| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3208996-3209349 | Common:1; Rare:65 | ||||
| chr20:3209433-3209548 | Common:1; Rare:40 | ||||
| chr20:3407899-3408014 | Rare:32 | ||||
| chr20:3470883-3471110 | Common:2; Rare:111 | ||||
| chr20:3681918-3682334 | Common:4; Rare:113 | ||||
| chr20:3767702-3768032 | Common:3; Rare:104 | ||||
| chr20:3795535-3795835 | Common:2; Rare:73 | ||||
| chr20:3796214-3796537 | Common:4; Rare:72 | ||||
| chr20:3802089-3802369 | Rare:67 | ||||
| chr20:3802924-3803135 | Common:2; Rare:58 | ||||
| chr20:3846695-3846894 | Rare:59 | ||||
| chr20:3888674-3888929 | Common:1; Rare:65 | ||||
| chr20:3889083-3889420 | Common:2; Rare:185; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr20:4148586-4148918 | Rare:90 | ||||
| chr20:4686108-4686508 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):2 |