| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29024876-29024979 | Rare:19 | ||||
| chr21:29073586-29073865 | Common:2; Rare:82 | ||||
| chr21:31659502-31659757 | Common:2; Rare:121; Clinvar:4; Clinvar (benign):4 | ||||
| chr21:32279017-32279214 | Common:3; Rare:84 | ||||
| chr21:32392940-32393179 | Common:2; Rare:101 | ||||
| chr21:32771841-32772167 | Common:13; Rare:135 | ||||
| chr21:33266262-33266434 | Rare:56; Clinvar:3 | ||||
| chr21:33324835-33325032 | Common:4; Rare:78 | ||||
| chr21:33491700-33491913 | Rare:48 | ||||
| chr21:33542080-33542183 | Rare:37 | ||||
| chr21:33542805-33543102 | Common:3; Rare:110 | ||||
| chr21:36060489-36060604 | Common:1; Rare:35 | ||||
| chr21:36320068-36320258 | Common:3; Rare:99 | ||||
| chr21:37072517-37072812 | Common:8; Rare:140 | ||||
| chr21:37073006-37073387 | Common:5; Rare:144 |