| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:48120160-48120397 | Common:1; Rare:54 | ||||
| chr20:48231631-48231806 | Common:1; Rare:33 | ||||
| chr20:48343193-48343296 | Rare:29 | ||||
| chr20:48359794-48359939 | Common:1; Rare:30 | ||||
| chr20:48406639-48406777 | Rare:33 | ||||
| chr20:48470993-48471368 | Common:1; Rare:67 | ||||
| chr20:48473504-48473531 | Rare:5 | ||||
| chr20:48498225-48498487 | Common:2; Rare:60 | ||||
| chr20:48499020-48499221 | Common:1; Rare:58 | ||||
| chr20:48499887-48500082 | Common:3; Rare:44 | ||||
| chr20:48500098-48500350 | Common:2; Rare:55 | ||||
| chr20:48516341-48516435 | Common:1; Rare:14 | ||||
| chr20:48516444-48516519 | Common:1; Rare:1 | ||||
| chr20:48989387-48989597 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:49094634-49094865 | Rare:47 |