Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68231370-68231760 | Common:1; Rare:131; Clinvar (pathogenic):2 | ||||
chr10:68331541-68331715 | Rare:36 | ||||
chr10:68331754-68332152 | Common:2; Rare:146 | ||||
chr10:68332874-68333030 | Common:1; Rare:40 | ||||
chr10:68407213-68407458 | Common:5; Rare:80 | ||||
chr10:68471706-68471863 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
chr10:68527419-68527686 | Common:3; Rare:93 | ||||
chr10:68560336-68560742 | Common:4; Rare:126 | ||||
chr10:68721018-68721331 | Common:2; Rare:101 | ||||
chr10:68827405-68827537 | Common:2; Rare:55 | ||||
chr10:68900747-68900884 | Common:1; Rare:44 | ||||
chr10:68900936-68901355 | Common:3; Rare:162 | ||||
chr10:68955789-68956222 | Common:1; Rare:117 | ||||
chr10:68956375-68956775 | Common:1; Rare:115 | ||||
chr10:69123425-69123539 | Common:1; Rare:26 |