| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:31659522-31659838 | Common:2; Rare:137; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:32279017-32279174 | Common:2; Rare:73 | ||||
| chr21:32392946-32393163 | Common:2; Rare:92 | ||||
| chr21:32411441-32411786 | Common:3; Rare:67 | ||||
| chr21:32612522-32612910 | Rare:95 | ||||
| chr21:32727889-32728129 | Rare:118; Clinvar:2 | ||||
| chr21:32771724-32772176 | Common:13; Rare:200 | ||||
| chr21:33266275-33266462 | Rare:61; Clinvar:3 | ||||
| chr21:33324854-33325032 | Common:4; Rare:71 | ||||
| chr21:33479831-33480190 | Common:1; Rare:116 | ||||
| chr21:33542080-33542206 | Rare:44 | ||||
| chr21:33542805-33543141 | Common:3; Rare:120 | ||||
| chr21:34073166-34073232 | Common:1; Rare:11 | ||||
| chr21:34526935-34527232 | Common:1; Rare:42 | ||||
| chr21:36060480-36060607 | Common:1; Rare:39 |