| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38501235-38501329 | Rare:35 | ||||
| chr22:38741552-38741765 | Rare:40 | ||||
| chr22:38953626-38953669 | Rare:6 | ||||
| chr22:38953678-38953754 | Common:1; Rare:22 | ||||
| chr22:38954023-38954109 | Common:1; Rare:15 | ||||
| chr22:38954121-38954158 | Rare:6 | ||||
| chr22:39066125-39066348 | Common:2; Rare:39 | ||||
| chr22:39145573-39145858 | Common:3; Rare:100 | ||||
| chr22:39446995-39447257 | Common:2; Rare:55 | ||||
| chr22:39920471-39920663 | Rare:31 | ||||
| chr22:41256019-41256214 | Rare:65 | ||||
| chr22:41413746-41414093 | Common:2; Rare:105 | ||||
| chr22:41444411-41444685 | Common:2; Rare:67 | ||||
| chr22:41518310-41518570 | Common:3; Rare:54; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:41530790-41531034 | Rare:80 |