| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87876324-87876614 | Common:2; Rare:124 | ||||
| chr7:91880658-91880804 | Common:1; Rare:41 | ||||
| chr7:92134442-92134567 | Rare:37 | ||||
| chr7:92245835-92246274 | Common:6; Rare:110; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92528528-92528831 | Common:3; Rare:98; Clinvar (benign):1 | ||||
| chr7:94394532-94395084 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:94413892-94414275 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:94421901-94422184 | Common:2; Rare:52; Clinvar (benign):1 | ||||
| chr7:94422490-94422779 | Common:2; Rare:42 | ||||
| chr7:94423040-94423536 | Common:5; Rare:100; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr7:94425040-94425225 | Rare:54; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:94425607-94425960 | Rare:116; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr7:94425993-94426299 | Common:1; Rare:55; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr7:94656047-94656374 | Common:2; Rare:91; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:98252133-98252372 | Common:1; Rare:54 |