| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:79453627-79454102 | Common:3; Rare:113 | ||||
| chr7:80918970-80919352 | Common:3; Rare:129 | ||||
| chr7:82443585-82443885 | Common:2; Rare:97 | ||||
| chr7:87152300-87152474 | Common:1; Rare:56 | ||||
| chr7:87345476-87345701 | Common:4; Rare:71 | ||||
| chr7:87876277-87876657 | Common:2; Rare:172 | ||||
| chr7:90211633-90211913 | Common:4; Rare:86 | ||||
| chr7:90346556-90346733 | Common:3; Rare:77 | ||||
| chr7:91880668-91880801 | Common:1; Rare:36 | ||||
| chr7:92134427-92134556 | Rare:36 | ||||
| chr7:92134717-92134923 | Common:3; Rare:61 | ||||
| chr7:92245894-92245974 | Rare:24; Clinvar:3 | ||||
| chr7:92528389-92528816 | Common:3; Rare:135; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92836438-92836509 | Rare:13 | ||||
| chr7:93117929-93118194 | Rare:40 |