| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4648986-4649158 | Common:2; Rare:59; Clinvar (benign):2 | ||||
| chr12:6493240-6493374 | Common:5; Rare:37 | ||||
| chr12:6493789-6494138 | Common:2; Rare:105 | ||||
| chr12:6635951-6636091 | Common:2; Rare:38 | ||||
| chr12:6663102-6663406 | Common:2; Rare:84 | ||||
| chr12:6723974-6724163 | Rare:49 | ||||
| chr12:6970621-6970952 | Common:3; Rare:103 | ||||
| chr12:7189549-7189726 | Rare:65; Clinvar:4 | ||||
| chr12:10613507-10613686 | Common:1; Rare:71 | ||||
| chr12:11171571-11171648 | Common:2; Rare:25 | ||||
| chr12:12891294-12891567 | Common:1; Rare:55 | ||||
| chr12:14771124-14771250 | Rare:40 | ||||
| chr12:14774183-14774422 | Common:2; Rare:59 | ||||
| chr12:14803426-14803695 | Common:1; Rare:73 | ||||
| chr12:15882272-15882415 | Rare:56 |