| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45407404-45407485 | Rare:16 | ||||
| chr20:45407868-45407972 | Common:2; Rare:20 | ||||
| chr20:45415982-45416159 | Rare:48 | ||||
| chr20:45416329-45416625 | Rare:89; Clinvar (pathogenic):2 | ||||
| chr20:45469427-45469777 | Common:1; Rare:90 | ||||
| chr20:45791813-45792028 | Common:2; Rare:76 | ||||
| chr20:45833292-45833456 | Common:1; Rare:27 | ||||
| chr20:45834018-45834235 | Rare:79 | ||||
| chr20:45857343-45857621 | Common:3; Rare:71 | ||||
| chr20:45891228-45891387 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45912141-45912303 | Common:3; Rare:37 | ||||
| chr20:45934647-45934731 | Rare:41 | ||||
| chr20:45935056-45935345 | Rare:111 | ||||
| chr20:45971799-45971905 | Common:2; Rare:37 | ||||
| chr20:46364369-46364551 | Rare:69 |