| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108731470-108731830 | Common:3; Rare:114 | ||||
| chr12:109020998-109021131 | Common:2; Rare:38 | ||||
| chr12:109093390-109093568 | Common:2; Rare:68 | ||||
| chr12:109098362-109098524 | Rare:71; Clinvar:1 | ||||
| chr12:109154528-109154686 | Common:1; Rare:41 | ||||
| chr12:109477287-109477653 | Common:3; Rare:90 | ||||
| chr12:109573435-109573845 | Common:3; Rare:133; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880327-109880650 | Common:1; Rare:104 | ||||
| chr12:109900195-109900345 | Rare:62 | ||||
| chr12:109996288-109996439 | Common:2; Rare:41 | ||||
| chr12:110281015-110281264 | Rare:92 | ||||
| chr12:110468702-110468929 | Rare:64 | ||||
| chr12:110502058-110502241 | Common:1; Rare:64 | ||||
| chr12:110613997-110614229 | Rare:71; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:111685769-111686110 | Rare:127 |