| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:169790017-169790392 | Common:2; Rare:130 | ||||
| chr7:149143-149272 | Common:2; Rare:47 | ||||
| chr7:193705-193757 | Rare:21 | ||||
| chr7:4973859-4974102 | Common:4; Rare:93 | ||||
| chr7:5427821-5427957 | Common:1; Rare:57 | ||||
| chr7:5570139-5570344 | Common:2; Rare:71 | ||||
| chr7:5823031-5823347 | Common:5; Rare:122 | ||||
| chr7:6729463-6729819 | Common:4; Rare:130 | ||||
| chr7:12504212-12504456 | Common:2; Rare:50 | ||||
| chr7:16420631-16420701 | Rare:22 | ||||
| chr7:22563293-22563377 | Common:1; Rare:23 | ||||
| chr7:23490417-23490580 | Common:3; Rare:71 | ||||
| chr7:23680813-23680873 | Common:1; Rare:17 | ||||
| chr7:25359906-25360003 | Common:1; Rare:16 | ||||
| chr7:26193249-26193696 | Rare:156; Clinvar (benign):2 |