| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:27113770-27113973 | Common:1; Rare:43 | ||||
| chr7:27119638-27119724 | Rare:12 | ||||
| chr7:27130122-27130430 | Common:3; Rare:94 | ||||
| chr7:27130660-27130898 | Rare:66 | ||||
| chr7:27140197-27140340 | Common:1; Rare:33 | ||||
| chr7:27143472-27143605 | Common:1; Rare:37 | ||||
| chr7:27143621-27143761 | Rare:29 | ||||
| chr7:27150744-27151038 | Common:2; Rare:72 | ||||
| chr7:27740063-27740254 | Common:6; Rare:54 | ||||
| chr7:28180474-28180696 | Common:1; Rare:69 | ||||
| chr7:28685885-28686185 | Common:1; Rare:67 | ||||
| chr7:29989625-29989845 | Rare:82 | ||||
| chr7:30026419-30026503 | Rare:29; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:30026583-30026857 | Rare:64 | ||||
| chr7:30478654-30478848 | Common:1; Rare:72; Clinvar:1 |