Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49877861-49878178 | Common:4; Rare:103 | ||||
chr19:49929096-49929224 | Common:3; Rare:38 | ||||
chr19:49929404-49929820 | Common:7; Rare:141 | ||||
chr19:50476425-50476573 | Rare:63 | ||||
chr19:50511068-50511574 | Common:4; Rare:163 | ||||
chr19:50804636-50804909 | Common:5; Rare:76 | ||||
chr19:51366272-51366562 | Common:5; Rare:89; Clinvar (benign):2 | ||||
chr19:51887897-51888046 | Rare:54 | ||||
chr19:52008195-52008305 | Rare:29 | ||||
chr19:52397719-52397881 | Common:3; Rare:48 | ||||
chr19:53254845-53255067 | Common:2; Rare:80 | ||||
chr19:53431875-53432000 | Common:3; Rare:35 | ||||
chr19:54115247-54115497 | Common:2; Rare:64; Clinvar (benign):2 | ||||
chr19:54115610-54115800 | Common:2; Rare:51; Clinvar:5 | ||||
chr19:54449039-54449253 | Common:2; Rare:64 |