| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37807736-37807977 | Common:4; Rare:88 | ||||
| chr22:37849316-37849480 | Rare:93 | ||||
| chr22:37953609-37953806 | Rare:76 | ||||
| chr22:38506281-38506510 | Rare:78 | ||||
| chr22:38570181-38570483 | Common:5; Rare:54 | ||||
| chr22:38656382-38656721 | Common:1; Rare:81 | ||||
| chr22:38681809-38682010 | Common:2; Rare:86 | ||||
| chr22:39349803-39350010 | Common:1; Rare:65 | ||||
| chr22:40044560-40044862 | Common:2; Rare:68 | ||||
| chr22:40346434-40346664 | Rare:106; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:40856434-40857160 | Common:3; Rare:295; Clinvar:4 | ||||
| chr22:41367395-41367455 | Rare:19 | ||||
| chr22:41446354-41446542 | Common:1; Rare:39 | ||||
| chr22:41446778-41446935 | Rare:58 | ||||
| chr22:41468638-41468762 | Common:2; Rare:36 |