Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1493206-1493599 | Common:4; Rare:117 | ||||
chr16:1706047-1706189 | Common:2; Rare:42 | ||||
chr16:1771502-1771868 | Common:3; Rare:144 | ||||
chr16:1773128-1773213 | Rare:20 | ||||
chr16:1782506-1783009 | Common:4; Rare:167 | ||||
chr16:1964818-1965067 | Common:6; Rare:106 | ||||
chr16:1971883-1972093 | Common:3; Rare:59 | ||||
chr16:2047777-2048034 | Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2268058-2268183 | Common:1; Rare:66 | ||||
chr16:2474916-2475151 | Rare:74 | ||||
chr16:2513631-2514035 | Rare:148 | ||||
chr16:2519364-2519641 | Common:1; Rare:100 | ||||
chr16:2520117-2520406 | Common:9; Rare:156 | ||||
chr16:2537691-2538088 | Common:4; Rare:152 | ||||
chr16:2758539-2758555 | Rare:6 |