| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108515007-108515333 | Common:1; Rare:100 | ||||
| chr12:108561118-108561498 | Common:4; Rare:100 | ||||
| chr12:108562390-108562733 | Common:9; Rare:141; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108857571-108857725 | Rare:86 | ||||
| chr12:109093626-109093903 | Common:2; Rare:62 | ||||
| chr12:109097252-109097633 | Rare:114; Clinvar:2 | ||||
| chr12:109097983-109098250 | Common:4; Rare:86 | ||||
| chr12:109154557-109154707 | Common:1; Rare:38 | ||||
| chr12:109458779-109459137 | Common:1; Rare:56 | ||||
| chr12:109476995-109477695 | Common:6; Rare:175 | ||||
| chr12:109573483-109573854 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:109880384-109880678 | Common:1; Rare:89 | ||||
| chr12:109996222-109996450 | Common:2; Rare:67 | ||||
| chr12:109999066-109999461 | Rare:92 | ||||
| chr12:110124128-110124446 | Common:2; Rare:104 |