| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91940735-91940984 | Common:4; Rare:79; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92134409-92134552 | Rare:40 | ||||
| chr7:92134744-92134888 | Common:2; Rare:42 | ||||
| chr7:92245871-92246237 | Common:5; Rare:91; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92528389-92528807 | Common:3; Rare:129; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93890720-93890942 | Common:3; Rare:53 | ||||
| chr7:93921650-93921964 | Common:3; Rare:63 | ||||
| chr7:94656114-94656374 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95434899-95435140 | Common:1; Rare:108; Clinvar (benign):1 | ||||
| chr7:97117523-97117724 | Common:1; Rare:79 | ||||
| chr7:97872382-97872627 | Common:2; Rare:74 | ||||
| chr7:99325786-99325961 | Common:1; Rare:70 | ||||
| chr7:99408537-99408694 | Common:2; Rare:50 | ||||
| chr7:99408702-99409063 | Common:1; Rare:99 | ||||
| chr7:99438731-99438977 | Common:1; Rare:76 |