Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43008431-43008842 | Rare:75 | ||||
chr1:43008870-43009048 | Rare:28 | ||||
chr1:43039341-43039425 | Rare:20 | ||||
chr1:43044951-43045209 | Common:2; Rare:68 | ||||
chr1:43052890-43053264 | Common:2; Rare:59 | ||||
chr1:43120498-43120536 | Rare:10 | ||||
chr1:43206721-43207209 | Common:1; Rare:119 | ||||
chr1:43348593-43348742 | Common:1; Rare:26 | ||||
chr1:43348811-43349310 | Common:2; Rare:157; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:43349324-43349650 | Common:1; Rare:74; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:43358154-43358275 | Rare:23 | ||||
chr1:43454501-43454892 | Common:1; Rare:90 | ||||
chr1:43531611-43531841 | Common:1; Rare:54 | ||||
chr1:43532135-43532199 | Common:1; Rare:22 | ||||
chr1:43548458-43548693 | Common:1; Rare:42 |