| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:31659509-31659835 | Common:2; Rare:144; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732017-31732298 | Common:4; Rare:128 | ||||
| chr21:32278985-32279205 | Common:3; Rare:101 | ||||
| chr21:32392940-32393171 | Common:2; Rare:98 | ||||
| chr21:32411718-32411822 | Rare:19 | ||||
| chr21:32412246-32412519 | Common:2; Rare:64 | ||||
| chr21:32412626-32412730 | Rare:23 | ||||
| chr21:32727889-32728122 | Rare:113; Clinvar:2 | ||||
| chr21:32771670-32772235 | Common:14; Rare:246 | ||||
| chr21:33266262-33266473 | Rare:68; Clinvar:3 | ||||
| chr21:33324863-33325032 | Common:4; Rare:67 | ||||
| chr21:33479820-33480204 | Common:1; Rare:119 | ||||
| chr21:33542778-33543163 | Common:4; Rare:133 | ||||
| chr21:34526819-34527130 | Common:1; Rare:45 | ||||
| chr21:34888218-34888342 | Common:1; Rare:22 |