| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34126561-34126778 | Rare:70 | ||||
| chr9:34178937-34179077 | Common:1; Rare:39 | ||||
| chr9:34329195-34329606 | Rare:130 | ||||
| chr9:34376831-34377235 | Common:1; Rare:93 | ||||
| chr9:34381453-34381694 | Rare:42 | ||||
| chr9:34458247-34458416 | Common:1; Rare:45 | ||||
| chr9:34458518-34459003 | Common:2; Rare:116; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:34590136-34590216 | Common:3; Rare:19 | ||||
| chr9:34612084-34612223 | Common:8; Rare:46 | ||||
| chr9:34620447-34620597 | Common:1; Rare:44 | ||||
| chr9:34646544-34646786 | Common:1; Rare:75; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr9:34665331-34665676 | Rare:102 | ||||
| chr9:34990070-34990440 | Common:1; Rare:101 | ||||
| chr9:34991117-34991370 | Rare:45 | ||||
| chr9:35072367-35072577 | Rare:51; Clinvar:2 |