| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74174114-74174386 | Common:1; Rare:143 | ||||
| chr7:74254366-74254497 | Rare:58 | ||||
| chr7:76047938-76048180 | Common:1; Rare:83 | ||||
| chr7:76302890-76302970 | Rare:34; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:77696236-77696460 | Rare:86 | ||||
| chr7:77798411-77798888 | Common:1; Rare:120 | ||||
| chr7:87152309-87152468 | Common:1; Rare:50 | ||||
| chr7:87876337-87876641 | Common:1; Rare:133 | ||||
| chr7:88220013-88220151 | Rare:69 | ||||
| chr7:90346596-90346733 | Common:3; Rare:59 | ||||
| chr7:91880682-91880791 | Common:1; Rare:29 | ||||
| chr7:92528434-92528808 | Common:3; Rare:117; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:94656122-94656387 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:96322016-96322188 | Rare:82; Clinvar:4 | ||||
| chr7:97117475-97117759 | Common:1; Rare:121 |