| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:37502961-37502968 | Rare:2 | ||||
| chr20:37507557-37507840 | Common:3; Rare:40 | ||||
| chr20:37508596-37508609 | Rare:2 | ||||
| chr20:37509798-37509919 | Rare:22 | ||||
| chr20:37526270-37526277 | Rare:1 | ||||
| chr20:38420618-38420653 | Rare:7 | ||||
| chr20:38450868-38450898 | Rare:7 | ||||
| chr20:38523452-38523519 | Rare:10 | ||||
| chr20:38570571-38570847 | Common:2; Rare:48 | ||||
| chr20:40686257-40686354 | Common:1; Rare:16; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:40687306-40687433 | Rare:23; Clinvar (benign):1 | ||||
| chr20:40688015-40688345 | Rare:74; Clinvar (benign):1 | ||||
| chr20:41097741-41097950 | Common:2; Rare:35 | ||||
| chr20:41199581-41199694 | Rare:20 | ||||
| chr20:41225476-41225646 | Rare:38 |