| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35284476-35284872 | Common:3; Rare:122 | ||||
| chr20:35411959-35412119 | Rare:57 | ||||
| chr20:35542385-35542595 | Rare:67 | ||||
| chr20:35556030-35556266 | Rare:73 | ||||
| chr20:35556712-35557487 | Common:3; Rare:228 | ||||
| chr20:35664804-35665045 | Common:1; Rare:63 | ||||
| chr20:35699186-35699647 | Rare:132; Clinvar (benign):3 | ||||
| chr20:35740823-35741135 | Common:3; Rare:84 | ||||
| chr20:35742097-35742651 | Common:5; Rare:177 | ||||
| chr20:36154500-36154890 | Common:1; Rare:78 | ||||
| chr20:36236429-36236535 | Rare:26 | ||||
| chr20:36461133-36461486 | Common:1; Rare:102 | ||||
| chr20:36541434-36541571 | Common:2; Rare:36 | ||||
| chr20:36573067-36573331 | Common:2; Rare:64 | ||||
| chr20:36573406-36573616 | Rare:94 |