| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89526022-89526090 | Rare:19 | ||||
| chr12:89708770-89709085 | Common:1; Rare:120 | ||||
| chr12:89709218-89709415 | Common:3; Rare:79 | ||||
| chr12:89709639-89709808 | Common:1; Rare:60 | ||||
| chr12:92929218-92929503 | Common:1; Rare:90 | ||||
| chr12:93377759-93377959 | Rare:63 | ||||
| chr12:93441855-93442173 | Common:2; Rare:100 | ||||
| chr12:93570280-93570389 | Common:1; Rare:21 | ||||
| chr12:93570865-93571075 | Rare:55 | ||||
| chr12:93571716-93571900 | Common:6; Rare:71 | ||||
| chr12:93677329-93677400 | Rare:15 | ||||
| chr12:94459833-94460043 | Common:2; Rare:61 | ||||
| chr12:95003593-95003833 | Common:3; Rare:100; Clinvar (benign):6 | ||||
| chr12:95073439-95073680 | Common:1; Rare:85 | ||||
| chr12:95217386-95217849 | Common:4; Rare:127 |