| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45340381-45340496 | Common:1; Rare:31; Clinvar:1 | ||||
| chr1:45500046-45500351 | Common:1; Rare:75; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521827-45522013 | Common:1; Rare:75 | ||||
| chr1:45550689-45551110 | Common:3; Rare:110 | ||||
| chr1:45566643-45566902 | Common:3; Rare:64 | ||||
| chr1:45583931-45584218 | Common:1; Rare:110 | ||||
| chr1:45686452-45686668 | Rare:78 | ||||
| chr1:45687054-45687365 | Common:1; Rare:84 | ||||
| chr1:45688049-45688239 | Common:1; Rare:53 | ||||
| chr1:45750607-45750823 | Rare:79 | ||||
| chr1:46133037-46133209 | Common:1; Rare:41 | ||||
| chr1:46198358-46198534 | Common:1; Rare:73; Clinvar:1 | ||||
| chr1:46303140-46303775 | Common:3; Rare:189 | ||||
| chr1:46339962-46340196 | Common:4; Rare:47 | ||||
| chr1:46340664-46340819 | Common:3; Rare:39 |