| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:30504758-30505079 | Common:2; Rare:106 | ||||
| chr7:30594717-30594980 | Common:3; Rare:124; Clinvar:6; Clinvar (benign):7 | ||||
| chr7:32070818-32071141 | Common:3; Rare:83 | ||||
| chr7:32495249-32495575 | Rare:84 | ||||
| chr7:33062707-33062934 | Common:3; Rare:95 | ||||
| chr7:33129227-33129586 | Common:5; Rare:101 | ||||
| chr7:35253529-35253651 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:35254049-35254327 | Common:1; Rare:101 | ||||
| chr7:35254552-35254711 | Rare:33 | ||||
| chr7:35694883-35695254 | Common:4; Rare:105 | ||||
| chr7:35800940-35801269 | Common:2; Rare:140 | ||||
| chr7:39085690-39085777 | Rare:15 | ||||
| chr7:39566295-39566450 | Common:1; Rare:75 | ||||
| chr7:40134570-40135026 | Rare:143; Clinvar:1 | ||||
| chr7:42932154-42932389 | Rare:86 |