| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63642490-63642890 | Common:2; Rare:128 | ||||
| chr20:63678534-63678777 | Common:4; Rare:64 | ||||
| chr20:63682211-63683018 | Common:10; Rare:575 | ||||
| chr20:63691328-63691966 | Common:6; Rare:297; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr20:63846425-63846951 | Rare:241 | ||||
| chr20:63863891-63864114 | Common:5; Rare:52 | ||||
| chr20:63864152-63864431 | Rare:100 | ||||
| chr20:63865823-63866003 | Common:3; Rare:113 | ||||
| chr20:63873500-63873940 | Common:2; Rare:218 | ||||
| chr20:63896680-63897000 | Rare:67 | ||||
| chr20:63954691-63955395 | Common:2; Rare:283 | ||||
| chr20:63973242-63973755 | Common:8; Rare:202 | ||||
| chr20:63978750-63979106 | Common:3; Rare:139 | ||||
| chr20:64083523-64083789 | Common:2; Rare:86 | ||||
| chr21:8397251-8398032 | Rare:4 |