| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:94459807-94460160 | Common:4; Rare:96 | ||||
| chr12:94460428-94460474 | Rare:11 | ||||
| chr12:95003390-95003446 | Rare:5 | ||||
| chr12:95003625-95003862 | Common:3; Rare:93; Clinvar (benign):4 | ||||
| chr12:95072922-95073152 | Common:2; Rare:79 | ||||
| chr12:95073495-95073730 | Common:1; Rare:76 | ||||
| chr12:95217347-95217906 | Common:6; Rare:144 | ||||
| chr12:95218467-95218599 | Rare:20 | ||||
| chr12:95473557-95473634 | Rare:13 | ||||
| chr12:95473851-95474224 | Common:3; Rare:153 | ||||
| chr12:95858830-95859067 | Common:3; Rare:71 | ||||
| chr12:95942554-95942727 | Common:1; Rare:36 | ||||
| chr12:95942747-95942781 | Common:1; Rare:8 | ||||
| chr12:95942800-95943355 | Common:3; Rare:106 | ||||
| chr12:95943419-95943563 | Common:1; Rare:38 |