| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17628647-17628866 | Common:2; Rare:76 | ||||
| chr22:17638696-17638830 | Rare:49 | ||||
| chr22:17774383-17774580 | Rare:66 | ||||
| chr22:18077800-18078058 | Common:5; Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18110625-18110846 | Rare:59 | ||||
| chr22:18149837-18150191 | Common:2; Rare:82 | ||||
| chr22:19122382-19122650 | Common:4; Rare:64 | ||||
| chr22:19178445-19178527 | Common:1; Rare:22 | ||||
| chr22:19291665-19291940 | Common:11; Rare:93 | ||||
| chr22:19431512-19431836 | Common:1; Rare:90 | ||||
| chr22:19431856-19431908 | Rare:8 | ||||
| chr22:19432279-19432614 | Common:4; Rare:143 | ||||
| chr22:19447495-19447878 | Common:3; Rare:169 | ||||
| chr22:19478947-19479064 | Rare:41 | ||||
| chr22:19479090-19479462 | Common:4; Rare:134 |