| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20116971-20117655 | Common:4; Rare:205 | ||||
| chr22:20319984-20320174 | Common:2; Rare:68 | ||||
| chr22:20394079-20394194 | Rare:28 | ||||
| chr22:20495775-20495993 | Common:2; Rare:82 | ||||
| chr22:20507496-20507652 | Rare:50 | ||||
| chr22:20917284-20917461 | Rare:72 | ||||
| chr22:20982159-20982358 | Common:2; Rare:54; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002029-21002289 | Common:6; Rare:99 | ||||
| chr22:21567500-21567768 | Common:3; Rare:75 | ||||
| chr22:21629943-21630065 | Common:1; Rare:60 | ||||
| chr22:21642034-21642372 | Common:2; Rare:106 | ||||
| chr22:21651981-21652192 | Common:1; Rare:49 | ||||
| chr22:21665934-21666076 | Rare:43 | ||||
| chr22:21867412-21867808 | Common:4; Rare:112 | ||||
| chr22:21982729-21982890 | Rare:46 |