| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107761102-107761253 | Common:3; Rare:59 | ||||
| chr12:108515021-108515305 | Common:1; Rare:85 | ||||
| chr12:108561150-108561461 | Common:4; Rare:73 | ||||
| chr12:108562394-108562651 | Common:6; Rare:103; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:108731480-108731678 | Common:2; Rare:74 | ||||
| chr12:109052465-109052638 | Common:2; Rare:43 | ||||
| chr12:109097465-109097613 | Rare:53; Clinvar:1 | ||||
| chr12:109477287-109477660 | Common:3; Rare:92 | ||||
| chr12:109573468-109573813 | Common:3; Rare:104; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:109900158-109900336 | Rare:62 | ||||
| chr12:109996288-109996434 | Common:2; Rare:39 | ||||
| chr12:110281003-110281186 | Common:1; Rare:73 | ||||
| chr12:110502051-110502195 | Common:1; Rare:53 | ||||
| chr12:110613997-110614224 | Rare:70; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:111685933-111686094 | Rare:56 |