| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108562427-108562699 | Common:9; Rare:117; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108730413-108730482 | Rare:20 | ||||
| chr12:108731502-108731703 | Common:2; Rare:73 | ||||
| chr12:109052470-109052638 | Common:2; Rare:41 | ||||
| chr12:109154557-109154713 | Common:1; Rare:40 | ||||
| chr12:109477279-109477662 | Common:3; Rare:96 | ||||
| chr12:109573478-109573826 | Common:3; Rare:102; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:109880374-109880678 | Common:1; Rare:92 | ||||
| chr12:109900159-109900332 | Rare:62 | ||||
| chr12:109996232-109996450 | Common:2; Rare:64 | ||||
| chr12:109999099-109999204 | Rare:15 | ||||
| chr12:110450257-110450408 | Common:2; Rare:56 | ||||
| chr12:110468702-110468929 | Rare:64 | ||||
| chr12:110502051-110502331 | Common:1; Rare:101 | ||||
| chr12:110613982-110614233 | Rare:77; Clinvar:3; Clinvar (benign):2 |