| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33473843-33474140 | Common:4; Rare:91 | ||||
| chr9:34048866-34048971 | Rare:42 | ||||
| chr9:34126665-34126786 | Rare:41 | ||||
| chr9:34178933-34179077 | Common:1; Rare:39 | ||||
| chr9:34329213-34329598 | Rare:119 | ||||
| chr9:34458521-34458778 | Common:1; Rare:67 | ||||
| chr9:34652016-34652200 | Rare:51 | ||||
| chr9:35103090-35103295 | Common:1; Rare:66 | ||||
| chr9:35161782-35162054 | Common:4; Rare:76 | ||||
| chr9:35489922-35490144 | Common:3; Rare:63 | ||||
| chr9:35657850-35658376 | Common:8; Rare:439; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35732041-35732344 | Common:2; Rare:82 | ||||
| chr9:35732365-35732700 | Common:3; Rare:86 | ||||
| chr9:35748882-35749395 | Common:3; Rare:168 | ||||
| chr9:35814983-35815293 | Rare:79 |