| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47355731-47355893 | Rare:26 | ||||
| chr20:47356638-47356899 | Rare:64 | ||||
| chr20:47501764-47502019 | Common:1; Rare:88 | ||||
| chr20:49046166-49046364 | Common:3; Rare:61 | ||||
| chr20:49219245-49219494 | Common:1; Rare:114 | ||||
| chr20:49278038-49278266 | Rare:64 | ||||
| chr20:49278275-49278716 | Common:13; Rare:147 | ||||
| chr20:49915496-49915818 | Common:4; Rare:88 | ||||
| chr20:50113128-50113272 | Common:6; Rare:66 | ||||
| chr20:50115926-50116092 | Common:2; Rare:38 | ||||
| chr20:50510087-50510411 | Common:3; Rare:123 | ||||
| chr20:50958496-50958869 | Common:1; Rare:132; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:53593808-53593894 | Common:1; Rare:31 | ||||
| chr20:54475358-54476114 | Common:7; Rare:212 | ||||
| chr20:56392187-56392479 | Common:2; Rare:84 |