Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1971865-1972141 | Common:3; Rare:83 | ||||
chr16:1990339-1990372 | Rare:7 | ||||
chr16:2009676-2009956 | Common:15; Rare:121 | ||||
chr16:2047804-2048063 | Rare:130; Clinvar:2; Clinvar (benign):7 | ||||
chr16:2155336-2155815 | Common:1; Rare:151 | ||||
chr16:2189281-2189478 | Common:1; Rare:81 | ||||
chr16:2205678-2205937 | Common:5; Rare:117 | ||||
chr16:2223304-2223688 | Rare:155 | ||||
chr16:2267763-2267887 | Common:3; Rare:42 | ||||
chr16:2268060-2268533 | Common:5; Rare:167 | ||||
chr16:2429114-2429484 | Common:3; Rare:121 | ||||
chr16:2459912-2460133 | Rare:67 | ||||
chr16:2475003-2475151 | Rare:50 | ||||
chr16:2513583-2514180 | Common:1; Rare:227 | ||||
chr16:2520244-2520456 | Common:7; Rare:132 |