| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43789377-43789617 | Common:1; Rare:87 | ||||
| chr21:44299979-44300100 | Rare:48 | ||||
| chr21:44339216-44339357 | Common:1; Rare:51 | ||||
| chr21:44353443-44353649 | Common:2; Rare:39 | ||||
| chr21:44873577-44874050 | Common:8; Rare:191 | ||||
| chr21:44928653-44928669 | Common:1; Rare:4 | ||||
| chr21:45287879-45288085 | Common:5; Rare:80 | ||||
| chr21:45981519-45981946 | Common:24; Rare:113; Clinvar:5; Clinvar (benign):4 | ||||
| chr21:45986611-45987072 | Common:6; Rare:155; Clinvar:27; Clinvar (benign):11 | ||||
| chr21:46097317-46097620 | Common:3; Rare:61 | ||||
| chr21:46184423-46184708 | Common:3; Rare:24 | ||||
| chr21:46286209-46286399 | Common:4; Rare:72 | ||||
| chr21:46286610-46286684 | Common:1; Rare:29 | ||||
| chr21:46323871-46324222 | Common:3; Rare:130; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458683-46459122 | Common:4; Rare:148 |