| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45727687-45728042 | Common:2; Rare:96 | ||||
| chr12:46266480-46266675 | Rare:28 | ||||
| chr12:53039138-53039341 | Common:4; Rare:47 | ||||
| chr12:53100703-53101080 | Common:3; Rare:123 | ||||
| chr12:54081850-54082002 | Common:1; Rare:34 | ||||
| chr12:54125915-54126234 | Common:2; Rare:60 | ||||
| chr12:54126470-54126557 | Rare:26 | ||||
| chr12:54429030-54429411 | Common:2; Rare:72 | ||||
| chr12:55697215-55697477 | Common:2; Rare:70; Clinvar (benign):3 | ||||
| chr12:55709769-55710014 | Common:1; Rare:34 | ||||
| chr12:56634987-56635089 | Rare:17 | ||||
| chr12:57162760-57162952 | Rare:48 | ||||
| chr12:57184130-57184450 | Rare:75 | ||||
| chr12:57195748-57196170 | Common:3; Rare:112 | ||||
| chr12:57204488-57204749 | Common:2; Rare:77 |