| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92134789-92134923 | Common:1; Rare:42 | ||||
| chr7:92245855-92246281 | Common:6; Rare:111; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92246620-92247020 | Common:1; Rare:87 | ||||
| chr7:92447276-92447515 | Common:3; Rare:77 | ||||
| chr7:92528385-92528814 | Common:3; Rare:134; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590009-92590144 | Rare:53 | ||||
| chr7:92590280-92590620 | Common:1; Rare:104 | ||||
| chr7:92833660-92834180 | Rare:115 | ||||
| chr7:92835157-92835413 | Common:2; Rare:62 | ||||
| chr7:92836544-92836872 | Rare:88 | ||||
| chr7:93232116-93232427 | Common:3; Rare:73 | ||||
| chr7:93890749-93890877 | Common:2; Rare:32 | ||||
| chr7:93921857-93922063 | Common:2; Rare:44 | ||||
| chr7:94004300-94004495 | Rare:54 | ||||
| chr7:94510002-94510103 | Rare:36 |