| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55728357-55728565 | Rare:48 | ||||
| chr12:55728940-55729214 | Rare:59 | ||||
| chr12:55729670-55729791 | Rare:28 | ||||
| chr12:55829498-55829793 | Rare:92 | ||||
| chr12:55830754-55830937 | Rare:57 | ||||
| chr12:55842925-55843014 | Rare:18 | ||||
| chr12:55931863-55932123 | Rare:62 | ||||
| chr12:55966665-55966843 | Rare:45 | ||||
| chr12:55997104-55997342 | Common:1; Rare:69; Clinvar:2 | ||||
| chr12:56041614-56041960 | Common:4; Rare:82; Clinvar (benign):1 | ||||
| chr12:56104367-56104657 | Common:4; Rare:100 | ||||
| chr12:56152470-56152630 | Rare:50 | ||||
| chr12:56157048-56157359 | Rare:56 | ||||
| chr12:56158233-56158407 | Rare:58 | ||||
| chr12:56221839-56222015 | Common:1; Rare:43 |