| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55966700-55966879 | Rare:46 | ||||
| chr12:55997081-55997330 | Common:1; Rare:72; Clinvar:2 | ||||
| chr12:56041614-56041968 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr12:56118004-56118278 | Rare:90 | ||||
| chr12:56152470-56152618 | Rare:44 | ||||
| chr12:56158237-56158428 | Rare:68 | ||||
| chr12:56221833-56222015 | Common:1; Rare:44 | ||||
| chr12:56300013-56300163 | Common:2; Rare:57 | ||||
| chr12:56315847-56316111 | Common:1; Rare:67 | ||||
| chr12:56333948-56334145 | Rare:58 | ||||
| chr12:56360081-56360250 | Common:3; Rare:42 | ||||
| chr12:56468425-56468584 | Common:1; Rare:73 | ||||
| chr12:56636303-56636455 | Rare:31 | ||||
| chr12:56645956-56646289 | Common:1; Rare:77 | ||||
| chr12:56688090-56688557 | Common:5; Rare:160 |