Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:62939369-62939622 | Common:1; Rare:67 | ||||
chr21:16194173-16194568 | Common:3; Rare:105 | ||||
chr21:16588576-16588730 | Common:1; Rare:45 | ||||
chr21:26844336-26844847 | Common:3; Rare:197 | ||||
chr21:26965487-26965547 | Common:1; Rare:26 | ||||
chr21:26967086-26967097 | Rare:3 | ||||
chr21:31667031-31667330 | Rare:71; Clinvar:1; Clinvar (pathogenic):7 | ||||
chr21:32360750-32360886 | Rare:16 | ||||
chr21:32508641-32508785 | Rare:34 | ||||
chr21:33436764-33436866 | Rare:21; Clinvar:1 | ||||
chr21:34887996-34888022 | Rare:3 | ||||
chr21:38907226-38907498 | Rare:48 | ||||
chr21:38913199-38913240 | Rare:13 | ||||
chr21:38913567-38913692 | Common:5; Rare:29 | ||||
chr21:41186620-41186629 | Rare:4 |