Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:84631288-84631477 | Common:4; Rare:54 | ||||
chr15:92724278-92724510 | Common:6; Rare:37 | ||||
chr16:399435-399736 | Common:4; Rare:107 | ||||
chr16:1961963-1962055 | Common:3; Rare:35 | ||||
chr16:11841804-11841943 | Common:2; Rare:53 | ||||
chr16:15701352-15701424 | Rare:15 | ||||
chr16:27243262-27243497 | Rare:38 | ||||
chr16:27718763-27719010 | Common:1; Rare:44 | ||||
chr16:30353067-30353236 | Rare:69 | ||||
chr16:30444521-30444569 | Rare:8 | ||||
chr16:30875333-30875557 | Rare:71 | ||||
chr16:53924326-53924492 | Rare:29 | ||||
chr16:56617439-56617587 | Common:2; Rare:32 | ||||
chr16:56834248-56834419 | Rare:48; Clinvar (pathogenic):1 | ||||
chr16:69318669-69318884 | Common:1; Rare:86 |