| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39020806-39020911 | Common:1; Rare:29 | ||||
| chr22:39152431-39152796 | Common:5; Rare:122 | ||||
| chr22:39319499-39319921 | Common:6; Rare:168 | ||||
| chr22:39349803-39350017 | Common:1; Rare:67 | ||||
| chr22:39502164-39502379 | Rare:60 | ||||
| chr22:39532707-39532888 | Common:2; Rare:77 | ||||
| chr22:40044166-40044341 | Common:2; Rare:36 | ||||
| chr22:40177763-40177946 | Rare:54 | ||||
| chr22:40346445-40346664 | Rare:101; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:40636659-40637033 | Common:2; Rare:102 | ||||
| chr22:40819266-40819495 | Common:11; Rare:112 | ||||
| chr22:40856369-40857154 | Common:3; Rare:324; Clinvar:3 | ||||
| chr22:40951611-40951716 | Common:1; Rare:29 | ||||
| chr22:41091413-41091862 | Common:6; Rare:166 | ||||
| chr22:41205102-41205365 | Common:1; Rare:81 |