| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:94150452-94150594 | Rare:26 | ||||
| chr12:94459276-94459558 | Common:1; Rare:56 | ||||
| chr12:94459771-94460106 | Common:4; Rare:95 | ||||
| chr12:94460425-94460503 | Rare:20 | ||||
| chr12:94615961-94616106 | Rare:27 | ||||
| chr12:94616440-94616532 | Rare:11 | ||||
| chr12:95003196-95003238 | Rare:6 | ||||
| chr12:95003383-95003484 | Rare:18 | ||||
| chr12:95003553-95003875 | Common:4; Rare:124; Clinvar (benign):6 | ||||
| chr12:95072884-95073241 | Common:3; Rare:116 | ||||
| chr12:95073366-95073488 | Common:2; Rare:27 | ||||
| chr12:95073491-95073782 | Common:1; Rare:93 | ||||
| chr12:95217182-95217216 | Rare:13 | ||||
| chr12:95217279-95217889 | Common:6; Rare:162 | ||||
| chr12:95218005-95218142 | Common:2; Rare:23 |