Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:29019312-29019407 | Common:5; Rare:38 | ||||
chr21:29024504-29024761 | Common:3; Rare:107 | ||||
chr21:31659502-31659806 | Common:2; Rare:138; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr21:32279017-32279205 | Common:3; Rare:83 | ||||
chr21:32392956-32393171 | Common:2; Rare:91 | ||||
chr21:32612548-32612895 | Rare:86 | ||||
chr21:32771724-32772237 | Common:14; Rare:220 | ||||
chr21:33266262-33266434 | Rare:56; Clinvar:3 | ||||
chr21:33324866-33325058 | Common:4; Rare:83 | ||||
chr21:33479836-33480167 | Common:1; Rare:109 | ||||
chr21:33491704-33491923 | Rare:51 | ||||
chr21:33542080-33542206 | Rare:44 | ||||
chr21:33542810-33543095 | Common:3; Rare:103 | ||||
chr21:36060503-36060604 | Common:1; Rare:30 | ||||
chr21:37072595-37072718 | Common:3; Rare:60 |