| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44723671-44723784 | Rare:22 | ||||
| chr1:44739667-44739889 | Common:1; Rare:84 | ||||
| chr1:44775499-44775610 | Rare:48 | ||||
| chr1:44775815-44776140 | Common:2; Rare:117 | ||||
| chr1:44808436-44808596 | Common:1; Rare:44 | ||||
| chr1:44986512-44986756 | Common:2; Rare:47; Clinvar (benign):1 | ||||
| chr1:45010967-45011211 | Common:2; Rare:67 | ||||
| chr1:45339938-45340047 | Common:1; Rare:41; Clinvar (benign):1 | ||||
| chr1:45340092-45340268 | Rare:75; Clinvar:13; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr1:45340381-45340566 | Common:1; Rare:47; Clinvar:1 | ||||
| chr1:45500040-45500365 | Common:1; Rare:79; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521688-45521761 | Rare:25 | ||||
| chr1:45521811-45522087 | Common:1; Rare:104 | ||||
| chr1:45550694-45551110 | Common:3; Rare:108 | ||||
| chr1:45583956-45584171 | Rare:84 |