| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:26200571-26200614 | Rare:20 | ||||
| chr7:26200616-26201159 | Common:3; Rare:250 | ||||
| chr7:26201215-26201557 | Rare:135 | ||||
| chr7:26201586-26201838 | Common:2; Rare:124 | ||||
| chr7:27113840-27113951 | Rare:26 | ||||
| chr7:27740070-27740212 | Common:5; Rare:36 | ||||
| chr7:28180518-28180735 | Common:1; Rare:73 | ||||
| chr7:30478716-30478779 | Common:1; Rare:24 | ||||
| chr7:30504717-30505027 | Common:3; Rare:107 | ||||
| chr7:30594722-30595117 | Common:6; Rare:180; Clinvar:10; Clinvar (benign):14 | ||||
| chr7:32495247-32495564 | Rare:80 | ||||
| chr7:32957832-32958037 | Common:3; Rare:49 | ||||
| chr7:35694883-35695268 | Common:4; Rare:110 | ||||
| chr7:35800716-35801258 | Common:2; Rare:204 | ||||
| chr7:39623500-39623820 | Rare:99 |