| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20507443-20507685 | Rare:88 | ||||
| chr22:20858223-20858613 | Common:3; Rare:106 | ||||
| chr22:20858748-20859146 | Common:8; Rare:192; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:20916947-20917542 | Common:1; Rare:175 | ||||
| chr22:20917784-20918013 | Rare:79 | ||||
| chr22:20981816-20982105 | Common:2; Rare:76; Clinvar (benign):1 | ||||
| chr22:20982108-20982414 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr22:21001543-21001956 | Common:2; Rare:139 | ||||
| chr22:21001977-21002446 | Common:7; Rare:168 | ||||
| chr22:21567628-21567820 | Common:2; Rare:72 | ||||
| chr22:21568137-21568369 | Common:3; Rare:60 | ||||
| chr22:21629345-21629577 | Common:2; Rare:66 | ||||
| chr22:21629914-21630202 | Common:3; Rare:112 | ||||
| chr22:21641916-21642416 | Common:2; Rare:146 | ||||
| chr22:21651752-21652288 | Common:2; Rare:116 |