| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104138158-104138384 | Common:1; Rare:60 | ||||
| chr12:104958309-104958380 | Rare:19 | ||||
| chr12:104986222-104986355 | Common:2; Rare:45 | ||||
| chr12:105107609-105107797 | Common:1; Rare:88 | ||||
| chr12:105236085-105236312 | Common:2; Rare:105 | ||||
| chr12:106955453-106955820 | Common:3; Rare:133 | ||||
| chr12:106987040-106987283 | Common:4; Rare:69 | ||||
| chr12:107093514-107093623 | Rare:43 | ||||
| chr12:107685679-107685895 | Common:1; Rare:73 | ||||
| chr12:108561153-108561481 | Common:4; Rare:79 | ||||
| chr12:108562380-108562654 | Common:7; Rare:109; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:108731499-108731644 | Common:2; Rare:53 | ||||
| chr12:109052466-109052638 | Common:2; Rare:42 | ||||
| chr12:109097433-109097644 | Rare:75; Clinvar:2 | ||||
| chr12:109097849-109098204 | Common:4; Rare:112 |