| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92325284-92325961 | Common:8; Rare:170 | ||||
| chr9:92764795-92765144 | Common:2; Rare:108 | ||||
| chr9:93451483-93451736 | Common:3; Rare:78 | ||||
| chr9:93453534-93453726 | Common:1; Rare:46 | ||||
| chr9:93576362-93576413 | Rare:13 | ||||
| chr9:94030693-94030813 | Rare:30 | ||||
| chr9:94374294-94374580 | Common:2; Rare:96 | ||||
| chr9:95875449-95875723 | Common:1; Rare:98 | ||||
| chr9:96383681-96383769 | Rare:27 | ||||
| chr9:96778042-96778156 | Rare:36 | ||||
| chr9:97013578-97013829 | Common:4; Rare:69 | ||||
| chr9:97633269-97633448 | Rare:46 | ||||
| chr9:97633478-97633895 | Common:6; Rare:136 | ||||
| chr9:98255578-98255899 | Common:3; Rare:98 | ||||
| chr9:99221892-99222349 | Common:2; Rare:179; Clinvar:3; Clinvar (benign):3 |