| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55842928-55843011 | Rare:17 | ||||
| chr12:55927872-55928215 | Rare:84 | ||||
| chr12:56079991-56080237 | Common:4; Rare:61 | ||||
| chr12:56087864-56088152 | Common:2; Rare:75; Clinvar (pathogenic):1 | ||||
| chr12:56104375-56104648 | Common:4; Rare:97 | ||||
| chr12:56116531-56116813 | Common:2; Rare:104 | ||||
| chr12:56137334-56137634 | Common:1; Rare:86 | ||||
| chr12:56152419-56152620 | Rare:59 | ||||
| chr12:56158233-56158428 | Rare:68 | ||||
| chr12:56221846-56222015 | Common:1; Rare:41 | ||||
| chr12:56258328-56258520 | Rare:67 | ||||
| chr12:56300021-56300163 | Common:2; Rare:53 | ||||
| chr12:56300275-56300395 | Rare:37 | ||||
| chr12:56315224-56315428 | Rare:56 | ||||
| chr12:56315851-56316142 | Common:2; Rare:76 |