| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24793017-24793485 | Rare:200; Clinvar:1 | ||||
| chr2:24971684-24971848 | Common:1; Rare:62 | ||||
| chr2:24971915-24972136 | Common:1; Rare:72 | ||||
| chr2:26244577-26244966 | Common:2; Rare:143; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345785-26346182 | Common:1; Rare:118 | ||||
| chr2:27032831-27033078 | Rare:92 | ||||
| chr2:27086527-27086801 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr2:27211774-27212047 | Common:3; Rare:97 | ||||
| chr2:27212231-27212370 | Common:1; Rare:73 | ||||
| chr2:27217270-27217515 | Rare:99 | ||||
| chr2:27356992-27357179 | Common:2; Rare:69 | ||||
| chr2:27369873-27370012 | Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:27370257-27370700 | Common:2; Rare:181 | ||||
| chr2:27583014-27583112 | Rare:38 | ||||
| chr2:27628981-27629100 | Common:1; Rare:66 |