| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44355270-44355404 | Common:1; Rare:31 | ||||
| chr1:44631922-44632088 | Common:1; Rare:56 | ||||
| chr1:44638160-44638296 | Rare:40 | ||||
| chr1:44674421-44674755 | Common:3; Rare:87 | ||||
| chr1:44739667-44739935 | Common:2; Rare:106 | ||||
| chr1:44746334-44746582 | Common:1; Rare:35 | ||||
| chr1:44760321-44760609 | Common:1; Rare:84 | ||||
| chr1:44762272-44762619 | Common:1; Rare:118 | ||||
| chr1:44775388-44775620 | Common:2; Rare:93 | ||||
| chr1:44775795-44776149 | Common:2; Rare:127 | ||||
| chr1:44777726-44778129 | Common:1; Rare:111 | ||||
| chr1:44843014-44843100 | Rare:9 | ||||
| chr1:44986532-44986714 | Common:2; Rare:34; Clinvar (benign):1 | ||||
| chr1:45012095-45012285 | Common:1; Rare:73; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:45206390-45206752 | Common:2; Rare:126 |