| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6568233-6568382 | Rare:55 | ||||
| chr12:6663100-6663295 | Rare:56 | ||||
| chr12:6688884-6689239 | Rare:110 | ||||
| chr12:6753038-6753189 | Common:4; Rare:53 | ||||
| chr12:6851243-6851497 | Rare:60 | ||||
| chr12:6851879-6852174 | Rare:78 | ||||
| chr12:6867381-6867561 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6970612-6970980 | Common:4; Rare:119; Clinvar (benign):1 | ||||
| chr12:7018468-7018580 | Common:1; Rare:30 | ||||
| chr12:7189556-7189731 | Rare:65; Clinvar:4 | ||||
| chr12:8697762-8698043 | Common:1; Rare:112 | ||||
| chr12:8914359-8914735 | Common:6; Rare:110 | ||||
| chr12:8949975-8950104 | Common:1; Rare:36 | ||||
| chr12:10613508-10613700 | Common:1; Rare:74 | ||||
| chr12:11171124-11171237 | Rare:42 |