| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44777609-44777985 | Common:2; Rare:98 | ||||
| chr1:44800182-44800385 | Common:1; Rare:47 | ||||
| chr1:44811259-44811630 | Common:2; Rare:68 | ||||
| chr1:44986534-44986802 | Common:2; Rare:55; Clinvar (benign):1 | ||||
| chr1:45339657-45339775 | Rare:27 | ||||
| chr1:45339987-45340240 | Rare:90; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr1:45340387-45340451 | Common:1; Rare:13; Clinvar:1 | ||||
| chr1:45491149-45491283 | Common:1; Rare:49 | ||||
| chr1:45499998-45500397 | Common:2; Rare:104; Clinvar:5; Clinvar (pathogenic):3 | ||||
| chr1:45521880-45522083 | Common:1; Rare:77 | ||||
| chr1:45550691-45550903 | Common:1; Rare:59 | ||||
| chr1:45566653-45567096 | Common:3; Rare:118 | ||||
| chr1:45567882-45568209 | Common:2; Rare:110 | ||||
| chr1:45583930-45584198 | Common:1; Rare:102 | ||||
| chr1:45687011-45687312 | Common:2; Rare:83 |