| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34646889-34647067 | Rare:42; Clinvar (benign):1 | ||||
| chr9:34651980-34652204 | Rare:69 | ||||
| chr9:34665280-34665680 | Rare:120 | ||||
| chr9:34666014-34666193 | Common:2; Rare:41 | ||||
| chr9:34989315-34989542 | Rare:57 | ||||
| chr9:34990128-34990293 | Rare:39 | ||||
| chr9:34991092-34991807 | Common:4; Rare:195 | ||||
| chr9:35072114-35072335 | Rare:73 | ||||
| chr9:35072547-35073013 | Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35079753-35079856 | Rare:18 | ||||
| chr9:35079932-35080223 | Common:5; Rare:78; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:35096050-35096400 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:35103094-35103318 | Common:1; Rare:74 | ||||
| chr9:35111545-35111886 | Common:1; Rare:85 | ||||
| chr9:35161773-35162049 | Common:4; Rare:77 |