| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:18507399-18507619 | Common:1; Rare:63; Clinvar:1 | ||||
| chr20:18567353-18567499 | Common:1; Rare:52 | ||||
| chr20:20017242-20017410 | Rare:63 | ||||
| chr20:21303252-21303429 | Rare:63 | ||||
| chr20:23049196-23049265 | Rare:30 | ||||
| chr20:23049383-23049445 | Rare:22 | ||||
| chr20:23049546-23049867 | Common:4; Rare:107; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:23086314-23086490 | Rare:36 | ||||
| chr20:23350555-23350861 | Common:1; Rare:99 | ||||
| chr20:23361888-23362215 | Common:3; Rare:110 | ||||
| chr20:24992684-24992847 | Common:5; Rare:76 | ||||
| chr20:25195596-25195806 | Common:2; Rare:68 | ||||
| chr20:25247826-25248124 | Common:1; Rare:100 | ||||
| chr20:25290239-25290611 | Common:3; Rare:129 | ||||
| chr20:25300942-25301139 | Common:1; Rare:50 |