| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:8857687-8857746 | Rare:20 | ||||
| chr9:8858014-8858110 | Common:2; Rare:35 | ||||
| chr9:14313603-14313753 | Common:1; Rare:38 | ||||
| chr9:14693244-14693438 | Common:1; Rare:87 | ||||
| chr9:14910219-14910275 | Common:1; Rare:10; Clinvar:2 | ||||
| chr9:15307133-15307444 | Common:2; Rare:145 | ||||
| chr9:15422580-15423048 | Common:1; Rare:217 | ||||
| chr9:16870661-16870856 | Rare:93 | ||||
| chr9:19049328-19049469 | Rare:65 | ||||
| chr9:19102893-19103051 | Common:2; Rare:65 | ||||
| chr9:19127402-19127566 | Common:2; Rare:43 | ||||
| chr9:19230353-19230849 | Common:8; Rare:210 | ||||
| chr9:19380178-19380339 | Common:4; Rare:81 | ||||
| chr9:21031616-21031691 | Common:1; Rare:26 | ||||
| chr9:21994329-21994396 | Rare:23; Clinvar:2; Clinvar (benign):6 |