| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52517588-52517978 | Common:1; Rare:111; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr12:53986203-53986299 | Common:1; Rare:32 | ||||
| chr12:54391271-54391464 | Rare:40 | ||||
| chr12:55728967-55729114 | Rare:27 | ||||
| chr12:55829539-55829793 | Rare:81 | ||||
| chr12:55931944-55932101 | Rare:41 | ||||
| chr12:56116259-56116710 | Common:3; Rare:162 | ||||
| chr12:56152481-56152608 | Rare:36 | ||||
| chr12:56189460-56189679 | Rare:77 | ||||
| chr12:56221856-56222015 | Common:1; Rare:37 | ||||
| chr12:56752313-56752466 | Rare:48 | ||||
| chr12:57111342-57111453 | Rare:27 | ||||
| chr12:57230002-57230215 | Rare:46 | ||||
| chr12:57772092-57772230 | Rare:50 | ||||
| chr12:62260070-62260411 | Common:1; Rare:125 |