| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38505992-38506028 | Rare:14 | ||||
| chr22:38506285-38506626 | Common:1; Rare:105 | ||||
| chr22:38570147-38570483 | Common:5; Rare:64 | ||||
| chr22:38656360-38656706 | Common:1; Rare:88 | ||||
| chr22:38681798-38682019 | Common:2; Rare:95 | ||||
| chr22:39244977-39245220 | Rare:55 | ||||
| chr22:40044234-40044346 | Common:1; Rare:25 | ||||
| chr22:40044552-40044929 | Common:2; Rare:85 | ||||
| chr22:40177752-40177983 | Rare:73 | ||||
| chr22:40346425-40346556 | Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40370443-40370664 | Rare:86 | ||||
| chr22:40636667-40637014 | Common:2; Rare:96 | ||||
| chr22:40856721-40857183 | Common:3; Rare:172; Clinvar:4 | ||||
| chr22:41091545-41091825 | Common:6; Rare:105 | ||||
| chr22:41286150-41286500 | Common:2; Rare:108 |