Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:31739098-31739301 | Common:1; Rare:46 | ||||
chr20:31819094-31819449 | Common:3; Rare:77; Clinvar (benign):1 | ||||
chr20:32207666-32207951 | Common:3; Rare:109 | ||||
chr20:33401476-33401618 | Rare:37 | ||||
chr20:33994042-33994128 | Rare:29 | ||||
chr20:34558560-34558767 | Common:1; Rare:57 | ||||
chr20:34677083-34677291 | Rare:55 | ||||
chr20:34872820-34872908 | Rare:33 | ||||
chr20:34955743-34955928 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
chr20:35556712-35557104 | Common:2; Rare:105 | ||||
chr20:35699158-35699221 | Rare:15 | ||||
chr20:35699234-35699264 | Rare:4 | ||||
chr20:35699292-35699481 | Rare:67; Clinvar (benign):3 | ||||
chr20:35742330-35742641 | Common:5; Rare:96 | ||||
chr20:35771784-35772064 | Common:2; Rare:86 |