| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6914209-6914358 | Rare:33 | ||||
| chr12:6914442-6914612 | Rare:46 | ||||
| chr12:6914625-6914657 | Common:1; Rare:9 | ||||
| chr12:6914807-6914935 | Rare:25 | ||||
| chr12:6915433-6915462 | Rare:2 | ||||
| chr12:6915465-6915659 | Common:1; Rare:38 | ||||
| chr12:6924901-6925166 | Common:11; Rare:64 | ||||
| chr12:6927544-6927991 | Common:1; Rare:116 | ||||
| chr12:6928380-6928473 | Common:1; Rare:21 | ||||
| chr12:6928502-6928767 | Rare:56 | ||||
| chr12:6937595-6937744 | Rare:38 | ||||
| chr12:6937902-6938274 | Common:1; Rare:141; Clinvar (benign):1 | ||||
| chr12:6938628-6938946 | Rare:88 | ||||
| chr12:6943460-6943860 | Common:5; Rare:195 | ||||
| chr12:6943921-6944637 | Common:13; Rare:461; Clinvar:15; Clinvar (benign):4; Clinvar (pathogenic):3 |