| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35699336-35699473 | Rare:44 | ||||
| chr20:35742170-35742651 | Common:5; Rare:154 | ||||
| chr20:35771790-35772061 | Common:2; Rare:84 | ||||
| chr20:36236454-36236493 | Rare:8 | ||||
| chr20:36541425-36541561 | Common:2; Rare:38 | ||||
| chr20:36573243-36573604 | Common:1; Rare:149 | ||||
| chr20:36746062-36746304 | Common:2; Rare:87 | ||||
| chr20:36773724-36773889 | Common:2; Rare:46 | ||||
| chr20:36951436-36951549 | Rare:28; Clinvar (benign):1 | ||||
| chr20:36951551-36951924 | Common:1; Rare:124; Clinvar:3; Clinvar (benign):5 | ||||
| chr20:37178877-37179173 | Rare:83 | ||||
| chr20:37289392-37289669 | Common:1; Rare:72 | ||||
| chr20:37521136-37521255 | Common:1; Rare:31 | ||||
| chr20:37527818-37528196 | Common:5; Rare:136 | ||||
| chr20:37693844-37694143 | Common:1; Rare:91 |