| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108515071-108515298 | Common:1; Rare:68 | ||||
| chr12:108561150-108561457 | Common:4; Rare:72 | ||||
| chr12:108562352-108562678 | Common:10; Rare:129; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108731510-108731680 | Common:2; Rare:63 | ||||
| chr12:109052466-109052638 | Common:2; Rare:42 | ||||
| chr12:109093423-109093617 | Common:2; Rare:71 | ||||
| chr12:109477272-109477660 | Common:3; Rare:100 | ||||
| chr12:109573430-109573813 | Common:3; Rare:126; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109900159-109900327 | Rare:59 | ||||
| chr12:109996299-109996450 | Common:2; Rare:42 | ||||
| chr12:110468671-110468938 | Rare:72 | ||||
| chr12:110502055-110502331 | Common:1; Rare:99 | ||||
| chr12:110613996-110614212 | Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:111685754-111686085 | Rare:124 | ||||
| chr12:111841845-111841986 | Common:2; Rare:46 |