| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34469809-34470087 | Common:1; Rare:53 | ||||
| chr20:34480513-34480688 | Rare:47; Clinvar (benign):1 | ||||
| chr20:34487364-34487381 | Rare:2 | ||||
| chr20:34488839-34489250 | Common:1; Rare:77 | ||||
| chr20:34497666-34497895 | Common:1; Rare:40 | ||||
| chr20:34686788-34686865 | Rare:12 | ||||
| chr20:34722504-34722681 | Common:1; Rare:28 | ||||
| chr20:34727686-34727710 | Rare:5 | ||||
| chr20:34903903-34904254 | Rare:66 | ||||
| chr20:34929551-34929883 | Common:1; Rare:61 | ||||
| chr20:34936762-34936952 | Rare:53; Clinvar:1 | ||||
| chr20:35003301-35003425 | Common:2; Rare:48 | ||||
| chr20:35029116-35029278 | Common:1; Rare:32 | ||||
| chr20:35049956-35050217 | Common:2; Rare:61 | ||||
| chr20:35248070-35248295 | Rare:40 |