| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44339216-44339357 | Common:1; Rare:51 | ||||
| chr21:44801707-44801880 | Rare:68 | ||||
| chr21:44817958-44818303 | Common:1; Rare:139 | ||||
| chr21:44873600-44874050 | Common:8; Rare:181 | ||||
| chr21:44939899-44940039 | Common:2; Rare:39 | ||||
| chr21:45287858-45288093 | Common:6; Rare:95 | ||||
| chr21:45534692-45534842 | Rare:34 | ||||
| chr21:45981519-45981873 | Common:24; Rare:88; Clinvar:3; Clinvar (benign):3 | ||||
| chr21:45986674-45987084 | Common:6; Rare:139; Clinvar:21; Clinvar (benign):12 | ||||
| chr21:46184402-46184722 | Common:3; Rare:29 | ||||
| chr21:46286209-46286396 | Common:4; Rare:72 | ||||
| chr21:46323809-46324224 | Common:3; Rare:157; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46436838-46437021 | Common:2; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr21:46458671-46459141 | Common:4; Rare:159 | ||||
| chr22:17159136-17159385 | Common:7; Rare:115 |