| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19408760-19409012 | Common:5; Rare:98 | ||||
| chr9:20622388-20622714 | Common:1; Rare:113 | ||||
| chr9:21802487-21802692 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:23826301-23826491 | Common:1; Rare:77 | ||||
| chr9:26892331-26892398 | Rare:27 | ||||
| chr9:26892404-26892456 | Rare:23 | ||||
| chr9:26892711-26892829 | Rare:63 | ||||
| chr9:26947094-26947237 | Common:1; Rare:52 | ||||
| chr9:26956255-26956470 | Common:2; Rare:80 | ||||
| chr9:27005607-27005710 | Rare:20 | ||||
| chr9:27109398-27109511 | Rare:25; Clinvar (benign):1 | ||||
| chr9:27529724-27529981 | Common:5; Rare:65 | ||||
| chr9:27573422-27573541 | Common:5; Rare:64 | ||||
| chr9:32384479-32384732 | Common:1; Rare:92 | ||||
| chr9:32573041-32573219 | Common:2; Rare:66 |