Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:13300056-13300189 | Rare:44; Clinvar:1 | ||||
chr10:14838056-14838318 | Common:2; Rare:71 | ||||
chr10:14878670-14878915 | Common:2; Rare:69 | ||||
chr10:14954030-14954220 | Rare:63 | ||||
chr10:15097312-15097401 | Common:1; Rare:42 | ||||
chr10:17228988-17229026 | Common:1; Rare:8 | ||||
chr10:17233574-17233929 | Common:3; Rare:112; Clinvar (benign):1 | ||||
chr10:17643894-17644281 | Common:2; Rare:114 | ||||
chr10:18659283-18659483 | Common:1; Rare:69 | ||||
chr10:27154217-27154493 | Rare:76 | ||||
chr10:28532635-28532812 | Common:1; Rare:73 | ||||
chr10:28533012-28533215 | Rare:82 | ||||
chr10:30434542-30434700 | Common:1; Rare:44 | ||||
chr10:31031850-31032088 | Common:2; Rare:107 | ||||
chr10:31318990-31319244 | Common:2; Rare:74 |