| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108562347-108562676 | Common:10; Rare:129; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:109052495-109052660 | Common:2; Rare:50 | ||||
| chr12:109093436-109093542 | Common:1; Rare:46 | ||||
| chr12:109154557-109154696 | Common:1; Rare:36 | ||||
| chr12:109175986-109176195 | Rare:65 | ||||
| chr12:109477272-109477656 | Common:3; Rare:99 | ||||
| chr12:109573443-109573840 | Common:3; Rare:126; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880337-109880678 | Common:1; Rare:104 | ||||
| chr12:109996304-109996436 | Common:2; Rare:34 | ||||
| chr12:110280973-110281164 | Common:1; Rare:82 | ||||
| chr12:110468705-110468909 | Rare:54 | ||||
| chr12:110502058-110502340 | Common:1; Rare:106 | ||||
| chr12:111685715-111686114 | Rare:142 | ||||
| chr12:111766837-111766982 | Rare:47 | ||||
| chr12:111841887-111842038 | Common:2; Rare:44 |