| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105107612-105107795 | Common:1; Rare:84 | ||||
| chr12:105236036-105236294 | Common:2; Rare:111 | ||||
| chr12:106955642-106955910 | Rare:97 | ||||
| chr12:106987048-106987286 | Common:4; Rare:67 | ||||
| chr12:108129676-108129845 | Common:1; Rare:35 | ||||
| chr12:108515038-108515313 | Common:1; Rare:83 | ||||
| chr12:108562394-108562686 | Common:9; Rare:123; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108730185-108730348 | Rare:28 | ||||
| chr12:108730421-108730457 | Rare:9 | ||||
| chr12:109093421-109093754 | Common:3; Rare:109 | ||||
| chr12:109098338-109098564 | Rare:102; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:109154557-109154799 | Common:2; Rare:59 | ||||
| chr12:109477260-109477656 | Common:3; Rare:104 | ||||
| chr12:109573421-109573813 | Common:5; Rare:134; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr12:109880371-109880673 | Common:1; Rare:93 |