| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:95290829-95291196 | Common:2; Rare:141 | ||||
| chr10:95384040-95384294 | Common:3; Rare:59 | ||||
| chr10:95561334-95561611 | Common:4; Rare:86 | ||||
| chr10:95693856-95694209 | Common:5; Rare:117; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95907826-95907915 | Rare:24 | ||||
| chr10:96129986-96130063 | Common:1; Rare:25 | ||||
| chr10:96130193-96130529 | Common:1; Rare:114 | ||||
| chr10:96586801-96587183 | Common:5; Rare:152 | ||||
| chr10:96832079-96832302 | Rare:86 | ||||
| chr10:97334694-97334830 | Common:1; Rare:59 | ||||
| chr10:97401232-97401462 | Rare:89 | ||||
| chr10:97426047-97426302 | Common:2; Rare:114 | ||||
| chr10:97445975-97446251 | Rare:73 | ||||
| chr10:97451922-97452191 | Rare:86 | ||||
| chr10:97498362-97498578 | Common:2; Rare:89 |