Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23980224-23980605 | Common:1; Rare:114 | ||||
chr1:24642973-24643329 | Common:2; Rare:112 | ||||
chr1:25232453-25232596 | Rare:57 | ||||
chr1:25247434-25247630 | Common:2; Rare:69 | ||||
chr1:25338214-25338447 | Common:1; Rare:80 | ||||
chr1:25800072-25800370 | Common:1; Rare:114; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
chr1:25819833-25820013 | Common:4; Rare:57 | ||||
chr1:25859353-25859549 | Common:3; Rare:82 | ||||
chr1:25906392-25906614 | Rare:84 | ||||
chr1:26234005-26234243 | Common:1; Rare:83 | ||||
chr1:26279923-26280158 | Rare:134 | ||||
chr1:26306626-26306860 | Common:13; Rare:73 | ||||
chr1:26432091-26432414 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472266-26472627 | Common:4; Rare:130 | ||||
chr1:26890023-26890369 | Common:3; Rare:129 |