| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37087266-37087569 | Common:1; Rare:56 | ||||
| chr9:37121225-37121374 | Rare:27 | ||||
| chr9:37506180-37506292 | Rare:20 | ||||
| chr9:37780812-37781165 | Common:3; Rare:83; Clinvar (benign):2 | ||||
| chr9:37859853-37860193 | Common:2; Rare:64 | ||||
| chr9:37899969-37899989 | Rare:2 | ||||
| chr9:37952918-37953019 | Rare:23 | ||||
| chr9:40106623-40106748 | Common:2; Rare:14 | ||||
| chr9:40992077-40992405 | Common:7; Rare:23 | ||||
| chr9:40992645-40992771 | Common:1; Rare:6 | ||||
| chr9:41074453-41074555 | Common:2; Rare:24 | ||||
| chr9:41074661-41074911 | Common:2; Rare:38 | ||||
| chr9:41074950-41075235 | Common:3; Rare:37 | ||||
| chr9:41358595-41358882 | Common:2; Rare:71 | ||||
| chr9:62801756-62802069 | Common:2; Rare:1 |