Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:42893050-42893365 | Common:4; Rare:110 | ||||
chr21:43659461-43659644 | Common:1; Rare:59 | ||||
chr21:43776258-43776385 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
chr21:43789375-43789629 | Common:1; Rare:93 | ||||
chr21:44339226-44339469 | Common:2; Rare:74 | ||||
chr21:44801774-44801874 | Rare:41 | ||||
chr21:44873618-44874040 | Common:8; Rare:170 | ||||
chr21:45287867-45288106 | Common:6; Rare:93 | ||||
chr21:45981524-45981947 | Common:24; Rare:113; Clinvar:5; Clinvar (benign):4 | ||||
chr21:45986935-45987175 | Common:2; Rare:93; Clinvar:20; Clinvar (benign):8 | ||||
chr21:46286268-46286400 | Common:3; Rare:45 | ||||
chr21:46323830-46324202 | Common:2; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
chr21:46458708-46459009 | Common:3; Rare:100 | ||||
chr22:17159187-17159373 | Common:5; Rare:84 | ||||
chr22:17628675-17628966 | Common:1; Rare:105 |