| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:174999344-174999479 | Rare:36 | ||||
| chr1:174999621-175000163 | Common:3; Rare:180 | ||||
| chr1:175006964-175007152 | Common:2; Rare:33 | ||||
| chr1:175023394-175023681 | Common:1; Rare:84 | ||||
| chr1:176207203-176207344 | Common:2; Rare:73 | ||||
| chr1:178093625-178093833 | Common:4; Rare:68 | ||||
| chr1:178094183-178094543 | Rare:127 | ||||
| chr1:178341332-178341551 | Common:1; Rare:42 | ||||
| chr1:178724992-178725316 | Common:11; Rare:109 | ||||
| chr1:179081798-179082114 | Common:3; Rare:84 | ||||
| chr1:179365947-179365978 | Rare:13 | ||||
| chr1:179877756-179877905 | Rare:32 | ||||
| chr1:179882214-179882349 | Rare:23 | ||||
| chr1:179882488-179882912 | Rare:212; Clinvar:9; Clinvar (benign):2 | ||||
| chr1:179954641-179954834 | Common:1; Rare:44 |