| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34329186-34329598 | Rare:131 | ||||
| chr9:34458533-34458826 | Common:1; Rare:70 | ||||
| chr9:34612062-34612238 | Common:9; Rare:68 | ||||
| chr9:34620391-34620639 | Common:1; Rare:77 | ||||
| chr9:34652001-34652223 | Rare:66 | ||||
| chr9:34665339-34665665 | Rare:99 | ||||
| chr9:34665976-34666078 | Common:1; Rare:29 | ||||
| chr9:34992740-34992917 | Common:1; Rare:43 | ||||
| chr9:35072336-35072448 | Rare:30; Clinvar:1 | ||||
| chr9:35072457-35072675 | Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:35079917-35080153 | Common:4; Rare:58; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:35101904-35102182 | Rare:64 | ||||
| chr9:35103082-35103295 | Common:1; Rare:72 | ||||
| chr9:35161819-35162152 | Common:4; Rare:95 | ||||
| chr9:35162286-35162327 | Rare:11 |