| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6766430-6766569 | Rare:36 | ||||
| chr12:6766827-6767043 | Common:2; Rare:53 | ||||
| chr12:6767051-6767245 | Common:1; Rare:39 | ||||
| chr12:6767895-6768211 | Common:1; Rare:48 | ||||
| chr12:6821745-6821877 | Common:1; Rare:38 | ||||
| chr12:6828104-6828445 | Common:7; Rare:62 | ||||
| chr12:6828554-6828684 | Rare:31 | ||||
| chr12:6829344-6829493 | Rare:38 | ||||
| chr12:6829624-6829734 | Common:1; Rare:17 | ||||
| chr12:6850823-6850843 | Rare:4 | ||||
| chr12:6850855-6851143 | Rare:72 | ||||
| chr12:6851230-6851526 | Common:1; Rare:69 | ||||
| chr12:6851865-6852264 | Common:1; Rare:105 | ||||
| chr12:6852265-6852837 | Common:1; Rare:151 | ||||
| chr12:6867317-6867695 | Common:2; Rare:167; Clinvar:2; Clinvar (benign):2 |