| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35604004-35604177 | Common:3; Rare:49 | ||||
| chr9:35657716-35657770 | Common:1; Rare:33; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:35679564-35679970 | Common:1; Rare:93 | ||||
| chr9:35706824-35707128 | Common:2; Rare:83 | ||||
| chr9:35711272-35711744 | Rare:109 | ||||
| chr9:35714793-35715063 | Rare:70 | ||||
| chr9:35717376-35717631 | Common:1; Rare:61 | ||||
| chr9:35723951-35724335 | Rare:95 | ||||
| chr9:35724571-35724960 | Common:1; Rare:86 | ||||
| chr9:35728226-35728450 | Rare:39 | ||||
| chr9:35736239-35736516 | Rare:104 | ||||
| chr9:35737892-35737984 | Rare:33 | ||||
| chr9:35740579-35740835 | Rare:78; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:35833777-35834108 | Common:6; Rare:71 | ||||
| chr9:36349688-36349746 | Rare:17 |