| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55728951-55729189 | Rare:48 | ||||
| chr12:55729661-55729819 | Rare:37 | ||||
| chr12:55829497-55829793 | Rare:92 | ||||
| chr12:55931939-55932101 | Rare:42 | ||||
| chr12:55966707-55966875 | Rare:45 | ||||
| chr12:56007616-56007825 | Common:2; Rare:45 | ||||
| chr12:56041558-56042002 | Common:4; Rare:94; Clinvar (benign):1 | ||||
| chr12:56104210-56104749 | Common:5; Rare:184 | ||||
| chr12:56117985-56118290 | Rare:98 | ||||
| chr12:56152419-56152630 | Rare:63 | ||||
| chr12:56158237-56158415 | Rare:63 | ||||
| chr12:56189466-56189749 | Common:1; Rare:95 | ||||
| chr12:56221839-56222019 | Common:1; Rare:44 | ||||
| chr12:56224153-56224435 | Common:1; Rare:85 | ||||
| chr12:56258310-56258514 | Rare:65 |