| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3767720-3767920 | Common:2; Rare:61 | ||||
| chr20:3820462-3820567 | Rare:45 | ||||
| chr20:3846740-3846891 | Rare:44 | ||||
| chr20:4686151-4686508 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:5112861-5112976 | Common:1; Rare:30 | ||||
| chr20:5112980-5113178 | Rare:83 | ||||
| chr20:5119907-5120174 | Common:1; Rare:90 | ||||
| chr20:5126699-5127081 | Common:3; Rare:132 | ||||
| chr20:5610913-5611169 | Common:2; Rare:91 | ||||
| chr20:5950410-5950689 | Common:8; Rare:86 | ||||
| chr20:6122994-6123128 | Common:2; Rare:34; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:13784889-13785080 | Common:2; Rare:83; Clinvar (benign):3 | ||||
| chr20:14337561-14337656 | Rare:21 | ||||
| chr20:16573308-16573541 | Common:1; Rare:64 | ||||
| chr20:17558417-17558563 | Common:1; Rare:23 |