| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4538444-4538927 | Common:3; Rare:109 | ||||
| chr12:6493224-6493394 | Common:6; Rare:47 | ||||
| chr12:6493778-6494140 | Common:2; Rare:108 | ||||
| chr12:6724196-6724285 | Rare:19 | ||||
| chr12:6753066-6753189 | Common:4; Rare:47 | ||||
| chr12:6851247-6851508 | Rare:60 | ||||
| chr12:6970621-6970977 | Common:4; Rare:115; Clinvar (benign):1 | ||||
| chr12:7189541-7189726 | Rare:67; Clinvar:4 | ||||
| chr12:10613533-10613703 | Common:1; Rare:69 | ||||
| chr12:11171574-11171630 | Common:1; Rare:21 | ||||
| chr12:12891314-12891567 | Common:1; Rare:49 | ||||
| chr12:14803462-14803658 | Common:1; Rare:49 | ||||
| chr12:15882263-15882544 | Common:1; Rare:97 | ||||
| chr12:21501556-21501835 | Common:2; Rare:71 | ||||
| chr12:22624946-22625252 | Common:1; Rare:139 |