| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31489920-31490164 | Common:3; Rare:100 | ||||
| chr22:31496409-31496589 | Common:1; Rare:51 | ||||
| chr22:31662192-31662326 | Common:1; Rare:57 | ||||
| chr22:31750066-31750214 | Common:3; Rare:52 | ||||
| chr22:31753761-31754059 | Common:1; Rare:106 | ||||
| chr22:32412188-32412275 | Common:1; Rare:33 | ||||
| chr22:33057541-33057635 | Common:1; Rare:13 | ||||
| chr22:35257403-35257510 | Common:1; Rare:29 | ||||
| chr22:35299666-35299931 | Common:3; Rare:72 | ||||
| chr22:35399918-35400183 | Rare:92 | ||||
| chr22:35839903-35839929 | Rare:4 | ||||
| chr22:35961523-35961723 | Rare:44 | ||||
| chr22:36239506-36239747 | Common:2; Rare:66 | ||||
| chr22:36387917-36388333 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481294-36481656 | Common:4; Rare:101 |