| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108562387-108562733 | Common:9; Rare:141; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108633762-108633962 | Rare:38 | ||||
| chr12:108730185-108730436 | Common:1; Rare:50 | ||||
| chr12:108857525-108857869 | Common:3; Rare:158 | ||||
| chr12:109093412-109093667 | Common:2; Rare:95 | ||||
| chr12:109098320-109098449 | Rare:52; Clinvar:1 | ||||
| chr12:109154557-109154798 | Common:2; Rare:58 | ||||
| chr12:109477259-109477664 | Common:3; Rare:109 | ||||
| chr12:109573431-109573814 | Common:3; Rare:126; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880371-109880673 | Common:1; Rare:93 | ||||
| chr12:109996257-109996439 | Common:2; Rare:54 | ||||
| chr12:110281024-110281222 | Rare:72 | ||||
| chr12:110468756-110468928 | Rare:54 | ||||
| chr12:110501443-110501641 | Common:1; Rare:58 | ||||
| chr12:110502047-110502241 | Common:1; Rare:67 |