| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:15307204-15307444 | Common:2; Rare:118 | ||||
| chr9:15422611-15422886 | Common:1; Rare:120 | ||||
| chr9:15510960-15511248 | Common:2; Rare:93 | ||||
| chr9:15552826-15553184 | Common:4; Rare:129 | ||||
| chr9:18473944-18474262 | Rare:90 | ||||
| chr9:19049291-19049405 | Rare:46 | ||||
| chr9:19102850-19103104 | Common:2; Rare:111 | ||||
| chr9:19127427-19127755 | Common:7; Rare:100 | ||||
| chr9:19230275-19230495 | Common:3; Rare:79 | ||||
| chr9:19379485-19379865 | Common:1; Rare:134 | ||||
| chr9:19380188-19380349 | Common:4; Rare:77 | ||||
| chr9:20622394-20622714 | Common:1; Rare:113 | ||||
| chr9:20658199-20658429 | Common:5; Rare:96 | ||||
| chr9:20684099-20684289 | Common:3; Rare:77 | ||||
| chr9:21802515-21802700 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):1 |