| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3159803-3160066 | Rare:81 | ||||
| chr20:3209433-3209566 | Common:1; Rare:47 | ||||
| chr20:3407538-3407704 | Common:2; Rare:49 | ||||
| chr20:3407928-3408056 | Rare:31 | ||||
| chr20:3470883-3471040 | Common:2; Rare:70 | ||||
| chr20:3681967-3682377 | Common:4; Rare:104 | ||||
| chr20:3767704-3767930 | Common:2; Rare:70 | ||||
| chr20:3795688-3795845 | Common:2; Rare:41 | ||||
| chr20:3820486-3820582 | Rare:39 | ||||
| chr20:3846724-3846894 | Rare:50 | ||||
| chr20:4015512-4015792 | Common:3; Rare:102 | ||||
| chr20:4148678-4148890 | Rare:67 | ||||
| chr20:4686268-4686704 | Common:3; Rare:112; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:5112721-5113178 | Common:2; Rare:147 | ||||
| chr20:5119922-5120185 | Common:1; Rare:87 |