| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:169751507-169751644 | Rare:49; Clinvar (benign):1 | ||||
| chr6:170306597-170306820 | Common:2; Rare:65 | ||||
| chr6:170554211-170554404 | Common:1; Rare:63 | ||||
| chr7:712434-712711 | Common:2; Rare:50 | ||||
| chr7:727236-727314 | Rare:26; Clinvar:1 | ||||
| chr7:975518-975674 | Common:1; Rare:61 | ||||
| chr7:1028303-1028495 | Common:1; Rare:71 | ||||
| chr7:1055273-1055393 | Rare:49 | ||||
| chr7:1138198-1138316 | Rare:42 | ||||
| chr7:1537318-1537450 | Rare:43 | ||||
| chr7:1570012-1570178 | Common:1; Rare:49 | ||||
| chr7:2242168-2242255 | Common:2; Rare:53 | ||||
| chr7:2314369-2314626 | Common:5; Rare:103 | ||||
| chr7:2403288-2403622 | Common:1; Rare:131 | ||||
| chr7:4775498-4775675 | Common:6; Rare:76; Clinvar:1 |