| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29298608-29298935 | Common:2; Rare:126 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732102-31732416 | Common:4; Rare:134 | ||||
| chr21:32279017-32279205 | Common:3; Rare:83 | ||||
| chr21:32392873-32393155 | Common:2; Rare:113 | ||||
| chr21:32411624-32411811 | Rare:44 | ||||
| chr21:32412607-32412750 | Rare:31 | ||||
| chr21:32612233-32612486 | Common:3; Rare:67 | ||||
| chr21:32727897-32728114 | Rare:107; Clinvar:2 | ||||
| chr21:32771724-32772171 | Common:13; Rare:197 | ||||
| chr21:33266262-33266434 | Rare:56; Clinvar:3 | ||||
| chr21:33324862-33325121 | Common:4; Rare:110 | ||||
| chr21:33542077-33542206 | Rare:44 | ||||
| chr21:33542814-33543169 | Common:2; Rare:117 | ||||
| chr21:34888214-34888326 | Common:1; Rare:22 |