Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:37073003-37073398 | Common:5; Rare:151 | ||||
chr21:37267463-37267740 | Common:3; Rare:103 | ||||
chr21:39387676-39387797 | Common:2; Rare:53 | ||||
chr21:39445751-39445919 | Common:3; Rare:55 | ||||
chr21:39612802-39612940 | Rare:45 | ||||
chr21:41508079-41508349 | Common:2; Rare:57 | ||||
chr21:41767037-41767176 | Common:3; Rare:66; Clinvar:1 | ||||
chr21:42315487-42315815 | Common:1; Rare:86 | ||||
chr21:42879527-42879625 | Common:3; Rare:37 | ||||
chr21:42893073-42893349 | Common:3; Rare:96 | ||||
chr21:43659468-43659592 | Common:1; Rare:43 | ||||
chr21:43776266-43776618 | Common:4; Rare:124; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr21:44339216-44339438 | Common:2; Rare:71 | ||||
chr21:44801766-44801880 | Rare:49 | ||||
chr21:44873554-44874040 | Common:8; Rare:190 |