| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104064327-104064555 | Common:1; Rare:57 | ||||
| chr12:104138164-104138560 | Common:1; Rare:114 | ||||
| chr12:104286741-104287135 | Common:3; Rare:72 | ||||
| chr12:104287204-104287322 | Rare:27 | ||||
| chr12:105107612-105107803 | Common:1; Rare:91; Clinvar:1 | ||||
| chr12:105236068-105236279 | Common:2; Rare:94 | ||||
| chr12:107093510-107093626 | Rare:46 | ||||
| chr12:107685689-107685895 | Rare:70 | ||||
| chr12:108561153-108561457 | Common:4; Rare:72 | ||||
| chr12:108562329-108562658 | Common:9; Rare:124; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:109052470-109052644 | Common:3; Rare:48 | ||||
| chr12:109097867-109098260 | Common:5; Rare:119 | ||||
| chr12:109477275-109477643 | Common:3; Rare:93 | ||||
| chr12:109573478-109573791 | Common:3; Rare:94; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:109900188-109900360 | Rare:64 |