| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42649333-42649459 | Common:1; Rare:55 | ||||
| chr22:42857178-42857430 | Common:3; Rare:105 | ||||
| chr22:42947028-42947076 | Rare:1 | ||||
| chr22:42959804-42959979 | Common:1; Rare:34 | ||||
| chr22:43015089-43015384 | Common:2; Rare:121 | ||||
| chr22:43812208-43812441 | Common:3; Rare:78 | ||||
| chr22:43955326-43955566 | Common:3; Rare:75 | ||||
| chr22:44024196-44024426 | Common:1; Rare:76 | ||||
| chr22:45163758-45164081 | Common:4; Rare:131 | ||||
| chr22:45413594-45413742 | Rare:58 | ||||
| chr22:46250260-46250423 | Common:3; Rare:53 | ||||
| chr22:46335621-46335776 | Common:4; Rare:66; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:46762506-46762669 | Common:3; Rare:58 | ||||
| chr22:49853601-49853899 | Common:2; Rare:106 | ||||
| chr22:49918436-49918796 | Common:4; Rare:133 |