| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50903892-50904137 | Rare:55 | ||||
| chr20:50958388-50958879 | Common:1; Rare:191; Clinvar:5; Clinvar (benign):5 | ||||
| chr20:51542681-51542849 | Common:6; Rare:58 | ||||
| chr20:52972631-52972828 | Common:2; Rare:39 | ||||
| chr20:53593775-53593922 | Common:1; Rare:57 | ||||
| chr20:56392187-56392687 | Common:6; Rare:129 | ||||
| chr20:56412073-56412204 | Common:2; Rare:23 | ||||
| chr20:56412253-56412453 | Rare:41 | ||||
| chr20:56468504-56468722 | Rare:86 | ||||
| chr20:57392531-57392649 | Common:1; Rare:32 | ||||
| chr20:58651112-58651318 | Common:2; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:58651484-58651678 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):3 | ||||
| chr20:58652321-58652599 | Common:2; Rare:89 | ||||
| chr20:58910331-58910623 | Common:2; Rare:63 | ||||
| chr20:58981168-58981344 | Common:2; Rare:86 |