Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:2508870-2509197 | Common:1; Rare:63 | ||||
chr20:2652455-2652648 | Common:7; Rare:64 | ||||
chr20:2664177-2664273 | Common:2; Rare:42 | ||||
chr20:2840624-2840771 | Common:1; Rare:58 | ||||
chr20:3209439-3209549 | Rare:40 | ||||
chr20:3767716-3768032 | Common:3; Rare:99 | ||||
chr20:3795730-3795804 | Common:1; Rare:20 | ||||
chr20:4686235-4686501 | Common:1; Rare:56; Clinvar (benign):1 | ||||
chr20:5112908-5113175 | Rare:108 | ||||
chr20:5119903-5120149 | Common:1; Rare:86 | ||||
chr20:5126692-5127065 | Common:3; Rare:124 | ||||
chr20:5950467-5950637 | Common:8; Rare:47 | ||||
chr20:13784878-13785080 | Common:2; Rare:90; Clinvar (benign):3 | ||||
chr20:16573305-16573540 | Common:1; Rare:65 | ||||
chr20:17558418-17558626 | Common:1; Rare:35 |