| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3786720-3787000 | Common:4; Rare:90 | ||||
| chr20:3795729-3795879 | Common:2; Rare:56 | ||||
| chr20:3796174-3796314 | Rare:33 | ||||
| chr20:3820060-3820370 | Common:2; Rare:82 | ||||
| chr20:3820442-3820926 | Common:2; Rare:166 | ||||
| chr20:3846652-3846906 | Common:2; Rare:70 | ||||
| chr20:3888665-3888952 | Common:1; Rare:72 | ||||
| chr20:3889148-3889450 | Common:2; Rare:167; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr20:4015496-4015777 | Common:4; Rare:102 | ||||
| chr20:4148686-4148864 | Rare:59 | ||||
| chr20:4249090-4249898 | Common:10; Rare:274 | ||||
| chr20:4686260-4686466 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr20:4823434-4823719 | Common:4; Rare:58 | ||||
| chr20:4824140-4824500 | Rare:61 | ||||
| chr20:5113044-5113218 | Rare:73 |