| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44475821-44475910 | Rare:34 | ||||
| chr20:44910012-44910096 | Common:1; Rare:37 | ||||
| chr20:44960340-44960514 | Common:1; Rare:72 | ||||
| chr20:44966357-44966571 | Common:2; Rare:85 | ||||
| chr20:45363108-45363238 | Rare:39 | ||||
| chr20:45363359-45363528 | Common:1; Rare:42 | ||||
| chr20:45406541-45406744 | Rare:52 | ||||
| chr20:45416013-45416178 | Rare:57 | ||||
| chr20:45416267-45416625 | Rare:106; Clinvar (pathogenic):2 | ||||
| chr20:45791870-45792030 | Common:2; Rare:59 | ||||
| chr20:45833718-45833937 | Common:7; Rare:53 | ||||
| chr20:45834080-45834209 | Rare:49 | ||||
| chr20:45857315-45857621 | Common:3; Rare:85 | ||||
| chr20:45891271-45891387 | Common:1; Rare:41; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45934510-45934714 | Common:1; Rare:92 |