chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176053775860537759TC8GENIChomozygous111072842
176053816760538168AC14GENIChomozygous111072844
176053862560538626CT13GENIChomozygous111353449
176053951260539513AG21GENIChomozygous111072845
176053979760539798TC21GENIChomozygous111072846
176054098060540981TC12GENICpossibly homozygous111209348
176053835860538359CT22GENIChomozygous111209345
176053883860538839TC20GENIChomozygous111209346
176054057460540575GC18GENIChomozygous111209347
176054100160541002TC11GENIChomozygous119347558
176054100960541010TC11GENICheterozygous119347560
176054102860541029TC11GENIChomozygous111209349
176054109260541093AG22GENIChomozygous111072850
176054121460541215GA23GENIChomozygous111072851
176054145260541453GA24GENIChomozygous111072852
176054160760541608TC19GENIChomozygous111072853
176054162860541629CG20GENIChomozygous111209350
176054230160542302CG21GENIChomozygous111209351
176054257360542574TC20GENIChomozygous111209352
176054282260542823AT23GENIChomozygous111072855
176054335960543360CT19GENIChomozygous111209353
176054352360543524AG25GENIChomozygous111072856
176054564860545649CT24GENIChomozygous111209354
176054705560547056CG31GENIChomozygous111072858
176054812760548128AC24GENIChomozygous111072859
176054952460549525TC29GENIChomozygous111072861
176055002960550030CA24GENIChomozygous111072862
176055008060550081GA27GENIChomozygous111209355
176055032260550323CA26GENIChomozygous111072863
176055076960550770TC20GENIChomozygous111072864
176055284060552841GT22GENIChomozygous111072865