| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:94004327-94004455 | Rare:40 | ||||
| chr7:94656114-94656374 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:96322031-96322197 | Rare:74; Clinvar:4 | ||||
| chr7:97117442-97117776 | Common:2; Rare:145 | ||||
| chr7:97872378-97872584 | Common:2; Rare:67 | ||||
| chr7:99325816-99325952 | Common:1; Rare:53 | ||||
| chr7:99408546-99408712 | Common:2; Rare:49 | ||||
| chr7:99408789-99409032 | Common:1; Rare:74 | ||||
| chr7:99438715-99438988 | Common:1; Rare:90 | ||||
| chr7:99466120-99466273 | Rare:53 | ||||
| chr7:99472646-99472949 | Common:4; Rare:94 | ||||
| chr7:99552084-99552197 | Rare:39 | ||||
| chr7:99558491-99558727 | Common:2; Rare:78 | ||||
| chr7:99616850-99616989 | Common:2; Rare:43 | ||||
| chr7:100015509-100015625 | Common:1; Rare:27 |