| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93442321-93442623 | Common:4; Rare:57 | ||||
| chr12:93467406-93467623 | Common:3; Rare:72 | ||||
| chr12:93467692-93467808 | Common:2; Rare:27 | ||||
| chr12:93570823-93570992 | Rare:41 | ||||
| chr12:93571547-93571712 | Common:1; Rare:53 | ||||
| chr12:93677225-93677606 | Common:1; Rare:88 | ||||
| chr12:94148579-94148732 | Rare:28 | ||||
| chr12:94459859-94460069 | Common:2; Rare:64 | ||||
| chr12:95003639-95003833 | Common:3; Rare:76; Clinvar (benign):3 | ||||
| chr12:95072961-95073090 | Common:1; Rare:41 | ||||
| chr12:95217218-95217339 | Rare:49 | ||||
| chr12:95217362-95217906 | Common:6; Rare:143 | ||||
| chr12:95218020-95218480 | Common:7; Rare:198 | ||||
| chr12:95473833-95474198 | Common:3; Rare:141 | ||||
| chr12:95547586-95547815 | Common:1; Rare:41 |