Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:56392425-56392687 | Common:5; Rare:61 | ||||
chr20:62386985-62387126 | Common:3; Rare:58 | ||||
chr21:25734865-25734983 | Common:2; Rare:55 | ||||
chr21:25735003-25735184 | Rare:59 | ||||
chr21:28992841-28993075 | Common:2; Rare:92 | ||||
chr21:32279028-32279191 | Common:3; Rare:71 | ||||
chr21:32392988-32393147 | Common:2; Rare:66 | ||||
chr21:33542088-33542259 | Rare:65 | ||||
chr21:33542832-33543081 | Common:2; Rare:86 | ||||
chr21:42893064-42893328 | Common:4; Rare:85 | ||||
chr21:44873672-44874032 | Common:7; Rare:147 | ||||
chr21:46635476-46635680 | Common:4; Rare:64 | ||||
chr22:19479125-19479457 | Common:4; Rare:117 | ||||
chr22:19941736-19941877 | Rare:59; Clinvar:4; Clinvar (benign):2 | ||||
chr22:20117246-20117600 | Common:3; Rare:114 |