| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16989820-16990290 | Common:5; Rare:163 | ||||
| chr7:17099440-17099870 | Common:8; Rare:174 | ||||
| chr7:22359322-22359730 | Common:3; Rare:77 | ||||
| chr7:22786280-22786770 | Common:9; Rare:141 | ||||
| chr7:23293672-23294072 | Common:4; Rare:122 | ||||
| chr7:23471213-23471475 | Common:3; Rare:138 | ||||
| chr7:23474334-23474815 | Common:2; Rare:255 | ||||
| chr7:25951143-25951470 | Common:3; Rare:99 | ||||
| chr7:26193370-26194051 | Common:2; Rare:306; Clinvar (benign):3 | ||||
| chr7:27122288-27122669 | Common:2; Rare:133 | ||||
| chr7:27617822-27617973 | Rare:33 | ||||
| chr7:28956010-28956320 | Common:2; Rare:173 | ||||
| chr7:29208990-29209260 | Common:1; Rare:63 | ||||
| chr7:29405980-29406501 | Common:2; Rare:134 | ||||
| chr7:29684680-29685330 | Common:14; Rare:336 |