| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53727403-53727714 | Rare:66 | ||||
| chr12:54053777-54053871 | Rare:11 | ||||
| chr12:54419182-54419662 | Common:1; Rare:107 | ||||
| chr12:55712066-55712261 | Common:5; Rare:54; Clinvar (benign):1 | ||||
| chr12:55715987-55716195 | Common:2; Rare:95 | ||||
| chr12:55716306-55716571 | Common:2; Rare:66 | ||||
| chr12:55720204-55720434 | Common:4; Rare:30; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:55728956-55729214 | Rare:55 | ||||
| chr12:55729659-55729799 | Rare:32 | ||||
| chr12:55829509-55829793 | Rare:92 | ||||
| chr12:55830782-55830968 | Common:1; Rare:51 | ||||
| chr12:55927759-55927805 | Rare:16 | ||||
| chr12:55931982-55932095 | Rare:32 | ||||
| chr12:55966720-55966904 | Rare:48 | ||||
| chr12:56041614-56041956 | Common:3; Rare:80 |