| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34872792-34872967 | Rare:63 | ||||
| chr20:34874909-34875097 | Common:2; Rare:40 | ||||
| chr20:34921216-34921462 | Common:1; Rare:73 | ||||
| chr20:34955725-34955868 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:35092634-35092958 | Common:2; Rare:132 | ||||
| chr20:35147121-35147159 | Rare:11 | ||||
| chr20:35284559-35284817 | Common:2; Rare:67 | ||||
| chr20:35304043-35304279 | Rare:62 | ||||
| chr20:35556043-35556259 | Rare:66 | ||||
| chr20:35556920-35557242 | Common:2; Rare:101 | ||||
| chr20:35664848-35665005 | Common:1; Rare:43 | ||||
| chr20:35699267-35699481 | Rare:74; Clinvar (benign):3 | ||||
| chr20:35740823-35741135 | Common:3; Rare:84 | ||||
| chr20:35742097-35742654 | Common:5; Rare:179 | ||||
| chr20:35771796-35772055 | Common:2; Rare:80 |