| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34329210-34329598 | Rare:121 | ||||
| chr9:34458555-34458778 | Rare:55 | ||||
| chr9:34612084-34612223 | Common:8; Rare:46 | ||||
| chr9:34637723-34637953 | Rare:68 | ||||
| chr9:34646294-34646800 | Common:2; Rare:124; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr9:34651900-34652201 | Rare:85 | ||||
| chr9:34653573-34653928 | Rare:54 | ||||
| chr9:34662562-34662721 | Rare:51 | ||||
| chr9:34665324-34665680 | Rare:106 | ||||
| chr9:34666025-34666062 | Rare:7 | ||||
| chr9:34989520-34989769 | Common:2; Rare:63 | ||||
| chr9:35072425-35072770 | Rare:84; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35103091-35103289 | Common:1; Rare:62 | ||||
| chr9:35161819-35162149 | Common:4; Rare:94 | ||||
| chr9:35162165-35162210 | Rare:9 |