| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3807694-3807717 | Rare:4 | ||||
| chr20:3885018-3885171 | Rare:37 | ||||
| chr20:3918128-3918239 | Rare:21 | ||||
| chr20:3921407-3921707 | Common:4; Rare:60 | ||||
| chr20:3972427-3972661 | Common:1; Rare:43 | ||||
| chr20:3985792-3985997 | Rare:37 | ||||
| chr20:4512969-4513190 | Common:1; Rare:35 | ||||
| chr20:4687171-4687522 | Common:4; Rare:93 | ||||
| chr20:4926533-4926616 | Common:3; Rare:13 | ||||
| chr20:5092292-5092574 | Common:1; Rare:63 | ||||
| chr20:5115205-5115542 | Rare:72; Clinvar (pathogenic):1 | ||||
| chr20:5118349-5118717 | Rare:62 | ||||
| chr20:5167719-5167878 | Common:1; Rare:30 | ||||
| chr20:5578566-5578672 | Common:2; Rare:37 | ||||
| chr20:5587282-5587371 | Rare:12 |