| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44299979-44300100 | Rare:48 | ||||
| chr21:44801774-44801870 | Rare:41 | ||||
| chr21:44873634-44874028 | Common:8; Rare:158 | ||||
| chr21:45287879-45288093 | Common:5; Rare:82 | ||||
| chr21:46184423-46184708 | Common:3; Rare:24 | ||||
| chr21:46286252-46286407 | Common:4; Rare:57 | ||||
| chr21:46323841-46324161 | Common:2; Rare:106; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46605058-46605233 | Common:2; Rare:37 | ||||
| chr21:46635457-46635744 | Common:6; Rare:99 | ||||
| chr22:17159175-17159385 | Common:6; Rare:99 | ||||
| chr22:17628697-17628860 | Common:1; Rare:53 | ||||
| chr22:17638696-17638817 | Rare:43 | ||||
| chr22:18077791-18078007 | Common:4; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19291707-19291921 | Common:9; Rare:64 | ||||
| chr22:19432400-19432574 | Common:1; Rare:66 |