| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63707855-63708104 | Rare:70 | ||||
| chr20:63865061-63865368 | Common:2; Rare:117 | ||||
| chr20:64079924-64080129 | Common:2; Rare:85 | ||||
| chr21:25734844-25735072 | Common:2; Rare:99 | ||||
| chr21:25735379-25735455 | Rare:20 | ||||
| chr21:25735521-25735721 | Rare:55 | ||||
| chr21:26170565-26170890 | Common:3; Rare:107; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:26845401-26845641 | Common:2; Rare:67 | ||||
| chr21:28885343-28885408 | Common:2; Rare:52 | ||||
| chr21:28992797-28993152 | Common:2; Rare:146 | ||||
| chr21:29019260-29019434 | Common:5; Rare:69 | ||||
| chr21:29024537-29024753 | Common:2; Rare:98 | ||||
| chr21:29073592-29073870 | Common:2; Rare:83 | ||||
| chr21:31659531-31659796 | Common:2; Rare:116; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr21:32279012-32279219 | Common:3; Rare:87 |