| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45981501-45981794 | Common:23; Rare:63; Clinvar (benign):2 | ||||
| chr21:46184392-46184753 | Common:4; Rare:34 | ||||
| chr21:46286233-46286392 | Common:4; Rare:61 | ||||
| chr21:46323841-46324202 | Common:2; Rare:125; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46458686-46459063 | Common:3; Rare:130 | ||||
| chr21:46635457-46635718 | Common:6; Rare:91 | ||||
| chr22:17159190-17159385 | Common:5; Rare:92 | ||||
| chr22:17628648-17628853 | Common:2; Rare:72 | ||||
| chr22:17774434-17774560 | Rare:51 | ||||
| chr22:18077820-18078035 | Common:4; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19122382-19122667 | Common:4; Rare:69 | ||||
| chr22:19178456-19178543 | Common:1; Rare:24 | ||||
| chr22:19291696-19291903 | Common:10; Rare:68 | ||||
| chr22:19432380-19432606 | Common:2; Rare:93 | ||||
| chr22:19447684-19447868 | Common:2; Rare:71 |