| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3795712-3795804 | Common:2; Rare:26 | ||||
| chr20:3820171-3820262 | Rare:24 | ||||
| chr20:3846724-3846900 | Common:1; Rare:51 | ||||
| chr20:3888710-3888927 | Common:1; Rare:52 | ||||
| chr20:3889083-3889412 | Common:2; Rare:181; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr20:4686139-4686505 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:4823402-4823709 | Common:4; Rare:61 | ||||
| chr20:4823785-4823898 | Rare:27 | ||||
| chr20:5112753-5113178 | Common:2; Rare:137 | ||||
| chr20:5119907-5120147 | Common:1; Rare:82 | ||||
| chr20:5126527-5126825 | Common:3; Rare:83 | ||||
| chr20:5950372-5950689 | Common:8; Rare:97 | ||||
| chr20:6122994-6123128 | Common:2; Rare:34; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:9166297-9166603 | Common:1; Rare:71 | ||||
| chr20:10218716-10218941 | Rare:48 |