| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109880430-109880676 | Common:1; Rare:66 | ||||
| chr12:109996294-109996429 | Common:2; Rare:37 | ||||
| chr12:109999066-109999223 | Rare:29 | ||||
| chr12:110468139-110468537 | Common:3; Rare:135 | ||||
| chr12:110468692-110468933 | Rare:66 | ||||
| chr12:110502040-110502240 | Common:1; Rare:68 | ||||
| chr12:110613979-110614191 | Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:110614306-110614399 | Rare:29; Clinvar:1 | ||||
| chr12:110641573-110641861 | Common:1; Rare:57 | ||||
| chr12:110742718-110742806 | Rare:23 | ||||
| chr12:110742871-110743177 | Common:2; Rare:107 | ||||
| chr12:111369019-111369228 | Common:1; Rare:58 | ||||
| chr12:111686006-111686110 | Rare:32 | ||||
| chr12:111766823-111767092 | Rare:86 | ||||
| chr12:111841875-111842260 | Common:3; Rare:107 |