| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19127476-19127581 | Common:1; Rare:34 | ||||
| chr9:19380184-19380339 | Common:4; Rare:76 | ||||
| chr9:19408789-19409012 | Common:3; Rare:90 | ||||
| chr9:20684086-20684269 | Common:3; Rare:74 | ||||
| chr9:21335369-21335526 | Common:2; Rare:57 | ||||
| chr9:21802540-21802691 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994338-21994828 | Common:2; Rare:144; Clinvar:2; Clinvar (benign):4 | ||||
| chr9:21995257-21995467 | Rare:56 | ||||
| chr9:26892737-26892887 | Common:1; Rare:76 | ||||
| chr9:26947127-26947323 | Rare:64 | ||||
| chr9:26956378-26956460 | Common:1; Rare:28 | ||||
| chr9:32384478-32384692 | Common:1; Rare:76 | ||||
| chr9:32573046-32573220 | Common:3; Rare:64 | ||||
| chr9:33001543-33001746 | Common:3; Rare:102; Clinvar (benign):4 | ||||
| chr9:33025090-33025324 | Common:6; Rare:103 |