| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26843032-26843169 | Common:3; Rare:21 | ||||
| chr21:26845391-26845521 | Common:1; Rare:29 | ||||
| chr21:28885312-28885396 | Common:1; Rare:62 | ||||
| chr21:28992797-28993088 | Common:2; Rare:121 | ||||
| chr21:29019297-29019434 | Common:5; Rare:56 | ||||
| chr21:29024537-29024771 | Common:2; Rare:102 | ||||
| chr21:29024876-29025012 | Rare:25 | ||||
| chr21:29073592-29073865 | Common:2; Rare:80 | ||||
| chr21:29298536-29298960 | Common:3; Rare:158 | ||||
| chr21:30215930-30216129 | Rare:45 | ||||
| chr21:31659531-31659838 | Common:2; Rare:132; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732047-31732311 | Common:4; Rare:126 | ||||
| chr21:32278982-32279214 | Common:3; Rare:103 | ||||
| chr21:32298637-32299001 | Common:2; Rare:105; Clinvar (pathogenic):1 | ||||
| chr21:32392906-32393197 | Common:4; Rare:123 |