Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23959641-23959854 | Common:2; Rare:57 | ||||
chr1:24112096-24112359 | Rare:68 | ||||
chr1:24319425-24319484 | Rare:15 | ||||
chr1:24642959-24643318 | Common:1; Rare:113 | ||||
chr1:25232463-25232657 | Rare:75 | ||||
chr1:25247431-25247679 | Common:3; Rare:96 | ||||
chr1:25338190-25338453 | Common:1; Rare:93 | ||||
chr1:25819832-25820021 | Common:4; Rare:60 | ||||
chr1:25906406-25906590 | Rare:71 | ||||
chr1:26067621-26067841 | Common:2; Rare:34 | ||||
chr1:26279928-26280139 | Rare:111 | ||||
chr1:26317902-26317959 | Common:1; Rare:6 | ||||
chr1:26432200-26432415 | Common:4; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26787865-26787974 | Common:1; Rare:36; Clinvar (benign):1 | ||||
chr1:26862838-26863203 | Rare:81 |