| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68319911-68319956 | Rare:19 | ||||
| chr2:68319962-68320268 | Rare:64 | ||||
| chr2:68467255-68467692 | Common:2; Rare:120 | ||||
| chr2:69012917-69013196 | Common:9; Rare:71 | ||||
| chr2:69387088-69387406 | Common:1; Rare:90; Clinvar:3 | ||||
| chr2:69437401-69437677 | Common:1; Rare:134; Clinvar:6; Clinvar (benign):3 | ||||
| chr2:69643605-69643829 | Rare:79 | ||||
| chr2:69741843-69742157 | Common:1; Rare:65 | ||||
| chr2:69829517-69829792 | Common:1; Rare:100 | ||||
| chr2:69914482-69914748 | Rare:70 | ||||
| chr2:70086931-70087117 | Common:1; Rare:93 | ||||
| chr2:70087309-70087904 | Common:2; Rare:213 | ||||
| chr2:70087906-70088012 | Rare:25 | ||||
| chr2:70190651-70190779 | Rare:36 | ||||
| chr2:70191012-70191152 | Common:1; Rare:39 |