chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176053775860537759TC17GENIChomozygous111072842
176053778160537782CT18GENIChomozygous111072843
176053816760538168AC38GENIChomozygous111072844
176053883860538839TC35GENIChomozygous111209346
176053951260539513AG21GENIChomozygous111072845
176053979760539798TC40GENIChomozygous111072846
176054032960540330CT27GENIChomozygous111072847
176054054860540549GA29GENIChomozygous111072849
176054098460540985TC17GENICheterozygous119452066
176054102860541029TC19GENICheterozygous111209349
176054109260541093AG20GENIChomozygous111072850
176054121460541215GA35GENIChomozygous111072851
176054145260541453GA30GENIChomozygous111072852
176054160760541608TC34GENIChomozygous111072853
176054254860542549GA19GENIChomozygous111072854
176054282260542823AT32GENIChomozygous111072855
176054352360543524AG13GENIChomozygous111072856
176054429260544293GA27GENIChomozygous111072857
176053862560538626CT47GENIChomozygous111353449
176054099360540994TC16GENICheterozygous119296669
176054705560547056CG30GENIChomozygous111072858
176054812760548128AC36GENIChomozygous111072859
176054844460548445AC35GENIChomozygous111072860
176054952460549525TC16GENIChomozygous111072861
176055002960550030CA26GENIChomozygous111072862
176055032260550323CA29GENIChomozygous111072863
176055076960550770TC25GENIChomozygous111072864
176055284060552841GT20GENIChomozygous111072865