| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19122343-19122626 | Common:5; Rare:80 | ||||
| chr22:19144632-19144879 | Common:8; Rare:154 | ||||
| chr22:19178350-19178522 | Common:3; Rare:83; Clinvar (benign):1 | ||||
| chr22:19178671-19179033 | Common:8; Rare:248; Clinvar (benign):3 | ||||
| chr22:19291659-19291947 | Common:21; Rare:185 | ||||
| chr22:19431677-19431858 | Rare:80 | ||||
| chr22:19432269-19432610 | Common:7; Rare:256 | ||||
| chr22:19446950-19447490 | Common:7; Rare:256 | ||||
| chr22:19447660-19447972 | Common:4; Rare:218 | ||||
| chr22:19479104-19479473 | Common:8; Rare:267 | ||||
| chr22:19479600-19479970 | Common:10; Rare:180 | ||||
| chr22:19854787-19855013 | Rare:156 | ||||
| chr22:19881156-19881503 | Common:3; Rare:135 | ||||
| chr22:19940990-19941450 | Common:9; Rare:157 | ||||
| chr22:19941582-19941888 | Common:1; Rare:176; Clinvar:10; Clinvar (benign):7 |