| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:14366008-14366048 | Rare:5 | ||||
| chr12:14567677-14567947 | Common:2; Rare:59 | ||||
| chr12:14771118-14771244 | Rare:45 | ||||
| chr12:14774184-14774473 | Common:3; Rare:75 | ||||
| chr12:14803403-14803720 | Common:2; Rare:86 | ||||
| chr12:15221394-15221418 | Rare:3 | ||||
| chr12:15789352-15789597 | Rare:88 | ||||
| chr12:15882263-15882813 | Common:1; Rare:184 | ||||
| chr12:16347482-16347732 | Common:4; Rare:46 | ||||
| chr12:19129405-19129829 | Common:3; Rare:172 | ||||
| chr12:19439311-19439503 | Common:1; Rare:61 | ||||
| chr12:21395375-21395557 | Common:6; Rare:90 | ||||
| chr12:21437592-21437671 | Common:3; Rare:30 | ||||
| chr12:21501513-21501880 | Common:4; Rare:103 | ||||
| chr12:21657754-21658003 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):1 |