| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:4148552-4148890 | Rare:91 | ||||
| chr20:4686200-4686508 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:4823608-4823730 | Common:1; Rare:21 | ||||
| chr20:5001443-5001639 | Common:1; Rare:57 | ||||
| chr20:5112737-5113184 | Common:2; Rare:145 | ||||
| chr20:5119576-5120195 | Common:1; Rare:194 | ||||
| chr20:5126677-5127081 | Common:3; Rare:135 | ||||
| chr20:5610904-5611122 | Common:2; Rare:70 | ||||
| chr20:5750314-5750642 | Common:4; Rare:83 | ||||
| chr20:5950368-5950746 | Common:8; Rare:117 | ||||
| chr20:8114346-8114551 | Common:9; Rare:74 | ||||
| chr20:8601108-8601356 | Common:1; Rare:52 | ||||
| chr20:9068504-9068842 | Common:2; Rare:84 | ||||
| chr20:10218696-10218876 | Rare:43 | ||||
| chr20:10434434-10434697 | Common:1; Rare:82 |