| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215430693-215431147 | Rare:97; Clinvar (pathogenic):1 | ||||
| chr2:215431555-215432057 | Common:1; Rare:117 | ||||
| chr2:215432714-215432885 | Rare:29 | ||||
| chr2:215432993-215433025 | Rare:5 | ||||
| chr2:215433312-215433589 | Common:3; Rare:72 | ||||
| chr2:215435095-215435275 | Rare:28 | ||||
| chr2:215563007-215563067 | Rare:4 | ||||
| chr2:215611172-215611394 | Common:1; Rare:40 | ||||
| chr2:215611576-215612020 | Common:2; Rare:74 | ||||
| chr2:215614371-215614684 | Common:4; Rare:63 | ||||
| chr2:215615864-215616052 | Common:1; Rare:44 | ||||
| chr2:215617210-215617314 | Rare:15 | ||||
| chr2:215619926-215620110 | Common:2; Rare:24 | ||||
| chr2:215620309-215620553 | Common:3; Rare:45 | ||||
| chr2:215621325-215621807 | Common:6; Rare:80 |