| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49936255-49936415 | Rare:64 | ||||
| chr20:50113112-50113250 | Common:5; Rare:66 | ||||
| chr20:50115932-50116079 | Common:1; Rare:33 | ||||
| chr20:50930268-50930635 | Common:4; Rare:131 | ||||
| chr20:50930870-50931026 | Rare:55 | ||||
| chr20:50931201-50931380 | Common:2; Rare:57 | ||||
| chr20:50958474-50958896 | Common:1; Rare:162; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:56392191-56392695 | Common:6; Rare:132 | ||||
| chr20:56468423-56468705 | Rare:102 | ||||
| chr20:57266106-57266295 | Common:1; Rare:55 | ||||
| chr20:58150787-58150967 | Rare:67 | ||||
| chr20:58651091-58651289 | Common:2; Rare:44; Clinvar (benign):1 | ||||
| chr20:58651624-58652058 | Common:1; Rare:94; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:58888788-58889005 | Common:1; Rare:65 | ||||
| chr20:58892354-58892480 | Rare:31 |