| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107093510-107093623 | Rare:44 | ||||
| chr12:107685689-107685934 | Rare:78 | ||||
| chr12:107761049-107761255 | Common:3; Rare:87 | ||||
| chr12:108515071-108515319 | Common:1; Rare:76 | ||||
| chr12:108561136-108561469 | Common:4; Rare:83 | ||||
| chr12:108562387-108562736 | Common:9; Rare:141; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108857550-108857850 | Common:3; Rare:144 | ||||
| chr12:109052434-109052660 | Common:3; Rare:64 | ||||
| chr12:109093399-109093903 | Common:4; Rare:146 | ||||
| chr12:109097899-109098249 | Common:5; Rare:110 | ||||
| chr12:109098343-109098443 | Rare:42 | ||||
| chr12:109154552-109154707 | Common:1; Rare:38 | ||||
| chr12:109477287-109477679 | Common:3; Rare:103 | ||||
| chr12:109573421-109573845 | Common:5; Rare:142; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr12:109880288-109880703 | Common:2; Rare:129 |