Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:101277425-101277625 | Common:2; Rare:101 | ||||
chr15:101295189-101295342 | Rare:46 | ||||
chr15:101652360-101652509 | Common:1; Rare:68 | ||||
chr16:53576-53870 | Common:6; Rare:98 | ||||
chr16:78111-78304 | Common:3; Rare:69 | ||||
chr16:740984-741152 | Rare:52 | ||||
chr16:1771521-1771630 | Rare:44 | ||||
chr16:1827135-1827220 | Common:1; Rare:36 | ||||
chr16:1943207-1943512 | Common:1; Rare:90 | ||||
chr16:1964818-1965061 | Common:6; Rare:106 | ||||
chr16:1971801-1972079 | Common:3; Rare:82 | ||||
chr16:2047810-2048033 | Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2777116-2777392 | Common:2; Rare:114 | ||||
chr16:2980410-2980630 | Common:2; Rare:78 | ||||
chr16:3443452-3443691 | Common:3; Rare:72 |