| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34049181-34049293 | Common:1; Rare:28 | ||||
| chr9:34178935-34179090 | Common:1; Rare:43 | ||||
| chr9:34329213-34329608 | Common:1; Rare:122 | ||||
| chr9:34458521-34458826 | Common:1; Rare:74 | ||||
| chr9:34652032-34652217 | Rare:53 | ||||
| chr9:34665339-34665683 | Rare:104 | ||||
| chr9:34992794-34992910 | Common:1; Rare:29 | ||||
| chr9:35161782-35162114 | Common:4; Rare:97 | ||||
| chr9:35489848-35490144 | Common:3; Rare:88 | ||||
| chr9:35657850-35658449 | Common:10; Rare:472; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35685432-35685783 | Common:1; Rare:81; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr9:35689702-35690152 | Common:4; Rare:136; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732074-35732339 | Common:2; Rare:72 | ||||
| chr9:35732362-35732693 | Common:3; Rare:84 | ||||
| chr9:35748957-35749371 | Common:2; Rare:150 |