| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:63050548-63050866 | Common:1; Rare:74 | ||||
| chr2:63588186-63588324 | Rare:60; Clinvar:2 | ||||
| chr2:63588356-63588527 | Common:1; Rare:45; Clinvar:5 | ||||
| chr2:63588584-63589070 | Common:1; Rare:152; Clinvar (benign):1 | ||||
| chr2:63840653-63841266 | Common:3; Rare:172 | ||||
| chr2:63841271-63841954 | Common:2; Rare:196 | ||||
| chr2:63842645-63842694 | Rare:10 | ||||
| chr2:64018712-64019018 | Common:1; Rare:62 | ||||
| chr2:64019057-64019723 | Common:1; Rare:185 | ||||
| chr2:64144250-64144693 | Common:4; Rare:123 | ||||
| chr2:64453991-64454197 | Rare:43 | ||||
| chr2:64524045-64524651 | Common:3; Rare:183 | ||||
| chr2:64524768-64525045 | Common:2; Rare:70 | ||||
| chr2:64653640-64654207 | Common:3; Rare:193 | ||||
| chr2:64750780-64750812 | Rare:12 |