| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67443429-67443722 | Common:3; Rare:163 | ||||
| chr11:67464620-67464852 | Rare:265 | ||||
| chr11:67469160-67469436 | Common:4; Rare:164 | ||||
| chr11:67482901-67483192 | Rare:124; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr11:67504250-67504710 | Common:4; Rare:205 | ||||
| chr11:67505259-67505485 | Rare:95 | ||||
| chr11:67505928-67506360 | Common:2; Rare:151 | ||||
| chr11:67508029-67508492 | Common:2; Rare:162 | ||||
| chr11:67508603-67508796 | Common:6; Rare:123 | ||||
| chr11:67629936-67630518 | Common:19; Rare:246 | ||||
| chr11:68003741-68004201 | Common:2; Rare:204; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68010119-68010455 | Common:2; Rare:128 | ||||
| chr11:68010834-68011233 | Common:3; Rare:124 | ||||
| chr11:68014320-68014720 | Common:2; Rare:112 | ||||
| chr11:68014800-68014958 | Rare:59 |