| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55830804-55830889 | Rare:35 | ||||
| chr12:55931948-55932101 | Rare:40 | ||||
| chr12:55997127-55997333 | Common:1; Rare:62; Clinvar:2 | ||||
| chr12:56041614-56041961 | Common:4; Rare:82; Clinvar (benign):1 | ||||
| chr12:56104344-56104670 | Common:4; Rare:112 | ||||
| chr12:56116290-56116736 | Common:3; Rare:157 | ||||
| chr12:56118126-56118283 | Rare:49 | ||||
| chr12:56152481-56152624 | Rare:43 | ||||
| chr12:56158001-56158428 | Common:1; Rare:126 | ||||
| chr12:56221855-56222019 | Common:1; Rare:38 | ||||
| chr12:56224264-56224465 | Common:1; Rare:58 | ||||
| chr12:56258329-56258494 | Rare:51 | ||||
| chr12:56300272-56300584 | Common:1; Rare:89 | ||||
| chr12:56315847-56316104 | Common:1; Rare:65 | ||||
| chr12:56333948-56334193 | Rare:78 |