| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42812752-42812821 | Common:1; Rare:12 | ||||
| chr21:43343358-43343434 | Common:1; Rare:11 | ||||
| chr21:43720039-43720178 | Rare:25 | ||||
| chr21:43774742-43774941 | Common:2; Rare:36; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr21:43800466-43800559 | Rare:38 | ||||
| chr21:43812213-43812488 | Common:3; Rare:61 | ||||
| chr21:43929280-43929388 | Rare:25 | ||||
| chr21:44335734-44335869 | Common:1; Rare:51 | ||||
| chr21:45041288-45041604 | Common:3; Rare:58 | ||||
| chr21:45319675-45319844 | Common:2; Rare:38 | ||||
| chr21:45487351-45487508 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:45509840-45510259 | Common:5; Rare:179; Clinvar:3; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr21:45590578-45590796 | Common:5; Rare:72 | ||||
| chr21:45992008-45992182 | Common:1; Rare:64; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr21:46636269-46636473 | Common:1; Rare:36 |