| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19431631-19431882 | Rare:123 | ||||
| chr22:19431807-19432076 | Rare:92 | ||||
| chr22:19432198-19432632 | Common:12; Rare:462 | ||||
| chr22:19447140-19447512 | Common:2; Rare:155 | ||||
| chr22:19447555-19447990 | Common:7; Rare:386 | ||||
| chr22:19479100-19479491 | Common:12; Rare:410 | ||||
| chr22:19479693-19479995 | Common:10; Rare:228 | ||||
| chr22:19714216-19714821 | Common:5; Rare:388 | ||||
| chr22:19718230-19718580 | Rare:165 | ||||
| chr22:19854745-19855170 | Common:11; Rare:371 | ||||
| chr22:19881174-19881458 | Common:2; Rare:83 | ||||
| chr22:19918700-19919000 | Common:6; Rare:101; Clinvar:4; Clinvar (benign):5 | ||||
| chr22:19937635-19937905 | Common:6; Rare:52 | ||||
| chr22:19940914-19941440 | Common:7; Rare:123 | ||||
| chr22:19941696-19941939 | Rare:251; Clinvar:16; Clinvar (benign):10 |