| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87345445-87345712 | Common:5; Rare:86 | ||||
| chr7:87876329-87876634 | Common:2; Rare:132 | ||||
| chr7:90346559-90346754 | Common:4; Rare:86 | ||||
| chr7:91880672-91880823 | Common:2; Rare:41 | ||||
| chr7:92134442-92134603 | Rare:50 | ||||
| chr7:92245886-92245994 | Rare:31; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528370-92528829 | Common:4; Rare:144; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93232189-93232389 | Common:2; Rare:39 | ||||
| chr7:94656100-94656374 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95434913-95435091 | Common:1; Rare:86; Clinvar (benign):1 | ||||
| chr7:95592509-95592945 | Common:2; Rare:128 | ||||
| chr7:95596144-95596634 | Common:5; Rare:136 | ||||
| chr7:95596637-95596811 | Common:2; Rare:33 | ||||
| chr7:95596835-95596899 | Rare:11 | ||||
| chr7:95596945-95597029 | Rare:6 |