| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46356988-46357232 | Common:1; Rare:88; Clinvar:6; Clinvar (benign):2 | ||||
| chr21:46368944-46369179 | Rare:34 | ||||
| chr21:46369733-46369756 | Rare:2 | ||||
| chr21:46458043-46458372 | Common:2; Rare:65 | ||||
| chr21:46551723-46551855 | Rare:46 | ||||
| chr21:46559301-46559381 | Rare:14 | ||||
| chr21:46559521-46559611 | Rare:25 | ||||
| chr21:46606188-46606360 | Rare:29 | ||||
| chr21:46608755-46608872 | Rare:18 | ||||
| chr21:46609022-46609303 | Common:2; Rare:53 | ||||
| chr21:46667272-46667421 | Common:3; Rare:55 | ||||
| chr22:17171519-17171710 | Common:2; Rare:44 | ||||
| chr22:17171793-17172058 | Common:4; Rare:70 | ||||
| chr22:17228677-17228865 | Rare:30 | ||||
| chr22:17236978-17237260 | Common:1; Rare:50 |