| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20116924-20117066 | Common:1; Rare:40 | ||||
| chr22:20117116-20117571 | Common:3; Rare:142 | ||||
| chr22:20319963-20320166 | Common:2; Rare:77 | ||||
| chr22:20393934-20394196 | Common:1; Rare:80 | ||||
| chr22:20495781-20495994 | Common:2; Rare:81 | ||||
| chr22:20507547-20507633 | Rare:24 | ||||
| chr22:20524172-20524301 | Rare:20 | ||||
| chr22:20736659-20737010 | Common:3; Rare:72 | ||||
| chr22:20742320-20742420 | Rare:27 | ||||
| chr22:20858704-20859111 | Common:8; Rare:205; Clinvar:3; Clinvar (benign):5 | ||||
| chr22:20859378-20859519 | Rare:33 | ||||
| chr22:20917191-20917461 | Rare:107 | ||||
| chr22:20979345-20979480 | Common:3; Rare:64 | ||||
| chr22:20981963-20981990 | Rare:10 | ||||
| chr22:20982196-20982396 | Common:2; Rare:53; Clinvar (benign):4; Clinvar (pathogenic):1 |