Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:53502921-53503039 | Rare:37 | ||||
chr16:53503141-53503564 | Common:10; Rare:134 | ||||
chr16:53503570-53503850 | Common:3; Rare:72 | ||||
chr16:53503881-53504142 | Common:5; Rare:55 | ||||
chr16:53703798-53704262 | Common:1; Rare:147; Clinvar:6; Clinvar (benign):2 | ||||
chr16:54930546-54930740 | Common:1; Rare:52 | ||||
chr16:56423695-56423782 | Rare:17 | ||||
chr16:56424819-56425052 | Common:1; Rare:59 | ||||
chr16:56425406-56425712 | Common:4; Rare:123 | ||||
chr16:56451203-56451619 | Common:2; Rare:146 | ||||
chr16:56451746-56451851 | Rare:28 | ||||
chr16:56519549-56519753 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
chr16:56519919-56520272 | Common:7; Rare:120; Clinvar:6; Clinvar (benign):5 | ||||
chr16:56608274-56608686 | Common:3; Rare:118 | ||||
chr16:56625574-56625833 | Common:1; Rare:78 |