| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122500838-122501170 | Common:3; Rare:89 | ||||
| chr12:122526846-122527260 | Common:4; Rare:146 | ||||
| chr12:122871960-122872124 | Rare:30 | ||||
| chr12:122896071-122896260 | Rare:94 | ||||
| chr12:122974566-122974761 | Rare:50 | ||||
| chr12:122975139-122975244 | Common:1; Rare:27 | ||||
| chr12:123233119-123233501 | Common:2; Rare:126; Clinvar:1 | ||||
| chr12:123364825-123364928 | Common:1; Rare:41 | ||||
| chr12:123436590-123436877 | Common:2; Rare:59 | ||||
| chr12:123584655-123584808 | Common:3; Rare:44 | ||||
| chr12:123602023-123602174 | Common:3; Rare:56 | ||||
| chr12:123633546-123633840 | Common:1; Rare:140; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:124914077-124914251 | Common:6; Rare:66 | ||||
| chr12:131929076-131929336 | Common:9; Rare:79; Clinvar:1 | ||||
| chr12:132144309-132144486 | Rare:72 |