| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104064435-104064555 | Rare:29 | ||||
| chr12:104138145-104138384 | Common:1; Rare:61 | ||||
| chr12:104287208-104287276 | Rare:12 | ||||
| chr12:104958254-104958380 | Common:3; Rare:35 | ||||
| chr12:104986151-104986353 | Common:3; Rare:67 | ||||
| chr12:105107612-105107795 | Common:1; Rare:84 | ||||
| chr12:105236066-105236294 | Common:2; Rare:104 | ||||
| chr12:106357692-106357819 | Common:3; Rare:29; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106582605-106582907 | Common:1; Rare:76 | ||||
| chr12:106955460-106955907 | Common:3; Rare:165 | ||||
| chr12:107093527-107093647 | Rare:42 | ||||
| chr12:107685706-107685893 | Rare:66 | ||||
| chr12:108515005-108515305 | Common:1; Rare:88 | ||||
| chr12:108561141-108561448 | Common:3; Rare:74 | ||||
| chr12:108562408-108562726 | Common:9; Rare:134; Clinvar:2; Clinvar (benign):6 |