| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44674421-44674722 | Common:3; Rare:79 | ||||
| chr1:44775426-44775599 | Common:1; Rare:69 | ||||
| chr1:44775797-44776140 | Common:2; Rare:121 | ||||
| chr1:44808383-44808581 | Common:1; Rare:47 | ||||
| chr1:44986522-44986741 | Common:2; Rare:44; Clinvar (benign):1 | ||||
| chr1:45339949-45340189 | Common:1; Rare:84; Clinvar (benign):1 | ||||
| chr1:45340386-45340466 | Common:1; Rare:19; Clinvar:1 | ||||
| chr1:45500056-45500384 | Common:1; Rare:91; Clinvar:5; Clinvar (pathogenic):3 | ||||
| chr1:45521827-45522087 | Common:1; Rare:101 | ||||
| chr1:45550730-45551086 | Common:3; Rare:87 | ||||
| chr1:45687059-45687357 | Common:1; Rare:77 | ||||
| chr1:45688091-45688237 | Common:1; Rare:46 | ||||
| chr1:45750621-45750821 | Rare:74 | ||||
| chr1:46198338-46198552 | Common:4; Rare:105; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:46303131-46303752 | Common:3; Rare:184 |