| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:64563032-64563223 | Common:2; Rare:52 | ||||
| chr7:64794282-64794471 | Common:4; Rare:53 | ||||
| chr7:65982188-65982353 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:66114768-66114963 | Common:1; Rare:89 | ||||
| chr7:66628676-66628984 | Common:2; Rare:113; Clinvar:5 | ||||
| chr7:66682024-66682184 | Common:5; Rare:77 | ||||
| chr7:66995474-66995754 | Rare:77 | ||||
| chr7:66996557-66996850 | Common:2; Rare:65 | ||||
| chr7:69599468-69599893 | Common:2; Rare:102; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr7:73683419-73683622 | Common:3; Rare:81 | ||||
| chr7:73719635-73719811 | Common:3; Rare:54 | ||||
| chr7:73738794-73739017 | Common:1; Rare:65 | ||||
| chr7:74174093-74174441 | Common:1; Rare:161 | ||||
| chr7:74254366-74254528 | Rare:75 | ||||
| chr7:74657472-74657722 | Common:2; Rare:77 |