| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:264559-264964 | Common:4; Rare:146 | ||||
| chr2:677376-677552 | Common:1; Rare:73 | ||||
| chr2:3377804-3378060 | Common:2; Rare:76 | ||||
| chr2:3379619-3379762 | Common:1; Rare:58 | ||||
| chr2:3558251-3558695 | Common:6; Rare:163 | ||||
| chr2:3575089-3575358 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423398-9423697 | Rare:92 | ||||
| chr2:9473759-9473841 | Rare:30 | ||||
| chr2:9474493-9474630 | Common:6; Rare:63 | ||||
| chr2:9555712-9555992 | Common:2; Rare:95 | ||||
| chr2:9843250-9843539 | Common:6; Rare:86 | ||||
| chr2:10689925-10690012 | Common:2; Rare:28 | ||||
| chr2:11466127-11466259 | Common:3; Rare:35 | ||||
| chr2:17753721-17754174 | Common:4; Rare:143; Clinvar (benign):1 | ||||
| chr2:19901667-19901743 | Common:1; Rare:36 |