| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:14546266-14546401 | Common:2; Rare:36 | ||||
| chr21:17819303-17819488 | Common:1; Rare:70 | ||||
| chr21:25607473-25607560 | Rare:47 | ||||
| chr21:25734853-25735242 | Common:2; Rare:153 | ||||
| chr21:25735246-25735478 | Common:3; Rare:62 | ||||
| chr21:25735568-25735625 | Rare:18 | ||||
| chr21:26845401-26845708 | Common:2; Rare:80 | ||||
| chr21:28885337-28885404 | Common:1; Rare:55 | ||||
| chr21:29019307-29019414 | Common:5; Rare:46 | ||||
| chr21:29024534-29024745 | Common:2; Rare:97 | ||||
| chr21:29024876-29024999 | Rare:23 | ||||
| chr21:29073586-29073854 | Common:2; Rare:80 | ||||
| chr21:29145403-29145639 | Rare:40 | ||||
| chr21:31659502-31659757 | Common:2; Rare:121; Clinvar:4; Clinvar (benign):4 | ||||
| chr21:32279016-32279214 | Common:3; Rare:85 |