Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25475459-25475683 | Common:5; Rare:32 | ||||
chr1:25557676-25557868 | Rare:40 | ||||
chr1:25568761-25569177 | Common:6; Rare:90 | ||||
chr1:25800780-25801161 | Common:1; Rare:83; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr1:25829326-25829652 | Rare:84 | ||||
chr1:25875509-25875764 | Rare:69 | ||||
chr1:25889169-25889229 | Rare:11 | ||||
chr1:26447334-26447641 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:26454942-26455240 | Common:2; Rare:57 | ||||
chr1:26457516-26457752 | Common:3; Rare:29 | ||||
chr1:26620388-26620669 | Common:1; Rare:117 | ||||
chr1:26697186-26697300 | Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
chr1:26715080-26715171 | Rare:15 | ||||
chr1:26720719-26720966 | Common:1; Rare:59 | ||||
chr1:26832541-26832863 | Rare:72 |