| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:108526039-108526203 | Rare:47 | ||||
| chr7:108526273-108526381 | Common:4; Rare:44 | ||||
| chr7:108569524-108570077 | Common:4; Rare:194 | ||||
| chr7:112206364-112206806 | Common:2; Rare:160 | ||||
| chr7:116499493-116499805 | Common:3; Rare:104 | ||||
| chr7:116524495-116525236 | Common:5; Rare:204; Clinvar (benign):2 | ||||
| chr7:116526172-116526683 | Common:3; Rare:143; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:116672085-116672573 | Common:1; Rare:107; Clinvar:4 | ||||
| chr7:116724493-116724561 | Rare:7 | ||||
| chr7:116862470-116862632 | Common:2; Rare:62 | ||||
| chr7:118183937-118184223 | Common:2; Rare:112 | ||||
| chr7:120951019-120951197 | Common:1; Rare:74 | ||||
| chr7:123748651-123748894 | Common:1; Rare:86 | ||||
| chr7:123748920-123749241 | Common:3; Rare:118 | ||||
| chr7:124929776-124929883 | Common:2; Rare:30 |