Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:63864983-63865340 | Common:2; Rare:124 | ||||
chr20:63980974-63981184 | Common:3; Rare:69; Clinvar:6; Clinvar (benign):3 | ||||
chr21:17819344-17819689 | Common:2; Rare:106 | ||||
chr21:25607468-25607560 | Rare:49 | ||||
chr21:25734855-25735239 | Common:2; Rare:151 | ||||
chr21:25735422-25735454 | Rare:8 | ||||
chr21:28885354-28885413 | Common:2; Rare:49 | ||||
chr21:28992825-28993152 | Common:2; Rare:134 | ||||
chr21:29019329-29019450 | Common:5; Rare:51 | ||||
chr21:29073597-29073864 | Common:2; Rare:76 | ||||
chr21:31659525-31659763 | Common:2; Rare:108; Clinvar:4; Clinvar (benign):4 | ||||
chr21:32392946-32393171 | Common:2; Rare:96 | ||||
chr21:33542096-33542236 | Rare:53 | ||||
chr21:33542805-33543095 | Common:3; Rare:106 | ||||
chr21:34526817-34527115 | Common:1; Rare:43 |