| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55716366-55716563 | Common:2; Rare:55 | ||||
| chr12:55728951-55729331 | Rare:75 | ||||
| chr12:55729660-55729827 | Rare:41 | ||||
| chr12:55829500-55829794 | Rare:92 | ||||
| chr12:55830737-55830937 | Rare:64 | ||||
| chr12:55931929-55932101 | Rare:43 | ||||
| chr12:55966700-55966865 | Rare:42 | ||||
| chr12:56007617-56007813 | Common:1; Rare:42 | ||||
| chr12:56041643-56041968 | Common:3; Rare:78; Clinvar (benign):1 | ||||
| chr12:56116321-56116806 | Common:3; Rare:173 | ||||
| chr12:56118004-56118283 | Rare:91 | ||||
| chr12:56152470-56152620 | Rare:46 | ||||
| chr12:56189465-56189645 | Rare:67 | ||||
| chr12:56221855-56222026 | Common:1; Rare:43 | ||||
| chr12:56224077-56224435 | Common:2; Rare:104 |