| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106083980-106084217 | Common:1; Rare:42 | ||||
| chr12:106987048-106987306 | Common:5; Rare:72 | ||||
| chr12:107685709-107685902 | Rare:68 | ||||
| chr12:108562387-108562651 | Common:6; Rare:104; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:108597993-108598246 | Rare:66 | ||||
| chr12:109097978-109098204 | Common:3; Rare:74 | ||||
| chr12:109477287-109477726 | Common:4; Rare:113 | ||||
| chr12:109573450-109573813 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880361-109880676 | Common:1; Rare:94 | ||||
| chr12:109996299-109996439 | Common:2; Rare:39 | ||||
| chr12:110450259-110450437 | Common:2; Rare:65 | ||||
| chr12:110468705-110468902 | Rare:53 | ||||
| chr12:110502058-110502244 | Common:1; Rare:66 | ||||
| chr12:111841894-111841998 | Common:2; Rare:35 | ||||
| chr12:112013129-112013460 | Common:1; Rare:114 |