| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:56051396-56051865 | Common:1; Rare:177; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106378-56106671 | Common:8; Rare:110 | ||||
| chr7:65982188-65982328 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:66075574-66075966 | Rare:105; Clinvar (benign):1 | ||||
| chr7:66114741-66114910 | Common:1; Rare:75 | ||||
| chr7:66115186-66115354 | Rare:38 | ||||
| chr7:66682024-66682241 | Common:6; Rare:97 | ||||
| chr7:66996564-66996901 | Common:2; Rare:78 | ||||
| chr7:73683396-73683659 | Common:3; Rare:120 | ||||
| chr7:73738786-73739028 | Common:1; Rare:71 | ||||
| chr7:73842506-73842686 | Common:6; Rare:25 | ||||
| chr7:74174102-74174441 | Common:1; Rare:160 | ||||
| chr7:74254351-74254535 | Rare:85 | ||||
| chr7:74453910-74454115 | Rare:53 | ||||
| chr7:75842950-75843184 | Common:2; Rare:38 |