| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6688843-6689089 | Rare:76 | ||||
| chr12:6689227-6689765 | Common:3; Rare:146 | ||||
| chr12:6723959-6724303 | Common:1; Rare:86 | ||||
| chr12:6752908-6753189 | Common:6; Rare:80 | ||||
| chr12:6765435-6765595 | Common:1; Rare:32 | ||||
| chr12:6766397-6766748 | Rare:101 | ||||
| chr12:6829675-6829883 | Common:2; Rare:56 | ||||
| chr12:6851247-6851481 | Rare:54 | ||||
| chr12:6851902-6852250 | Common:1; Rare:88 | ||||
| chr12:6867398-6867604 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868919-6869181 | Rare:78; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6869418-6869773 | Common:1; Rare:100; Clinvar (pathogenic):1 | ||||
| chr12:6873274-6873680 | Common:4; Rare:118 | ||||
| chr12:6904793-6904890 | Rare:21 | ||||
| chr12:6914406-6914657 | Common:1; Rare:66 |