| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:17819324-17819415 | Rare:35 | ||||
| chr21:25607456-25607544 | Rare:51 | ||||
| chr21:25734853-25735239 | Common:2; Rare:152 | ||||
| chr21:25735359-25735700 | Common:2; Rare:92 | ||||
| chr21:26845385-26845641 | Common:2; Rare:70 | ||||
| chr21:28885310-28885413 | Common:3; Rare:77 | ||||
| chr21:28992801-28993049 | Common:1; Rare:112 | ||||
| chr21:29019287-29019387 | Common:5; Rare:44 | ||||
| chr21:29024537-29024747 | Common:2; Rare:96 | ||||
| chr21:29024876-29024997 | Rare:22 | ||||
| chr21:29077473-29077491 | Rare:3 | ||||
| chr21:29130352-29130672 | Common:1; Rare:52 | ||||
| chr21:29298642-29298947 | Common:3; Rare:124 | ||||
| chr21:31659502-31659833 | Common:2; Rare:148; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr21:32279010-32279215 | Common:3; Rare:87 |