| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19144639-19144831 | Common:3; Rare:67 | ||||
| chr22:19178437-19178516 | Common:1; Rare:23 | ||||
| chr22:19432284-19432599 | Common:4; Rare:136 | ||||
| chr22:19447677-19447954 | Common:2; Rare:114 | ||||
| chr22:19479090-19479477 | Common:4; Rare:141 | ||||
| chr22:19479687-19479971 | Common:4; Rare:79 | ||||
| chr22:19854795-19854983 | Rare:64 | ||||
| chr22:20020895-20021145 | Common:1; Rare:83 | ||||
| chr22:20079921-20080249 | Common:1; Rare:103 | ||||
| chr22:20117159-20117652 | Common:4; Rare:162 | ||||
| chr22:20319989-20320107 | Common:2; Rare:47 | ||||
| chr22:20858696-20859066 | Common:5; Rare:178; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:20917278-20917431 | Rare:56 | ||||
| chr22:20982209-20982317 | Common:2; Rare:19; Clinvar (benign):2 | ||||
| chr22:21002092-21002195 | Common:3; Rare:35 |