| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:84194887-84195203 | Common:6; Rare:62 | ||||
| chr7:87152309-87152468 | Common:1; Rare:50 | ||||
| chr7:87345443-87345730 | Common:5; Rare:90 | ||||
| chr7:87876342-87876653 | Common:1; Rare:135 | ||||
| chr7:90346571-90346749 | Common:4; Rare:80 | ||||
| chr7:91880668-91880751 | Common:1; Rare:23 | ||||
| chr7:91940735-91940881 | Common:1; Rare:40 | ||||
| chr7:92134381-92134598 | Rare:72 | ||||
| chr7:92134721-92134890 | Common:3; Rare:50 | ||||
| chr7:92528402-92528816 | Common:3; Rare:130; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93232189-93232396 | Common:2; Rare:40 | ||||
| chr7:94004321-94004505 | Rare:52 | ||||
| chr7:94656100-94656391 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:94907547-94907681 | Rare:32 | ||||
| chr7:95434938-95435143 | Common:1; Rare:101; Clinvar (benign):1 |