| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:677378-677515 | Rare:30 | ||||
| chr12:685459-685591 | Common:1; Rare:27 | ||||
| chr12:719496-719814 | Rare:59 | ||||
| chr12:720431-720602 | Common:1; Rare:24 | ||||
| chr12:749960-750246 | Common:3; Rare:50 | ||||
| chr12:751117-751525 | Common:1; Rare:103 | ||||
| chr12:754231-754270 | Common:1; Rare:7; Clinvar (benign):2 | ||||
| chr12:948623-948908 | Common:4; Rare:58 | ||||
| chr12:1532174-1532381 | Common:1; Rare:39 | ||||
| chr12:1533166-1533193 | Rare:2 | ||||
| chr12:1533398-1533434 | Rare:9 | ||||
| chr12:1533463-1533663 | Common:1; Rare:39 | ||||
| chr12:1533684-1533894 | Common:1; Rare:36 | ||||
| chr12:1534002-1534160 | Common:1; Rare:32 | ||||
| chr12:1534804-1535021 | Common:1; Rare:54 |