Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73625968-73626106 | Rare:23 | ||||
chr10:73743996-73744436 | Common:1; Rare:112 | ||||
chr10:73781957-73782345 | Common:1; Rare:122 | ||||
chr10:73874485-73874732 | Rare:61 | ||||
chr10:74151061-74151268 | Common:1; Rare:63 | ||||
chr10:74176321-74176558 | Common:3; Rare:59 | ||||
chr10:74176663-74176806 | Rare:37; Clinvar:2 | ||||
chr10:75210461-75210867 | Common:1; Rare:142 | ||||
chr10:78029477-78029643 | Common:1; Rare:49; Clinvar (benign):1 | ||||
chr10:78035349-78035715 | Common:1; Rare:88; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr10:79445436-79445737 | Rare:91 | ||||
chr10:80079062-80079286 | Common:2; Rare:94 | ||||
chr10:80205446-80205648 | Common:3; Rare:74 | ||||
chr10:84424855-84424953 | Rare:12 | ||||
chr10:86521759-86521960 | Rare:64 |