| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3209433-3209542 | Common:1; Rare:37 | ||||
| chr20:3470877-3471039 | Common:2; Rare:75 | ||||
| chr20:3767720-3768051 | Common:4; Rare:105 | ||||
| chr20:3795654-3795835 | Common:2; Rare:48 | ||||
| chr20:3888705-3888923 | Common:1; Rare:51 | ||||
| chr20:4148586-4148907 | Rare:89 | ||||
| chr20:4686234-4686508 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:5112972-5113171 | Rare:86 | ||||
| chr20:5119899-5120174 | Common:1; Rare:92 | ||||
| chr20:5126686-5127067 | Common:3; Rare:126 | ||||
| chr20:5950410-5950720 | Common:8; Rare:98 | ||||
| chr20:10218638-10218876 | Rare:61 | ||||
| chr20:13784884-13785080 | Common:2; Rare:87; Clinvar (benign):3 | ||||
| chr20:16573288-16573547 | Common:1; Rare:76 | ||||
| chr20:16729905-16730089 | Common:1; Rare:59 |