| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2840631-2840771 | Common:1; Rare:56 | ||||
| chr20:3045887-3046098 | Common:1; Rare:57 | ||||
| chr20:3173526-3173699 | Common:1; Rare:62 | ||||
| chr20:3209447-3209542 | Rare:32 | ||||
| chr20:3407909-3408002 | Rare:24 | ||||
| chr20:3470915-3471039 | Common:1; Rare:48 | ||||
| chr20:3732570-3732733 | Rare:36 | ||||
| chr20:3767720-3768052 | Common:4; Rare:106 | ||||
| chr20:3795705-3795799 | Common:2; Rare:29 | ||||
| chr20:3846723-3846886 | Rare:48 | ||||
| chr20:4148719-4148883 | Rare:52 | ||||
| chr20:4686166-4686499 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:4823580-4823815 | Common:1; Rare:52 | ||||
| chr20:5001451-5001639 | Common:1; Rare:56 | ||||
| chr20:5112846-5113246 | Common:1; Rare:140 |