| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108562394-108562715 | Common:9; Rare:136; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108731465-108731664 | Common:2; Rare:78 | ||||
| chr12:109052466-109052653 | Common:3; Rare:54 | ||||
| chr12:109093404-109093524 | Rare:47 | ||||
| chr12:109097476-109097629 | Rare:55; Clinvar:1 | ||||
| chr12:109097867-109098275 | Common:5; Rare:121 | ||||
| chr12:109154541-109154686 | Common:1; Rare:38 | ||||
| chr12:109477273-109477657 | Common:3; Rare:98 | ||||
| chr12:109573443-109573852 | Common:3; Rare:131; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880370-109880665 | Common:1; Rare:90 | ||||
| chr12:109900216-109900365 | Rare:57 | ||||
| chr12:109996294-109996439 | Common:2; Rare:40 | ||||
| chr12:110280983-110281167 | Common:1; Rare:80 | ||||
| chr12:110450253-110450383 | Common:2; Rare:53 | ||||
| chr12:110468650-110468938 | Rare:81 |