| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25696814-25697053 | Common:3; Rare:69 | ||||
| chr20:31547316-31547437 | Rare:30 | ||||
| chr20:31722851-31722956 | Rare:26 | ||||
| chr20:31739107-31739357 | Common:1; Rare:63 | ||||
| chr20:32207712-32207876 | Common:1; Rare:47 | ||||
| chr20:34112161-34112423 | Rare:79 | ||||
| chr20:35092787-35092962 | Common:1; Rare:73 | ||||
| chr20:35455059-35455214 | Common:1; Rare:56 | ||||
| chr20:35699305-35699481 | Rare:62; Clinvar (benign):3 | ||||
| chr20:36236254-36236491 | Common:2; Rare:48 | ||||
| chr20:36573388-36573493 | Rare:36 | ||||
| chr20:37178865-37179144 | Rare:80 | ||||
| chr20:37289578-37289669 | Common:1; Rare:28 | ||||
| chr20:38033415-38033556 | Common:1; Rare:45 | ||||
| chr20:38962150-38962382 | Common:1; Rare:96 |