Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54251673-54251886 | Common:1; Rare:70 | ||||
chr1:54542050-54542289 | Common:3; Rare:70 | ||||
chr1:54641652-54641837 | Common:2; Rare:39 | ||||
chr1:54715471-54715916 | Common:6; Rare:126 | ||||
chr1:54764477-54764845 | Common:7; Rare:108 | ||||
chr1:54806012-54806148 | Common:4; Rare:48 | ||||
chr1:54887120-54887469 | Common:3; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
chr1:56645244-56645390 | Common:1; Rare:55 | ||||
chr1:58546694-58546874 | Common:4; Rare:81 | ||||
chr1:58784020-58784204 | Rare:45 | ||||
chr1:59296504-59297137 | Common:15; Rare:177 | ||||
chr1:59814535-59815099 | Common:7; Rare:158 | ||||
chr1:60008830-60008902 | Rare:10 | ||||
chr1:60073735-60073845 | Rare:25 | ||||
chr1:61077015-61077224 | Common:3; Rare:56 |