| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33290350-33290563 | Common:2; Rare:78 | ||||
| chr9:33473863-33474131 | Common:2; Rare:80 | ||||
| chr9:34048870-34049267 | Common:2; Rare:126 | ||||
| chr9:34126604-34126795 | Common:1; Rare:59 | ||||
| chr9:34178932-34179078 | Common:1; Rare:39 | ||||
| chr9:34329186-34329606 | Rare:134 | ||||
| chr9:34458539-34458833 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:34612084-34612219 | Common:8; Rare:45 | ||||
| chr9:34620457-34620651 | Common:1; Rare:46 | ||||
| chr9:34637600-34637953 | Common:1; Rare:105; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:34646561-34646814 | Common:1; Rare:82; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr9:34665373-34665646 | Rare:89 | ||||
| chr9:34665929-34666075 | Common:1; Rare:38 | ||||
| chr9:34989395-34989790 | Common:2; Rare:103 | ||||
| chr9:34990088-34990354 | Common:1; Rare:70 |