| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5115300-5115532 | Rare:49; Clinvar (pathogenic):1 | ||||
| chr20:5609860-5610024 | Common:1; Rare:29 | ||||
| chr20:8238775-8238916 | Common:5; Rare:35 | ||||
| chr20:8317870-8317946 | Common:1; Rare:14 | ||||
| chr20:8557944-8558053 | Common:1; Rare:23 | ||||
| chr20:10660071-10660444 | Common:6; Rare:72 | ||||
| chr20:18705600-18705729 | Rare:27 | ||||
| chr20:18793966-18794086 | Rare:39 | ||||
| chr20:19757532-19757664 | Common:2; Rare:37 | ||||
| chr20:19993418-19993523 | Rare:23 | ||||
| chr20:25562901-25563105 | Rare:57 | ||||
| chr20:26009664-26009876 | Common:1; Rare:52 | ||||
| chr20:26135726-26136054 | Rare:86 | ||||
| chr20:26136273-26136591 | Common:2; Rare:62 | ||||
| chr20:26174231-26174564 | Common:3; Rare:74 |