| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19941752-19941877 | Rare:50; Clinvar:4 | ||||
| chr22:20020873-20021116 | Common:1; Rare:75 | ||||
| chr22:20319992-20320151 | Common:2; Rare:53 | ||||
| chr22:20495781-20495985 | Common:2; Rare:78 | ||||
| chr22:20507496-20507643 | Rare:42 | ||||
| chr22:20734126-20734413 | Rare:75 | ||||
| chr22:21002092-21002211 | Common:3; Rare:45 | ||||
| chr22:21938159-21938300 | Rare:49 | ||||
| chr22:23894234-23894504 | Common:3; Rare:95 | ||||
| chr22:23894577-23894868 | Common:3; Rare:113; Clinvar:1 | ||||
| chr22:24555884-24556045 | Rare:51 | ||||
| chr22:26483752-26483964 | Common:4; Rare:91; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512428-26512550 | Common:1; Rare:55 | ||||
| chr22:27919195-27919527 | Common:5; Rare:149 | ||||
| chr22:28741791-28742074 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 |