Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:2777235-2777377 | Common:1; Rare:57 | ||||
chr16:2980417-2980619 | Common:2; Rare:72 | ||||
chr16:3305394-3305514 | Common:1; Rare:41 | ||||
chr16:3400984-3401226 | Common:6; Rare:88 | ||||
chr16:3443461-3443732 | Common:3; Rare:93 | ||||
chr16:3611581-3611804 | Rare:95 | ||||
chr16:4476273-4476452 | Common:3; Rare:66 | ||||
chr16:4538413-4538621 | Common:2; Rare:74 | ||||
chr16:4538763-4538894 | Rare:54 | ||||
chr16:4734232-4734298 | Rare:19 | ||||
chr16:4767126-4767321 | Common:1; Rare:64 | ||||
chr16:5097737-5098007 | Common:4; Rare:98 | ||||
chr16:8797621-8797877 | Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
chr16:11851517-11851635 | Rare:57 | ||||
chr16:11976628-11976782 | Rare:61 |