| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:169701993-169702347 | Common:5; Rare:149 | ||||
| chr6:169751515-169751644 | Rare:48; Clinvar (benign):1 | ||||
| chr6:170306548-170306824 | Common:3; Rare:90 | ||||
| chr6:170554221-170554424 | Common:1; Rare:65 | ||||
| chr7:602601-602712 | Rare:34 | ||||
| chr7:1044414-1044634 | Common:4; Rare:90 | ||||
| chr7:1055274-1055393 | Rare:48 | ||||
| chr7:1504329-1504526 | Common:3; Rare:90 | ||||
| chr7:1537318-1537465 | Rare:49 | ||||
| chr7:1570018-1570151 | Common:1; Rare:45 | ||||
| chr7:2242168-2242268 | Common:2; Rare:60 | ||||
| chr7:2354056-2354127 | Rare:35 | ||||
| chr7:2403288-2403628 | Common:1; Rare:134 | ||||
| chr7:4775521-4775691 | Common:4; Rare:81; Clinvar:1 | ||||
| chr7:4882214-4882295 | Rare:12 |