| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54259517-54259724 | Rare:40 | ||||
| chr12:54279691-54279929 | Common:2; Rare:76 | ||||
| chr12:54419449-54419662 | Rare:36 | ||||
| chr12:55716014-55716194 | Common:1; Rare:85 | ||||
| chr12:55716403-55716577 | Common:2; Rare:45 | ||||
| chr12:55728294-55728521 | Rare:68 | ||||
| chr12:55728952-55729122 | Rare:29 | ||||
| chr12:55729670-55729807 | Rare:32 | ||||
| chr12:55829506-55829793 | Rare:92 | ||||
| chr12:55830752-55830960 | Common:1; Rare:61 | ||||
| chr12:55931944-55932095 | Rare:41 | ||||
| chr12:55966037-55966294 | Common:1; Rare:51 | ||||
| chr12:55966708-55966865 | Rare:40 | ||||
| chr12:55997127-55997352 | Common:2; Rare:68; Clinvar:2 | ||||
| chr12:56041613-56041982 | Common:4; Rare:83; Clinvar (benign):1 |