Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:684326-684479 | Common:3; Rare:86 | ||||
chr16:1351870-1351999 | Common:1; Rare:71; Clinvar:6; Clinvar (benign):1 | ||||
chr16:1420714-1420937 | Common:1; Rare:90 | ||||
chr16:1533492-1533694 | Common:1; Rare:39 | ||||
chr16:1782510-1782743 | Common:4; Rare:76 | ||||
chr16:1827179-1827232 | Rare:29 | ||||
chr16:1943160-1943481 | Common:1; Rare:102 | ||||
chr16:1964823-1964992 | Common:6; Rare:71 | ||||
chr16:1971938-1972110 | Common:1; Rare:48 | ||||
chr16:2009674-2009914 | Common:15; Rare:101 | ||||
chr16:2047795-2048038 | Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2268072-2268178 | Common:1; Rare:51 | ||||
chr16:2459954-2460147 | Common:1; Rare:55 | ||||
chr16:2474983-2475151 | Rare:53 | ||||
chr16:2682367-2682608 | Rare:106 |