Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:63865042-63865338 | Common:2; Rare:103 | ||||
chr21:25734870-25734993 | Common:2; Rare:58 | ||||
chr21:25735046-25735104 | Rare:19 | ||||
chr21:26170619-26170895 | Common:3; Rare:93; Clinvar:5; Clinvar (benign):2 | ||||
chr21:28992833-28993052 | Common:1; Rare:97 | ||||
chr21:33324674-33325032 | Common:4; Rare:123 | ||||
chr21:33479890-33480189 | Common:1; Rare:97 | ||||
chr21:33542823-33543090 | Common:2; Rare:95 | ||||
chr21:33588628-33588798 | Rare:76 | ||||
chr21:37073023-37073245 | Common:4; Rare:81 | ||||
chr21:41361857-41362030 | Common:1; Rare:23 | ||||
chr21:42879524-42879665 | Common:3; Rare:48 | ||||
chr21:42893017-42893375 | Common:5; Rare:131 | ||||
chr21:44299979-44300117 | Rare:55; Clinvar (benign):1 | ||||
chr21:44873618-44874053 | Common:8; Rare:174 |