| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:95561320-95561576 | Common:3; Rare:69 | ||||
| chr10:95656623-95656931 | Common:1; Rare:86; Clinvar:6; Clinvar (benign):2 | ||||
| chr10:95907816-95907931 | Common:2; Rare:32 | ||||
| chr10:96130155-96130522 | Common:2; Rare:122 | ||||
| chr10:96271480-96271815 | Common:1; Rare:63 | ||||
| chr10:96720380-96720616 | Common:1; Rare:59 | ||||
| chr10:96832047-96832299 | Rare:99 | ||||
| chr10:97334686-97334876 | Common:2; Rare:75 | ||||
| chr10:97425904-97426298 | Common:15; Rare:178 | ||||
| chr10:97445973-97446229 | Rare:69 | ||||
| chr10:97498381-97498560 | Common:2; Rare:70 | ||||
| chr10:97584172-97584424 | Rare:47 | ||||
| chr10:97687133-97687532 | Common:6; Rare:118 | ||||
| chr10:98268183-98268482 | Common:3; Rare:75 | ||||
| chr10:98446870-98447025 | Rare:45 |