| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120725963-120726076 | Rare:30 | ||||
| chr12:120903360-120903675 | Common:2; Rare:67 | ||||
| chr12:120904144-120904534 | Common:4; Rare:141 | ||||
| chr12:120978231-120978820 | Common:4; Rare:153; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr12:121016383-121016594 | Common:5; Rare:90 | ||||
| chr12:121209900-121210305 | Common:5; Rare:145 | ||||
| chr12:121210349-121210460 | Rare:27 | ||||
| chr12:121296257-121296445 | Rare:31 | ||||
| chr12:121296615-121297046 | Common:3; Rare:125 | ||||
| chr12:121297073-121297191 | Rare:26 | ||||
| chr12:121297260-121297393 | Common:2; Rare:27 | ||||
| chr12:121297767-121297941 | Common:2; Rare:35 | ||||
| chr12:121352140-121352676 | Common:3; Rare:192 | ||||
| chr12:121352745-121352884 | Rare:28 | ||||
| chr12:121399584-121400208 | Common:6; Rare:193 |