| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97497772-97497948 | Common:1; Rare:60 | ||||
| chr10:97498321-97498637 | Common:6; Rare:294 | ||||
| chr10:97498610-97499051 | Common:6; Rare:319 | ||||
| chr10:97584030-97584450 | Common:4; Rare:207; Clinvar (benign):1 | ||||
| chr10:97633330-97633780 | Common:7; Rare:240 | ||||
| chr10:97640393-97640856 | Common:2; Rare:235 | ||||
| chr10:97686951-97687774 | Common:25; Rare:612 | ||||
| chr10:97713072-97713472 | Rare:86 | ||||
| chr10:97713578-97713843 | Rare:148 | ||||
| chr10:97714071-97714590 | Common:2; Rare:335 | ||||
| chr10:97736928-97737271 | Common:4; Rare:265 | ||||
| chr10:97849640-97850020 | Common:1; Rare:161 | ||||
| chr10:98134503-98134749 | Common:3; Rare:245 | ||||
| chr10:98415030-98415323 | Common:3; Rare:190 | ||||
| chr10:98446834-98447068 | Rare:170; Clinvar:1 |