| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100285735-100285909 | Common:1; Rare:30 | ||||
| chr10:100286018-100286502 | Rare:114 | ||||
| chr10:100286593-100286925 | Common:5; Rare:127 | ||||
| chr10:100286941-100287039 | Common:1; Rare:16 | ||||
| chr10:100346869-100347208 | Common:1; Rare:86 | ||||
| chr10:100347352-100347614 | Common:4; Rare:78 | ||||
| chr10:100528998-100529107 | Rare:15 | ||||
| chr10:100529278-100529461 | Common:1; Rare:51; Clinvar (pathogenic):1 | ||||
| chr10:100529469-100529531 | Rare:27 | ||||
| chr10:100529675-100530041 | Common:2; Rare:105 | ||||
| chr10:100535707-100536011 | Common:6; Rare:117 | ||||
| chr10:100536078-100536200 | Rare:29 | ||||
| chr10:100912602-100913046 | Common:1; Rare:121 | ||||
| chr10:100913311-100913461 | Rare:40 | ||||
| chr10:100987376-100987646 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):2 |