| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39319594-39319851 | Common:3; Rare:107 | ||||
| chr22:39349810-39349998 | Common:1; Rare:61 | ||||
| chr22:39399644-39399799 | Common:3; Rare:62 | ||||
| chr22:39502088-39502393 | Rare:87 | ||||
| chr22:39532698-39533046 | Common:2; Rare:131 | ||||
| chr22:40044121-40044341 | Common:2; Rare:50 | ||||
| chr22:40044528-40044871 | Common:2; Rare:80 | ||||
| chr22:40177793-40177970 | Rare:54 | ||||
| chr22:40346441-40346564 | Rare:51; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:40636668-40637008 | Common:2; Rare:95 | ||||
| chr22:40819298-40819526 | Common:11; Rare:109 | ||||
| chr22:40856584-40857154 | Common:2; Rare:220; Clinvar:3 | ||||
| chr22:41286168-41286392 | Common:2; Rare:64 | ||||
| chr22:41446789-41446979 | Rare:81 | ||||
| chr22:41468657-41468747 | Common:2; Rare:29 |