| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2664186-2664243 | Rare:29 | ||||
| chr20:2840629-2840771 | Common:1; Rare:56 | ||||
| chr20:3045892-3046134 | Common:1; Rare:71 | ||||
| chr20:3071789-3072157 | Common:4; Rare:92 | ||||
| chr20:3159800-3159941 | Rare:51 | ||||
| chr20:3173526-3173696 | Common:1; Rare:62 | ||||
| chr20:3209075-3209342 | Common:1; Rare:48 | ||||
| chr20:3209433-3209542 | Common:1; Rare:37 | ||||
| chr20:3470914-3471040 | Common:2; Rare:49 | ||||
| chr20:3767716-3767985 | Common:3; Rare:84 | ||||
| chr20:3795725-3795835 | Common:1; Rare:27 | ||||
| chr20:3846722-3846891 | Rare:51 | ||||
| chr20:3888832-3888939 | Rare:26 | ||||
| chr20:3889155-3889387 | Common:1; Rare:120; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:4183182-4183446 | Common:2; Rare:61 |