| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3173542-3173722 | Common:1; Rare:56 | ||||
| chr20:3209405-3209542 | Common:1; Rare:46 | ||||
| chr20:3767720-3768093 | Common:5; Rare:116 | ||||
| chr20:3846737-3846885 | Rare:44 | ||||
| chr20:4148615-4148889 | Rare:77 | ||||
| chr20:4686292-4686481 | Rare:44 | ||||
| chr20:5113015-5113178 | Rare:75 | ||||
| chr20:5119677-5120185 | Common:1; Rare:159 | ||||
| chr20:5610904-5611150 | Common:2; Rare:85 | ||||
| chr20:5750314-5750462 | Rare:35 | ||||
| chr20:5950401-5950720 | Common:8; Rare:99 | ||||
| chr20:10435040-10435335 | Rare:70 | ||||
| chr20:11890659-11890879 | Common:2; Rare:82 | ||||
| chr20:13638904-13639041 | Common:1; Rare:39 | ||||
| chr20:13784884-13785094 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):3 |