| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35699286-35699528 | Rare:80; Clinvar (benign):3 | ||||
| chr20:35741616-35741699 | Common:1; Rare:26 | ||||
| chr20:35741939-35742657 | Common:6; Rare:235 | ||||
| chr20:35771839-35772050 | Common:2; Rare:69 | ||||
| chr20:36236441-36236547 | Rare:26 | ||||
| chr20:36541296-36541594 | Common:3; Rare:83 | ||||
| chr20:36573326-36573729 | Common:2; Rare:158 | ||||
| chr20:36574388-36574567 | Rare:68 | ||||
| chr20:36605496-36605796 | Common:2; Rare:105 | ||||
| chr20:36746044-36746321 | Common:3; Rare:96 | ||||
| chr20:36951670-36951911 | Common:1; Rare:62; Clinvar (benign):4 | ||||
| chr20:37095939-37096033 | Rare:42 | ||||
| chr20:37178865-37179238 | Rare:109 | ||||
| chr20:37179495-37179575 | Rare:29 | ||||
| chr20:37289577-37289732 | Common:2; Rare:61 |