| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107685709-107685950 | Rare:80 | ||||
| chr12:108515006-108515313 | Common:1; Rare:93 | ||||
| chr12:108562347-108562686 | Common:10; Rare:133; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108633780-108633992 | Rare:41 | ||||
| chr12:108730192-108730443 | Common:1; Rare:50 | ||||
| chr12:109052256-109052667 | Common:3; Rare:101 | ||||
| chr12:109131124-109131423 | Common:1; Rare:54 | ||||
| chr12:109154516-109154714 | Common:1; Rare:51 | ||||
| chr12:109477260-109477660 | Common:3; Rare:105 | ||||
| chr12:109573430-109573852 | Common:3; Rare:137; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109996201-109996456 | Common:2; Rare:72 | ||||
| chr12:110281673-110281896 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr12:110502051-110502332 | Common:1; Rare:102 | ||||
| chr12:110742662-110742671 | Rare:1 | ||||
| chr12:110742762-110743139 | Common:3; Rare:144 |