| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:16728035-16728195 | Rare:29 | ||||
| chr9:16868043-16868341 | Common:1; Rare:62 | ||||
| chr9:16870652-16870854 | Rare:99 | ||||
| chr9:16871211-16871537 | Common:2; Rare:96 | ||||
| chr9:19049291-19049402 | Rare:45 | ||||
| chr9:19102877-19103042 | Common:2; Rare:69 | ||||
| chr9:19127417-19127581 | Common:2; Rare:50 | ||||
| chr9:19379485-19379750 | Common:1; Rare:99 | ||||
| chr9:19380154-19380330 | Common:5; Rare:94 | ||||
| chr9:19408826-19409019 | Common:3; Rare:76 | ||||
| chr9:20622446-20622667 | Rare:77 | ||||
| chr9:20684087-20684282 | Common:3; Rare:76 | ||||
| chr9:21031602-21031775 | Common:1; Rare:55 | ||||
| chr9:21335313-21335526 | Common:4; Rare:71 | ||||
| chr9:21802540-21802687 | Rare:44; Clinvar:1; Clinvar (benign):1 |