chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96557048765570488GA14GENICpossibly homozygous52007874
96557146065571461GGA35GENICpossibly homozygous52007875
96557187665571878TT--32GENIChomozygous52007876
96557399065573991GA28GENIChomozygous52007877
96557433465574335AG37GENIChomozygous52007878
96557434865574349AT38GENICpossibly homozygous52007879
96557465965574660TC47GENICheterozygous52007880
96557466665574667CG46GENICheterozygous52007881
96557482365574824AC16GENIChomozygous52007882
96557482365574824AG23GENIChomozygous52007883
96557483465574835CG34GENIChomozygous52007884
96557484665574847GC31GENICheterozygous52007885
96557494965574950CG23GENIChomozygous52007886
96557503065575031CG17GENICheterozygous52007887
96557506465575065GC16GENICheterozygous52007888
96557523765575238GC56GENICheterozygous52007889
96557526065575261CG54GENICheterozygous52007890
96557604365576044CG9GENICheterozygous52007891
96557605265576053GC9GENICheterozygous52007892
96557607065576071CT18GENICheterozygous52007893
96557688465576885AAC48GENIChomozygous52007894
96557770665577707TG36GENICpossibly homozygous52007895
96557816365578164GGA21GENICheterozygous52007896
96557821765578218GGGAAAA24GENIChomozygous52007897
96558190765581908AG33GENIChomozygous52007898
96558529165585292TC26GENICpossibly homozygous52007899
96558762565587626TTAC7GENICheterozygous52007900
96558790865587910GT--25GENIChomozygous52007901