| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19102863-19103065 | Common:2; Rare:87 | ||||
| chr9:19127420-19127605 | Common:4; Rare:57 | ||||
| chr9:19380191-19380339 | Common:4; Rare:74 | ||||
| chr9:20684058-20684283 | Common:3; Rare:90 | ||||
| chr9:21802515-21802687 | Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994350-21994577 | Rare:71; Clinvar:1; Clinvar (benign):4 | ||||
| chr9:26892738-26892895 | Common:1; Rare:77 | ||||
| chr9:26947024-26947287 | Common:1; Rare:101 | ||||
| chr9:32384537-32384726 | Common:1; Rare:75 | ||||
| chr9:32573041-32573243 | Common:3; Rare:74 | ||||
| chr9:33025081-33025383 | Common:7; Rare:125 | ||||
| chr9:33076583-33076861 | Common:2; Rare:87 | ||||
| chr9:33166890-33166951 | Rare:28 | ||||
| chr9:33167322-33167587 | Rare:100 | ||||
| chr9:33290255-33290565 | Common:3; Rare:104 |