| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19479693-19479956 | Common:4; Rare:70 | ||||
| chr22:19854782-19855055 | Common:2; Rare:101 | ||||
| chr22:19881155-19881567 | Common:3; Rare:112 | ||||
| chr22:19941708-19942124 | Common:2; Rare:121; Clinvar:6; Clinvar (benign):4 | ||||
| chr22:20020897-20021202 | Common:2; Rare:96 | ||||
| chr22:20079955-20080301 | Common:1; Rare:118 | ||||
| chr22:20116898-20117656 | Common:5; Rare:229 | ||||
| chr22:20319928-20320151 | Common:2; Rare:89 | ||||
| chr22:20491757-20492008 | Rare:40 | ||||
| chr22:20495768-20496007 | Common:2; Rare:85 | ||||
| chr22:20507518-20507725 | Rare:77 | ||||
| chr22:20507938-20508355 | Common:1; Rare:96 | ||||
| chr22:20553161-20553291 | Rare:24 | ||||
| chr22:20573430-20573590 | Common:1; Rare:27 | ||||
| chr22:20858657-20859108 | Common:9; Rare:232; Clinvar:3; Clinvar (benign):5 |