| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106955472-106955907 | Common:3; Rare:162 | ||||
| chr12:106987029-106987258 | Common:4; Rare:65 | ||||
| chr12:107093477-107093623 | Rare:55 | ||||
| chr12:107318169-107318492 | Common:6; Rare:72 | ||||
| chr12:107320260-107320469 | Rare:37 | ||||
| chr12:107581037-107581200 | Rare:54 | ||||
| chr12:107685689-107685895 | Rare:70 | ||||
| chr12:108131651-108131799 | Common:3; Rare:26 | ||||
| chr12:108515032-108515313 | Common:1; Rare:85 | ||||
| chr12:108562394-108562715 | Common:9; Rare:136; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:109097867-109098335 | Common:5; Rare:145 | ||||
| chr12:109115912-109116210 | Common:3; Rare:56 | ||||
| chr12:109116485-109116674 | Rare:31 | ||||
| chr12:109130749-109131255 | Common:2; Rare:90 | ||||
| chr12:109131289-109131423 | Rare:24 |