| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3972548-3972661 | Common:1; Rare:25 | ||||
| chr20:3985937-3985997 | Rare:14 | ||||
| chr20:4687230-4687533 | Common:3; Rare:76 | ||||
| chr20:4688371-4688447 | Common:1; Rare:14 | ||||
| chr20:4694151-4694178 | Rare:4 | ||||
| chr20:4697448-4697467 | Rare:4 | ||||
| chr20:4859282-4859489 | Common:1; Rare:48 | ||||
| chr20:5092292-5092574 | Common:1; Rare:63 | ||||
| chr20:5115299-5115483 | Rare:38; Clinvar (pathogenic):1 | ||||
| chr20:5167719-5167805 | Common:1; Rare:18 | ||||
| chr20:5551695-5551704 | Rare:3 | ||||
| chr20:5609688-5609710 | Rare:2 | ||||
| chr20:6081295-6081380 | Rare:16 | ||||
| chr20:6097491-6097802 | Common:3; Rare:90; Clinvar (pathogenic):3 | ||||
| chr20:9491711-9491952 | Rare:43 |