| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45340381-45340466 | Common:1; Rare:21; Clinvar:1 | ||||
| chr1:45499998-45500335 | Common:2; Rare:75; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr1:45521827-45522077 | Common:1; Rare:99 | ||||
| chr1:45550689-45550903 | Common:1; Rare:60 | ||||
| chr1:45583927-45584078 | Rare:59 | ||||
| chr1:45687059-45687318 | Common:1; Rare:70 | ||||
| chr1:45688079-45688219 | Common:1; Rare:40 | ||||
| chr1:45750607-45750814 | Rare:75 | ||||
| chr1:46133037-46133203 | Common:1; Rare:41 | ||||
| chr1:46198346-46198491 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:46303138-46303769 | Common:3; Rare:188 | ||||
| chr1:46340708-46340846 | Common:3; Rare:44 | ||||
| chr1:46604186-46604403 | Common:1; Rare:61 | ||||
| chr1:46810864-46811179 | Common:2; Rare:88 | ||||
| chr1:47333797-47333972 | Common:2; Rare:61 |