| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:76637496-76637616 | Rare:23 | ||||
| chr9:77370216-77370529 | Common:2; Rare:110; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:77387597-77387768 | Rare:39 | ||||
| chr9:77945684-77946100 | Rare:91 | ||||
| chr9:81655947-81656196 | Common:1; Rare:49 | ||||
| chr9:83219209-83219357 | Common:2; Rare:38 | ||||
| chr9:83920762-83920771 | Rare:5 | ||||
| chr9:85805079-85805222 | Common:3; Rare:48 | ||||
| chr9:86025685-86025956 | Common:2; Rare:60 | ||||
| chr9:86033361-86033578 | Rare:63 | ||||
| chr9:86288699-86289038 | Rare:58 | ||||
| chr9:86299179-86299251 | Rare:11 | ||||
| chr9:87524125-87524338 | Common:4; Rare:35 | ||||
| chr9:88387523-88387650 | Common:1; Rare:30 | ||||
| chr9:89358181-89358429 | Rare:48 |