| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20016821-20017027 | Common:3; Rare:66 | ||||
| chr22:20020877-20021151 | Common:2; Rare:175 | ||||
| chr22:20079893-20080302 | Common:2; Rare:263 | ||||
| chr22:20116956-20117616 | Common:7; Rare:355 | ||||
| chr22:20131511-20131860 | Common:6; Rare:83 | ||||
| chr22:20319995-20320217 | Common:4; Rare:133 | ||||
| chr22:20393996-20394203 | Rare:96 | ||||
| chr22:20495754-20496016 | Common:4; Rare:173 | ||||
| chr22:20507458-20507676 | Rare:125 | ||||
| chr22:20858701-20859108 | Common:13; Rare:391; Clinvar:6; Clinvar (benign):8 | ||||
| chr22:20917286-20917516 | Rare:158 | ||||
| chr22:20982170-20982387 | Common:4; Rare:114; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr22:21002032-21002302 | Common:10; Rare:159 | ||||
| chr22:21014710-21015190 | Common:2; Rare:114 | ||||
| chr22:21567638-21567781 | Common:1; Rare:52 |