chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152467268524672686GA11GENIChomozygous139686845
152467326024673261AC19GENIChomozygous139686846
152467456124674562CT21GENIChomozygous139686847
152467505924675060AC4GENIChomozygous139686849
152467700124677002TC20GENIChomozygous139686850
152467868924678690CT23GENIChomozygous139686851
152467927324679274TC20GENICpossibly homozygous139686852
152467930324679304TC20GENICpossibly homozygous139686853
152467963324679634GA17GENICpossibly homozygous139686854
152468035024680351CT16GENIChomozygous139686855
152468039524680396GA12GENIChomozygous139686856
152468039724680398GA12GENIChomozygous139686857
152468039924680400GA12GENIChomozygous139686858
152468040124680402GA12GENIChomozygous139686859
152468049924680500TC24GENIChomozygous139686860
152468065124680652CT12GENIChomozygous139686861
152468133924681340AC18GENIChomozygous139686862
152468154324681544CT11GENIChomozygous139686863
152468181824681819GA15GENIChomozygous139686864
152468237524682376CT15GENIChomozygous139686865
152468412724684128TC14GENIChomozygous139686866
152468621424686215AG18GENIChomozygous139686867
152468767824687679AG11GENIChomozygous139686868
152468768424687685AG8GENIChomozygous139686869
152468871024688711GT25GENIChomozygous139686870
152468914224689142GGTTGGGGATTTA13GENIChomozygous139622903
152468767324687673CGCG7GENIChomozygous139622901
152468177724681780AAG9GENICheterozygous139622899
152468579424685794AGAAAGAAAGAA6GENIChomozygous139622900
152468769724687699CC9GENIChomozygous139622902
152469096224690963T7GENIChomozygous139622904
152469250824692509GA17GENIChomozygous139686871
152469270124692702CA17GENIChomozygous139686872
152469272124692722CA17GENIChomozygous139686873
152469480324694804T17GENIChomozygous139622905
152469270124692702C17GENICheterozygous403375386