Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:26170568-26170890 | Common:3; Rare:107; Clinvar:5; Clinvar (benign):2 | ||||
chr21:29019289-29019414 | Common:5; Rare:51 | ||||
chr21:29024869-29024991 | Rare:20 | ||||
chr21:31659519-31659837 | Common:2; Rare:138; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
chr21:31660017-31660172 | Rare:39 | ||||
chr21:31731946-31732256 | Common:4; Rare:131 | ||||
chr21:32392968-32393164 | Common:2; Rare:83 | ||||
chr21:33266275-33266446 | Rare:56; Clinvar:3 | ||||
chr21:33542067-33542191 | Rare:46 | ||||
chr21:33542805-33543109 | Common:3; Rare:114 | ||||
chr21:33642192-33642614 | Common:2; Rare:158 | ||||
chr21:33774730-33775086 | Common:1; Rare:109 | ||||
chr21:37072995-37073477 | Common:5; Rare:168 | ||||
chr21:37267332-37267645 | Common:3; Rare:102 | ||||
chr21:42879520-42879674 | Common:3; Rare:53 |