| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29019257-29019610 | Common:36; Rare:507 | ||||
| chr21:29024157-29024798 | Common:14; Rare:630 | ||||
| chr21:29024731-29025157 | Common:6; Rare:362 | ||||
| chr21:29072758-29073158 | Common:3; Rare:84 | ||||
| chr21:29073563-29073963 | Common:12; Rare:594 | ||||
| chr21:29298629-29299939 | Common:18; Rare:1124 | ||||
| chr21:29300021-29300149 | Rare:30 | ||||
| chr21:29300201-29300426 | Common:1; Rare:99 | ||||
| chr21:29939910-29940260 | Common:3; Rare:90 | ||||
| chr21:31659340-31659838 | Common:14; Rare:981; Clinvar:29; Clinvar (benign):30; Clinvar (pathogenic):15 | ||||
| chr21:31659885-31660591 | Common:1; Rare:300 | ||||
| chr21:31731185-31731692 | Common:3; Rare:205 | ||||
| chr21:31731893-31733006 | Common:31; Rare:1163 | ||||
| chr21:32278520-32278920 | Common:2; Rare:169 | ||||
| chr21:32278932-32279374 | Common:21; Rare:782 |