| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26956255-26956475 | Common:2; Rare:82 | ||||
| chr9:27529764-27529899 | Common:4; Rare:43 | ||||
| chr9:33025071-33025382 | Common:7; Rare:127 | ||||
| chr9:33076610-33076823 | Common:2; Rare:74 | ||||
| chr9:33166785-33166958 | Rare:62; Clinvar:2 | ||||
| chr9:33167150-33167514 | Common:1; Rare:124; Clinvar:5 | ||||
| chr9:33290350-33290578 | Common:2; Rare:84 | ||||
| chr9:33473845-33474092 | Common:4; Rare:80 | ||||
| chr9:33817633-33817775 | Common:1; Rare:51 | ||||
| chr9:34178857-34179096 | Common:1; Rare:66 | ||||
| chr9:34329270-34329588 | Rare:86 | ||||
| chr9:34458555-34458833 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:34652017-34652227 | Rare:58 | ||||
| chr9:34665363-34665660 | Rare:96 | ||||
| chr9:34992814-34992859 | Common:1; Rare:14 |