Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23825382-23825555 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:25232445-25232642 | Rare:81 | ||||
chr1:25819887-25820013 | Common:2; Rare:38 | ||||
chr1:26695581-26695758 | Rare:62 | ||||
chr1:28505857-28506062 | Common:1; Rare:88 | ||||
chr1:28552803-28553113 | Common:2; Rare:106 | ||||
chr1:28643024-28643224 | Rare:78 | ||||
chr1:31296725-31297071 | Common:5; Rare:115 | ||||
chr1:32200402-32200664 | Rare:51 | ||||
chr1:32650929-32651247 | Common:2; Rare:111 | ||||
chr1:32817270-32817686 | Rare:111; Clinvar:5; Clinvar (benign):1 | ||||
chr1:34985298-34985389 | Common:1; Rare:31 | ||||
chr1:35557374-35557486 | Common:1; Rare:24 | ||||
chr1:35557649-35557863 | Common:2; Rare:87 | ||||
chr1:37474389-37474581 | Common:1; Rare:78 |