| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:70258254-70258316 | Rare:12 | ||||
| chr9:72305213-72305441 | Common:2; Rare:38 | ||||
| chr9:72918722-72918976 | Common:1; Rare:47 | ||||
| chr9:83219195-83219357 | Common:2; Rare:40 | ||||
| chr9:83920762-83920773 | Rare:5 | ||||
| chr9:86948574-86948760 | Common:1; Rare:54 | ||||
| chr9:87041867-87041886 | Rare:5 | ||||
| chr9:87042092-87042294 | Common:1; Rare:92 | ||||
| chr9:88387451-88387695 | Common:2; Rare:57 | ||||
| chr9:94459006-94459298 | Common:2; Rare:88 | ||||
| chr9:94700062-94700276 | Rare:24 | ||||
| chr9:97238260-97238504 | Common:5; Rare:73 | ||||
| chr9:97238660-97238787 | Rare:36 | ||||
| chr9:99819882-99820075 | Common:1; Rare:61 | ||||
| chr9:101426553-101426732 | Rare:60; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 |