| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68406955-68407138 | Common:3; Rare:76 | ||||
| chr10:68407161-68407464 | Common:14; Rare:259 | ||||
| chr10:68471600-68472099 | Common:6; Rare:413; Clinvar:2; Clinvar (benign):8 | ||||
| chr10:68527293-68527725 | Common:8; Rare:309 | ||||
| chr10:68720898-68721311 | Common:8; Rare:317 | ||||
| chr10:68721420-68721720 | Common:3; Rare:95 | ||||
| chr10:68826890-68827290 | Common:3; Rare:125 | ||||
| chr10:68827370-68827593 | Common:5; Rare:156 | ||||
| chr10:68900751-68900921 | Common:2; Rare:90 | ||||
| chr10:68900976-68901466 | Common:9; Rare:476 | ||||
| chr10:68955982-68956470 | Common:5; Rare:306 | ||||
| chr10:68956634-68956745 | Rare:30 | ||||
| chr10:68988540-68988889 | Common:2; Rare:143; Clinvar:1; Clinvar (benign):4 | ||||
| chr10:68988850-68989130 | Common:4; Rare:126; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr10:68989200-68989393 | Rare:77 |