Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:636258-636441 | Common:4; Rare:57 | ||||
chr16:740951-741144 | Rare:64 | ||||
chr16:1420712-1420918 | Common:1; Rare:84 | ||||
chr16:1493263-1493572 | Common:4; Rare:97 | ||||
chr16:1533492-1533688 | Common:1; Rare:39 | ||||
chr16:1706047-1706304 | Common:2; Rare:80 | ||||
chr16:1771502-1771833 | Common:3; Rare:129 | ||||
chr16:1782646-1783009 | Common:1; Rare:113 | ||||
chr16:1827179-1827232 | Rare:29 | ||||
chr16:1971904-1972110 | Common:1; Rare:59 | ||||
chr16:2047804-2048043 | Rare:112; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2155571-2155820 | Common:1; Rare:76 | ||||
chr16:2268055-2268186 | Common:1; Rare:69 | ||||
chr16:2340742-2341086 | Common:3; Rare:121; Clinvar (benign):1 | ||||
chr16:2682359-2682598 | Rare:109 |