| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:31659531-31659829 | Common:2; Rare:129; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr21:31732064-31732327 | Common:5; Rare:121 | ||||
| chr21:32278848-32279168 | Common:3; Rare:137 | ||||
| chr21:32392899-32393139 | Common:1; Rare:98 | ||||
| chr21:32612553-32612886 | Rare:82 | ||||
| chr21:32771844-32772167 | Common:12; Rare:131 | ||||
| chr21:33324813-33325016 | Common:4; Rare:75 | ||||
| chr21:33479899-33480190 | Common:1; Rare:92 | ||||
| chr21:33542066-33542191 | Rare:46 | ||||
| chr21:33542805-33543152 | Common:3; Rare:120 | ||||
| chr21:33931013-33931237 | Common:2; Rare:55 | ||||
| chr21:36060470-36060613 | Common:4; Rare:47 | ||||
| chr21:36060792-36061019 | Common:2; Rare:41 | ||||
| chr21:36134931-36135087 | Rare:41 | ||||
| chr21:36320061-36320258 | Common:3; Rare:100 |