| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:95561285-95561631 | Common:4; Rare:104 | ||||
| chr10:95656419-95656555 | Common:1; Rare:35 | ||||
| chr10:95656589-95657002 | Common:1; Rare:111; Clinvar:6; Clinvar (benign):3 | ||||
| chr10:95657017-95657087 | Rare:10 | ||||
| chr10:95693842-95694067 | Common:2; Rare:92; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95755477-95755752 | Common:1; Rare:47 | ||||
| chr10:95907745-95907966 | Common:3; Rare:67 | ||||
| chr10:95908107-95908271 | Rare:27 | ||||
| chr10:96043211-96043722 | Common:3; Rare:160 | ||||
| chr10:96043931-96044410 | Common:2; Rare:134 | ||||
| chr10:96129406-96129469 | Rare:10 | ||||
| chr10:96129608-96129830 | Common:1; Rare:51 | ||||
| chr10:96129857-96130105 | Common:2; Rare:87 | ||||
| chr10:96130175-96130789 | Common:2; Rare:201 | ||||
| chr10:96130898-96131033 | Rare:35 |