Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1943131-1943574 | Common:1; Rare:139 | ||||
chr16:1964792-1965003 | Common:10; Rare:101 | ||||
chr16:1971853-1972131 | Common:3; Rare:85 | ||||
chr16:2047731-2048033 | Rare:144; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2268084-2268207 | Common:1; Rare:47 | ||||
chr16:2474992-2475151 | Rare:51 | ||||
chr16:2682370-2682540 | Rare:68 | ||||
chr16:2777243-2777366 | Common:1; Rare:48 | ||||
chr16:3134821-3135141 | Common:3; Rare:86 | ||||
chr16:3305261-3305514 | Common:4; Rare:78 | ||||
chr16:3400967-3401251 | Common:6; Rare:103 | ||||
chr16:4425780-4425879 | Common:1; Rare:46 | ||||
chr16:4476331-4476476 | Rare:58 | ||||
chr16:4538417-4538636 | Common:2; Rare:79 | ||||
chr16:4693476-4693759 | Common:3; Rare:128 |