| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106774509-106774715 | Common:1; Rare:61 | ||||
| chr12:106955460-106955925 | Common:3; Rare:172 | ||||
| chr12:107093490-107093642 | Rare:57 | ||||
| chr12:107685709-107685905 | Rare:68 | ||||
| chr12:108562394-108562751 | Common:9; Rare:142; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108857580-108857883 | Common:3; Rare:131 | ||||
| chr12:109052457-109052667 | Common:3; Rare:64 | ||||
| chr12:109097847-109098250 | Common:5; Rare:126 | ||||
| chr12:109116484-109116704 | Rare:38 | ||||
| chr12:109154524-109154691 | Common:1; Rare:43 | ||||
| chr12:109477269-109477664 | Common:3; Rare:106 | ||||
| chr12:109573466-109573841 | Common:3; Rare:112; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109900159-109900356 | Rare:67 | ||||
| chr12:109996220-109996434 | Common:2; Rare:62 | ||||
| chr12:110124123-110124455 | Common:2; Rare:106 |