Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:25735491-25735715 | Rare:58 | ||||
chr21:26170565-26170926 | Common:5; Rare:116; Clinvar:5; Clinvar (benign):2 | ||||
chr21:26845405-26845649 | Common:2; Rare:65 | ||||
chr21:28885337-28885431 | Common:2; Rare:71 | ||||
chr21:29019307-29019400 | Common:5; Rare:41 | ||||
chr21:29024534-29024776 | Common:2; Rare:104 | ||||
chr21:29073592-29073850 | Common:2; Rare:76 | ||||
chr21:32278985-32279205 | Common:3; Rare:101 | ||||
chr21:32392946-32393191 | Common:4; Rare:105 | ||||
chr21:32411636-32411786 | Rare:36 | ||||
chr21:32612305-32612638 | Common:1; Rare:79 | ||||
chr21:32727889-32728122 | Rare:113; Clinvar:2 | ||||
chr21:32771724-32772167 | Common:13; Rare:196 | ||||
chr21:33266262-33266473 | Rare:68; Clinvar:3 | ||||
chr21:33324813-33325073 | Common:4; Rare:106 |