| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:175000219-175000619 | Common:2; Rare:135 | ||||
| chr1:175014646-175015222 | Common:19; Rare:311; Clinvar (pathogenic):2 | ||||
| chr1:175022990-175023200 | Common:2; Rare:72 | ||||
| chr1:175023354-175023740 | Common:3; Rare:265 | ||||
| chr1:175192679-175193340 | Common:13; Rare:330 | ||||
| chr1:176206064-176206314 | Rare:56 | ||||
| chr1:176206334-176206471 | Rare:25 | ||||
| chr1:176207039-176207818 | Common:16; Rare:678 | ||||
| chr1:177170762-177171000 | Common:1; Rare:49 | ||||
| chr1:177256200-177256730 | Common:1; Rare:102 | ||||
| chr1:178093568-178093872 | Common:9; Rare:195 | ||||
| chr1:178093966-178094141 | Common:2; Rare:85 | ||||
| chr1:178094310-178094590 | Rare:188 | ||||
| chr1:178341194-178341594 | Common:2; Rare:142 | ||||
| chr1:178725036-178725400 | Common:30; Rare:297 |