| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106774509-106774731 | Common:1; Rare:66 | ||||
| chr12:107093510-107093626 | Rare:46 | ||||
| chr12:107685689-107685895 | Rare:70 | ||||
| chr12:108561120-108561488 | Common:4; Rare:97 | ||||
| chr12:108562387-108562673 | Common:8; Rare:119; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:108648972-108649218 | Rare:41 | ||||
| chr12:108731476-108731820 | Common:3; Rare:112 | ||||
| chr12:109097393-109097645 | Rare:86; Clinvar:2 | ||||
| chr12:109097847-109098248 | Common:5; Rare:126 | ||||
| chr12:109154557-109154686 | Common:1; Rare:34 | ||||
| chr12:109458933-109459114 | Common:1; Rare:29 | ||||
| chr12:109477275-109477650 | Common:3; Rare:95 | ||||
| chr12:109573476-109573852 | Common:3; Rare:111; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:109880370-109880668 | Common:1; Rare:91 | ||||
| chr12:110281024-110281189 | Rare:65 |