| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161721252-161722322 | Common:52; Rare:526 | ||||
| chr1:161725892-161726250 | Rare:249 | ||||
| chr1:161726187-161726970 | Common:3; Rare:295 | ||||
| chr1:161749380-161749919 | Common:4; Rare:514 | ||||
| chr1:161749940-161750608 | Common:3; Rare:475 | ||||
| chr1:161766104-161766720 | Common:25; Rare:597; Clinvar (pathogenic):3 | ||||
| chr1:162069458-162069858 | Common:3; Rare:279 | ||||
| chr1:162366804-162366938 | Rare:26 | ||||
| chr1:162412020-162412400 | Common:1; Rare:73 | ||||
| chr1:162497589-162497989 | Common:20; Rare:507 | ||||
| chr1:162498198-162498887 | Common:2; Rare:177 | ||||
| chr1:162561239-162561990 | Common:28; Rare:1167 | ||||
| chr1:162562166-162562566 | Common:4; Rare:124 | ||||
| chr1:162631447-162631885 | Rare:131 | ||||
| chr1:162632880-162633170 | Rare:52 |