| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:17612772-17613110 | Common:2; Rare:273 | ||||
| chr21:17818440-17818806 | Common:1; Rare:114 | ||||
| chr21:17819265-17819870 | Common:4; Rare:321 | ||||
| chr21:20998144-20998667 | Common:1; Rare:544 | ||||
| chr21:21238940-21239412 | Common:9; Rare:189 | ||||
| chr21:25607421-25607653 | Common:1; Rare:251 | ||||
| chr21:25639750-25640250 | Common:4; Rare:120 | ||||
| chr21:25734820-25735492 | Common:14; Rare:643 | ||||
| chr21:25735507-25735744 | Rare:163 | ||||
| chr21:26168880-26169370 | Rare:132 | ||||
| chr21:26169598-26169841 | Common:2; Rare:113 | ||||
| chr21:26169951-26170196 | Common:3; Rare:65 | ||||
| chr21:26170514-26170958 | Common:12; Rare:337; Clinvar:15; Clinvar (benign):6 | ||||
| chr21:26842995-26843223 | Common:5; Rare:38 | ||||
| chr21:26843506-26843809 | Common:7; Rare:92 |