| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:4793727-4793813 | Common:1; Rare:20 | ||||
| chr9:5629682-5629890 | Rare:56 | ||||
| chr9:5768906-5769029 | Rare:40 | ||||
| chr9:5799001-5799264 | Rare:64 | ||||
| chr9:14993186-14993326 | Common:3; Rare:47 | ||||
| chr9:15478476-15478637 | Common:1; Rare:49 | ||||
| chr9:19050203-19050469 | Rare:49 | ||||
| chr9:19378362-19378924 | Common:1; Rare:163 | ||||
| chr9:19788790-19789159 | Common:5; Rare:132 | ||||
| chr9:20684756-20685076 | Rare:71 | ||||
| chr9:20981048-20981384 | Rare:72 | ||||
| chr9:25677425-25677691 | Common:3; Rare:118 | ||||
| chr9:32550811-32551159 | Common:1; Rare:138; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33923226-33923431 | Common:2; Rare:75 | ||||
| chr9:34380783-34380900 | Common:1; Rare:41 |