| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19854787-19854979 | Rare:65 | ||||
| chr22:19941774-19941889 | Rare:48; Clinvar:2 | ||||
| chr22:20117237-20117571 | Common:3; Rare:108 | ||||
| chr22:20319999-20320133 | Common:1; Rare:49 | ||||
| chr22:20495781-20495920 | Common:1; Rare:54 | ||||
| chr22:20982196-20982358 | Common:2; Rare:37; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002092-21002195 | Common:3; Rare:35 | ||||
| chr22:23894576-23894695 | Common:3; Rare:47 | ||||
| chr22:24555895-24556066 | Rare:50 | ||||
| chr22:26512434-26512550 | Common:1; Rare:52 | ||||
| chr22:26590103-26590220 | Common:3; Rare:49 | ||||
| chr22:27919195-27919437 | Common:4; Rare:110 | ||||
| chr22:28741798-28742090 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:28742408-28742701 | Common:1; Rare:73 | ||||
| chr22:29267835-29268339 | Common:2; Rare:148 |