| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43789112-43789157 | Rare:14 | ||||
| chr21:43789286-43789664 | Common:1; Rare:140 | ||||
| chr21:43866275-43866472 | Common:1; Rare:43 | ||||
| chr21:43866523-43866598 | Rare:23 | ||||
| chr21:43866757-43867017 | Common:1; Rare:54 | ||||
| chr21:43916732-43916808 | Rare:16 | ||||
| chr21:44012090-44012392 | Common:2; Rare:106 | ||||
| chr21:44012775-44013125 | Rare:95 | ||||
| chr21:44107270-44107401 | Common:1; Rare:28 | ||||
| chr21:44299617-44299777 | Common:1; Rare:46 | ||||
| chr21:44299855-44300134 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr21:44300531-44300699 | Common:1; Rare:49 | ||||
| chr21:44339082-44339207 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr21:44339209-44339584 | Common:3; Rare:103 | ||||
| chr21:44353128-44353298 | Common:1; Rare:37 |