| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:52602463-52602542 | Rare:19 | ||||
| chr1:52632939-52633205 | Common:2; Rare:53 | ||||
| chr1:52697546-52697678 | Common:2; Rare:27 | ||||
| chr1:52698264-52698547 | Common:3; Rare:92; Clinvar (pathogenic):1 | ||||
| chr1:52726319-52726596 | Common:9; Rare:112 | ||||
| chr1:52842522-52842983 | Common:8; Rare:148 | ||||
| chr1:52843036-52843291 | Common:4; Rare:67 | ||||
| chr1:52921482-52921841 | Common:2; Rare:123 | ||||
| chr1:52927152-52927374 | Common:4; Rare:71 | ||||
| chr1:53014791-53015033 | Rare:72; Clinvar (benign):1 | ||||
| chr1:53196641-53196957 | Common:1; Rare:118; Clinvar:6; Clinvar (benign):1 | ||||
| chr1:53220152-53220867 | Common:3; Rare:287 | ||||
| chr1:53238460-53238772 | Common:2; Rare:105 | ||||
| chr1:53327373-53327518 | Common:1; Rare:39 | ||||
| chr1:53328057-53328297 | Rare:53 |