| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136996554-136996914 | Common:2; Rare:99 | ||||
| chr9:137086747-137087110 | Common:1; Rare:139; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:137112544-137112997 | Common:2; Rare:168 | ||||
| chr9:137113115-137113214 | Rare:50 | ||||
| chr9:137176705-137176781 | Common:1; Rare:24 | ||||
| chr9:137188502-137188781 | Common:2; Rare:135 | ||||
| chr9:137188934-137189113 | Rare:67 | ||||
| chr9:137204554-137204840 | Common:2; Rare:50 | ||||
| chr9:137204852-137205211 | Rare:95 | ||||
| chr9:137205575-137205767 | Rare:82 | ||||
| chr9:137277787-137277886 | Common:1; Rare:22 | ||||
| chr9:137423131-137423383 | Common:1; Rare:83 | ||||
| chr9:137454462-137454543 | Rare:31 | ||||
| chr9:137551581-137551955 | Common:29; Rare:155 | ||||
| chr9:137578559-137579069 | Common:2; Rare:153 |