| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44406979-44407136 | Common:1; Rare:25 | ||||
| chr20:44407260-44407471 | Rare:46; Clinvar:1 | ||||
| chr20:44422246-44422289 | Rare:12 | ||||
| chr20:45419363-45419586 | Common:2; Rare:87; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr20:45824182-45824442 | Common:2; Rare:71 | ||||
| chr20:45894582-45894661 | Common:1; Rare:19 | ||||
| chr20:47282198-47282443 | Common:1; Rare:50 | ||||
| chr20:47339767-47339902 | Rare:25 | ||||
| chr20:50415697-50415966 | Common:2; Rare:78 | ||||
| chr20:50914256-50914551 | Common:3; Rare:60 | ||||
| chr20:56483865-56484148 | Common:1; Rare:75 | ||||
| chr20:57541045-57541157 | Common:2; Rare:22 | ||||
| chr20:57580506-57580741 | Common:3; Rare:60 | ||||
| chr20:58995712-58995879 | Common:3; Rare:66 | ||||
| chr20:58997621-58998013 | Common:3; Rare:107 |