Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235328142-235328525 | Common:3; Rare:112 | ||||
chr1:235504426-235504653 | Common:2; Rare:60 | ||||
chr1:236065072-236065283 | Common:2; Rare:88; Clinvar (pathogenic):1 | ||||
chr1:236281920-236282242 | Common:6; Rare:96 | ||||
chr1:236523861-236524034 | Common:2; Rare:45 | ||||
chr1:236604478-236604629 | Common:4; Rare:44 | ||||
chr1:239386453-239386684 | Rare:34 | ||||
chr1:239386823-239387107 | Common:1; Rare:100 | ||||
chr1:243255201-243255339 | Common:1; Rare:28 | ||||
chr1:243255783-243256113 | Rare:91; Clinvar:4 | ||||
chr1:244451879-244452219 | Common:1; Rare:112 | ||||
chr1:244461244-244461319 | Common:1; Rare:23 | ||||
chr1:244835562-244835747 | Common:2; Rare:82; Clinvar (benign):5 | ||||
chr1:244856527-244856823 | Common:1; Rare:68; Clinvar (benign):2 | ||||
chr1:244864370-244864686 | Rare:122 |