| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46113342-46113627 | Rare:65 | ||||
| chr21:46184400-46184753 | Common:4; Rare:33 | ||||
| chr21:46286222-46286396 | Common:4; Rare:66 | ||||
| chr21:46323790-46324237 | Common:3; Rare:173; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458686-46459084 | Common:4; Rare:136 | ||||
| chr21:46635474-46635778 | Common:6; Rare:98 | ||||
| chr21:46636158-46636466 | Common:2; Rare:62 | ||||
| chr22:17158973-17159393 | Common:10; Rare:173 | ||||
| chr22:17628602-17628872 | Common:2; Rare:87 | ||||
| chr22:17638689-17638845 | Rare:57 | ||||
| chr22:17774390-17774585 | Rare:68 | ||||
| chr22:18077814-18078135 | Common:5; Rare:104; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:18149796-18150134 | Common:2; Rare:77 | ||||
| chr22:18150137-18150194 | Rare:10 | ||||
| chr22:19122338-19122573 | Common:5; Rare:73 |