| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:29603268-29603780 | Common:4; Rare:116; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:29603795-29603876 | Rare:19 | ||||
| chr22:29766910-29767422 | Common:5; Rare:155 | ||||
| chr22:30356828-30356992 | Common:1; Rare:58 | ||||
| chr22:30425728-30425823 | Common:1; Rare:26 | ||||
| chr22:30607105-30607216 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):2 | ||||
| chr22:31160124-31160227 | Rare:40 | ||||
| chr22:31399383-31399655 | Common:1; Rare:78 | ||||
| chr22:31489827-31490164 | Common:3; Rare:130 | ||||
| chr22:31496215-31496565 | Common:2; Rare:98 | ||||
| chr22:31630795-31630975 | Common:4; Rare:48 | ||||
| chr22:31750046-31750328 | Common:3; Rare:80 | ||||
| chr22:31753759-31753982 | Rare:77 | ||||
| chr22:32474627-32475044 | Common:4; Rare:136; Clinvar:6; Clinvar (benign):2 | ||||
| chr22:35257397-35257508 | Common:1; Rare:28 |