| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134224530-134224695 | Rare:62 | ||||
| chr11:134225441-134225635 | Rare:59 | ||||
| chr11:134253217-134253608 | Common:2; Rare:129; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:134410103-134410314 | Common:2; Rare:43 | ||||
| chr12:389230-389400 | Common:1; Rare:67 | ||||
| chr12:389481-389643 | Common:5; Rare:70 | ||||
| chr12:401446-401669 | Rare:60 | ||||
| chr12:459895-460009 | Rare:52 | ||||
| chr12:460159-460513 | Common:2; Rare:93 | ||||
| chr12:460736-460821 | Common:3; Rare:14 | ||||
| chr12:610367-610516 | Common:2; Rare:15 | ||||
| chr12:643609-643941 | Common:2; Rare:70 | ||||
| chr12:752343-752624 | Common:1; Rare:87 | ||||
| chr12:907677-908034 | Common:4; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:914111-914399 | Rare:65; Clinvar:1 |