Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:50623887-50624129 | Common:1; Rare:95 | ||||
chr10:52314163-52314291 | Rare:29 | ||||
chr10:56361238-56361461 | Common:5; Rare:70 | ||||
chr10:60944175-60944278 | Rare:33 | ||||
chr10:68332884-68333102 | Common:1; Rare:50 | ||||
chr10:71819465-71819895 | Common:1; Rare:172; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71851183-71851452 | Common:5; Rare:115; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72273911-72274354 | Common:2; Rare:148 | ||||
chr10:73096777-73097018 | Common:3; Rare:76 | ||||
chr10:73167948-73168158 | Rare:55 | ||||
chr10:73252594-73252734 | Rare:43; Clinvar:4 | ||||
chr10:73495818-73496131 | Common:2; Rare:88 | ||||
chr10:73744008-73744104 | Rare:27 | ||||
chr10:73744254-73744424 | Common:1; Rare:47 | ||||
chr10:73771984-73772328 | Common:3; Rare:98 |