| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:4823402-4823800 | Common:5; Rare:89 | ||||
| chr20:5112962-5113178 | Rare:92 | ||||
| chr20:5119906-5120155 | Common:1; Rare:85 | ||||
| chr20:5126616-5126825 | Common:3; Rare:56 | ||||
| chr20:5610898-5611154 | Common:2; Rare:89 | ||||
| chr20:5750324-5750461 | Rare:32 | ||||
| chr20:5911318-5911672 | Common:3; Rare:104 | ||||
| chr20:5950414-5950718 | Common:8; Rare:94 | ||||
| chr20:8019956-8020004 | Rare:5 | ||||
| chr20:9068575-9068846 | Rare:70 | ||||
| chr20:10218727-10219159 | Rare:79 | ||||
| chr20:13638898-13639029 | Common:1; Rare:36 | ||||
| chr20:13784878-13785080 | Common:2; Rare:90; Clinvar (benign):3 | ||||
| chr20:13995246-13995603 | Rare:102 | ||||
| chr20:14337561-14337871 | Common:1; Rare:64 |