| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:93232288-93232417 | Common:2; Rare:30 | ||||
| chr7:93890743-93890942 | Common:2; Rare:45 | ||||
| chr7:93921867-93922188 | Common:4; Rare:82 | ||||
| chr7:94425766-94426050 | Rare:87; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:94656049-94656601 | Common:2; Rare:95; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:94908399-94908436 | Rare:5 | ||||
| chr7:95396354-95396508 | Common:2; Rare:66 | ||||
| chr7:95485830-95486156 | Common:1; Rare:96 | ||||
| chr7:95592755-95593198 | Rare:122 | ||||
| chr7:95596155-95596449 | Common:1; Rare:93 | ||||
| chr7:95596452-95596689 | Common:5; Rare:44 | ||||
| chr7:95596692-95596753 | Common:1; Rare:14 | ||||
| chr7:95596867-95597079 | Common:3; Rare:28 | ||||
| chr7:97117481-97117644 | Rare:44 | ||||
| chr7:97117648-97117834 | Common:1; Rare:110 |