| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3209258-3209348 | Common:1; Rare:16 | ||||
| chr20:3209439-3209542 | Rare:36 | ||||
| chr20:3767720-3768070 | Common:5; Rare:111 | ||||
| chr20:3846684-3846912 | Common:1; Rare:65 | ||||
| chr20:3889160-3889401 | Common:1; Rare:123; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:4015520-4015793 | Common:3; Rare:101 | ||||
| chr20:4148559-4148890 | Rare:91 | ||||
| chr20:4686268-4686502 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:5112852-5113178 | Common:1; Rare:118 | ||||
| chr20:5119576-5120185 | Common:1; Rare:189 | ||||
| chr20:5126725-5127081 | Common:3; Rare:123 | ||||
| chr20:5610924-5611154 | Common:2; Rare:81 | ||||
| chr20:5750309-5750453 | Rare:35 | ||||
| chr20:5950410-5950720 | Common:8; Rare:98 | ||||
| chr20:10034854-10035155 | Common:6; Rare:113 |