Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93909369-93909760 | Common:5; Rare:126 | ||||
chr1:94418050-94418508 | Common:3; Rare:157 | ||||
chr1:94926988-94927347 | Common:4; Rare:118 | ||||
chr1:95072600-95072742 | Rare:40 | ||||
chr1:95072881-95073069 | Common:3; Rare:67 | ||||
chr1:95233959-95234347 | Common:6; Rare:120 | ||||
chr1:95234437-95234507 | Common:1; Rare:14 | ||||
chr1:96721523-96721819 | Common:3; Rare:124 | ||||
chr1:97920944-97921156 | Rare:89; Clinvar:3 | ||||
chr1:98661510-98661752 | Common:3; Rare:80 | ||||
chr1:98661998-98662194 | Rare:48 | ||||
chr1:99766500-99766734 | Common:1; Rare:43 | ||||
chr1:99849869-99850277 | Common:2; Rare:117; Clinvar:1 | ||||
chr1:99850295-99850414 | Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
chr1:99969836-99970103 | Rare:60 |