Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32817270-32817686 | Rare:111; Clinvar:5; Clinvar (benign):1 | ||||
chr1:33036817-33037104 | Rare:105; Clinvar (pathogenic):1 | ||||
chr1:33080944-33081167 | Common:2; Rare:57 | ||||
chr1:33472355-33472673 | Rare:72 | ||||
chr1:35031682-35031817 | Rare:41 | ||||
chr1:35079316-35079422 | Common:3; Rare:30 | ||||
chr1:35193092-35193345 | Common:1; Rare:92 | ||||
chr1:35557360-35557442 | Rare:20 | ||||
chr1:35557636-35557852 | Common:2; Rare:87 | ||||
chr1:35641406-35641647 | Common:1; Rare:57 | ||||
chr1:35769951-35770130 | Rare:43 | ||||
chr1:36088778-36088922 | Common:1; Rare:59 | ||||
chr1:36149439-36149802 | Common:2; Rare:99 | ||||
chr1:36224123-36224495 | Common:1; Rare:120 | ||||
chr1:36397869-36398036 | Common:2; Rare:43 |