| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108827370-108827403 | Rare:10 | ||||
| chr12:108827405-108827666 | Rare:47 | ||||
| chr12:109097867-109098221 | Common:5; Rare:110 | ||||
| chr12:109098343-109098435 | Rare:41 | ||||
| chr12:109154557-109154866 | Common:3; Rare:70 | ||||
| chr12:109175986-109176212 | Rare:73 | ||||
| chr12:109477260-109477666 | Common:3; Rare:108 | ||||
| chr12:109573421-109573813 | Common:5; Rare:134; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr12:110502058-110502331 | Common:1; Rare:99 | ||||
| chr12:110614004-110614193 | Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:110742789-110743139 | Common:3; Rare:139 | ||||
| chr12:111685739-111686119 | Rare:136 | ||||
| chr12:111766853-111767035 | Rare:59 | ||||
| chr12:111841910-111842224 | Common:2; Rare:84 | ||||
| chr12:112013119-112013468 | Common:1; Rare:124 |