| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55997127-55997333 | Common:1; Rare:62; Clinvar:2 | ||||
| chr12:56007616-56007902 | Common:2; Rare:73 | ||||
| chr12:56041562-56042203 | Common:6; Rare:172; Clinvar:3; Clinvar (benign):6 | ||||
| chr12:56104196-56104749 | Common:5; Rare:186 | ||||
| chr12:56104751-56104828 | Rare:15 | ||||
| chr12:56116293-56116854 | Common:4; Rare:191 | ||||
| chr12:56116858-56117242 | Common:4; Rare:103 | ||||
| chr12:56117961-56118283 | Rare:103 | ||||
| chr12:56152425-56152625 | Rare:61 | ||||
| chr12:56158211-56158401 | Rare:61 | ||||
| chr12:56189442-56189749 | Common:1; Rare:100 | ||||
| chr12:56221839-56222045 | Common:1; Rare:56 | ||||
| chr12:56224006-56224435 | Common:3; Rare:114 | ||||
| chr12:56258322-56258494 | Rare:54 | ||||
| chr12:56267056-56267302 | Common:2; Rare:63 |