| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45363364-45363527 | Common:1; Rare:40 | ||||
| chr20:45416035-45416159 | Rare:34 | ||||
| chr20:45791912-45792014 | Common:1; Rare:40 | ||||
| chr20:45857320-45857624 | Common:3; Rare:85 | ||||
| chr20:45881079-45881241 | Common:2; Rare:37 | ||||
| chr20:45891269-45891387 | Common:1; Rare:41; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45910965-45911184 | Common:3; Rare:70 | ||||
| chr20:45912143-45912303 | Common:3; Rare:37 | ||||
| chr20:45934545-45934730 | Common:1; Rare:88 | ||||
| chr20:45971828-45971948 | Common:1; Rare:43 | ||||
| chr20:46363962-46364087 | Common:1; Rare:25 | ||||
| chr20:46364362-46364551 | Rare:72 | ||||
| chr20:46406570-46406814 | Common:2; Rare:64 | ||||
| chr20:46513536-46513708 | Common:3; Rare:64 | ||||
| chr20:46709521-46709695 | Rare:52; Clinvar:1 |