| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2658714-2658940 | Common:2; Rare:88; Clinvar:4 | ||||
| chr20:3200075-3200354 | Common:1; Rare:70 | ||||
| chr20:3203859-3204075 | Common:5; Rare:54 | ||||
| chr20:3218384-3218561 | Rare:48; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:3671235-3671555 | Common:1; Rare:105 | ||||
| chr20:3784338-3784558 | Rare:47 | ||||
| chr20:3800208-3800322 | Common:1; Rare:47 | ||||
| chr20:3804361-3804914 | Common:4; Rare:154 | ||||
| chr20:3808164-3808348 | Common:3; Rare:36 | ||||
| chr20:4162173-4162290 | Common:4; Rare:29 | ||||
| chr20:4822540-4822776 | Common:2; Rare:50 | ||||
| chr20:5592689-5592831 | Rare:20 | ||||
| chr20:6025589-6025709 | Common:1; Rare:19 | ||||
| chr20:6768406-6768621 | Common:1; Rare:54 | ||||
| chr20:8488377-8488569 | Common:2; Rare:22 |