| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34049361-34049585 | Common:1; Rare:68 | ||||
| chr9:34126622-34126813 | Common:1; Rare:56 | ||||
| chr9:34178933-34179063 | Common:1; Rare:34 | ||||
| chr9:34329186-34329598 | Rare:131 | ||||
| chr9:34458539-34458833 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:34612073-34612177 | Rare:36 | ||||
| chr9:34637718-34637953 | Rare:69 | ||||
| chr9:34646519-34646692 | Common:1; Rare:49; Clinvar:2 | ||||
| chr9:34652049-34652217 | Rare:50 | ||||
| chr9:34666012-34666156 | Common:1; Rare:31 | ||||
| chr9:35071970-35072132 | Common:1; Rare:51 | ||||
| chr9:35072525-35072675 | Rare:43; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:35079990-35080100 | Common:3; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:35103080-35103214 | Common:1; Rare:46 | ||||
| chr9:35646835-35646951 | Rare:24 |