| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35699118-35699260 | Rare:25 | ||||
| chr20:35699267-35699587 | Rare:94; Clinvar (benign):3 | ||||
| chr20:35741567-35741693 | Common:1; Rare:39 | ||||
| chr20:35741933-35742630 | Common:6; Rare:223 | ||||
| chr20:35771824-35772055 | Common:2; Rare:74 | ||||
| chr20:35855163-35855282 | Common:1; Rare:23 | ||||
| chr20:35968556-35968619 | Rare:12 | ||||
| chr20:36092342-36092791 | Common:1; Rare:106 | ||||
| chr20:36236391-36236539 | Common:1; Rare:40 | ||||
| chr20:36461160-36461498 | Common:1; Rare:99 | ||||
| chr20:36541181-36541560 | Common:3; Rare:99 | ||||
| chr20:36573376-36573622 | Rare:102 | ||||
| chr20:36605544-36605961 | Common:2; Rare:144 | ||||
| chr20:36700540-36700697 | Rare:37 | ||||
| chr20:36746044-36746311 | Common:2; Rare:95 |