chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148117249681172496C14GENIChomozygous129177967
148117374381173744C11GENIChomozygous129177968
148117374881173748AC11GENIChomozygous129177969
148117375481173757GGT10GENIChomozygous129177970
148117377281173772C9GENIChomozygous129177971
148117378081173780CA11GENIChomozygous129177972
148117378481173785A11GENIChomozygous129177973
148119219981192199T19GENIChomozygous129177974
148120486881204869AC17GENIChomozygous118703707
148121009181210092AG22GENICheterozygous129212795
148121012181210122AC25GENICheterozygous129212796
148121012881210129GA23GENICheterozygous129212797
148121013781210138GT22GENICheterozygous129212798
148121014081210141GA22GENICheterozygous129212799
148121016081210161GT24GENICheterozygous118703730
148121018981210190AG20GENICheterozygous130145286
148121021381210214CG18GENICheterozygous131151478
148121057281210573CT20GENIChomozygous113501556
148123237681232377AG18GENIChomozygous113501558
148123291981232921AG10GENICheterozygous130428413
148124513081245131TC1GENIChomozygous134348012