| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17563276-17563623 | Common:2; Rare:74 | ||||
| chr22:17628706-17628866 | Common:1; Rare:51 | ||||
| chr22:17638684-17638818 | Rare:46 | ||||
| chr22:18077814-18078028 | Common:4; Rare:70; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19144646-19144868 | Common:3; Rare:75 | ||||
| chr22:19291662-19291917 | Common:11; Rare:91 | ||||
| chr22:19432283-19432593 | Common:4; Rare:130 | ||||
| chr22:19447667-19447960 | Common:2; Rare:122 | ||||
| chr22:19479142-19479462 | Common:4; Rare:109 | ||||
| chr22:19479675-19479960 | Common:4; Rare:78 | ||||
| chr22:19524408-19524643 | Rare:74 | ||||
| chr22:19854787-19854997 | Rare:73 | ||||
| chr22:19941722-19941877 | Rare:66; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20079921-20080292 | Common:1; Rare:120 | ||||
| chr22:20319992-20320174 | Common:2; Rare:62 |