| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53499442-53499557 | Rare:28 | ||||
| chr12:53676057-53676416 | Common:3; Rare:156 | ||||
| chr12:53985000-53985227 | Common:2; Rare:56 | ||||
| chr12:54009209-54009434 | Rare:82 | ||||
| chr12:55725836-55725942 | Rare:19 | ||||
| chr12:55726755-55726962 | Common:1; Rare:71 | ||||
| chr12:55727030-55727244 | Rare:66 | ||||
| chr12:55728895-55729275 | Common:1; Rare:78 | ||||
| chr12:55729520-55729790 | Common:1; Rare:55 | ||||
| chr12:55829506-55829793 | Rare:92 | ||||
| chr12:55966702-55966875 | Rare:45 | ||||
| chr12:56041690-56041984 | Common:3; Rare:70; Clinvar (benign):1 | ||||
| chr12:56116523-56116800 | Common:2; Rare:108 | ||||
| chr12:56152491-56152618 | Rare:36 | ||||
| chr12:56221862-56221992 | Common:1; Rare:34 |