| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6869445-6869773 | Common:1; Rare:92; Clinvar (pathogenic):1 | ||||
| chr12:6869892-6870133 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6873274-6873721 | Common:4; Rare:124 | ||||
| chr12:6914408-6914635 | Rare:61 | ||||
| chr12:6928231-6928380 | Common:2; Rare:35 | ||||
| chr12:6943531-6943817 | Common:4; Rare:116 | ||||
| chr12:6943905-6944154 | Common:10; Rare:254; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6944173-6944497 | Common:3; Rare:151; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6946347-6946585 | Common:1; Rare:62 | ||||
| chr12:6959224-6959333 | Rare:24 | ||||
| chr12:6967508-6967632 | Rare:47 | ||||
| chr12:6970519-6971009 | Common:4; Rare:158; Clinvar (benign):1 | ||||
| chr12:7018396-7018713 | Common:1; Rare:93 | ||||
| chr12:7108412-7108695 | Common:1; Rare:86 | ||||
| chr12:7109124-7109275 | Rare:50 |