| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:113966006-113966115 | Rare:25 | ||||
| chr12:113966214-113966553 | Common:10; Rare:111 | ||||
| chr12:114683482-114683516 | Rare:3 | ||||
| chr12:114683958-114684219 | Common:3; Rare:83; Clinvar:2 | ||||
| chr12:114684315-114684415 | Common:1; Rare:24 | ||||
| chr12:114684491-114684816 | Common:2; Rare:94 | ||||
| chr12:116276431-116276614 | Rare:58 | ||||
| chr12:116276779-116277222 | Common:2; Rare:133; Clinvar (benign):2 | ||||
| chr12:116277345-116277473 | Rare:33 | ||||
| chr12:116277532-116277935 | Common:1; Rare:134 | ||||
| chr12:116559481-116559673 | Common:2; Rare:31 | ||||
| chr12:116737953-116738366 | Common:5; Rare:139 | ||||
| chr12:116738524-116738621 | Common:1; Rare:17 | ||||
| chr12:116881089-116881224 | Common:1; Rare:37 | ||||
| chr12:116881362-116881625 | Common:3; Rare:61 |