| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38656364-38656714 | Common:1; Rare:89 | ||||
| chr22:38681858-38682239 | Common:2; Rare:147 | ||||
| chr22:38739743-38740093 | Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:38742513-38742637 | Common:1; Rare:44 | ||||
| chr22:39021069-39021182 | Common:1; Rare:26 | ||||
| chr22:39152460-39152798 | Common:5; Rare:114 | ||||
| chr22:39472570-39472828 | Rare:42 | ||||
| chr22:40346441-40346578 | Rare:61; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40405877-40406173 | Common:1; Rare:96 | ||||
| chr22:40636659-40637014 | Common:2; Rare:96 | ||||
| chr22:40856434-40856724 | Rare:130 | ||||
| chr22:40856919-40857154 | Common:1; Rare:94; Clinvar:3 | ||||
| chr22:40951035-40951404 | Common:2; Rare:129 | ||||
| chr22:40951600-40951716 | Common:1; Rare:34 | ||||
| chr22:41091456-41091850 | Common:6; Rare:142 |