| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33025060-33025354 | Common:7; Rare:124 | ||||
| chr9:33076610-33076877 | Common:2; Rare:93 | ||||
| chr9:33166788-33166966 | Rare:62; Clinvar:2 | ||||
| chr9:33290353-33290575 | Common:2; Rare:83 | ||||
| chr9:33402458-33402664 | Rare:35 | ||||
| chr9:34048836-34049014 | Common:2; Rare:79 | ||||
| chr9:34049186-34049315 | Common:1; Rare:31 | ||||
| chr9:34178937-34179078 | Common:1; Rare:39 | ||||
| chr9:34329189-34329595 | Rare:127 | ||||
| chr9:34652039-34652217 | Rare:53 | ||||
| chr9:34665379-34665655 | Rare:89 | ||||
| chr9:35103073-35103288 | Common:1; Rare:76 | ||||
| chr9:35657846-35658376 | Common:8; Rare:441; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35689702-35690009 | Common:3; Rare:99; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35690014-35690111 | Common:1; Rare:26; Clinvar:1 |