| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:18150040-18150181 | Common:1; Rare:37 | ||||
| chr22:19291700-19291992 | Common:9; Rare:98 | ||||
| chr22:19432303-19432614 | Common:4; Rare:131 | ||||
| chr22:19447690-19447966 | Common:2; Rare:105 | ||||
| chr22:19479702-19479963 | Common:4; Rare:72 | ||||
| chr22:19854787-19854972 | Rare:63 | ||||
| chr22:19941722-19941881 | Rare:66; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20020880-20021125 | Common:1; Rare:79 | ||||
| chr22:20079955-20080292 | Common:1; Rare:113 | ||||
| chr22:20319994-20320174 | Common:2; Rare:60 | ||||
| chr22:20495771-20495994 | Common:2; Rare:82 | ||||
| chr22:20773805-20774124 | Common:2; Rare:53 | ||||
| chr22:20858821-20859100 | Common:4; Rare:142; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:20917313-20917469 | Rare:57 | ||||
| chr22:21002059-21002251 | Common:4; Rare:73 |