chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152467268524672686GA57GENIChomozygous139686845
152467326024673261AC59GENIChomozygous139686846
152467456124674562CT65GENIChomozygous139686847
152467505924675060AC17GENIChomozygous139686849
152467700124677002TC70GENIChomozygous139686850
152467868924678690CT53GENIChomozygous139686851
152467927324679274TC42GENIChomozygous139686852
152468035024680351CT48GENIChomozygous139686855
152467930324679304TC41GENIChomozygous139686853
152467963324679634GA60GENIChomozygous139686854
152468039524680396GA22GENIChomozygous139686856
152468039724680398GA22GENIChomozygous139686857
152468039924680400GA22GENIChomozygous139686858
152468040124680402GA22GENIChomozygous139686859
152468049924680500TC46GENIChomozygous139686860
152468065124680652CT42GENICpossibly homozygous139686861
152468133924681340AC44GENIChomozygous139686862
152468154324681544CT34GENIChomozygous139686863
152468181824681819GA26GENIChomozygous139686864
152468237524682376CT32GENIChomozygous139686865
152468412724684128TC53GENIChomozygous139686866
152468621424686215AG63GENIChomozygous139686867
152468767824687679AG32GENIChomozygous139686868
152468768424687685AG22GENICpossibly homozygous139686869
152468871024688711GT41GENIChomozygous139686870
152468914224689142GGTTGGGGATTTA39GENIChomozygous139622903
152468189924681900T9GENICheterozygous141045903
152468858724688589TC34GENICheterozygous145190020
152468177724681780AAG12GENICheterozygous139622899
152468579424685794AGAAAGAAAGAA24GENIChomozygous139622900
152468767324687673CGCG20GENICpossibly homozygous139622901
152468769724687699CC19GENICheterozygous139622902
152469096224690963T47GENIChomozygous139622904
152469250824692509GA60GENICpossibly homozygous139686871
152469270124692702CA56GENICpossibly homozygous139686872
152469272124692722CA57GENICpossibly homozygous139686873
152469480324694804T54GENIChomozygous139622905
152469270124692702C56GENICheterozygous403375386
152468768624687687AG20GENICheterozygous403375385