| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33001519-33001751 | Common:3; Rare:120; Clinvar (benign):4 | ||||
| chr9:33025052-33025407 | Common:7; Rare:139 | ||||
| chr9:33076597-33076865 | Common:2; Rare:89 | ||||
| chr9:33166884-33166952 | Rare:31 | ||||
| chr9:33167112-33167502 | Common:1; Rare:135; Clinvar:6 | ||||
| chr9:33264590-33264947 | Common:1; Rare:101 | ||||
| chr9:33290349-33290578 | Common:2; Rare:85 | ||||
| chr9:33290856-33291180 | Common:2; Rare:65 | ||||
| chr9:33473826-33474149 | Common:4; Rare:99 | ||||
| chr9:34048839-34049003 | Common:2; Rare:73 | ||||
| chr9:34049170-34049588 | Common:2; Rare:122 | ||||
| chr9:34126622-34126809 | Common:1; Rare:56 | ||||
| chr9:34178929-34179096 | Common:1; Rare:47 | ||||
| chr9:34329181-34329638 | Common:1; Rare:142 | ||||
| chr9:34458539-34458787 | Rare:63 |