Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24556031-24556149 | Common:2; Rare:34 | ||||
chr1:24642890-24643329 | Common:2; Rare:146 | ||||
chr1:24745587-24745611 | Rare:6 | ||||
chr1:25232442-25232657 | Rare:87 | ||||
chr1:25247076-25247132 | Rare:13 | ||||
chr1:25247413-25247673 | Common:3; Rare:103 | ||||
chr1:25337838-25337915 | Rare:9 | ||||
chr1:25338184-25338466 | Common:2; Rare:98 | ||||
chr1:25819913-25820029 | Common:2; Rare:34 | ||||
chr1:26279933-26280160 | Rare:127 | ||||
chr1:26432229-26432414 | Common:4; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472303-26472521 | Common:4; Rare:70 | ||||
chr1:26473047-26473251 | Rare:104 | ||||
chr1:26787877-26788214 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26900420-26900492 | Rare:31 |