| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2840631-2840771 | Common:1; Rare:56 | ||||
| chr20:3173532-3173705 | Common:1; Rare:58 | ||||
| chr20:3209224-3209331 | Rare:20 | ||||
| chr20:3209439-3209542 | Rare:36 | ||||
| chr20:3407528-3407756 | Common:3; Rare:64 | ||||
| chr20:3470945-3471039 | Common:1; Rare:30 | ||||
| chr20:3795630-3795799 | Common:2; Rare:49 | ||||
| chr20:3846604-3846894 | Common:3; Rare:74 | ||||
| chr20:3889151-3889406 | Common:1; Rare:137; Clinvar:6; Clinvar (benign):2 | ||||
| chr20:5112846-5113178 | Common:1; Rare:120 | ||||
| chr20:5119883-5120049 | Common:1; Rare:65 | ||||
| chr20:5126527-5127081 | Common:4; Rare:176 | ||||
| chr20:5610880-5611177 | Common:2; Rare:107 | ||||
| chr20:5750354-5750461 | Rare:30 | ||||
| chr20:5911307-5911517 | Common:2; Rare:54 |