| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3046123-3046367 | Common:1; Rare:99 | ||||
| chr20:3173538-3173696 | Common:1; Rare:53 | ||||
| chr20:3209439-3209552 | Rare:40 | ||||
| chr20:3767733-3768067 | Common:5; Rare:105 | ||||
| chr20:3889160-3889417 | Common:1; Rare:134; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr20:4686212-4686478 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr20:4823588-4823959 | Common:1; Rare:75 | ||||
| chr20:5112874-5113194 | Common:1; Rare:123 | ||||
| chr20:5119914-5120168 | Common:1; Rare:85 | ||||
| chr20:5126569-5126786 | Common:3; Rare:59 | ||||
| chr20:5610879-5611148 | Common:2; Rare:93 | ||||
| chr20:5950278-5950689 | Common:8; Rare:122 | ||||
| chr20:10435036-10435328 | Rare:69 | ||||
| chr20:13784882-13785065 | Common:2; Rare:76; Clinvar (benign):2 | ||||
| chr20:16573333-16573539 | Common:1; Rare:54 |