| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108562361-108562751 | Common:9; Rare:149; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108632093-108632220 | Common:1; Rare:30 | ||||
| chr12:108633741-108634024 | Rare:57 | ||||
| chr12:108731456-108731690 | Common:2; Rare:85 | ||||
| chr12:109052259-109052653 | Common:3; Rare:94 | ||||
| chr12:109097902-109098252 | Common:5; Rare:108 | ||||
| chr12:109098362-109098533 | Rare:74; Clinvar:2 | ||||
| chr12:109154546-109154707 | Common:1; Rare:40 | ||||
| chr12:109477260-109477664 | Common:3; Rare:108 | ||||
| chr12:109573433-109573813 | Common:3; Rare:125; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880370-109880668 | Common:1; Rare:91 | ||||
| chr12:109900159-109900360 | Rare:67 | ||||
| chr12:109908291-109908603 | Common:3; Rare:63 | ||||
| chr12:109908698-109908893 | Common:1; Rare:57 | ||||
| chr12:109996212-109996393 | Common:2; Rare:60 |