| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33402439-33402615 | Rare:32 | ||||
| chr9:34048866-34048982 | Common:1; Rare:45 | ||||
| chr9:34049186-34049267 | Common:1; Rare:19 | ||||
| chr9:34126375-34126425 | Rare:19 | ||||
| chr9:34329303-34329614 | Common:1; Rare:85 | ||||
| chr9:34458563-34458789 | Rare:57 | ||||
| chr9:34652015-34652217 | Rare:58 | ||||
| chr9:34665373-34665655 | Rare:92 | ||||
| chr9:35071938-35072316 | Common:1; Rare:133 | ||||
| chr9:35072500-35072937 | Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35161808-35162114 | Common:4; Rare:91 | ||||
| chr9:35657857-35658392 | Common:9; Rare:442; Clinvar:41; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35705751-35705977 | Common:1; Rare:59 | ||||
| chr9:35732037-35732334 | Common:2; Rare:77 | ||||
| chr9:35732373-35732775 | Common:4; Rare:102 |