| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:41163169-41163323 | Rare:55 | ||||
| chr20:43457802-43457907 | Rare:47 | ||||
| chr20:43590650-43590986 | Rare:74 | ||||
| chr20:44210701-44211102 | Common:5; Rare:145 | ||||
| chr20:44475770-44475935 | Rare:74 | ||||
| chr20:44521981-44522180 | Common:2; Rare:68 | ||||
| chr20:44531772-44531978 | Common:1; Rare:66 | ||||
| chr20:44582309-44582667 | Rare:56 | ||||
| chr20:44651688-44651822 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr20:44714561-44714892 | Rare:69 | ||||
| chr20:44885602-44885785 | Common:4; Rare:70 | ||||
| chr20:44909809-44910087 | Common:1; Rare:87 | ||||
| chr20:44966370-44966571 | Common:1; Rare:78 | ||||
| chr20:45348418-45348591 | Common:1; Rare:48 | ||||
| chr20:45363346-45363494 | Rare:28 |