| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6924405-6924528 | Common:1; Rare:31 | ||||
| chr12:6943517-6943818 | Common:4; Rare:126 | ||||
| chr12:6943847-6944131 | Common:14; Rare:310; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:6970612-6971009 | Common:4; Rare:129; Clinvar (benign):1 | ||||
| chr12:7018425-7018617 | Common:1; Rare:55 | ||||
| chr12:7108468-7108681 | Common:1; Rare:62 | ||||
| chr12:7109132-7109228 | Rare:35 | ||||
| chr12:7128885-7129122 | Common:2; Rare:29 | ||||
| chr12:7189049-7189213 | Common:2; Rare:32 | ||||
| chr12:7189519-7189953 | Common:6; Rare:145; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:7751616-7751778 | Common:2; Rare:59 | ||||
| chr12:7862944-7863024 | Rare:23 | ||||
| chr12:7872740-7872941 | Rare:43 | ||||
| chr12:7873029-7873156 | Common:2; Rare:29 | ||||
| chr12:8032523-8032798 | Common:5; Rare:87 |