| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17578268-17578462 | Rare:24 | ||||
| chr22:17639549-17639574 | Rare:8 | ||||
| chr22:17639577-17639888 | Common:5; Rare:83 | ||||
| chr22:18068506-18068613 | Common:2; Rare:18 | ||||
| chr22:19142579-19142817 | Common:1; Rare:94 | ||||
| chr22:19171600-19171724 | Rare:40 | ||||
| chr22:19176461-19176586 | Rare:62; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:19935587-19935619 | Common:1; Rare:8 | ||||
| chr22:19968294-19968686 | Common:3; Rare:127 | ||||
| chr22:20126257-20126364 | Common:1; Rare:34 | ||||
| chr22:21477895-21478002 | Common:1; Rare:28 | ||||
| chr22:21693684-21693757 | Rare:17 | ||||
| chr22:22098559-22098739 | Common:1; Rare:43 | ||||
| chr22:22298008-22298210 | Common:10; Rare:93 | ||||
| chr22:22303938-22303962 | Rare:4 |