| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:173825076-173825124 | Rare:7 | ||||
| chr1:173867948-173868380 | Common:3; Rare:157 | ||||
| chr1:174022282-174022557 | Rare:70 | ||||
| chr1:174999629-175000318 | Common:3; Rare:244 | ||||
| chr1:175947226-175947269 | Rare:18 | ||||
| chr1:176207248-176207345 | Common:1; Rare:50 | ||||
| chr1:178094008-178094106 | Common:1; Rare:19 | ||||
| chr1:178341317-178341563 | Common:1; Rare:49 | ||||
| chr1:178877310-178877568 | Common:1; Rare:58 | ||||
| chr1:179081912-179082104 | Common:1; Rare:60 | ||||
| chr1:179142978-179143235 | Common:1; Rare:52 | ||||
| chr1:179229655-179229816 | Common:3; Rare:22 | ||||
| chr1:179293667-179293930 | Common:3; Rare:75 | ||||
| chr1:179882038-179882356 | Common:2; Rare:71 | ||||
| chr1:179882520-179882957 | Common:1; Rare:223; Clinvar:10; Clinvar (benign):4 |