Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11805935-11806247 | Common:2; Rare:84; Clinvar:1 | ||||
chr1:11934485-11934790 | Common:6; Rare:98; Clinvar:6; Clinvar (benign):1 | ||||
chr1:15526583-15526905 | Common:2; Rare:102 | ||||
chr1:16352420-16352575 | Common:2; Rare:84 | ||||
chr1:19210254-19210410 | Rare:60 | ||||
chr1:19251505-19251874 | Common:6; Rare:122 | ||||
chr1:19312033-19312333 | Common:8; Rare:149 | ||||
chr1:19596742-19597068 | Common:3; Rare:120 | ||||
chr1:20508113-20508189 | Common:1; Rare:23 | ||||
chr1:20661359-20661703 | Common:3; Rare:124; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20787234-20787447 | Rare:102 | ||||
chr1:21345476-21345655 | Common:1; Rare:70 | ||||
chr1:23791066-23791187 | Rare:37 | ||||
chr1:23959641-23959899 | Common:2; Rare:71 | ||||
chr1:25232453-25232657 | Rare:81 |