| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105236025-105236294 | Common:2; Rare:115 | ||||
| chr12:106955650-106955925 | Rare:97 | ||||
| chr12:106985496-106985614 | Rare:24 | ||||
| chr12:107093477-107093661 | Rare:66 | ||||
| chr12:107093818-107093857 | Common:2; Rare:10 | ||||
| chr12:107685709-107685950 | Rare:80 | ||||
| chr12:107761036-107761273 | Common:3; Rare:95 | ||||
| chr12:108515038-108515313 | Common:1; Rare:83 | ||||
| chr12:108562380-108562731 | Common:9; Rare:141; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108633750-108633992 | Rare:46 | ||||
| chr12:108648961-108649173 | Rare:34 | ||||
| chr12:108730413-108730443 | Rare:6 | ||||
| chr12:108731470-108731832 | Common:3; Rare:116 | ||||
| chr12:109052259-109052676 | Common:3; Rare:103 | ||||
| chr12:109097904-109098242 | Common:5; Rare:106 |