| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:86868488-86868567 | Rare:25 | ||||
| chr10:86875852-86876073 | Common:2; Rare:56; Clinvar:11; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr10:86918102-86918365 | Common:1; Rare:48 | ||||
| chr10:86966639-86966766 | Rare:25 | ||||
| chr10:86971165-86971498 | Common:2; Rare:107 | ||||
| chr10:87025778-87025876 | Common:3; Rare:16 | ||||
| chr10:87054692-87054771 | Rare:15 | ||||
| chr10:87082565-87082581 | Rare:3 | ||||
| chr10:87093150-87093292 | Common:1; Rare:24 | ||||
| chr10:87203640-87203713 | Common:2; Rare:26 | ||||
| chr10:87342279-87342950 | Common:6; Rare:206 | ||||
| chr10:87343154-87343247 | Rare:21 | ||||
| chr10:87505418-87505514 | Rare:33 | ||||
| chr10:87767420-87767449 | Rare:4 | ||||
| chr10:87850786-87851031 | Rare:46 |