| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44133550-44133709 | Common:3; Rare:40 | ||||
| chr21:44299992-44300159 | Rare:58; Clinvar (benign):1 | ||||
| chr21:44305081-44305244 | Common:3; Rare:26 | ||||
| chr21:44339209-44339473 | Common:3; Rare:80 | ||||
| chr21:44801739-44801919 | Rare:79 | ||||
| chr21:44817948-44818253 | Common:1; Rare:127 | ||||
| chr21:44818730-44818876 | Rare:38 | ||||
| chr21:44872349-44872688 | Common:2; Rare:79 | ||||
| chr21:44873506-44873587 | Rare:21 | ||||
| chr21:44873593-44874113 | Common:9; Rare:199 | ||||
| chr21:45073543-45073845 | Common:5; Rare:69 | ||||
| chr21:45283397-45283699 | Common:1; Rare:81 | ||||
| chr21:45287867-45288108 | Common:6; Rare:93 | ||||
| chr21:45505129-45505371 | Common:4; Rare:135; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr21:45981507-45981897 | Common:24; Rare:100; Clinvar:3; Clinvar (benign):3 |