| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68383817-68384123 | Common:1; Rare:74 | ||||
| chr10:68544042-68544353 | Rare:53 | ||||
| chr10:68747220-68747334 | Rare:21 | ||||
| chr10:69170545-69170681 | Common:1; Rare:32 | ||||
| chr10:70161035-70161103 | Rare:15 | ||||
| chr10:70163752-70163802 | Rare:10 | ||||
| chr10:70164226-70164417 | Common:1; Rare:42 | ||||
| chr10:71651392-71651502 | Common:1; Rare:14 | ||||
| chr10:71822983-71823155 | Common:2; Rare:27 | ||||
| chr10:71823837-71823905 | Rare:23 | ||||
| chr10:71825817-71825913 | Rare:28; Clinvar (pathogenic):1 | ||||
| chr10:71889087-71889315 | Common:6; Rare:40 | ||||
| chr10:71965225-71965370 | Common:1; Rare:30 | ||||
| chr10:72352548-72352601 | Common:1; Rare:7 | ||||
| chr10:72407993-72408189 | Common:1; Rare:42; Clinvar (benign):1; Clinvar (pathogenic):1 |