| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6867459-6867671 | Common:2; Rare:109; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6869118-6869293 | Rare:53; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6869576-6869771 | Rare:67; Clinvar (pathogenic):1 | ||||
| chr12:6870028-6870309 | Common:3; Rare:82; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6873274-6873721 | Common:4; Rare:124 | ||||
| chr12:6927232-6927830 | Rare:136 | ||||
| chr12:6928010-6928372 | Common:2; Rare:79 | ||||
| chr12:6942797-6942927 | Common:1; Rare:23 | ||||
| chr12:6943912-6944172 | Common:10; Rare:260; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970185-6970370 | Rare:64 | ||||
| chr12:6970372-6971094 | Common:10; Rare:229; Clinvar (benign):2 | ||||
| chr12:7060762-7060853 | Rare:13 | ||||
| chr12:7062750-7062932 | Common:1; Rare:40 | ||||
| chr12:7108468-7108744 | Common:1; Rare:74 | ||||
| chr12:7109125-7109280 | Rare:52 |