| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92670024-92670351 | Common:1; Rare:98 | ||||
| chr9:93134201-93134352 | Common:2; Rare:57 | ||||
| chr9:93451444-93451679 | Common:3; Rare:62 | ||||
| chr9:93452292-93452388 | Rare:15 | ||||
| chr9:93453544-93453687 | Rare:32 | ||||
| chr9:95003683-95004052 | Common:3; Rare:69 | ||||
| chr9:95505882-95506216 | Common:2; Rare:115 | ||||
| chr9:95506592-95506672 | Rare:34; Clinvar:1; Clinvar (benign):4 | ||||
| chr9:95507368-95507669 | Rare:88 | ||||
| chr9:95875441-95875703 | Common:1; Rare:90 | ||||
| chr9:95875961-95876058 | Common:5; Rare:50; Clinvar (pathogenic):1 | ||||
| chr9:96655296-96655424 | Rare:34 | ||||
| chr9:96778048-96778154 | Rare:33 | ||||
| chr9:97411897-97412210 | Common:4; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:97633267-97633466 | Common:1; Rare:54 |