Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44674411-44674724 | Common:3; Rare:84 | ||||
chr1:44739667-44739887 | Common:1; Rare:83 | ||||
chr1:44775462-44775607 | Rare:55 | ||||
chr1:44775795-44776143 | Common:2; Rare:124 | ||||
chr1:45339938-45340178 | Common:1; Rare:81; Clinvar (benign):1 | ||||
chr1:45500046-45500359 | Common:1; Rare:76; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521871-45522089 | Common:1; Rare:83 | ||||
chr1:45550730-45550874 | Common:1; Rare:41 | ||||
chr1:45583930-45584061 | Rare:48 | ||||
chr1:45687059-45687353 | Common:1; Rare:77 | ||||
chr1:45688055-45688243 | Common:1; Rare:54 | ||||
chr1:45750615-45750821 | Rare:77 | ||||
chr1:46198426-46198620 | Common:7; Rare:90 | ||||
chr1:46303341-46303740 | Common:2; Rare:106 | ||||
chr1:46340666-46340819 | Common:3; Rare:39 |