Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:185157434-185157504 | Common:1; Rare:21 | ||||
chr1:185317196-185317567 | Common:2; Rare:109 | ||||
chr1:186375104-186375499 | Rare:112 | ||||
chr1:186375673-186375899 | Common:1; Rare:60 | ||||
chr1:190475810-190475857 | Common:2; Rare:9 | ||||
chr1:190477606-190477753 | Common:2; Rare:42 | ||||
chr1:190477853-190477875 | Rare:2 | ||||
chr1:190478078-190478353 | Rare:73 | ||||
chr1:190478674-190478993 | Common:6; Rare:82 | ||||
chr1:192808908-192809049 | Common:3; Rare:52 | ||||
chr1:193059253-193059755 | Common:1; Rare:234 | ||||
chr1:193105375-193105523 | Common:3; Rare:63 | ||||
chr1:193121769-193122120 | Common:1; Rare:118; Clinvar:4; Clinvar (benign):1 | ||||
chr1:193186056-193186277 | Rare:41 | ||||
chr1:193186386-193186659 | Common:3; Rare:50 |