| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50115889-50116144 | Common:3; Rare:59 | ||||
| chr20:50153610-50154001 | Common:3; Rare:152 | ||||
| chr20:50154039-50154101 | Common:1; Rare:12 | ||||
| chr20:50190706-50190871 | Rare:34 | ||||
| chr20:50510027-50510052 | Rare:3 | ||||
| chr20:50510062-50510497 | Common:3; Rare:166 | ||||
| chr20:50510834-50511061 | Rare:45 | ||||
| chr20:50730936-50731733 | Common:4; Rare:246 | ||||
| chr20:50794789-50795128 | Common:2; Rare:116 | ||||
| chr20:50795534-50795658 | Common:4; Rare:38 | ||||
| chr20:50930688-50930755 | Rare:28 | ||||
| chr20:50931104-50931927 | Common:5; Rare:303 | ||||
| chr20:50958437-50958872 | Common:1; Rare:166; Clinvar:4; Clinvar (benign):5 | ||||
| chr20:51542364-51542559 | Rare:73 | ||||
| chr20:51542623-51542835 | Common:6; Rare:68 |