| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42514418-42514498 | Rare:16 | ||||
| chr21:42879527-42879665 | Common:3; Rare:46 | ||||
| chr21:42893050-42893342 | Common:4; Rare:97 | ||||
| chr21:43659468-43659631 | Common:1; Rare:54 | ||||
| chr21:43776204-43776470 | Common:4; Rare:92; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr21:43789389-43789630 | Common:1; Rare:92 | ||||
| chr21:44299992-44300123 | Rare:52; Clinvar (benign):1 | ||||
| chr21:44425567-44425772 | Common:1; Rare:83 | ||||
| chr21:44872590-44872690 | Rare:24 | ||||
| chr21:44873605-44874050 | Common:8; Rare:180 | ||||
| chr21:45287851-45288108 | Common:6; Rare:100 | ||||
| chr21:45981527-45981785 | Common:23; Rare:51; Clinvar (benign):1 | ||||
| chr21:46184423-46184632 | Common:3; Rare:22 | ||||
| chr21:46286233-46286392 | Common:4; Rare:61 | ||||
| chr21:46323817-46324224 | Common:3; Rare:152; Clinvar:3; Clinvar (benign):2 |