| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3786238-3786340 | Common:2; Rare:23 | ||||
| chr20:3786682-3786952 | Common:4; Rare:97 | ||||
| chr20:3795607-3795951 | Common:3; Rare:80 | ||||
| chr20:3796089-3796333 | Common:1; Rare:62 | ||||
| chr20:3820105-3820352 | Common:2; Rare:64 | ||||
| chr20:3820362-3820955 | Common:2; Rare:189 | ||||
| chr20:3846593-3846923 | Common:4; Rare:82 | ||||
| chr20:3847091-3847125 | Rare:9 | ||||
| chr20:3847277-3847318 | Rare:10 | ||||
| chr20:3888956-3889450 | Common:3; Rare:259; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr20:4015494-4015785 | Common:4; Rare:106 | ||||
| chr20:4686297-4686476 | Rare:42 | ||||
| chr20:4814746-4815324 | Common:15; Rare:134 | ||||
| chr20:4823418-4823709 | Common:3; Rare:58 | ||||
| chr20:5001421-5001515 | Common:1; Rare:26 |