| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6375338-6375668 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6376155-6376426 | Common:3; Rare:57 | ||||
| chr12:6383980-6384382 | Common:2; Rare:97 | ||||
| chr12:6444875-6445003 | Rare:26 | ||||
| chr12:6452016-6452150 | Common:1; Rare:29 | ||||
| chr12:6470672-6470884 | Rare:50 | ||||
| chr12:6493107-6493502 | Common:8; Rare:124 | ||||
| chr12:6493778-6494146 | Common:2; Rare:109 | ||||
| chr12:6534287-6534629 | Common:5; Rare:138 | ||||
| chr12:6568245-6568393 | Rare:57 | ||||
| chr12:6601446-6601742 | Rare:69 | ||||
| chr12:6663090-6663400 | Common:2; Rare:88 | ||||
| chr12:6688870-6689089 | Rare:69 | ||||
| chr12:6689091-6689345 | Rare:73 | ||||
| chr12:6689350-6689778 | Common:3; Rare:111 |