| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35732073-35732344 | Common:2; Rare:75 | ||||
| chr9:35732399-35732704 | Common:3; Rare:74 | ||||
| chr9:35748946-35749371 | Common:2; Rare:152 | ||||
| chr9:35814983-35815302 | Rare:82 | ||||
| chr9:36036795-36036967 | Common:1; Rare:61 | ||||
| chr9:36190681-36190978 | Common:1; Rare:99 | ||||
| chr9:36258386-36258636 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36400310-36400579 | Common:1; Rare:80 | ||||
| chr9:36400841-36400989 | Common:3; Rare:70 | ||||
| chr9:36572750-36572975 | Common:2; Rare:71 | ||||
| chr9:37120126-37120614 | Common:2; Rare:152 | ||||
| chr9:37422563-37422749 | Common:2; Rare:96 | ||||
| chr9:37464970-37465156 | Common:2; Rare:63 | ||||
| chr9:37465172-37465538 | Common:3; Rare:117 | ||||
| chr9:37485728-37486050 | Common:3; Rare:118 |