| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37576238-37576524 | Common:1; Rare:85 | ||||
| chr9:37592417-37592693 | Common:3; Rare:95 | ||||
| chr9:37650725-37651089 | Common:2; Rare:109 | ||||
| chr9:37753685-37753836 | Common:6; Rare:90 | ||||
| chr9:37784841-37785155 | Common:1; Rare:140; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr9:37800682-37800794 | Common:1; Rare:34 | ||||
| chr9:37904076-37904476 | Common:3; Rare:130 | ||||
| chr9:38392581-38392758 | Common:1; Rare:49 | ||||
| chr9:38424452-38424617 | Rare:46 | ||||
| chr9:65675706-65675957 | Rare:57 | ||||
| chr9:66900574-66900804 | Common:3; Rare:73 | ||||
| chr9:68779944-68780094 | Common:2; Rare:51 | ||||
| chr9:69173885-69174308 | Common:6; Rare:131 | ||||
| chr9:69672255-69672570 | Common:1; Rare:89 | ||||
| chr9:69759863-69760157 | Common:3; Rare:115 |