| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:80205348-80205656 | Common:4; Rare:96 | ||||
| chr10:80408352-80408623 | Common:2; Rare:83 | ||||
| chr10:84139306-84139593 | Common:4; Rare:79 | ||||
| chr10:86521754-86521967 | Rare:67 | ||||
| chr10:86756250-86756621 | Common:4; Rare:127 | ||||
| chr10:86957540-86957781 | Rare:61 | ||||
| chr10:86968312-86968583 | Common:4; Rare:69 | ||||
| chr10:87094042-87094336 | Rare:88 | ||||
| chr10:87094351-87094462 | Common:1; Rare:28; Clinvar (benign):2 | ||||
| chr10:87094483-87094689 | Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:87094864-87095235 | Common:1; Rare:89; Clinvar:3 | ||||
| chr10:87504822-87505137 | Common:1; Rare:157; Clinvar (pathogenic):1 | ||||
| chr10:87817972-87818359 | Common:2; Rare:126 | ||||
| chr10:87863285-87863664 | Common:2; Rare:129; Clinvar:78; Clinvar (benign):8 | ||||
| chr10:87864058-87864538 | Common:2; Rare:143; Clinvar:18; Clinvar (benign):12; Clinvar (pathogenic):1 |