Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73495553-73495763 | Rare:44 | ||||
chr10:73495814-73496130 | Common:2; Rare:88 | ||||
chr10:73625955-73626060 | Rare:14 | ||||
chr10:73744214-73744440 | Common:1; Rare:64 | ||||
chr10:73781945-73782084 | Common:1; Rare:45 | ||||
chr10:74150755-74151295 | Common:3; Rare:134 | ||||
chr10:77926743-77926779 | Rare:6 | ||||
chr10:78035368-78035585 | Rare:56; Clinvar (pathogenic):1 | ||||
chr10:80078631-80078708 | Rare:30 | ||||
chr10:80079002-80079298 | Common:2; Rare:118 | ||||
chr10:80157702-80157992 | Common:4; Rare:86 | ||||
chr10:86521745-86521960 | Rare:71 | ||||
chr10:86756404-86756683 | Common:2; Rare:86 | ||||
chr10:86968373-86968501 | Common:3; Rare:23 | ||||
chr10:87094818-87095240 | Common:1; Rare:101; Clinvar:3 |