Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:2652455-2652661 | Common:8; Rare:72 | ||||
chr20:2664157-2664333 | Common:5; Rare:77 | ||||
chr20:2840436-2840759 | Common:3; Rare:104 | ||||
chr20:3209254-3209534 | Common:3; Rare:71 | ||||
chr20:3846705-3846886 | Rare:55 | ||||
chr20:5112977-5113161 | Rare:76 | ||||
chr20:5950410-5950723 | Common:8; Rare:99 | ||||
chr20:13784884-13785091 | Common:2; Rare:96; Clinvar (benign):3 | ||||
chr20:16573313-16573540 | Common:1; Rare:61 | ||||
chr20:17968459-17968594 | Common:4; Rare:57 | ||||
chr20:17968784-17969129 | Common:3; Rare:122 | ||||
chr20:18467132-18467439 | Common:1; Rare:64 | ||||
chr20:18507785-18507951 | Common:1; Rare:51; Clinvar:5; Clinvar (benign):1 | ||||
chr20:18567321-18567499 | Common:2; Rare:62 | ||||
chr20:21303214-21303385 | Rare:67 |