| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45889975-45890311 | Common:1; Rare:83 | ||||
| chr20:45891014-45891387 | Common:3; Rare:114; Clinvar:8; Clinvar (benign):3 | ||||
| chr20:45934373-45934730 | Common:2; Rare:148 | ||||
| chr20:46363962-46364069 | Common:1; Rare:20 | ||||
| chr20:46364350-46364535 | Common:1; Rare:67 | ||||
| chr20:46406565-46406787 | Common:2; Rare:60 | ||||
| chr20:46513497-46513691 | Common:3; Rare:75 | ||||
| chr20:47319040-47319135 | Common:1; Rare:32 | ||||
| chr20:47352310-47352650 | Common:1; Rare:58 | ||||
| chr20:47356664-47356887 | Rare:51 | ||||
| chr20:47501710-47502086 | Common:1; Rare:127 | ||||
| chr20:47786560-47786731 | Common:5; Rare:23 | ||||
| chr20:49046179-49046364 | Common:3; Rare:57 | ||||
| chr20:49219255-49219541 | Common:1; Rare:127 | ||||
| chr20:49278027-49278278 | Rare:68 |