| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:33229739-33229964 | Common:5; Rare:102 | ||||
| chr21:33266253-33266473 | Rare:68; Clinvar:3 | ||||
| chr21:33324866-33325065 | Common:4; Rare:83 | ||||
| chr21:33325367-33325515 | Common:2; Rare:25 | ||||
| chr21:33403290-33403544 | Common:1; Rare:62 | ||||
| chr21:33479819-33480204 | Common:1; Rare:120 | ||||
| chr21:33491700-33491877 | Rare:41 | ||||
| chr21:33542073-33542248 | Rare:70 | ||||
| chr21:33542805-33543169 | Common:3; Rare:122 | ||||
| chr21:33641703-33641944 | Common:1; Rare:61 | ||||
| chr21:33642203-33642671 | Common:2; Rare:166 | ||||
| chr21:33642674-33642711 | Rare:14 | ||||
| chr21:33799452-33799892 | Common:3; Rare:92; Clinvar (pathogenic):1 | ||||
| chr21:34526796-34527077 | Common:1; Rare:47 | ||||
| chr21:34887170-34887291 | Common:2; Rare:32 |