Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:397106-397298 | Common:4; Rare:54 | ||||
chr16:740944-741141 | Rare:67 | ||||
chr16:1420722-1420902 | Common:1; Rare:74 | ||||
chr16:1493263-1493587 | Common:4; Rare:98 | ||||
chr16:1612032-1612354 | Common:1; Rare:105; Clinvar:1 | ||||
chr16:1771515-1771865 | Common:3; Rare:136 | ||||
chr16:1782509-1782883 | Common:4; Rare:122 | ||||
chr16:1827166-1827232 | Common:1; Rare:32 | ||||
chr16:1943155-1943489 | Common:1; Rare:105 | ||||
chr16:1954510-1954829 | Common:3; Rare:87 | ||||
chr16:1964823-1964978 | Common:5; Rare:63 | ||||
chr16:1971884-1972084 | Common:3; Rare:57 | ||||
chr16:2047791-2048033 | Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2268072-2268193 | Common:1; Rare:53 | ||||
chr16:2682367-2682674 | Rare:140 |