| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43955213-43955598 | Common:10; Rare:293 | ||||
| chr22:44024050-44024410 | Common:3; Rare:172 | ||||
| chr22:44498026-44498552 | Common:9; Rare:485 | ||||
| chr22:44668546-44668950 | Common:9; Rare:279 | ||||
| chr22:44701872-44702339 | Common:20; Rare:265 | ||||
| chr22:44752365-44752816 | Common:14; Rare:259 | ||||
| chr22:45008772-45009180 | Common:3; Rare:295 | ||||
| chr22:45009873-45010250 | Common:4; Rare:358 | ||||
| chr22:45163632-45164073 | Common:15; Rare:433 | ||||
| chr22:45164570-45164681 | Common:1; Rare:39 | ||||
| chr22:45240809-45241101 | Common:5; Rare:159 | ||||
| chr22:45284781-45285014 | Common:6; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:45309398-45310180 | Common:5; Rare:612 | ||||
| chr22:45317786-45318072 | Common:1; Rare:68 | ||||
| chr22:45413589-45413786 | Common:2; Rare:135 |