Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:43370314-43370473 | Rare:29 | ||||
chr21:43800414-43800611 | Common:1; Rare:68 | ||||
chr21:43812070-43812314 | Common:2; Rare:44 | ||||
chr21:43812533-43812673 | Common:1; Rare:34 | ||||
chr21:43813001-43813068 | Rare:15 | ||||
chr21:45988940-45989091 | Common:1; Rare:37; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr21:46207471-46207675 | Common:1; Rare:63 | ||||
chr21:46243695-46243835 | Rare:41 | ||||
chr22:16603057-16603275 | Rare:46 | ||||
chr22:17866202-17866376 | Rare:34 | ||||
chr22:19171615-19171722 | Rare:35 | ||||
chr22:19434611-19434839 | Rare:56 | ||||
chr22:19758620-19758774 | Rare:44 | ||||
chr22:20303851-20304138 | Rare:39 | ||||
chr22:20656930-20657219 | Common:3; Rare:75 |