| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12696074-12696318 | Common:1; Rare:57 | ||||
| chr12:12696668-12696752 | Rare:31 | ||||
| chr12:12715374-12715610 | Common:2; Rare:32 | ||||
| chr12:12716959-12717547 | Common:3; Rare:185; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12717591-12717731 | Rare:38; Clinvar (benign):2 | ||||
| chr12:12725489-12726059 | Common:6; Rare:136 | ||||
| chr12:12726086-12726127 | Common:1; Rare:11 | ||||
| chr12:12813164-12813416 | Common:2; Rare:74 | ||||
| chr12:13000249-13000511 | Common:2; Rare:68 | ||||
| chr12:13095349-13095577 | Common:2; Rare:42 | ||||
| chr12:14365429-14365763 | Common:1; Rare:108 | ||||
| chr12:14367166-14367397 | Common:1; Rare:47 | ||||
| chr12:14367435-14367517 | Rare:16 | ||||
| chr12:14385090-14385388 | Rare:57 | ||||
| chr12:14567429-14567487 | Common:1; Rare:12 |