| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46497430-46497577 | Rare:28 | ||||
| chr22:46768516-46768527 | Rare:1 | ||||
| chr22:46806163-46806331 | Rare:35 | ||||
| chr22:46976003-46976165 | Rare:30 | ||||
| chr22:47097879-47097883 | |||||
| chr22:47689614-47689829 | Rare:38 | ||||
| chr22:47789676-47789785 | Common:1; Rare:17 | ||||
| chr22:47823431-47823725 | Common:2; Rare:70 | ||||
| chr22:49757760-49757771 | Rare:3 | ||||
| chr22:49962283-49962614 | Common:4; Rare:150 | ||||
| chr22:50217713-50218015 | Common:1; Rare:156; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr22:50526960-50527222 | Common:1; Rare:90; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:50527588-50527966 | Common:3; Rare:131; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr22:50539662-50539916 | Common:3; Rare:42 | ||||
| chr22:50560149-50560431 | Common:2; Rare:63 |