| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171688148-171688305 | Rare:32 | ||||
| chr2:171894204-171894456 | Common:2; Rare:112; Clinvar:2 | ||||
| chr2:171894500-171894623 | Rare:28 | ||||
| chr2:171922212-171922593 | Rare:130 | ||||
| chr2:171922663-171922787 | Rare:39 | ||||
| chr2:171922811-171922842 | Rare:4 | ||||
| chr2:171922900-171922966 | Rare:12 | ||||
| chr2:171922968-171923437 | Common:5; Rare:103 | ||||
| chr2:171999759-172000110 | Common:4; Rare:126 | ||||
| chr2:172000120-172000285 | Common:1; Rare:33 | ||||
| chr2:172084389-172084433 | Rare:10 | ||||
| chr2:172084611-172084838 | Rare:50 | ||||
| chr2:172085002-172085053 | Rare:8 | ||||
| chr2:172085083-172085763 | Common:3; Rare:165 | ||||
| chr2:172102856-172103108 | Common:2; Rare:67 |