Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42683286-42683477 | Common:3; Rare:73 | ||||
chr1:42767028-42767301 | Common:3; Rare:78 | ||||
chr1:42846420-42846649 | Common:1; Rare:61 | ||||
chr1:42931157-42931475 | Rare:71; Clinvar:5 | ||||
chr1:42958648-42959078 | Common:4; Rare:112; Clinvar:6; Clinvar (benign):8 | ||||
chr1:43367946-43368129 | Rare:44 | ||||
chr1:43389763-43389945 | Common:3; Rare:78 | ||||
chr1:43946597-43946966 | Rare:98 | ||||
chr1:43974778-43975011 | Common:3; Rare:62 | ||||
chr1:44674453-44674722 | Common:2; Rare:62 | ||||
chr1:44723647-44723790 | Rare:27 | ||||
chr1:44986543-44986748 | Common:2; Rare:35; Clinvar (benign):1 | ||||
chr1:45012002-45012272 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45339987-45340048 | Rare:18 | ||||
chr1:45340103-45340192 | Rare:38 |