| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33290280-33290570 | Common:2; Rare:103 | ||||
| chr9:33750577-33750721 | Rare:44 | ||||
| chr9:34048870-34048966 | Rare:40 | ||||
| chr9:34049168-34049273 | Common:1; Rare:26 | ||||
| chr9:34126631-34126809 | Common:1; Rare:53 | ||||
| chr9:34178933-34179096 | Common:1; Rare:46 | ||||
| chr9:34329181-34329608 | Common:1; Rare:134 | ||||
| chr9:34458546-34458826 | Rare:64 | ||||
| chr9:34652015-34652207 | Rare:55 | ||||
| chr9:34665373-34665665 | Rare:94 | ||||
| chr9:35103080-35103293 | Common:1; Rare:72 | ||||
| chr9:35489924-35490133 | Common:2; Rare:60 | ||||
| chr9:35657857-35658392 | Common:9; Rare:442; Clinvar:41; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35665193-35665313 | Common:1; Rare:41 | ||||
| chr9:35689692-35690120 | Common:4; Rare:133; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 |