| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:991090-991296 | Common:4; Rare:95 | ||||
| chr12:1690871-1691050 | Common:1; Rare:56 | ||||
| chr12:1811699-1811939 | Common:2; Rare:60; Clinvar:1 | ||||
| chr12:2004411-2004669 | Common:2; Rare:87 | ||||
| chr12:2812492-2812714 | Common:1; Rare:52 | ||||
| chr12:2876938-2877260 | Rare:97 | ||||
| chr12:2959783-2959944 | Common:2; Rare:44 | ||||
| chr12:3077267-3077428 | Common:5; Rare:71 | ||||
| chr12:3753064-3753236 | Common:1; Rare:42 | ||||
| chr12:3873355-3873514 | Common:1; Rare:36 | ||||
| chr12:4273742-4273762 | Rare:4 | ||||
| chr12:4320943-4321265 | Common:5; Rare:123 | ||||
| chr12:4538436-4538934 | Common:3; Rare:113 | ||||
| chr12:4649045-4649168 | Common:1; Rare:50; Clinvar (benign):2 | ||||
| chr12:6383976-6384250 | Common:1; Rare:63 |