Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91021941-91022213 | Rare:79 | ||||
chr1:91022285-91022418 | Common:1; Rare:21 | ||||
chr1:91404408-91404693 | Common:2; Rare:85 | ||||
chr1:91500703-91500926 | Common:2; Rare:72 | ||||
chr1:91501032-91501162 | Rare:40 | ||||
chr1:91501276-91501539 | Rare:62 | ||||
chr1:91886114-91886393 | Rare:105 | ||||
chr1:92030406-92030541 | Common:9; Rare:25 | ||||
chr1:92080004-92080371 | Common:1; Rare:68 | ||||
chr1:92080407-92080572 | Common:2; Rare:47 | ||||
chr1:92298659-92299097 | Common:2; Rare:149; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92484769-92485197 | Common:6; Rare:105 | ||||
chr1:92485679-92486076 | Common:1; Rare:72 | ||||
chr1:92486887-92487062 | Common:1; Rare:46 | ||||
chr1:92785066-92785439 | Common:7; Rare:119 |