| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91264150-91264600 | Common:3; Rare:189 | ||||
| chr7:91880654-91880822 | Common:3; Rare:90 | ||||
| chr7:91940729-91941002 | Common:6; Rare:129; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134284-92134908 | Common:8; Rare:315 | ||||
| chr7:92245401-92245808 | Rare:194; Clinvar (benign):2 | ||||
| chr7:92245826-92246281 | Common:8; Rare:168; Clinvar:7; Clinvar (benign):9 | ||||
| chr7:92528370-92528829 | Common:7; Rare:264; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr7:92589890-92590200 | Common:6; Rare:204 | ||||
| chr7:92833830-92834212 | Rare:147 | ||||
| chr7:92835296-92835700 | Common:3; Rare:152 | ||||
| chr7:92836458-92836656 | Rare:90 | ||||
| chr7:93232139-93232390 | Common:2; Rare:53 | ||||
| chr7:94004212-94004495 | Rare:148 | ||||
| chr7:94509491-94510131 | Common:6; Rare:292 | ||||
| chr7:94655501-94655901 | Common:3; Rare:90 |