| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:23048208-23048365 | Rare:41; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:23048879-23048919 | Rare:14 | ||||
| chr20:23084358-23084651 | Common:1; Rare:106 | ||||
| chr20:23084859-23085175 | Common:3; Rare:123 | ||||
| chr20:23349921-23350186 | Common:5; Rare:66 | ||||
| chr20:23358119-23358234 | Common:1; Rare:36 | ||||
| chr20:23633583-23633709 | Common:2; Rare:29 | ||||
| chr20:23981111-23981304 | Common:2; Rare:36 | ||||
| chr20:24932229-24932287 | Rare:19 | ||||
| chr20:24958864-24958963 | Common:1; Rare:31 | ||||
| chr20:25278212-25278399 | Common:2; Rare:76 | ||||
| chr20:25306909-25307135 | Common:1; Rare:46 | ||||
| chr20:25854000-25854082 | Common:3; Rare:31 | ||||
| chr20:29497213-29497443 | |||||
| chr20:30376925-30377326 | Common:9; Rare:73 |