| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108562387-108562713 | Common:9; Rare:135; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108633769-108633992 | Rare:43 | ||||
| chr12:108648961-108649173 | Rare:34 | ||||
| chr12:108730182-108730425 | Common:1; Rare:46 | ||||
| chr12:108857580-108857845 | Common:3; Rare:122 | ||||
| chr12:109052268-109052667 | Common:3; Rare:98 | ||||
| chr12:109097849-109098329 | Common:5; Rare:150 | ||||
| chr12:109098333-109098533 | Rare:85; Clinvar:2 | ||||
| chr12:109154557-109154869 | Common:3; Rare:71 | ||||
| chr12:109457795-109458022 | Common:1; Rare:41 | ||||
| chr12:109477275-109477660 | Common:3; Rare:98 | ||||
| chr12:109573430-109573845 | Common:3; Rare:134; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880361-109880658 | Common:1; Rare:91 | ||||
| chr12:109900202-109900360 | Rare:62 | ||||
| chr12:109914052-109914549 | Rare:104 |