Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236523700-236524111 | Common:4; Rare:105 | ||||
chr1:236524133-236524340 | Common:2; Rare:74 | ||||
chr1:236524365-236524700 | Common:3; Rare:85 | ||||
chr1:236524717-236524787 | Rare:15 | ||||
chr1:236525004-236525044 | Rare:3 | ||||
chr1:236603994-236604216 | Common:1; Rare:74 | ||||
chr1:236604401-236604696 | Common:5; Rare:90 | ||||
chr1:236604763-236604938 | Rare:38 | ||||
chr1:239386423-239386669 | Common:1; Rare:34 | ||||
chr1:241519067-241519194 | Common:1; Rare:28 | ||||
chr1:241519205-241519326 | Rare:20 | ||||
chr1:241519460-241519562 | Common:1; Rare:32 | ||||
chr1:241519596-241520053 | Common:3; Rare:139; Clinvar:15; Clinvar (benign):15; Clinvar (pathogenic):4 | ||||
chr1:241639601-241639911 | Common:4; Rare:82 | ||||
chr1:241639996-241640155 | Common:1; Rare:62 |