Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42846405-42846635 | Common:1; Rare:61 | ||||
chr1:42958834-42959078 | Common:4; Rare:69; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43358645-43359016 | Common:7; Rare:120 | ||||
chr1:43367965-43368208 | Rare:67 | ||||
chr1:43389766-43389955 | Common:3; Rare:83 | ||||
chr1:43946634-43946954 | Rare:84 | ||||
chr1:44213380-44213492 | Common:1; Rare:23 | ||||
chr1:44674421-44674769 | Common:3; Rare:90 | ||||
chr1:44775473-44775607 | Rare:54 | ||||
chr1:45339961-45340178 | Rare:68 | ||||
chr1:45500046-45500328 | Common:1; Rare:64; Clinvar:4 | ||||
chr1:45521833-45522089 | Common:1; Rare:100 | ||||
chr1:45522828-45522925 | Rare:15 | ||||
chr1:45550730-45550831 | Common:1; Rare:27 | ||||
chr1:45686515-45686651 | Rare:43 |