| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:100352809-100353094 | Rare:102 | ||||
| chr9:100427890-100428259 | Common:1; Rare:74 | ||||
| chr9:101398511-101398970 | Common:1; Rare:155 | ||||
| chr9:101533748-101533914 | Rare:53 | ||||
| chr9:104093977-104094327 | Common:3; Rare:84 | ||||
| chr9:104094486-104094604 | Common:2; Rare:37 | ||||
| chr9:104747604-104747799 | Common:1; Rare:60 | ||||
| chr9:104764051-104764211 | Common:2; Rare:37 | ||||
| chr9:105447972-105448153 | Common:2; Rare:67 | ||||
| chr9:105558079-105558170 | Rare:23; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:105694430-105694627 | Common:3; Rare:88 | ||||
| chr9:106862959-106863180 | Rare:74 | ||||
| chr9:106863365-106863630 | Common:1; Rare:55 | ||||
| chr9:107282940-107283639 | Common:6; Rare:206 | ||||
| chr9:107284042-107284141 | Common:1; Rare:21 |