| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45363353-45363528 | Common:1; Rare:43 | ||||
| chr20:45406580-45406697 | Rare:30 | ||||
| chr20:45791881-45791981 | Rare:35 | ||||
| chr20:45827245-45827510 | Common:2; Rare:43 | ||||
| chr20:45857348-45857622 | Common:3; Rare:70 | ||||
| chr20:45891005-45891379 | Common:3; Rare:117; Clinvar:8; Clinvar (benign):3 | ||||
| chr20:45912140-45912273 | Common:3; Rare:32 | ||||
| chr20:45971823-45972073 | Common:2; Rare:72 | ||||
| chr20:46363931-46364069 | Common:1; Rare:25 | ||||
| chr20:46364371-46364572 | Common:1; Rare:75 | ||||
| chr20:46406565-46406798 | Common:2; Rare:63 | ||||
| chr20:46709474-46709687 | Rare:60; Clinvar:1 | ||||
| chr20:47356646-47356887 | Rare:56 | ||||
| chr20:47501720-47502009 | Common:1; Rare:101 | ||||
| chr20:49046176-49046372 | Common:3; Rare:62 |