| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:20684125-20684282 | Common:2; Rare:61 | ||||
| chr9:21994329-21994598 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):6 | ||||
| chr9:26892771-26892885 | Common:1; Rare:48 | ||||
| chr9:26947146-26947255 | Rare:38 | ||||
| chr9:32573076-32573299 | Common:4; Rare:80 | ||||
| chr9:33025098-33025294 | Common:5; Rare:78 | ||||
| chr9:34178952-34179058 | Common:1; Rare:28 | ||||
| chr9:34329203-34329615 | Common:1; Rare:129 | ||||
| chr9:34612090-34612219 | Common:8; Rare:42 | ||||
| chr9:35657970-35658366 | Common:6; Rare:300; Clinvar:20; Clinvar (benign):11; Clinvar (pathogenic):34 | ||||
| chr9:35673854-35673954 | Common:2; Rare:25 | ||||
| chr9:35732095-35732320 | Rare:65 | ||||
| chr9:35732373-35732676 | Common:2; Rare:76 | ||||
| chr9:37785055-37785132 | Rare:23 | ||||
| chr9:37904091-37904453 | Common:3; Rare:114 |