| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26573116-26573406 | Rare:88 | ||||
| chr21:26843538-26843720 | Common:3; Rare:44 | ||||
| chr21:26845401-26845655 | Common:2; Rare:69 | ||||
| chr21:28884960-28885250 | Common:3; Rare:77 | ||||
| chr21:28885312-28885480 | Common:3; Rare:103 | ||||
| chr21:28992784-28993177 | Common:2; Rare:154 | ||||
| chr21:29019304-29019457 | Common:5; Rare:69 | ||||
| chr21:29024489-29024710 | Common:3; Rare:85 | ||||
| chr21:29024845-29025139 | Common:2; Rare:56 | ||||
| chr21:29073599-29073927 | Common:2; Rare:102 | ||||
| chr21:29298708-29298948 | Common:2; Rare:104 | ||||
| chr21:31559044-31559289 | Common:3; Rare:78 | ||||
| chr21:31559432-31559669 | Common:1; Rare:72 | ||||
| chr21:31659531-31659744 | Common:2; Rare:93; Clinvar:3; Clinvar (benign):4 | ||||
| chr21:31660070-31660470 | Rare:164 |