| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124861890-124862134 | Common:1; Rare:103 | ||||
| chr9:124862325-124862427 | Common:1; Rare:24 | ||||
| chr9:124940952-124941152 | Common:3; Rare:71 | ||||
| chr9:125189719-125190044 | Common:1; Rare:145 | ||||
| chr9:125200287-125200590 | Common:1; Rare:102 | ||||
| chr9:125241282-125241686 | Common:3; Rare:123 | ||||
| chr9:125261691-125261854 | Common:1; Rare:64 | ||||
| chr9:126805314-126805516 | Common:1; Rare:42 | ||||
| chr9:127424253-127424467 | Common:1; Rare:69 | ||||
| chr9:127449614-127449939 | Rare:89 | ||||
| chr9:127451274-127451562 | Common:3; Rare:119; Clinvar (benign):1 | ||||
| chr9:127568818-127569374 | Common:6; Rare:135 | ||||
| chr9:127579007-127579347 | Common:4; Rare:65 | ||||
| chr9:127611996-127612328 | Common:1; Rare:125; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127802719-127803056 | Common:4; Rare:89 |