Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1975690-1975825 | Common:2; Rare:57 | ||||
chr16:1984031-1984350 | Common:3; Rare:108; Clinvar (benign):4 | ||||
chr16:1990338-1990412 | Common:1; Rare:15 | ||||
chr16:1992752-1992965 | Rare:86 | ||||
chr16:2009762-2009906 | Common:7; Rare:53 | ||||
chr16:2047724-2048058 | Rare:170; Clinvar:2; Clinvar (benign):5 | ||||
chr16:2155096-2155280 | Common:1; Rare:61 | ||||
chr16:2155330-2155861 | Common:2; Rare:168 | ||||
chr16:2205695-2205868 | Common:4; Rare:81 | ||||
chr16:2214732-2215072 | Common:3; Rare:124 | ||||
chr16:2223304-2223693 | Rare:156 | ||||
chr16:2267841-2268210 | Common:1; Rare:160 | ||||
chr16:2340675-2340936 | Common:2; Rare:106; Clinvar:3; Clinvar (benign):2 | ||||
chr16:2429084-2429489 | Common:3; Rare:134 | ||||
chr16:2459909-2460197 | Common:2; Rare:95 |