| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92482459-92482803 | Rare:43 | ||||
| chr9:92535978-92536001 | Rare:2 | ||||
| chr9:92536600-92536606 | |||||
| chr9:92670051-92670314 | Common:1; Rare:79 | ||||
| chr9:92877953-92878195 | Common:2; Rare:71 | ||||
| chr9:93453546-93453687 | Rare:31 | ||||
| chr9:95317663-95317816 | Common:1; Rare:48; Clinvar:2 | ||||
| chr9:95516772-95517091 | Common:3; Rare:89; Clinvar (pathogenic):1 | ||||
| chr9:95875453-95875703 | Common:1; Rare:82 | ||||
| chr9:96778048-96778154 | Rare:33 | ||||
| chr9:97501488-97501791 | Common:6; Rare:77 | ||||
| chr9:97633267-97633428 | Rare:39 | ||||
| chr9:97633497-97633841 | Common:4; Rare:110 | ||||
| chr9:97697304-97697469 | Common:1; Rare:88; Clinvar:5 | ||||
| chr9:97922471-97922609 | Common:3; Rare:64 |