Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52921562-52921872 | Common:1; Rare:93 | ||||
chr1:52927219-52927385 | Common:3; Rare:61 | ||||
chr1:53014801-53015039 | Rare:71; Clinvar (benign):1 | ||||
chr1:53196639-53197050 | Common:1; Rare:156; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr1:53220150-53220498 | Rare:149 | ||||
chr1:53220539-53220822 | Common:2; Rare:116 | ||||
chr1:53238445-53238774 | Common:2; Rare:112 | ||||
chr1:53326883-53326980 | Common:1; Rare:23 | ||||
chr1:53327042-53327332 | Common:5; Rare:59 | ||||
chr1:53327352-53327531 | Common:1; Rare:46 | ||||
chr1:53328033-53328252 | Rare:52 | ||||
chr1:53838127-53838381 | Common:1; Rare:90 | ||||
chr1:53838450-53838742 | Rare:67 | ||||
chr1:53889668-53890241 | Common:5; Rare:135 | ||||
chr1:53945332-53945416 | Rare:19 |