| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:94425779-94426050 | Rare:84; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:94656118-94656411 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95396354-95396528 | Common:2; Rare:74 | ||||
| chr7:95434884-95435222 | Common:1; Rare:130; Clinvar (benign):1 | ||||
| chr7:95596512-95596718 | Common:2; Rare:39 | ||||
| chr7:96322049-96322331 | Rare:95; Clinvar:3 | ||||
| chr7:97117454-97117802 | Common:2; Rare:153 | ||||
| chr7:99325584-99325946 | Common:1; Rare:123 | ||||
| chr7:99408545-99408670 | Common:2; Rare:42 | ||||
| chr7:99408811-99409022 | Common:1; Rare:67 | ||||
| chr7:99438732-99438976 | Common:1; Rare:76 | ||||
| chr7:99466130-99466206 | Rare:34 | ||||
| chr7:99472646-99472934 | Common:4; Rare:90 | ||||
| chr7:99500249-99500402 | Common:1; Rare:44 | ||||
| chr7:99558486-99558727 | Common:2; Rare:80 |