| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104064435-104064614 | Rare:47 | ||||
| chr12:104138157-104138403 | Common:1; Rare:65 | ||||
| chr12:104287204-104287350 | Rare:36 | ||||
| chr12:105107612-105107795 | Common:1; Rare:84 | ||||
| chr12:105236066-105236331 | Common:2; Rare:125 | ||||
| chr12:106357660-106357812 | Common:3; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106955502-106955908 | Common:1; Rare:151 | ||||
| chr12:106987040-106987277 | Common:4; Rare:69 | ||||
| chr12:107093510-107093626 | Rare:46 | ||||
| chr12:107093829-107093920 | Common:2; Rare:18 | ||||
| chr12:107685737-107685934 | Rare:64 | ||||
| chr12:108515047-108515313 | Common:1; Rare:80 | ||||
| chr12:108561141-108561488 | Common:4; Rare:85 | ||||
| chr12:108562361-108562733 | Common:9; Rare:147; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108730185-108730443 | Common:1; Rare:50 |