| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55728940-55729302 | Rare:74 | ||||
| chr12:55729657-55729791 | Rare:29 | ||||
| chr12:55829509-55829793 | Rare:92 | ||||
| chr12:55830739-55830937 | Rare:63 | ||||
| chr12:55927862-55928166 | Rare:80 | ||||
| chr12:55966700-55966849 | Rare:36 | ||||
| chr12:56041614-56041961 | Common:4; Rare:82; Clinvar (benign):1 | ||||
| chr12:56116271-56116710 | Common:3; Rare:159 | ||||
| chr12:56152484-56152624 | Rare:41 | ||||
| chr12:56221846-56222026 | Common:1; Rare:47 | ||||
| chr12:56300079-56300163 | Common:2; Rare:32 | ||||
| chr12:56315828-56316102 | Common:1; Rare:68 | ||||
| chr12:56333948-56334161 | Rare:62 | ||||
| chr12:56645947-56646260 | Common:1; Rare:73 | ||||
| chr12:56752294-56752453 | Rare:54 |