g0314 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18954 | hp2 | a0001 | c0002 | t0014 | g0012 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18959 | hp2 | a0001 | c0002 | t0014 | g0012 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18967 | hp2 | a0002 | c0004 | t0002 | g0151 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18968 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18971 | hp2 | a0001 | c0001 | t0031 | g0001 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18974 | hp2 | a0001 | c0001 | t0011 | g0126 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18981 | hp1 | a0001 | c0001 | t0026 | g0307 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19003 | hp1 | a0001 | c0001 | t0030 | g0238 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19010 | hp2 | a0001 | c0001 | t0011 | g0123 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | LWK | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0224 | AFR | LWK | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19063 | hp1 | a0001 | c0001 | t0023 | g0143 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19074 | hp1 | a0009 | c0012 | t0004 | g0208 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | YRI | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | ASW | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0055 | AFR | ASW | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0162 | EUR | TSI | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA20805 | hp2 | a0001 | c0001 | t0032 | g0220 | EUR | TSI | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | GIH | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0287 | SAS | GIH | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0294 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02109 | hp1 | a0003 | c0006 | t0017 | g0215 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02109 | hp2 | a0005 | c0013 | t0006 | g0259 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0183 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | ACB | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0284 | AFR | MSL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG03471 | hp2 | a0001 | c0003 | t0006 | g0255 | AFR | MSL | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0054 | AFR | USA | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| HG06807 | hp2 | a0001 | c0001 | t0019 | g0212 | AFR | USA | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA21309 | hp1 | a0010 | c0011 | t0007 | g0221 | AFR | LWK | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | LWK | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0065 | REF | REF | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0017 | REF | REF | NR1D2_chr3_23940286_23985617 | NR1D2 | chr3 | 23940286 | 23985617 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:23962073 | G | A | 1 | a0003 | 2 | HG02109.hp1 HG02922.hp1 |
missense_variant | MODERATE | c.614G>A | p.Gly205Asp | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/8 | 907/5231 | 614/1740 | 205/579 | chr3 | 23962073 | |||
| chr3:23962099 | G | A | 1 | a0007 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.640G>A | p.Glu214Lys | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/8 | 933/5231 | 640/1740 | 214/579 | chr3 | 23962099 | |||
| chr3:23962155 | A | C | 1 | a0009 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.696A>C | p.Gln232His | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/8 | 989/5231 | 696/1740 | 232/579 | chr3 | 23962155 | |||
| chr3:23962330 | A | G | 1 | a0010 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.871A>G | p.Met291Val | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/8 | 1164/5231 | 871/1740 | 291/579 | chr3 | 23962330 | |||
| chr3:23962417 | G | A | 1 | a0004 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.958G>A | p.Gly320Arg | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/8 | 1251/5231 | 958/1740 | 320/579 | chr3 | 23962417 | |||
| chr3:23962454 | A | G | 1 | a0006 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.995A>G | p.Asn332Ser | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/8 | 1288/5231 | 995/1740 | 332/579 | chr3 | 23962454 | |||
| chr3:23962468 | T | G | 1 | a0005 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1009T>G | p.Cys337Gly | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/8 | 1302/5231 | 1009/1740 | 337/579 | chr3 | 23962468 | |||
| chr3:23965137 | A | G | 1 | a0008 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.1307A>G | p.Asn436Ser | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/8 | 1600/5231 | 1307/1740 | 436/579 | chr3 | 23965137 | |||
| chr3:23967831 | G | A | 1 | a0002 | 3 | HG00609.hp1 NA18946.hp2 NA18967.hp2 |
missense_variant | MODERATE | c.1351G>A | p.Ala451Thr | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/8 | 1644/5231 | 1351/1740 | 451/579 | chr3 | 23967831 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:23945593 | A | G | 1 | a0001c0007 | 2 | HG00642.hp2 HG01993.hp1 |
splice_region_variant&synonymous_variant | LOW | c.15A>G | p.Ala5Ala | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | 308/5231 | 15/1740 | 5/579 | chr3 | 23945593 | |||
| chr3:23954565 | C | T | 1 | a0001c0002 | 10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
synonymous_variant | LOW | c.45C>T | p.Ser15Ser | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 2/8 | 338/5231 | 45/1740 | 15/579 | chr3 | 23954565 | |||
| chr3:23956056 | A | G | 1 | a0001c0005 | 3 | HG00639.hp2 HG00738.hp1 HG01070.hp2 |
synonymous_variant | LOW | c.303A>G | p.Leu101Leu | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/8 | 596/5231 | 303/1740 | 101/579 | chr3 | 23956056 | |||
| chr3:23956113 | C | T | 3 | a0001c0003 a0005c0013 a0006c0014 |
11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
synonymous_variant | LOW | c.360C>T | p.Cys120Cys | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/8 | 653/5231 | 360/1740 | 120/579 | chr3 | 23956113 | |||
| chr3:23965006 | G | A | 1 | a0001c0002 | 10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
synonymous_variant | LOW | c.1176G>A | p.Val392Val | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/8 | 1469/5231 | 1176/1740 | 392/579 | chr3 | 23965006 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:23945329 | G | A | 1 | a0001c0001t0013 | 3 | HG02717.hp1 HG02809.hp1 HG02818.hp1 |
5_prime_UTR_variant | MODIFIER | c.-250G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | 250 | chr3 | 23945329 | ||||||
| chr3:23945356 | A | T | 4 | a0001c0001t0033 a0001c0002t0010 a0001c0002t0014 others(1): Show |
11 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-223A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | 223 | chr3 | 23945356 | ||||||
| chr3:23945368 | G | A | 1 | a0001c0001t0020 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-211G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | 211 | chr3 | 23945368 | ||||||
| chr3:23945393 | C | G | 1 | a0001c0001t0032 | 1 | NA20805.hp2 | 5_prime_UTR_variant | MODIFIER | c.-186C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | 186 | chr3 | 23945393 | ||||||
| chr3:23945404 | C | T | 1 | a0001c0001t0031 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-175C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | 175 | chr3 | 23945404 | ||||||
| chr3:23945439 | A | C | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(38): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
5_prime_UTR_variant | MODIFIER | c.-140A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | 140 | chr3 | 23945439 | ||||||
| chr3:23945456 | C | T | 4 | a0001c0001t0013 a0001c0002t0010 a0001c0002t0014 others(1): Show |
13 | HG00558.hp2 HG02602.hp1 HG02717.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-123C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | 123 | chr3 | 23945456 | ||||||
| chr3:23945492 | C | G | 16 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0018 others(13): Show |
86 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(83): Show |
5_prime_UTR_variant | MODIFIER | c.-87C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | 87 | chr3 | 23945492 | ||||||
| chr3:23945508 | C | T | 1 | a0001c0001t0019 | 2 | HG02615.hp1 HG06807.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-71C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | chr3 | 23945508 | |||||||
| chr3:23945511 | A | AGGC | 16 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(13): Show |
141 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(138): Show |
5_prime_UTR_variant | MODIFIER | c.-54_-52dupGCG | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | 51 | INFO_REALIGN_3_PRIME | chr3 | 23945511 | |||||
| chr3:23945511 | A | AGGCGGC | 2 | a0001c0001t0013 a0001c0001t0027 |
4 | HG02717.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-57_-52dupGCGGCG | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | 51 | INFO_REALIGN_3_PRIME | chr3 | 23945511 | |||||
| chr3:23945534 | C | G | 1 | a0001c0001t0016 | 2 | HG01081.hp2 HG01261.hp1 |
5_prime_UTR_variant | MODIFIER | c.-45C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/8 | 45 | chr3 | 23945534 | ||||||
| chr3:23977470 | A | G | 2 | a0001c0001t0018 a0001c0001t0022 |
3 | HG02886.hp2 HG02976.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*51A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 51 | chr3 | 23977470 | ||||||
| chr3:23977836 | A | C | 5 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0015 others(2): Show |
38 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*417A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 417 | chr3 | 23977836 | ||||||
| chr3:23977892 | TTACTC | T | 2 | a0001c0001t0018 a0001c0001t0022 |
3 | HG02886.hp2 HG02976.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*477_*481delTCTAC | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 477 | INFO_REALIGN_3_PRIME | chr3 | 23977892 | |||||
| chr3:23977977 | C | T | 1 | a0001c0001t0030 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*558C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 558 | chr3 | 23977977 | ||||||
| chr3:23978087 | TTTTCTTA others(45): Show |
T | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*671_*722delTCTTAT others(46): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 671 | INFO_REALIGN_3_PRIME | chr3 | 23978087 | |||||
| chr3:23978202 | T | A | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*783T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 783 | chr3 | 23978202 | ||||||
| chr3:23978218 | A | G | 1 | a0001c0001t0004 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 799 | chr3 | 23978218 | ||||||
| chr3:23978226 | T | G | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*807T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 807 | chr3 | 23978226 | ||||||
| chr3:23978228 | T | C | 1 | a0001c0001t0028 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*809T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 809 | chr3 | 23978228 | ||||||
| chr3:23978240 | A | C | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*821A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 821 | chr3 | 23978240 | ||||||
| chr3:23978241 | T | A | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*822T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 822 | chr3 | 23978241 | ||||||
| chr3:23978243 | T | G | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*824T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 824 | chr3 | 23978243 | ||||||
| chr3:23978244 | G | T | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*825G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 825 | chr3 | 23978244 | ||||||
| chr3:23978252 | T | C | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*833T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 833 | chr3 | 23978252 | ||||||
| chr3:23978254 | A | T | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*835A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 835 | chr3 | 23978254 | ||||||
| chr3:23978257 | T | C | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*838T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 838 | chr3 | 23978257 | ||||||
| chr3:23978259 | T | G | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*840T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 840 | chr3 | 23978259 | ||||||
| chr3:23978265 | T | A | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*846T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 846 | chr3 | 23978265 | ||||||
| chr3:23978274 | T | A | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*855T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 855 | chr3 | 23978274 | ||||||
| chr3:23978275 | T | A | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*856T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 856 | chr3 | 23978275 | ||||||
| chr3:23978276 | T | A | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*857T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 857 | chr3 | 23978276 | ||||||
| chr3:23978277 | T | A | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*858T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 858 | chr3 | 23978277 | ||||||
| chr3:23978282 | T | C | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*863T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 863 | chr3 | 23978282 | ||||||
| chr3:23978283 | G | T | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*864G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 864 | chr3 | 23978283 | ||||||
| chr3:23978284 | T | A | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 865 | chr3 | 23978284 | ||||||
| chr3:23978285 | G | A | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*866G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 866 | chr3 | 23978285 | ||||||
| chr3:23978286 | A | C | 1 | a0001c0001t0023 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*867A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 867 | chr3 | 23978286 | ||||||
| chr3:23978471 | C | G | 1 | a0001c0001t0011 | 4 | HG00408.hp1 NA18968.hp2 NA18974.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1052C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 1052 | chr3 | 23978471 | ||||||
| chr3:23978485 | CA | C | 17 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0012 others(14): Show |
113 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1078delA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 1078 | INFO_REALIGN_3_PRIME | chr3 | 23978485 | |||||
| chr3:23978485 | CAA | C | 4 | a0001c0001t0029 a0001c0003t0006 a0005c0013t0006 others(1): Show |
12 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1077_*1078delAA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 1077 | INFO_REALIGN_3_PRIME | chr3 | 23978485 | |||||
| chr3:23978668 | G | T | 2 | a0001c0001t0013 a0003c0006t0017 |
5 | HG02109.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1249G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 1249 | chr3 | 23978668 | ||||||
| chr3:23978713 | C | T | 1 | a0001c0002t0014 | 3 | NA18950.hp2 NA18954.hp2 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1294C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 1294 | chr3 | 23978713 | ||||||
| chr3:23978961 | C | T | 1 | a0001c0002t0034 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1542C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 1542 | chr3 | 23978961 | ||||||
| chr3:23979243 | A | G | 1 | a0001c0001t0026 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1824A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 1824 | chr3 | 23979243 | ||||||
| chr3:23979401 | A | G | 1 | a0001c0001t0025 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1982A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 1982 | chr3 | 23979401 | ||||||
| chr3:23979479 | CAATT | C | 3 | a0001c0002t0010 a0001c0002t0014 a0001c0002t0034 |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2063_*2066delTTAA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 2063 | INFO_REALIGN_3_PRIME | chr3 | 23979479 | |||||
| chr3:23979498 | G | T | 2 | a0001c0001t0021 a0001c0001t0024 |
2 | HG01346.hp2 HG01496.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2079G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 2079 | chr3 | 23979498 | ||||||
| chr3:23979699 | A | G | 1 | a0001c0001t0012 | 4 | HG01070.hp1 HG01071.hp2 HG02300.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2280A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 2280 | chr3 | 23979699 | ||||||
| chr3:23980285 | A | G | 5 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0021 others(2): Show |
60 | HG00423.hp1 HG00438.hp1 HG00673.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2866A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 2866 | chr3 | 23980285 | ||||||
| chr3:23980445 | T | C | 3 | a0001c0003t0006 a0005c0013t0006 a0006c0014t0006 |
11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3026T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 8/8 | 3026 | chr3 | 23980445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:23945662 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.16+68G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23945662 | |||||||
| chr3:23945727 | C | T | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | NA18612.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.16+133C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23945727 | |||||||
| chr3:23945735 | G | T | 1 | a0001c0001t0003g0316 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.16+141G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23945735 | |||||||
| chr3:23945770 | C | T | 47 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(44): Show |
51 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.16+176C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23945770 | |||||||
| chr3:23945810 | C | G | 47 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(44): Show |
51 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.16+216C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23945810 | |||||||
| chr3:23945825 | G | GC | 24 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(21): Show |
25 | HG00741.hp1 HG01109.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.16+239dupC | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23945825 | ||||||
| chr3:23945833 | C | T | 1 | a0001c0001t0012g0032 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.16+239C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23945833 | |||||||
| chr3:23945904 | C | T | 1 | a0001c0001t0005g0315 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.16+310C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23945904 | |||||||
| chr3:23946026 | C | CG | 10 | a0001c0001t0001g0265 a0001c0001t0003g0272 a0001c0001t0003g0273 others(7): Show |
11 | HG01109.hp2 HG01261.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.16+437dupG | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23946026 | ||||||
| chr3:23946030 | G | GGC | 7 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0001g0059 others(4): Show |
7 | HG00408.hp1 HG00408.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.16+451_16+452dupGC | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23946030 | ||||||
| chr3:23946047 | T | C | 2 | a0001c0001t0007g0054 a0001c0001t0007g0055 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.16+453T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946047 | |||||||
| chr3:23946090 | G | T | 4 | a0001c0001t0003g0053 a0001c0001t0003g0262 a0001c0001t0003g0263 others(1): Show |
4 | HG02280.hp1 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+496G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946090 | |||||||
| chr3:23946098 | G | A | 1 | a0001c0001t0003g0063 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.16+504G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946098 | |||||||
| chr3:23946147 | T | A | 1 | a0001c0001t0003g0064 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.16+553T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946147 | |||||||
| chr3:23946264 | G | A | 7 | a0001c0001t0004g0004 a0001c0001t0004g0013 a0001c0001t0004g0029 others(4): Show |
11 | HG00673.hp2 NA18940.hp1 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.16+670G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946264 | |||||||
| chr3:23946274 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.16+680C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946274 | |||||||
| chr3:23946351 | A | G | 120 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0026 others(117): Show |
138 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.16+757A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946351 | |||||||
| chr3:23946417 | G | T | 12 | a0001c0003t0006g0061 a0001c0003t0006g0062 a0001c0003t0006g0252 others(9): Show |
12 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.16+823G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946417 | |||||||
| chr3:23946441 | C | G | 47 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(44): Show |
51 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.16+847C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946441 | |||||||
| chr3:23946455 | T | G | 47 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(44): Show |
51 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.16+861T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946455 | |||||||
| chr3:23946503 | C | CA | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
19 | HG00609.hp1 HG00735.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.16+917dupA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23946503 | ||||||
| chr3:23946511 | A | G | 36 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0027 others(33): Show |
49 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+917A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946511 | |||||||
| chr3:23946512 | C | G | 1 | a0001c0001t0002g0210 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.16+918C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946512 | |||||||
| chr3:23946518 | G | T | 47 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(44): Show |
51 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.16+924G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946518 | |||||||
| chr3:23946543 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.16+949C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946543 | |||||||
| chr3:23946622 | G | C | 41 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0026 others(38): Show |
55 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.16+1028G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946622 | |||||||
| chr3:23946689 | G | T | 1 | a0001c0001t0001g0209 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.16+1095G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23946689 | |||||||
| chr3:23947046 | T | C | 49 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(46): Show |
53 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.16+1452T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947046 | |||||||
| chr3:23947065 | T | A | 49 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(46): Show |
53 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.16+1471T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947065 | |||||||
| chr3:23947133 | A | T | 2 | a0001c0001t0007g0225 a0001c0001t0007g0226 |
2 | HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.16+1539A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947133 | |||||||
| chr3:23947194 | C | T | 49 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(46): Show |
53 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.16+1600C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947194 | |||||||
| chr3:23947260 | T | G | 1 | a0001c0001t0003g0049 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.16+1666T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947260 | |||||||
| chr3:23947325 | CATT | C | 3 | a0001c0001t0012g0032 a0001c0001t0012g0279 a0001c0001t0012g0280 |
4 | HG01070.hp1 HG01071.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+1734_16+1736del others(3): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23947325 | ||||||
| chr3:23947420 | G | GT | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.16+1832dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23947420 | ||||||
| chr3:23947461 | G | A | 49 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(46): Show |
53 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.16+1867G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947461 | |||||||
| chr3:23947513 | G | A | 1 | a0001c0001t0003g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.16+1919G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947513 | |||||||
| chr3:23947559 | C | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | NA19056.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.16+1965C>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947559 | |||||||
| chr3:23947689 | A | AGTGTAGG others(100): Show |
1 | a0001c0001t0002g0186 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.16+2096_16+2202dup others(107): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23947689 | ||||||
| chr3:23947723 | T | G | 4 | a0001c0001t0002g0037 a0001c0001t0002g0082 a0001c0001t0002g0083 others(1): Show |
4 | HG02145.hp1 HG02615.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+2129T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947723 | |||||||
| chr3:23947724 | C | T | 11 | a0001c0001t0007g0054 a0001c0001t0007g0055 a0001c0001t0007g0219 others(8): Show |
11 | HG00639.hp1 HG00738.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.16+2130C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947724 | |||||||
| chr3:23947745 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.16+2151G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947745 | |||||||
| chr3:23947763 | C | G | 1 | a0001c0001t0004g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.16+2169C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947763 | |||||||
| chr3:23947792 | T | C | 120 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0026 others(117): Show |
138 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.16+2198T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947792 | |||||||
| chr3:23947795 | C | CT | 43 | a0001c0001t0002g0199 a0001c0001t0004g0003 a0001c0001t0004g0004 others(40): Show |
59 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.16+2202dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23947795 | ||||||
| chr3:23947797 | A | G | 38 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0027 others(35): Show |
51 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.16+2203A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947797 | |||||||
| chr3:23947800 | A | T | 120 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0026 others(117): Show |
138 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.16+2206A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947800 | |||||||
| chr3:23947827 | C | A | 5 | a0001c0001t0007g0054 a0001c0001t0007g0055 a0001c0001t0007g0219 others(2): Show |
5 | HG00639.hp1 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+2233C>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947827 | |||||||
| chr3:23947851 | C | G | 1 | a0001c0001t0002g0085 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.16+2257C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23947851 | |||||||
| chr3:23948118 | CA | C | 71 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0026 others(68): Show |
85 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.16+2538delA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23948118 | ||||||
| chr3:23948146 | C | A | 8 | a0001c0001t0003g0053 a0001c0001t0003g0262 a0001c0001t0003g0263 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.16+2552C>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23948146 | |||||||
| chr3:23948146 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.16+2552C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23948146 | |||||||
| chr3:23948375 | C | T | 11 | a0001c0003t0006g0061 a0001c0003t0006g0062 a0001c0003t0006g0252 others(8): Show |
11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.16+2781C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23948375 | |||||||
| chr3:23948385 | G | A | 1 | a0001c0001t0002g0086 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.16+2791G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23948385 | |||||||
| chr3:23948425 | T | C | 35 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(32): Show |
38 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.16+2831T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23948425 | |||||||
| chr3:23948750 | A | G | 76 | a0001c0001t0002g0035 a0001c0001t0002g0178 a0001c0001t0002g0179 others(73): Show |
90 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.16+3156A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23948750 | |||||||
| chr3:23948793 | T | C | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.16+3199T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23948793 | |||||||
| chr3:23948923 | A | G | 125 | a0001c0001t0002g0035 a0001c0001t0002g0178 a0001c0001t0002g0179 others(122): Show |
143 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.16+3329A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23948923 | |||||||
| chr3:23948968 | C | G | 11 | a0001c0001t0007g0054 a0001c0001t0007g0055 a0001c0001t0007g0219 others(8): Show |
11 | HG00639.hp1 HG00738.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.16+3374C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23948968 | |||||||
| chr3:23949078 | C | T | 2 | a0001c0001t0005g0315 a0001c0001t0020g0218 |
2 | HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.16+3484C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949078 | |||||||
| chr3:23949085 | G | A | 1 | a0001c0002t0034g0311 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.16+3491G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949085 | |||||||
| chr3:23949095 | G | A | 76 | a0001c0001t0002g0035 a0001c0001t0002g0178 a0001c0001t0002g0179 others(73): Show |
90 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.16+3501G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949095 | |||||||
| chr3:23949142 | G | A | 3 | a0001c0003t0006g0253 a0001c0003t0006g0254 a0001c0003t0006g0255 |
3 | HG02258.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.16+3548G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949142 | |||||||
| chr3:23949338 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0177 |
2 | HG02523.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.16+3744C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949338 | |||||||
| chr3:23949364 | G | GA | 10 | a0001c0001t0001g0087 a0001c0001t0002g0034 a0001c0003t0006g0061 others(7): Show |
10 | HG01243.hp1 HG02258.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.16+3781dupA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23949364 | ||||||
| chr3:23949400 | T | C | 1 | a0001c0001t0003g0230 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.16+3806T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949400 | |||||||
| chr3:23949517 | T | C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG01516.hp2 HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.16+3923T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949517 | |||||||
| chr3:23949533 | C | T | 1 | a0001c0001t0004g0025 | 2 | HG00423.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.16+3939C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949533 | |||||||
| chr3:23949535 | A | G | 35 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(32): Show |
38 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.16+3941A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949535 | |||||||
| chr3:23949595 | C | G | 1 | a0001c0003t0006g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.16+4001C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949595 | |||||||
| chr3:23949737 | C | T | 1 | a0001c0001t0003g0316 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.16+4143C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949737 | |||||||
| chr3:23949792 | GACTTGAA others(4): Show |
G | 1 | a0001c0001t0005g0281 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.16+4200_16+4210del others(11): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23949792 | ||||||
| chr3:23949806 | C | A | 22 | a0001c0001t0007g0054 a0001c0001t0007g0055 a0001c0001t0007g0219 others(19): Show |
22 | HG00639.hp1 HG00738.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.16+4212C>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949806 | |||||||
| chr3:23949837 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.16+4243G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949837 | |||||||
| chr3:23949891 | A | G | 1 | a0001c0001t0007g0219 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.16+4297A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23949891 | |||||||
| chr3:23950174 | A | T | 1 | a0001c0001t0005g0275 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.17-4363A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950174 | |||||||
| chr3:23950212 | A | G | 1 | a0001c0001t0004g0024 | 2 | HG02015.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.17-4325A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950212 | |||||||
| chr3:23950226 | C | G | 120 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0026 others(117): Show |
138 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.17-4311C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950226 | |||||||
| chr3:23950399 | A | G | 4 | a0001c0001t0007g0054 a0001c0001t0007g0055 a0001c0001t0007g0225 others(1): Show |
4 | HG02809.hp2 HG02976.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-4138A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950399 | |||||||
| chr3:23950405 | C | T | 1 | a0001c0001t0008g0076 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.17-4132C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950405 | |||||||
| chr3:23950438 | C | T | 44 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(41): Show |
48 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.17-4099C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950438 | |||||||
| chr3:23950514 | A | C | 4 | a0001c0001t0002g0037 a0001c0001t0002g0082 a0001c0001t0002g0083 others(1): Show |
4 | HG02145.hp1 HG02615.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-4023A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950514 | |||||||
| chr3:23950577 | A | G | 1 | a0001c0001t0026g0307 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.17-3960A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950577 | |||||||
| chr3:23950885 | C | CTTTTCT | 12 | a0001c0001t0005g0274 a0001c0001t0005g0282 a0001c0001t0005g0284 others(9): Show |
12 | HG02109.hp1 HG02717.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.17-3651_17-3646dup others(6): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23950885 | ||||||
| chr3:23950892 | C | T | 120 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0026 others(117): Show |
138 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.17-3645C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950892 | |||||||
| chr3:23950902 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.17-3635C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950902 | |||||||
| chr3:23950902 | CT | C | 15 | a0001c0001t0001g0177 a0001c0001t0002g0093 a0001c0001t0002g0094 others(12): Show |
15 | HG01074.hp1 HG01243.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.17-3616delT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23950902 | ||||||
| chr3:23950902 | CTT | C | 60 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0026 others(57): Show |
74 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.17-3617_17-3616del others(2): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23950902 | ||||||
| chr3:23950903 | T | TTTTTC | 33 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0275 others(30): Show |
37 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.17-3630_17-3629ins others(5): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23950903 | ||||||
| chr3:23950908 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.17-3629T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950908 | |||||||
| chr3:23950909 | T | C | 2 | a0001c0001t0005g0287 a0001c0001t0027g0288 |
2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.17-3628T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950909 | |||||||
| chr3:23950924 | G | T | 35 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(32): Show |
38 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.17-3613G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950924 | |||||||
| chr3:23950998 | C | G | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.17-3539C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23950998 | |||||||
| chr3:23951052 | T | C | 4 | a0001c0001t0002g0038 a0001c0001t0002g0070 a0001c0001t0002g0095 others(1): Show |
4 | HG00735.hp2 HG01261.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-3485T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23951052 | |||||||
| chr3:23951228 | T | G | 1 | a0001c0001t0002g0039 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.17-3309T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23951228 | |||||||
| chr3:23951252 | T | C | 2 | a0001c0001t0002g0097 a0008c0010t0002g0098 |
2 | HG02083.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.17-3285T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23951252 | |||||||
| chr3:23951314 | A | G | 4 | a0001c0001t0003g0028 a0001c0001t0003g0250 a0001c0001t0003g0251 others(1): Show |
5 | HG00642.hp1 HG00741.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-3223A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23951314 | |||||||
| chr3:23951448 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.17-3089A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23951448 | |||||||
| chr3:23951568 | A | G | 1 | a0001c0003t0006g0252 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.17-2969A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23951568 | |||||||
| chr3:23951677 | C | G | 1 | a0001c0001t0008g0076 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.17-2860C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23951677 | |||||||
| chr3:23951697 | G | A | 35 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(32): Show |
38 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.17-2840G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23951697 | |||||||
| chr3:23951771 | TTCC | T | 10 | a0001c0001t0007g0054 a0001c0001t0007g0055 a0001c0001t0007g0219 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.17-2764_17-2762del others(3): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23951771 | ||||||
| chr3:23951789 | C | T | 1 | a0006c0014t0006g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.17-2748C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23951789 | |||||||
| chr3:23951941 | A | G | 1 | a0001c0001t0003g0249 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.17-2596A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23951941 | |||||||
| chr3:23951946 | A | G | 248 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0014 others(245): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.17-2591A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23951946 | |||||||
| chr3:23952017 | A | G | 14 | a0001c0001t0013g0308 a0001c0001t0013g0309 a0001c0001t0013g0310 others(11): Show |
15 | HG00558.hp2 HG02109.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.17-2520A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952017 | |||||||
| chr3:23952020 | G | A | 1 | a0001c0002t0034g0311 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.17-2517G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952020 | |||||||
| chr3:23952094 | G | A | 1 | a0001c0001t0004g0190 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.17-2443G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952094 | |||||||
| chr3:23952124 | T | A | 1 | a0001c0001t0003g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.17-2413T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952124 | |||||||
| chr3:23952150 | C | A | 1 | a0001c0001t0001g0265 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.17-2387C>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952150 | |||||||
| chr3:23952151 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.17-2386A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952151 | |||||||
| chr3:23952154 | G | C | 1 | a0001c0001t0001g0265 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.17-2383G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952154 | |||||||
| chr3:23952305 | T | C | 1 | a0006c0014t0006g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.17-2232T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952305 | |||||||
| chr3:23952333 | A | G | 1 | a0007c0008t0007g0260 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.17-2204A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952333 | |||||||
| chr3:23952334 | T | G | 5 | a0001c0001t0003g0049 a0001c0001t0003g0053 a0001c0001t0003g0262 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-2203T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952334 | |||||||
| chr3:23952441 | G | C | 4 | a0001c0001t0001g0040 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | HG01069.hp2 HG01361.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-2096G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952441 | |||||||
| chr3:23952481 | G | C | 1 | a0001c0001t0032g0220 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.17-2056G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952481 | |||||||
| chr3:23952545 | A | G | 1 | a0001c0001t0003g0251 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.17-1992A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952545 | |||||||
| chr3:23952587 | G | A | 39 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0027 others(36): Show |
52 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.17-1950G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952587 | |||||||
| chr3:23952704 | C | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0211 |
3 | HG01934.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.17-1833C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952704 | |||||||
| chr3:23952725 | C | CA | 44 | a0001c0001t0002g0060 a0001c0001t0002g0085 a0001c0001t0002g0133 others(41): Show |
46 | HG00609.hp1 HG00639.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.17-1796dupA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23952725 | ||||||
| chr3:23952725 | C | CAA | 9 | a0001c0001t0005g0315 a0001c0003t0006g0061 a0001c0003t0006g0062 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.17-1797_17-1796dup others(2): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23952725 | ||||||
| chr3:23952725 | CA | C | 7 | a0001c0001t0001g0265 a0001c0001t0003g0248 a0001c0001t0004g0069 others(4): Show |
7 | HG00558.hp2 HG01070.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.17-1796delA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23952725 | ||||||
| chr3:23952855 | G | C | 2 | a0001c0001t0009g0136 a0001c0001t0033g0135 |
2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.17-1682G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952855 | |||||||
| chr3:23952911 | A | T | 2 | a0001c0001t0018g0217 a0001c0001t0018g0271 |
2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.17-1626A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23952911 | |||||||
| chr3:23952956 | GT | G | 12 | a0001c0001t0001g0102 a0001c0001t0007g0054 a0001c0001t0007g0055 others(9): Show |
12 | HG00639.hp1 HG00738.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.17-1570delT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23952956 | ||||||
| chr3:23953005 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.17-1532G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23953005 | |||||||
| chr3:23953050 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.17-1487A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23953050 | |||||||
| chr3:23953297 | T | C | 5 | a0001c0001t0007g0222 a0001c0001t0007g0223 a0001c0001t0007g0224 others(2): Show |
5 | HG00738.hp2 HG03669.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-1240T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23953297 | |||||||
| chr3:23953342 | C | CA | 47 | a0001c0001t0001g0005 a0001c0001t0001g0056 a0001c0001t0001g0071 others(44): Show |
50 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.17-1166dupA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23953342 | ||||||
| chr3:23953342 | CA | C | 67 | a0001c0001t0001g0125 a0001c0001t0002g0094 a0001c0001t0002g0134 others(64): Show |
83 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.17-1166delA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23953342 | ||||||
| chr3:23953342 | CAA | C | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0059 others(44): Show |
67 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.17-1167_17-1166del others(2): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23953342 | ||||||
| chr3:23953342 | CAAAAAAA others(1): Show |
C | 33 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(30): Show |
35 | HG01123.hp1 HG01192.hp1 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.17-1173_17-1166del others(8): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23953342 | ||||||
| chr3:23953342 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0012g0032 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.17-1182_17-1166del others(17): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 23953342 | ||||||
| chr3:23953348 | A | C | 1 | a0001c0002t0034g0311 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.17-1189A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23953348 | |||||||
| chr3:23953406 | A | G | 1 | a0001c0001t0001g0007 | 3 | NA18945.hp2 NA18986.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.17-1131A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23953406 | |||||||
| chr3:23953425 | G | A | 1 | a0001c0003t0006g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.17-1112G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23953425 | |||||||
| chr3:23953486 | A | G | 176 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0014 others(173): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.17-1051A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23953486 | |||||||
| chr3:23953603 | T | C | 19 | a0001c0001t0007g0054 a0001c0001t0007g0055 a0001c0001t0007g0219 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.17-934T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23953603 | |||||||
| chr3:23953665 | G | T | 1 | a0001c0001t0032g0220 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.17-872G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23953665 | |||||||
| chr3:23953688 | C | T | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.17-849C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23953688 | |||||||
| chr3:23954167 | G | A | 35 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(32): Show |
38 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.17-370G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23954167 | |||||||
| chr3:23954272 | A | G | 1 | a0001c0003t0006g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.17-265A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23954272 | |||||||
| chr3:23954359 | G | A | 1 | a0001c0002t0010g0313 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.17-178G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23954359 | |||||||
| chr3:23954482 | T | C | 1 | a0001c0002t0034g0311 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.17-55T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23954482 | |||||||
| chr3:23954522 | C | G | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.17-15C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 1/7 | chr3 | 23954522 | |||||||
| chr3:23954880 | T | G | 230 | a0001c0001t0001g0125 a0001c0001t0002g0008 a0001c0001t0002g0009 others(227): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.283+77T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 2/7 | chr3 | 23954880 | |||||||
| chr3:23954906 | T | G | 35 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(32): Show |
38 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.283+103T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 2/7 | chr3 | 23954906 | |||||||
| chr3:23955037 | C | T | 1 | a0001c0001t0005g0275 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.283+234C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 2/7 | chr3 | 23955037 | |||||||
| chr3:23955097 | A | G | 1 | a0001c0003t0006g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.283+294A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 2/7 | chr3 | 23955097 | |||||||
| chr3:23955779 | C | A | 3 | a0001c0001t0018g0217 a0001c0001t0018g0271 a0001c0001t0022g0216 |
3 | HG02886.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.284-258C>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 2/7 | chr3 | 23955779 | |||||||
| chr3:23955779 | C | T | 1 | a0001c0001t0009g0136 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.284-258C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 2/7 | chr3 | 23955779 | |||||||
| chr3:23955817 | T | C | 3 | a0001c0001t0018g0217 a0001c0001t0018g0271 a0001c0001t0022g0216 |
3 | HG02886.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.284-220T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 2/7 | chr3 | 23955817 | |||||||
| chr3:23955837 | G | A | 233 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(230): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.284-200G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 2/7 | chr3 | 23955837 | |||||||
| chr3:23955951 | G | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0059 a0001c0001t0001g0125 others(11): Show |
17 | HG00621.hp2 HG02015.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-86G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 2/7 | chr3 | 23955951 | |||||||
| chr3:23956017 | C | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0209 a0010c0011t0007g0221 |
3 | NA18951.hp1 NA19082.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.284-20C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 2/7 | chr3 | 23956017 | |||||||
| chr3:23956033 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA18952.hp1 | splice_region_variant&intron_variant | LOW | c.284-4C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 2/7 | chr3 | 23956033 | |||||||
| chr3:23956218 | G | C | 1 | a0001c0001t0001g0091 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.372+93G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23956218 | |||||||
| chr3:23956390 | G | T | 1 | a0001c0001t0011g0123 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.372+265G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23956390 | |||||||
| chr3:23956401 | G | A | 6 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0178 others(3): Show |
7 | HG01256.hp2 HG01258.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.372+276G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23956401 | |||||||
| chr3:23956487 | G | T | 233 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(230): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.372+362G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23956487 | |||||||
| chr3:23956565 | C | T | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.372+440C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23956565 | |||||||
| chr3:23956609 | A | G | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.372+484A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23956609 | |||||||
| chr3:23956837 | T | C | 35 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(32): Show |
38 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.372+712T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23956837 | |||||||
| chr3:23956844 | A | G | 1 | a0001c0001t0007g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.372+719A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23956844 | |||||||
| chr3:23957049 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.372+924C>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957049 | |||||||
| chr3:23957159 | T | C | 74 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0027 others(71): Show |
90 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.372+1034T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957159 | |||||||
| chr3:23957172 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.372+1047G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957172 | |||||||
| chr3:23957213 | C | T | 1 | a0006c0014t0006g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.372+1088C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957213 | |||||||
| chr3:23957240 | C | T | 28 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0002g0038 others(25): Show |
29 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.372+1115C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957240 | |||||||
| chr3:23957272 | G | A | 3 | a0001c0001t0007g0222 a0001c0001t0007g0223 a0001c0001t0032g0220 |
3 | HG00738.hp2 HG03669.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.372+1147G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957272 | |||||||
| chr3:23957282 | A | G | 1 | a0001c0001t0002g0179 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.372+1157A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957282 | |||||||
| chr3:23957373 | T | A | 1 | a0001c0001t0002g0082 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.372+1248T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957373 | |||||||
| chr3:23957390 | C | CT | 21 | a0001c0001t0001g0019 a0001c0001t0001g0087 a0001c0001t0001g0101 others(18): Show |
22 | HG00621.hp1 HG01123.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.372+1290dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23957390 | ||||||
| chr3:23957390 | CTTT | C | 10 | a0001c0001t0005g0302 a0001c0001t0026g0307 a0001c0002t0010g0012 others(7): Show |
11 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.372+1288_372+1290d others(5): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23957390 | ||||||
| chr3:23957390 | CTTTT | C | 10 | a0001c0001t0003g0247 a0001c0001t0003g0251 a0001c0001t0003g0273 others(7): Show |
10 | HG00741.hp2 HG01891.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.372+1287_372+1290d others(6): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23957390 | ||||||
| chr3:23957390 | CTTTTT | C | 61 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0026 others(58): Show |
78 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.372+1286_372+1290d others(7): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23957390 | ||||||
| chr3:23957390 | CTTTTTT | C | 19 | a0001c0001t0002g0039 a0001c0001t0002g0134 a0001c0001t0002g0161 others(16): Show |
19 | HG00140.hp1 HG00733.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.372+1285_372+1290d others(8): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23957390 | ||||||
| chr3:23957390 | CTTTTTTT | C | 110 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(107): Show |
130 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.372+1284_372+1290d others(9): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23957390 | ||||||
| chr3:23957454 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.372+1329C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957454 | |||||||
| chr3:23957482 | C | T | 1 | a0001c0001t0013g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.372+1357C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957482 | |||||||
| chr3:23957512 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.372+1387C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957512 | |||||||
| chr3:23957545 | T | C | 1 | a0001c0001t0003g0251 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.372+1420T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957545 | |||||||
| chr3:23957560 | C | CA | 6 | a0001c0001t0001g0071 a0001c0001t0001g0089 a0001c0001t0001g0109 others(3): Show |
6 | HG00639.hp1 HG01175.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.372+1448dupA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23957560 | ||||||
| chr3:23957586 | A | G | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.372+1461A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957586 | |||||||
| chr3:23957591 | T | G | 2 | a0001c0001t0015g0283 a0001c0001t0015g0290 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.372+1466T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957591 | |||||||
| chr3:23957596 | G | A | 2 | a0001c0001t0002g0086 a0001c0001t0002g0148 |
2 | HG00423.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.372+1471G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957596 | |||||||
| chr3:23957630 | G | T | 1 | a0001c0001t0002g0172 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.372+1505G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957630 | |||||||
| chr3:23957639 | C | A | 2 | a0001c0001t0003g0262 a0001c0001t0003g0263 |
2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.372+1514C>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957639 | |||||||
| chr3:23957647 | C | T | 5 | a0001c0001t0007g0222 a0001c0001t0007g0223 a0001c0001t0007g0224 others(2): Show |
5 | HG00738.hp2 HG03669.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+1522C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957647 | |||||||
| chr3:23957754 | A | C | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.372+1629A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957754 | |||||||
| chr3:23957847 | C | G | 1 | a0001c0001t0016g0132 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.372+1722C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957847 | |||||||
| chr3:23957863 | C | T | 1 | a0001c0001t0005g0298 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.372+1738C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23957863 | |||||||
| chr3:23958265 | C | T | 35 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(32): Show |
38 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.373-1406C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23958265 | |||||||
| chr3:23958323 | CAA | C | 2 | a0001c0001t0003g0026 a0001c0001t0003g0211 |
3 | HG01934.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.373-1346_373-1345d others(4): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23958323 | ||||||
| chr3:23958348 | TAAG | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0211 |
3 | HG01934.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.373-1319_373-1317d others(5): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23958348 | ||||||
| chr3:23958453 | T | G | 1 | a0001c0001t0001g0080 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.373-1218T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23958453 | |||||||
| chr3:23958458 | A | C | 2 | a0001c0001t0003g0026 a0001c0001t0003g0211 |
3 | HG01934.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.373-1213A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23958458 | |||||||
| chr3:23958612 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.373-1059C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23958612 | |||||||
| chr3:23958642 | T | TA | 20 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0099 others(17): Show |
21 | HG00609.hp2 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.373-1006dupA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23958642 | ||||||
| chr3:23958642 | TA | T | 139 | a0001c0001t0001g0120 a0001c0001t0002g0008 a0001c0001t0002g0009 others(136): Show |
163 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.373-1006delA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23958642 | ||||||
| chr3:23958642 | TAA | T | 7 | a0001c0001t0002g0153 a0001c0001t0002g0163 a0001c0001t0004g0067 others(4): Show |
7 | HG01070.hp2 HG02451.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-1007_373-1006d others(4): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23958642 | ||||||
| chr3:23958791 | T | C | 2 | a0001c0001t0009g0136 a0001c0001t0033g0135 |
2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.373-880T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23958791 | |||||||
| chr3:23958806 | A | G | 228 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0014 others(225): Show |
269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.373-865A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23958806 | |||||||
| chr3:23958817 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.373-854C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23958817 | |||||||
| chr3:23959004 | C | T | 1 | a0001c0001t0027g0288 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.373-667C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23959004 | |||||||
| chr3:23959005 | A | G | 248 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0014 others(245): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.373-666A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23959005 | |||||||
| chr3:23959025 | C | G | 5 | a0001c0001t0013g0308 a0001c0001t0013g0309 a0001c0001t0013g0310 others(2): Show |
5 | HG02109.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-646C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23959025 | |||||||
| chr3:23959058 | T | C | 1 | a0001c0005t0002g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.373-613T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23959058 | |||||||
| chr3:23959077 | A | T | 1 | a0001c0001t0002g0060 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.373-594A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23959077 | |||||||
| chr3:23959179 | A | AATTG | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.373-490_373-487dup others(4): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23959179 | ||||||
| chr3:23959181 | T | G | 75 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0026 others(72): Show |
92 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.373-490T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23959181 | |||||||
| chr3:23959263 | C | CA | 8 | a0001c0001t0001g0104 a0001c0001t0001g0124 a0001c0001t0001g0209 others(5): Show |
8 | HG01081.hp2 HG01261.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.373-390dupA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23959263 | ||||||
| chr3:23959263 | CA | C | 58 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0026 others(55): Show |
72 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.373-390delA | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23959263 | ||||||
| chr3:23959263 | CAA | C | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.373-391_373-390del others(2): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 23959263 | ||||||
| chr3:23959460 | A | T | 5 | a0001c0001t0003g0049 a0001c0001t0003g0053 a0001c0001t0003g0262 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-211A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23959460 | |||||||
| chr3:23959478 | A | G | 2 | a0001c0001t0003g0227 a0001c0001t0029g0228 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.373-193A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23959478 | |||||||
| chr3:23959587 | C | T | 224 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(221): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.373-84C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 3/7 | chr3 | 23959587 | |||||||
| chr3:23960111 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.517+296A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23960111 | |||||||
| chr3:23960279 | C | T | 1 | a0001c0001t0028g0246 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.517+464C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23960279 | |||||||
| chr3:23960298 | G | A | 5 | a0001c0001t0013g0308 a0001c0001t0013g0309 a0001c0001t0013g0310 others(2): Show |
5 | HG02109.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+483G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23960298 | |||||||
| chr3:23960321 | C | T | 1 | a0001c0001t0005g0299 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.517+506C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23960321 | |||||||
| chr3:23960458 | G | C | 1 | a0001c0001t0004g0189 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.517+643G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23960458 | |||||||
| chr3:23960479 | C | T | 2 | a0001c0001t0019g0212 a0001c0001t0019g0213 |
2 | HG02615.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.517+664C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23960479 | |||||||
| chr3:23960570 | G | A | 2 | a0001c0001t0021g0200 a0001c0001t0024g0195 |
2 | HG01346.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.517+755G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23960570 | |||||||
| chr3:23960577 | C | A | 8 | a0001c0003t0006g0061 a0001c0003t0006g0062 a0001c0003t0006g0252 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+762C>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23960577 | |||||||
| chr3:23960583 | C | T | 1 | a0001c0005t0002g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.517+768C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23960583 | |||||||
| chr3:23960727 | A | C | 218 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0014 others(215): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.517+912A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23960727 | |||||||
| chr3:23960850 | G | A | 1 | a0001c0001t0005g0291 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.517+1035G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23960850 | |||||||
| chr3:23961047 | T | C | 5 | a0001c0001t0007g0222 a0001c0001t0007g0223 a0001c0001t0007g0224 others(2): Show |
5 | HG00738.hp2 HG03669.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-930T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23961047 | |||||||
| chr3:23961089 | T | C | 1 | a0001c0003t0006g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.518-888T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23961089 | |||||||
| chr3:23961112 | A | AT | 7 | a0001c0001t0001g0018 a0001c0001t0003g0063 a0001c0001t0013g0308 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.518-855dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 23961112 | ||||||
| chr3:23961123 | A | T | 1 | a0001c0001t0004g0206 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.518-854A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23961123 | |||||||
| chr3:23961192 | A | G | 5 | a0001c0001t0005g0031 a0001c0001t0005g0303 a0001c0001t0005g0304 others(2): Show |
6 | HG02257.hp2 HG02622.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-785A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23961192 | |||||||
| chr3:23961318 | G | A | 2 | a0001c0003t0006g0061 a0001c0003t0006g0062 |
2 | HG02818.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.518-659G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23961318 | |||||||
| chr3:23961389 | C | CT | 46 | a0001c0001t0001g0058 a0001c0001t0001g0131 a0001c0001t0001g0265 others(43): Show |
47 | HG00423.hp2 HG00639.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.518-564dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 23961389 | ||||||
| chr3:23961389 | C | CTT | 19 | a0001c0001t0005g0030 a0001c0001t0005g0287 a0001c0001t0005g0291 others(16): Show |
22 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.518-565_518-564dup others(2): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 23961389 | ||||||
| chr3:23961389 | CT | C | 58 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0156 others(55): Show |
70 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.518-564delT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 23961389 | ||||||
| chr3:23961395 | T | C | 2 | a0001c0001t0009g0136 a0001c0001t0033g0135 |
2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.518-582T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23961395 | |||||||
| chr3:23961584 | C | T | 1 | a0006c0014t0006g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.518-393C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23961584 | |||||||
| chr3:23961587 | G | C | 4 | a0001c0001t0004g0010 a0001c0001t0004g0022 a0001c0001t0004g0077 others(1): Show |
7 | NA18945.hp1 NA18972.hp1 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-390G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23961587 | |||||||
| chr3:23961870 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0110 |
2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.518-107T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23961870 | |||||||
| chr3:23961901 | A | G | 2 | a0001c0003t0006g0256 a0001c0003t0006g0257 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.518-76A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 4/7 | chr3 | 23961901 | |||||||
| chr3:23962796 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1146+191C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23962796 | |||||||
| chr3:23962816 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1146+211T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23962816 | |||||||
| chr3:23962862 | G | A | 3 | a0001c0003t0006g0253 a0001c0003t0006g0254 a0001c0003t0006g0255 |
3 | HG02258.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1146+257G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23962862 | |||||||
| chr3:23963015 | G | GT | 7 | a0001c0001t0001g0127 a0001c0001t0002g0181 a0001c0001t0003g0026 others(4): Show |
8 | HG00621.hp2 HG01934.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1146+424dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 23963015 | ||||||
| chr3:23963208 | A | T | 1 | a0008c0010t0002g0098 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1146+603A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23963208 | |||||||
| chr3:23963281 | A | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0211 |
3 | HG01934.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1146+676A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23963281 | |||||||
| chr3:23963458 | G | GT | 16 | a0001c0001t0001g0265 a0001c0001t0002g0150 a0001c0001t0004g0067 others(13): Show |
17 | HG00558.hp2 HG02109.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.1146+864dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 23963458 | ||||||
| chr3:23963599 | A | G | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1146+994A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23963599 | |||||||
| chr3:23963608 | C | T | 3 | a0001c0001t0018g0217 a0001c0001t0018g0271 a0001c0001t0022g0216 |
3 | HG02886.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1146+1003C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23963608 | |||||||
| chr3:23963641 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1146+1036G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23963641 | |||||||
| chr3:23963650 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1146+1045C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23963650 | |||||||
| chr3:23963700 | C | T | 8 | a0001c0001t0003g0049 a0001c0001t0003g0053 a0001c0001t0003g0262 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1146+1095C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23963700 | |||||||
| chr3:23963919 | GT | G | 224 | a0001c0001t0001g0265 a0001c0001t0002g0009 a0001c0001t0002g0020 others(221): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1147-1042delT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 23963919 | ||||||
| chr3:23963919 | GTT | G | 10 | a0001c0001t0001g0182 a0001c0001t0005g0303 a0001c0002t0010g0012 others(7): Show |
11 | HG02572.hp1 HG02602.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1147-1043_1147-104 others(6): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 23963919 | ||||||
| chr3:23963934 | T | G | 39 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0027 others(36): Show |
52 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1147-1043T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23963934 | |||||||
| chr3:23963955 | A | G | 1 | a0001c0001t0020g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1147-1022A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23963955 | |||||||
| chr3:23964095 | T | C | 8 | a0001c0001t0003g0049 a0001c0001t0003g0053 a0001c0001t0003g0262 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1147-882T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23964095 | |||||||
| chr3:23964130 | G | A | 3 | a0001c0001t0018g0217 a0001c0001t0018g0271 a0001c0001t0022g0216 |
3 | HG02886.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1147-847G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23964130 | |||||||
| chr3:23964167 | C | T | 3 | a0001c0003t0006g0253 a0001c0003t0006g0254 a0001c0003t0006g0255 |
3 | HG02258.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1147-810C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23964167 | |||||||
| chr3:23964262 | A | G | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1147-715A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23964262 | |||||||
| chr3:23964268 | A | G | 249 | a0001c0001t0001g0182 a0001c0001t0002g0008 a0001c0001t0002g0009 others(246): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1147-709A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23964268 | |||||||
| chr3:23964285 | G | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0119 |
2 | HG01167.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1147-692G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23964285 | |||||||
| chr3:23964357 | G | A | 1 | a0001c0001t0009g0267 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1147-620G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23964357 | |||||||
| chr3:23964431 | G | A | 1 | a0001c0001t0007g0219 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1147-546G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23964431 | |||||||
| chr3:23964458 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1147-519A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23964458 | |||||||
| chr3:23964845 | A | G | 5 | a0001c0001t0007g0222 a0001c0001t0007g0223 a0001c0001t0007g0224 others(2): Show |
5 | HG00738.hp2 HG03669.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-132A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23964845 | |||||||
| chr3:23964894 | G | T | 2 | a0001c0001t0019g0212 a0001c0001t0019g0213 |
2 | HG02615.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1147-83G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 5/7 | chr3 | 23964894 | |||||||
| chr3:23965192 | C | G | 1 | a0001c0001t0002g0210 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1332+30C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23965192 | |||||||
| chr3:23965235 | C | CT | 152 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0071 others(149): Show |
177 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.1332+95dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 23965235 | ||||||
| chr3:23965235 | C | CTT | 21 | a0001c0001t0002g0034 a0001c0001t0002g0147 a0001c0001t0002g0170 others(18): Show |
24 | HG00673.hp2 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1332+94_1332+95dup others(2): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 23965235 | ||||||
| chr3:23965235 | CT | C | 11 | a0001c0001t0001g0124 a0001c0001t0003g0239 a0001c0001t0013g0308 others(8): Show |
11 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1332+95delT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 23965235 | ||||||
| chr3:23965300 | C | T | 1 | a0001c0001t0007g0223 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1332+138C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23965300 | |||||||
| chr3:23965362 | C | T | 1 | a0001c0001t0008g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1332+200C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23965362 | |||||||
| chr3:23965363 | T | C | 2 | a0001c0001t0019g0212 a0001c0001t0019g0213 |
2 | HG02615.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1332+201T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23965363 | |||||||
| chr3:23965400 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1332+238G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23965400 | |||||||
| chr3:23965414 | G | GT | 17 | a0001c0001t0001g0044 a0001c0001t0001g0118 a0001c0001t0001g0182 others(14): Show |
18 | HG01081.hp1 HG01934.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1332+265dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 23965414 | ||||||
| chr3:23965535 | A | G | 8 | a0001c0003t0006g0061 a0001c0003t0006g0062 a0001c0003t0006g0252 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1332+373A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23965535 | |||||||
| chr3:23965584 | C | G | 11 | a0001c0003t0006g0061 a0001c0003t0006g0062 a0001c0003t0006g0252 others(8): Show |
11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1332+422C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23965584 | |||||||
| chr3:23965685 | T | TA | 9 | a0001c0001t0003g0049 a0001c0001t0003g0053 a0001c0001t0003g0262 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1332+523_1332+524i others(3): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23965685 | |||||||
| chr3:23965723 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1332+561C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23965723 | |||||||
| chr3:23965800 | A | C | 5 | a0001c0001t0013g0308 a0001c0001t0013g0309 a0001c0001t0013g0310 others(2): Show |
5 | HG02109.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332+638A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23965800 | |||||||
| chr3:23966013 | T | C | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1332+851T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23966013 | |||||||
| chr3:23966075 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1332+913G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23966075 | |||||||
| chr3:23966348 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1332+1186T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23966348 | |||||||
| chr3:23966415 | C | G | 2 | a0001c0001t0003g0027 a0001c0001t0028g0246 |
3 | HG02132.hp1 NA18951.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1332+1253C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23966415 | |||||||
| chr3:23966549 | A | T | 228 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0014 others(225): Show |
269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1333-1264A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23966549 | |||||||
| chr3:23966828 | G | A | 3 | a0001c0003t0006g0253 a0001c0003t0006g0254 a0001c0003t0006g0255 |
3 | HG02258.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1333-985G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23966828 | |||||||
| chr3:23967032 | A | G | 1 | a0001c0001t0004g0067 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1333-781A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23967032 | |||||||
| chr3:23967133 | C | G | 1 | a0001c0003t0006g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1333-680C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23967133 | |||||||
| chr3:23967192 | G | A | 3 | a0001c0001t0012g0032 a0001c0001t0012g0279 a0001c0001t0012g0280 |
4 | HG01070.hp1 HG01071.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1333-621G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23967192 | |||||||
| chr3:23967364 | C | T | 8 | a0001c0001t0003g0049 a0001c0001t0003g0053 a0001c0001t0003g0262 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1333-449C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23967364 | |||||||
| chr3:23967485 | G | A | 1 | a0001c0001t0007g0219 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1333-328G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23967485 | |||||||
| chr3:23967583 | T | A | 1 | a0001c0001t0001g0081 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1333-230T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23967583 | |||||||
| chr3:23967591 | G | A | 5 | a0001c0001t0013g0308 a0001c0001t0013g0309 a0001c0001t0013g0310 others(2): Show |
5 | HG02109.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333-222G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23967591 | |||||||
| chr3:23967614 | G | C | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1333-199G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23967614 | |||||||
| chr3:23967788 | A | C | 128 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0014 others(125): Show |
151 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1333-25A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 6/7 | chr3 | 23967788 | |||||||
| chr3:23968121 | G | A | 1 | a0001c0001t0004g0207 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1543+98G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23968121 | |||||||
| chr3:23968294 | G | A | 1 | a0001c0001t0005g0289 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1543+271G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23968294 | |||||||
| chr3:23968428 | G | A | 233 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(230): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1543+405G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23968428 | |||||||
| chr3:23968643 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1543+620G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23968643 | |||||||
| chr3:23968649 | C | T | 233 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(230): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1543+626C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23968649 | |||||||
| chr3:23968934 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1543+911A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23968934 | |||||||
| chr3:23969000 | T | C | 1 | a0001c0001t0005g0294 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1543+977T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969000 | |||||||
| chr3:23969050 | T | C | 2 | a0001c0001t0007g0054 a0001c0001t0007g0055 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1543+1027T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969050 | |||||||
| chr3:23969288 | A | G | 40 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0010 others(37): Show |
56 | HG00423.hp1 HG00438.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.1543+1265A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969288 | |||||||
| chr3:23969288 | AAAAAAC | A | 3 | a0001c0002t0010g0276 a0001c0002t0010g0277 a0001c0002t0010g0313 |
3 | HG02738.hp1 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1543+1280_1543+128 others(10): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23969288 | ||||||
| chr3:23969301 | A | G | 41 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0026 others(38): Show |
55 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1543+1278A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969301 | |||||||
| chr3:23969319 | A | T | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1543+1296A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969319 | |||||||
| chr3:23969372 | C | G | 5 | a0001c0001t0003g0049 a0001c0001t0003g0053 a0001c0001t0003g0262 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1543+1349C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969372 | |||||||
| chr3:23969436 | A | G | 5 | a0001c0001t0013g0308 a0001c0001t0013g0309 a0001c0001t0013g0310 others(2): Show |
5 | HG02109.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543+1413A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969436 | |||||||
| chr3:23969471 | A | G | 1 | a0001c0001t0005g0289 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1543+1448A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969471 | |||||||
| chr3:23969691 | C | T | 124 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(121): Show |
144 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1543+1668C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969691 | |||||||
| chr3:23969757 | G | A | 1 | a0001c0001t0005g0294 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1543+1734G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969757 | |||||||
| chr3:23969769 | G | A | 2 | a0001c0001t0005g0286 a0001c0001t0005g0315 |
2 | HG02630.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1543+1746G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969769 | |||||||
| chr3:23969830 | A | G | 1 | a0001c0001t0005g0293 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1543+1807A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969830 | |||||||
| chr3:23969881 | G | A | 237 | a0001c0001t0001g0041 a0001c0001t0001g0110 a0001c0001t0001g0112 others(234): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1543+1858G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969881 | |||||||
| chr3:23969905 | A | G | 233 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(230): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1543+1882A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969905 | |||||||
| chr3:23969968 | G | A | 3 | a0001c0002t0010g0276 a0001c0002t0010g0277 a0001c0002t0010g0313 |
3 | HG02738.hp1 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1543+1945G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23969968 | |||||||
| chr3:23970145 | T | G | 1 | a0002c0004t0002g0151 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1543+2122T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23970145 | |||||||
| chr3:23970221 | G | T | 38 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0002g0037 others(35): Show |
39 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1543+2198G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23970221 | |||||||
| chr3:23970655 | C | G | 1 | a0001c0001t0013g0309 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1543+2632C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23970655 | |||||||
| chr3:23970721 | A | G | 1 | a0001c0001t0005g0298 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1543+2698A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23970721 | |||||||
| chr3:23970752 | G | C | 5 | a0001c0001t0007g0222 a0001c0001t0007g0223 a0001c0001t0007g0224 others(2): Show |
5 | HG00738.hp2 HG03669.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.1543+2729G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23970752 | |||||||
| chr3:23970771 | GTTGT | G | 10 | a0001c0001t0005g0274 a0001c0001t0005g0281 a0001c0001t0005g0282 others(7): Show |
10 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.1543+2755_1543+275 others(8): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23970771 | ||||||
| chr3:23970898 | C | T | 113 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(110): Show |
133 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1543+2875C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23970898 | |||||||
| chr3:23971169 | A | G | 1 | a0001c0001t0002g0149 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1543+3146A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23971169 | |||||||
| chr3:23971301 | C | CCA | 8 | a0001c0001t0002g0034 a0001c0001t0002g0094 a0001c0001t0002g0150 others(5): Show |
8 | HG02165.hp2 HG02735.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1543+3278_1543+327 others(6): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23971301 | |||||||
| chr3:23971302 | T | C | 116 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(113): Show |
136 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1543+3279T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23971302 | |||||||
| chr3:23971303 | A | AT | 181 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(178): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1543+3300dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23971303 | ||||||
| chr3:23971303 | A | ATT | 15 | a0001c0001t0003g0051 a0001c0001t0003g0227 a0001c0001t0003g0235 others(12): Show |
16 | HG01109.hp1 HG01993.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1543+3299_1543+330 others(6): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23971303 | ||||||
| chr3:23971303 | A | ATTTTT | 8 | a0001c0002t0010g0012 a0001c0002t0010g0277 a0001c0002t0010g0278 others(5): Show |
9 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1543+3296_1543+330 others(9): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23971303 | ||||||
| chr3:23971303 | A | T | 8 | a0001c0001t0002g0034 a0001c0001t0002g0094 a0001c0001t0002g0150 others(5): Show |
8 | HG02165.hp2 HG02735.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1543+3280A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23971303 | |||||||
| chr3:23971303 | AT | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0090 a0001c0001t0001g0127 others(2): Show |
7 | HG00621.hp2 HG01516.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.1543+3300delT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23971303 | ||||||
| chr3:23971461 | G | A | 1 | a0001c0001t0033g0135 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1543+3438G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23971461 | |||||||
| chr3:23971676 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1543+3653G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23971676 | |||||||
| chr3:23971697 | G | T | 233 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(230): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1543+3674G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23971697 | |||||||
| chr3:23971705 | C | CCTTTA | 225 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(222): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1543+3685_1543+368 others(9): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23971705 | ||||||
| chr3:23971759 | G | GAC | 234 | a0001c0001t0001g0182 a0001c0001t0002g0009 a0001c0001t0002g0020 others(231): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.1543+3738_1543+373 others(6): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23971759 | ||||||
| chr3:23971851 | T | C | 2 | a0001c0001t0009g0136 a0001c0001t0033g0135 |
2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1543+3828T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23971851 | |||||||
| chr3:23971865 | A | G | 248 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0014 others(245): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1543+3842A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23971865 | |||||||
| chr3:23971908 | A | T | 2 | a0001c0001t0002g0093 a0001c0001t0002g0166 |
2 | NA19011.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1543+3885A>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23971908 | |||||||
| chr3:23971974 | C | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0113 |
2 | NA18940.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.1543+3951C>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23971974 | |||||||
| chr3:23971980 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1543+3957C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23971980 | |||||||
| chr3:23972031 | T | A | 1 | a0001c0003t0006g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1543+4008T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23972031 | |||||||
| chr3:23972067 | T | G | 2 | a0001c0001t0003g0227 a0001c0001t0029g0228 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1543+4044T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23972067 | |||||||
| chr3:23972095 | C | T | 2 | a0001c0003t0006g0256 a0001c0003t0006g0257 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1543+4072C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23972095 | |||||||
| chr3:23972146 | A | G | 8 | a0001c0003t0006g0061 a0001c0003t0006g0062 a0001c0003t0006g0252 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1543+4123A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23972146 | |||||||
| chr3:23972394 | C | G | 1 | a0001c0001t0001g0128 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1543+4371C>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23972394 | |||||||
| chr3:23972402 | T | G | 2 | a0001c0007t0003g0233 a0001c0007t0003g0240 |
2 | HG00642.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1543+4379T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23972402 | |||||||
| chr3:23972454 | T | C | 1 | a0001c0001t0004g0191 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1543+4431T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23972454 | |||||||
| chr3:23972568 | C | T | 224 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(221): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1543+4545C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23972568 | |||||||
| chr3:23972579 | AT | A | 35 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(32): Show |
38 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.1543+4557delT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23972579 | |||||||
| chr3:23972742 | G | A | 2 | a0001c0003t0006g0256 a0001c0003t0006g0257 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1544-4481G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23972742 | |||||||
| chr3:23972823 | G | A | 221 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(218): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.1544-4400G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23972823 | |||||||
| chr3:23973238 | A | G | 1 | a0001c0001t0003g0242 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1544-3985A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23973238 | |||||||
| chr3:23973288 | T | C | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1544-3935T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23973288 | |||||||
| chr3:23973481 | T | C | 1 | a0001c0001t0003g0316 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1544-3742T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23973481 | |||||||
| chr3:23973489 | A | G | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1544-3734A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23973489 | |||||||
| chr3:23973636 | C | T | 35 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(32): Show |
38 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.1544-3587C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23973636 | |||||||
| chr3:23973649 | A | G | 74 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0027 others(71): Show |
90 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.1544-3574A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23973649 | |||||||
| chr3:23973650 | A | C | 5 | a0001c0001t0013g0308 a0001c0001t0013g0309 a0001c0001t0013g0310 others(2): Show |
5 | HG02109.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1544-3573A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23973650 | |||||||
| chr3:23973683 | A | G | 1 | a0001c0001t0002g0169 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1544-3540A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23973683 | |||||||
| chr3:23973697 | G | A | 1 | a0001c0001t0003g0049 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1544-3526G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23973697 | |||||||
| chr3:23973786 | A | G | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1544-3437A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23973786 | |||||||
| chr3:23973882 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1544-3341G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23973882 | |||||||
| chr3:23973956 | C | T | 11 | a0001c0003t0006g0061 a0001c0003t0006g0062 a0001c0003t0006g0252 others(8): Show |
11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1544-3267C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23973956 | |||||||
| chr3:23974088 | C | CT | 23 | a0001c0001t0001g0043 a0001c0001t0001g0072 a0001c0001t0001g0089 others(20): Show |
23 | HG00099.hp1 HG01069.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1544-3109dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23974088 | ||||||
| chr3:23974088 | C | CTT | 61 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0027 others(58): Show |
77 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.1544-3110_1544-310 others(6): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23974088 | ||||||
| chr3:23974088 | C | CTTT | 15 | a0001c0001t0002g0142 a0001c0001t0002g0166 a0001c0001t0002g0172 others(12): Show |
15 | HG00642.hp2 HG01891.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.1544-3111_1544-310 others(7): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23974088 | ||||||
| chr3:23974088 | C | CTTTT | 76 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0014 others(73): Show |
96 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1544-3112_1544-310 others(8): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23974088 | ||||||
| chr3:23974088 | C | CTTTTT | 49 | a0001c0001t0002g0021 a0001c0001t0002g0038 a0001c0001t0002g0039 others(46): Show |
53 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1544-3113_1544-310 others(9): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23974088 | ||||||
| chr3:23974088 | C | CTTTTTT | 14 | a0001c0001t0002g0034 a0001c0001t0002g0037 a0001c0001t0002g0082 others(11): Show |
14 | HG00639.hp1 HG01516.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1544-3114_1544-310 others(10): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23974088 | ||||||
| chr3:23974088 | C | CTTTTTTT others(14): Show |
1 | a0001c0002t0034g0311 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1544-3129_1544-310 others(25): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23974088 | ||||||
| chr3:23974088 | CT | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0104 a0001c0001t0001g0107 others(6): Show |
10 | HG00408.hp1 HG00733.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1544-3109delT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23974088 | ||||||
| chr3:23974088 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | NA18612.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1544-3119_1544-310 others(15): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23974088 | ||||||
| chr3:23974320 | C | A | 2 | a0001c0001t0015g0283 a0001c0001t0015g0290 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1544-2903C>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23974320 | |||||||
| chr3:23974360 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0130 |
5 | HG00558.hp1 NA18942.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1544-2863A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23974360 | |||||||
| chr3:23974636 | T | A | 35 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0274 others(32): Show |
38 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.1544-2587T>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23974636 | |||||||
| chr3:23974791 | C | A | 1 | a0001c0001t0002g0149 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1544-2432C>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23974791 | |||||||
| chr3:23974818 | A | AT | 12 | a0001c0001t0001g0209 a0001c0001t0002g0034 a0001c0001t0002g0210 others(9): Show |
13 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1544-2387dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23974818 | ||||||
| chr3:23974818 | AT | A | 6 | a0001c0001t0001g0114 a0001c0001t0001g0119 a0001c0001t0002g0157 others(3): Show |
6 | HG00735.hp1 HG01167.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1544-2387delT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23974818 | ||||||
| chr3:23974888 | G | A | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1544-2335G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23974888 | |||||||
| chr3:23975152 | G | A | 2 | a0001c0001t0007g0225 a0001c0001t0007g0226 |
2 | HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1544-2071G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975152 | |||||||
| chr3:23975152 | G | T | 5 | a0001c0001t0005g0030 a0001c0001t0005g0292 a0001c0001t0005g0293 others(2): Show |
6 | HG01192.hp1 HG01358.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1544-2071G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975152 | |||||||
| chr3:23975232 | C | T | 2 | a0001c0001t0016g0132 a0001c0001t0016g0266 |
2 | HG01081.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1544-1991C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975232 | |||||||
| chr3:23975289 | A | AT | 54 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0027 others(51): Show |
67 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.1544-1919dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23975289 | ||||||
| chr3:23975311 | A | G | 37 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0027 others(34): Show |
50 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1544-1912A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975311 | |||||||
| chr3:23975465 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1544-1758A>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975465 | |||||||
| chr3:23975537 | C | T | 1 | a0010c0011t0007g0221 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1544-1686C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975537 | |||||||
| chr3:23975538 | G | A | 10 | a0001c0001t0002g0021 a0001c0002t0010g0012 a0001c0002t0010g0276 others(7): Show |
12 | HG00558.hp2 HG02602.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.1544-1685G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975538 | |||||||
| chr3:23975604 | C | T | 318 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(315): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1544-1619C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975604 | |||||||
| chr3:23975778 | T | C | 8 | a0001c0003t0006g0061 a0001c0003t0006g0062 a0001c0003t0006g0252 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1544-1445T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975778 | |||||||
| chr3:23975801 | G | C | 1 | a0001c0001t0002g0021 | 2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1544-1422G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975801 | |||||||
| chr3:23975803 | G | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0173 |
2 | HG02735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1544-1420G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975803 | |||||||
| chr3:23975877 | G | T | 5 | a0001c0001t0005g0030 a0001c0001t0005g0292 a0001c0001t0005g0293 others(2): Show |
6 | HG01192.hp1 HG01358.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1544-1346G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975877 | |||||||
| chr3:23975899 | T | C | 1 | a0001c0001t0001g0018 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1544-1324T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975899 | |||||||
| chr3:23975963 | A | C | 253 | a0001c0001t0001g0019 a0001c0001t0001g0080 a0001c0001t0001g0107 others(250): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1544-1260A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23975963 | |||||||
| chr3:23976123 | T | G | 1 | a0001c0003t0006g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1544-1100T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23976123 | |||||||
| chr3:23976175 | G | A | 1 | a0001c0001t0003g0241 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1544-1048G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23976175 | |||||||
| chr3:23976344 | AGATAT | A | 2 | a0001c0001t0003g0026 a0001c0001t0003g0211 |
3 | HG01934.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1544-871_1544-867d others(7): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23976344 | ||||||
| chr3:23976464 | G | C | 2 | a0001c0001t0009g0136 a0001c0001t0033g0135 |
2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1544-759G>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23976464 | |||||||
| chr3:23976508 | A | C | 2 | a0001c0001t0003g0026 a0001c0001t0003g0211 |
3 | HG01934.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1544-715A>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23976508 | |||||||
| chr3:23976522 | G | GC | 9 | a0001c0002t0010g0012 a0001c0002t0010g0276 a0001c0002t0010g0277 others(6): Show |
10 | HG00558.hp2 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1544-700dupC | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23976522 | ||||||
| chr3:23976643 | G | A | 1 | a0001c0001t0003g0241 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1544-580G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23976643 | |||||||
| chr3:23976688 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1544-535C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23976688 | |||||||
| chr3:23976753 | T | G | 6 | a0001c0001t0004g0068 a0001c0001t0013g0308 a0001c0001t0013g0309 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1544-470T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23976753 | |||||||
| chr3:23976767 | G | A | 2 | a0001c0001t0015g0283 a0001c0001t0015g0290 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1544-456G>A | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23976767 | |||||||
| chr3:23976767 | G | T | 143 | a0001c0001t0001g0019 a0001c0001t0001g0107 a0001c0001t0001g0113 others(140): Show |
167 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.1544-456G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23976767 | |||||||
| chr3:23976776 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1544-447C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23976776 | |||||||
| chr3:23976932 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1544-291C>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23976932 | |||||||
| chr3:23976997 | TTTGA | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0211 |
3 | HG01934.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1544-220_1544-217d others(6): Show |
NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23976997 | ||||||
| chr3:23977003 | T | G | 5 | a0001c0001t0013g0308 a0001c0001t0013g0309 a0001c0001t0013g0310 others(2): Show |
5 | HG02109.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1544-220T>G | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23977003 | |||||||
| chr3:23977012 | G | GT | 222 | a0001c0001t0001g0019 a0001c0001t0001g0107 a0001c0001t0001g0113 others(219): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1544-207dupT | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 23977012 | ||||||
| chr3:23977101 | T | C | 1 | a0001c0001t0005g0302 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1544-122T>C | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23977101 | |||||||
| chr3:23977105 | G | T | 1 | a0001c0001t0002g0014 | 2 | NA18966.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1544-118G>T | NR1D2 | ENSG00000174738.13 | transcript | ENST00000312521.9 | protein_coding | 7/7 | chr3 | 23977105 |