| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20917169-20917413 | Rare:86 | ||||
| chr22:20982190-20982325 | Common:2; Rare:32; Clinvar (benign):2 | ||||
| chr22:21002088-21002257 | Common:4; Rare:63 | ||||
| chr22:21014877-21015175 | Common:1; Rare:66 | ||||
| chr22:21642015-21642339 | Common:2; Rare:96 | ||||
| chr22:21651922-21652224 | Common:2; Rare:65 | ||||
| chr22:21665934-21666085 | Rare:47 | ||||
| chr22:21982754-21982870 | Rare:29 | ||||
| chr22:23786874-23787032 | Common:1; Rare:59; Clinvar:3 | ||||
| chr22:23894237-23894487 | Common:3; Rare:87 | ||||
| chr22:24011228-24011466 | Rare:84 | ||||
| chr22:24270644-24270911 | Common:3; Rare:105 | ||||
| chr22:24555829-24556066 | Rare:72 | ||||
| chr22:25741839-25742235 | Common:2; Rare:86 | ||||
| chr22:26483763-26484012 | Common:6; Rare:103; Clinvar:5; Clinvar (benign):1 |