| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44210701-44211170 | Common:6; Rare:167 | ||||
| chr20:44475867-44475954 | Common:1; Rare:35 | ||||
| chr20:44521713-44521925 | Common:1; Rare:56 | ||||
| chr20:44651687-44651839 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr20:44960329-44960474 | Common:1; Rare:64 | ||||
| chr20:44966328-44966597 | Common:2; Rare:105 | ||||
| chr20:45115000-45115292 | Common:3; Rare:64 | ||||
| chr20:45124451-45124575 | Rare:31 | ||||
| chr20:45363353-45363527 | Common:1; Rare:42 | ||||
| chr20:45406376-45406754 | Rare:103 | ||||
| chr20:45407404-45407576 | Rare:37 | ||||
| chr20:45791837-45792014 | Common:1; Rare:65 | ||||
| chr20:45833292-45833369 | Common:1; Rare:11 | ||||
| chr20:45833752-45833940 | Common:7; Rare:43 | ||||
| chr20:45857342-45857602 | Common:3; Rare:67 |