| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23145178-23145567 | Common:3; Rare:131 | ||||
| chr22:23767940-23768016 | Rare:21 | ||||
| chr22:23786900-23787095 | Common:2; Rare:75; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:23857539-23857932 | Common:7; Rare:170 | ||||
| chr22:23893939-23893976 | Rare:3 | ||||
| chr22:23894235-23894549 | Common:3; Rare:114 | ||||
| chr22:23894553-23894915 | Common:3; Rare:152; Clinvar:1 | ||||
| chr22:23966638-23966908 | |||||
| chr22:23974356-23974690 | Common:1; Rare:4 | ||||
| chr22:23979725-23980006 | Common:1; Rare:1 | ||||
| chr22:24011098-24011454 | Common:42; Rare:201 | ||||
| chr22:24245062-24245228 | Rare:27 | ||||
| chr22:24270649-24270911 | Common:3; Rare:105 | ||||
| chr22:24555878-24556071 | Rare:56 | ||||
| chr22:24952616-24952737 | Rare:36 |