| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17159185-17159385 | Common:5; Rare:93 | ||||
| chr22:17628602-17628861 | Common:2; Rare:80 | ||||
| chr22:17638696-17638830 | Rare:49 | ||||
| chr22:17706638-17706823 | Common:1; Rare:43 | ||||
| chr22:18077814-18078026 | Common:4; Rare:68; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18110650-18110846 | Rare:51 | ||||
| chr22:19178449-19178510 | Common:1; Rare:15 | ||||
| chr22:19291696-19291907 | Common:10; Rare:69 | ||||
| chr22:19432302-19432567 | Common:3; Rare:107 | ||||
| chr22:19447509-19447786 | Common:2; Rare:134 | ||||
| chr22:19524378-19524655 | Common:1; Rare:87 | ||||
| chr22:19854787-19854997 | Rare:73 | ||||
| chr22:19941728-19941886 | Rare:67; Clinvar:4; Clinvar (benign):4 | ||||
| chr22:20020891-20021145 | Common:1; Rare:84 | ||||
| chr22:20079921-20080304 | Common:1; Rare:125 |