| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:24952598-24952717 | Rare:32 | ||||
| chr22:26476992-26477238 | Rare:68; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr22:26479307-26479476 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:26479577-26479720 | Rare:34 | ||||
| chr22:26479805-26479870 | Rare:15 | ||||
| chr22:26479937-26480205 | Common:1; Rare:45 | ||||
| chr22:26483511-26484114 | Common:14; Rare:226; Clinvar:7; Clinvar (benign):3 | ||||
| chr22:26512413-26512568 | Common:2; Rare:65 | ||||
| chr22:26590095-26590220 | Common:3; Rare:51 | ||||
| chr22:27919195-27919569 | Common:5; Rare:161 | ||||
| chr22:28741787-28742090 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):4 | ||||
| chr22:28742397-28742709 | Common:1; Rare:75 | ||||
| chr22:28800044-28800751 | Common:7; Rare:236 | ||||
| chr22:29267835-29268348 | Common:2; Rare:150 | ||||
| chr22:29553543-29553880 | Common:1; Rare:111 |