| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:20684115-20684285 | Common:2; Rare:65 | ||||
| chr9:21335347-21335504 | Common:3; Rare:60 | ||||
| chr9:21802515-21802677 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:26892738-26892828 | Rare:53 | ||||
| chr9:26947019-26947304 | Common:1; Rare:104 | ||||
| chr9:26947403-26947570 | Common:1; Rare:54 | ||||
| chr9:26956295-26956472 | Common:2; Rare:63 | ||||
| chr9:27529598-27529831 | Common:5; Rare:55 | ||||
| chr9:27573429-27573513 | Common:2; Rare:43 | ||||
| chr9:33025083-33025357 | Common:7; Rare:118 | ||||
| chr9:33166767-33166956 | Rare:63; Clinvar:3 | ||||
| chr9:33264528-33264894 | Common:2; Rare:104 | ||||
| chr9:33401366-33401687 | Common:3; Rare:62 | ||||
| chr9:33402464-33402766 | Rare:60 | ||||
| chr9:34048866-34048992 | Common:1; Rare:51 |