| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17628698-17628843 | Common:1; Rare:48 | ||||
| chr22:17638672-17638818 | Rare:50 | ||||
| chr22:17706675-17706795 | Common:1; Rare:33 | ||||
| chr22:18077820-18078038 | Common:4; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19144647-19144902 | Common:4; Rare:88 | ||||
| chr22:19178449-19178527 | Common:1; Rare:19 | ||||
| chr22:19291707-19291925 | Common:9; Rare:64 | ||||
| chr22:19432303-19432612 | Common:4; Rare:131 | ||||
| chr22:19447667-19447904 | Common:2; Rare:99 | ||||
| chr22:19479093-19479474 | Common:4; Rare:140 | ||||
| chr22:19479698-19479960 | Common:4; Rare:72 | ||||
| chr22:19854791-19854995 | Rare:69 | ||||
| chr22:19881155-19881484 | Common:2; Rare:92 | ||||
| chr22:19941746-19941881 | Rare:53; Clinvar:4 | ||||
| chr22:20020899-20021141 | Common:1; Rare:79 |