| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50930829-50930989 | Rare:52 | ||||
| chr20:50931066-50931254 | Common:1; Rare:56 | ||||
| chr20:50931294-50931466 | Rare:68 | ||||
| chr20:50931589-50931717 | Rare:55 | ||||
| chr20:50958456-50958896 | Common:1; Rare:174; Clinvar:4; Clinvar (benign):4 | ||||
| chr20:51802246-51802754 | Common:2; Rare:142; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:52105252-52105380 | Rare:40 | ||||
| chr20:52191678-52191815 | Rare:27 | ||||
| chr20:52192183-52192452 | Rare:52 | ||||
| chr20:52972238-52972358 | Common:1; Rare:24 | ||||
| chr20:53593827-53593909 | Common:1; Rare:37 | ||||
| chr20:54208044-54208148 | Rare:34 | ||||
| chr20:56392120-56392723 | Common:6; Rare:163 | ||||
| chr20:56468504-56468761 | Rare:94 | ||||
| chr20:57350899-57351327 | Common:6; Rare:113 |