| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55716403-55716607 | Common:3; Rare:53 | ||||
| chr12:55728327-55728518 | Rare:51 | ||||
| chr12:55728952-55729214 | Rare:55 | ||||
| chr12:55729660-55729807 | Rare:33 | ||||
| chr12:55829506-55829793 | Rare:92 | ||||
| chr12:55830804-55830924 | Rare:40 | ||||
| chr12:55927739-55928005 | Rare:72 | ||||
| chr12:55931944-55932068 | Rare:36 | ||||
| chr12:55966653-55966875 | Rare:59 | ||||
| chr12:55997127-55997339 | Common:1; Rare:65; Clinvar:2 | ||||
| chr12:56021232-56021367 | Common:9; Rare:20 | ||||
| chr12:56041613-56041968 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr12:56042248-56042601 | Common:1; Rare:91; Clinvar (benign):1 | ||||
| chr12:56079769-56079880 | Rare:28 | ||||
| chr12:56104367-56104670 | Common:4; Rare:107 |