| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:754019-754316 | Common:1; Rare:85; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:4275433-4275563 | Common:2; Rare:16 | ||||
| chr12:6934275-6934576 | Common:1; Rare:81 | ||||
| chr12:7089291-7089746 | Common:3; Rare:146 | ||||
| chr12:8242940-8243175 | Common:5; Rare:70 | ||||
| chr12:9065054-9065181 | Rare:14 | ||||
| chr12:9070486-9070787 | Common:1; Rare:58 | ||||
| chr12:9072482-9072572 | Rare:20 | ||||
| chr12:9076874-9077190 | Common:1; Rare:54 | ||||
| chr12:9089200-9089538 | Rare:59 | ||||
| chr12:9093512-9093805 | Common:3; Rare:72; Clinvar (benign):1 | ||||
| chr12:9094981-9095226 | Rare:44; Clinvar (benign):1 | ||||
| chr12:9109318-9109607 | Rare:62 | ||||
| chr12:9109865-9110173 | Common:1; Rare:82 | ||||
| chr12:9112187-9112537 | Common:1; Rare:84 |