| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26845395-26845641 | Common:2; Rare:68 | ||||
| chr21:28885312-28885394 | Common:1; Rare:62 | ||||
| chr21:29019312-29019400 | Common:5; Rare:37 | ||||
| chr21:29024534-29024726 | Common:2; Rare:85 | ||||
| chr21:29024876-29025012 | Rare:25 | ||||
| chr21:29073592-29073811 | Common:2; Rare:64 | ||||
| chr21:29077208-29077537 | Rare:86 | ||||
| chr21:29298711-29298960 | Common:2; Rare:107 | ||||
| chr21:30215993-30216378 | Common:2; Rare:74 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732017-31732306 | Common:4; Rare:136 | ||||
| chr21:32279017-32279205 | Common:3; Rare:83 | ||||
| chr21:32392931-32393171 | Common:2; Rare:102 | ||||
| chr21:32411634-32411780 | Rare:37 | ||||
| chr21:32412347-32412524 | Common:1; Rare:38 |