| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:18497171-18497287 | Common:1; Rare:46 | ||||
| chr20:18507431-18507603 | Rare:44; Clinvar:1 | ||||
| chr20:18507798-18507951 | Common:1; Rare:49; Clinvar:5; Clinvar (benign):1 | ||||
| chr20:20017279-20017388 | Rare:43 | ||||
| chr20:21303158-21303385 | Rare:85 | ||||
| chr20:23350629-23350822 | Common:1; Rare:65 | ||||
| chr20:23421391-23421684 | Common:5; Rare:121 | ||||
| chr20:24992702-24992827 | Common:3; Rare:56 | ||||
| chr20:25195630-25195775 | Common:2; Rare:55 | ||||
| chr20:25407586-25407771 | Common:1; Rare:65 | ||||
| chr20:25623952-25624140 | Common:1; Rare:63 | ||||
| chr20:25696766-25697098 | Common:3; Rare:94 | ||||
| chr20:31514332-31514514 | Common:6; Rare:89 | ||||
| chr20:31547272-31547438 | Rare:45 | ||||
| chr20:31739093-31739362 | Common:2; Rare:69 |