| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128702458-128702566 | Rare:22 | ||||
| chr9:128724010-128724430 | Common:1; Rare:159 | ||||
| chr9:128771750-128772190 | Common:4; Rare:111 | ||||
| chr9:128787023-128787354 | Common:4; Rare:102 | ||||
| chr9:128818261-128818556 | Common:3; Rare:87 | ||||
| chr9:128829710-128829967 | Common:2; Rare:92 | ||||
| chr9:128881902-128882197 | Common:2; Rare:96 | ||||
| chr9:128922006-128922314 | Common:1; Rare:72 | ||||
| chr9:128922624-128922724 | Common:1; Rare:21 | ||||
| chr9:128947514-128947728 | Common:1; Rare:95; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:129027860-129028260 | Common:5; Rare:146 | ||||
| chr9:129036330-129036672 | Common:2; Rare:94 | ||||
| chr9:129080725-129081148 | Common:2; Rare:113 | ||||
| chr9:129110663-129110966 | Common:4; Rare:69 | ||||
| chr9:129111291-129111447 | Common:2; Rare:57 |