Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:3717509-3717618 | Rare:57 | ||||
chr16:4425763-4425902 | Common:1; Rare:73 | ||||
chr16:4476271-4476476 | Common:3; Rare:79 | ||||
chr16:4614877-4615096 | Common:1; Rare:65 | ||||
chr16:4693489-4693729 | Common:2; Rare:106 | ||||
chr16:4734151-4734278 | Common:1; Rare:45 | ||||
chr16:4767134-4767398 | Common:1; Rare:84 | ||||
chr16:4795316-4795426 | Rare:38 | ||||
chr16:5033933-5033955 | Rare:6 | ||||
chr16:8797628-8797877 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
chr16:11797151-11797538 | Common:4; Rare:148 | ||||
chr16:11851506-11851653 | Rare:71 | ||||
chr16:11915391-11915728 | Common:5; Rare:126 | ||||
chr16:11915889-11916212 | Common:2; Rare:133 | ||||
chr16:11976628-11976761 | Rare:48 |