| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69387147-69387367 | Rare:58; Clinvar:2 | ||||
| chr2:69829524-69829716 | Rare:83 | ||||
| chr2:70087423-70087746 | Rare:128 | ||||
| chr2:70087911-70088167 | Rare:61 | ||||
| chr2:70257902-70258167 | Common:1; Rare:83 | ||||
| chr2:70293650-70293848 | Common:2; Rare:68 | ||||
| chr2:71068539-71068681 | Rare:61 | ||||
| chr2:71130225-71130659 | Common:6; Rare:120; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276450-71276599 | Rare:44 | ||||
| chr2:73233195-73233495 | Common:1; Rare:87 | ||||
| chr2:73385689-73386070 | Common:4; Rare:184; Clinvar:16; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr2:73828804-73828999 | Common:1; Rare:43 | ||||
| chr2:74147832-74148100 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74421567-74421771 | Rare:68 | ||||
| chr2:74482921-74483093 | Common:1; Rare:55 |