Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24642880-24643335 | Common:2; Rare:151 | ||||
chr1:25232427-25232702 | Rare:108 | ||||
chr1:25247040-25247151 | Rare:36 | ||||
chr1:25247445-25247639 | Common:2; Rare:69 | ||||
chr1:25338188-25338466 | Common:2; Rare:96 | ||||
chr1:25430914-25431063 | Common:1; Rare:58 | ||||
chr1:25819812-25820013 | Common:4; Rare:63 | ||||
chr1:25859348-25859580 | Common:3; Rare:99 | ||||
chr1:25906392-25906611 | Rare:83 | ||||
chr1:25998047-25998254 | Common:1; Rare:42 | ||||
chr1:26233873-26234254 | Common:3; Rare:119 | ||||
chr1:26279917-26280171 | Rare:145 | ||||
chr1:26306590-26306861 | Common:13; Rare:87 | ||||
chr1:26432111-26432414 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472237-26472539 | Common:4; Rare:105 |