| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132900889-132900963 | Common:1; Rare:10 | ||||
| chr9:132902603-132902969 | Rare:63; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr9:132903780-132904044 | Rare:51; Clinvar:5; Clinvar (benign):4 | ||||
| chr9:133119463-133119582 | Common:2; Rare:35 | ||||
| chr9:133127417-133127772 | Common:1; Rare:61 | ||||
| chr9:133127874-133127945 | Common:1; Rare:16 | ||||
| chr9:133133750-133133976 | Common:3; Rare:46 | ||||
| chr9:133147617-133147828 | Common:1; Rare:41 | ||||
| chr9:134350571-134350615 | Rare:12 | ||||
| chr9:134354003-134354288 | Common:4; Rare:67 | ||||
| chr9:134366008-134366168 | Rare:33 | ||||
| chr9:134368374-134368429 | Rare:18 | ||||
| chr9:134376620-134376652 | Common:1; Rare:1 | ||||
| chr9:134408464-134408787 | Common:2; Rare:72 | ||||
| chr9:136243815-136243889 | Rare:15 |