| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:26483779-26483935 | Common:4; Rare:57; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:26512428-26512550 | Common:1; Rare:55 | ||||
| chr22:26590095-26590220 | Common:3; Rare:51 | ||||
| chr22:27919187-27919527 | Common:5; Rare:152 | ||||
| chr22:28741780-28742087 | Common:2; Rare:101; Clinvar:2; Clinvar (benign):6 | ||||
| chr22:28742492-28742702 | Common:1; Rare:48 | ||||
| chr22:28800564-28800714 | Common:2; Rare:45 | ||||
| chr22:29267894-29268339 | Common:2; Rare:128 | ||||
| chr22:29766935-29767401 | Common:5; Rare:132 | ||||
| chr22:29838219-29838442 | Common:4; Rare:71 | ||||
| chr22:30356846-30357004 | Common:1; Rare:59 | ||||
| chr22:30591825-30592217 | Common:5; Rare:115 | ||||
| chr22:30607105-30607195 | Common:1; Rare:25; Clinvar:1; Clinvar (benign):2 | ||||
| chr22:31081139-31081346 | Common:1; Rare:53 | ||||
| chr22:31160124-31160227 | Rare:40 |