| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44651658-44651869 | Common:2; Rare:100; Clinvar (benign):2 | ||||
| chr20:44714677-44714935 | Rare:112 | ||||
| chr20:44715091-44715397 | Common:59; Rare:154 | ||||
| chr20:44745739-44745998 | Rare:112 | ||||
| chr20:44746100-44746760 | Common:4; Rare:172 | ||||
| chr20:44885419-44885862 | Common:14; Rare:259 | ||||
| chr20:44960334-44960591 | Common:2; Rare:166 | ||||
| chr20:44966313-44966578 | Common:4; Rare:193 | ||||
| chr20:45174707-45174907 | Rare:49 | ||||
| chr20:45254456-45254734 | Rare:127 | ||||
| chr20:45348369-45348595 | Common:2; Rare:116 | ||||
| chr20:45362916-45363257 | Common:2; Rare:198 | ||||
| chr20:45363361-45363537 | Common:2; Rare:86 | ||||
| chr20:45406537-45406678 | Rare:74 | ||||
| chr20:45415999-45416173 | Rare:99 |