| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68721401-68721612 | Common:2; Rare:72 | ||||
| chr10:68721639-68721686 | Rare:16 | ||||
| chr10:68827405-68827561 | Common:2; Rare:65 | ||||
| chr10:68900733-68900921 | Common:1; Rare:57 | ||||
| chr10:68900924-68901458 | Common:3; Rare:206 | ||||
| chr10:68901471-68901600 | Rare:36 | ||||
| chr10:68955777-68956450 | Common:4; Rare:175 | ||||
| chr10:68956539-68956676 | Rare:26 | ||||
| chr10:68988577-68988949 | Common:3; Rare:91; Clinvar:1; Clinvar (benign):4 | ||||
| chr10:68988998-68989129 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:68989208-68989272 | Rare:25 | ||||
| chr10:69087490-69087715 | Common:4; Rare:31 | ||||
| chr10:69087868-69088240 | Rare:80 | ||||
| chr10:69123404-69123540 | Common:1; Rare:30 | ||||
| chr10:69123643-69124013 | Common:1; Rare:88 |