Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:31659515-31659752 | Common:2; Rare:108; Clinvar:4; Clinvar (benign):4 | ||||
chr21:31732054-31732311 | Common:4; Rare:122 | ||||
chr21:32279017-32279205 | Common:3; Rare:83 | ||||
chr21:32392873-32393187 | Common:3; Rare:129 | ||||
chr21:32412344-32412519 | Common:1; Rare:38 | ||||
chr21:32771715-32772176 | Common:13; Rare:203 | ||||
chr21:33266262-33266426 | Rare:52; Clinvar:3 | ||||
chr21:33324862-33325010 | Common:3; Rare:53 | ||||
chr21:33479822-33480124 | Rare:105 | ||||
chr21:33542069-33542179 | Rare:43 | ||||
chr21:33542805-33543158 | Common:3; Rare:121 | ||||
chr21:36060503-36060574 | Common:1; Rare:22 | ||||
chr21:36134961-36135087 | Rare:30 | ||||
chr21:36320044-36320267 | Common:3; Rare:107 | ||||
chr21:37073040-37073348 | Common:5; Rare:122 |