chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140656801140656802CT31GENIChomozygous112857908
4140656891140656892AG28GENIChomozygous112857912
4140661355140661356GA27GENIChomozygous112857914
4140661785140661786AG19GENIChomozygous112857916
4140662303140662304TC35GENIChomozygous112857918
4140662477140662478CT27GENIChomozygous112857920
4140662763140662764CT33GENIChomozygous113057220
4140662825140662826CT29GENIChomozygous119281316
4140662826140662827TC28GENIChomozygous119281318
4140663099140663100CT26GENIChomozygous112857922
4140663448140663449CG27GENIChomozygous112857924
4140663577140663578TC27GENIChomozygous112857926
4140663588140663589AG27GENIChomozygous112857928
4140663960140663961GC28GENIChomozygous112857930
4140665166140665167GA32GENIChomozygous112857932
4140665547140665548GA22GENIChomozygous113057228
4140665560140665561AG22GENIChomozygous112857938
4140665968140665969GA19GENIChomozygous112857940
4140666487140666488CT22GENIChomozygous113057230
4140666532140666533TC25GENIChomozygous112857942