| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19380165-19380425 | Common:7; Rare:124 | ||||
| chr9:19408772-19409030 | Common:4; Rare:98 | ||||
| chr9:20621384-20621844 | Common:6; Rare:159 | ||||
| chr9:20621815-20622219 | Common:7; Rare:279 | ||||
| chr9:20622446-20622810 | Common:3; Rare:114 | ||||
| chr9:20683969-20684301 | Common:5; Rare:120 | ||||
| chr9:21335344-21335597 | Common:3; Rare:98 | ||||
| chr9:21802424-21802671 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994310-21994570 | Rare:79; Clinvar:3; Clinvar (benign):6 | ||||
| chr9:21995311-21995482 | Rare:50 | ||||
| chr9:22009291-22009487 | Common:1; Rare:58 | ||||
| chr9:22446600-22446860 | Common:6; Rare:67 | ||||
| chr9:23779214-23779614 | Common:2; Rare:140 | ||||
| chr9:23820770-23820920 | Rare:78 | ||||
| chr9:23821310-23821740 | Rare:171 |