chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107022294370222944TC52GENIChomozygous116627275
107022327770223278TA49GENIChomozygous116627277
107022354570223546GA18GENICheterozygous118042672
107022560770225608AC70GENIChomozygous116627279
107022622670226227AG69GENIChomozygous116627281
107022663670226637AG60GENIChomozygous116627283
107022663770226638AG60GENIChomozygous116627286
107022942570229426TC52GENIChomozygous116627288
107022963670229637TC47GENICpossibly homozygous116627290
107023057070230571GA78GENIChomozygous116627294
107023075670230757AC47GENIChomozygous116627296
107023093370230934TC58GENICpossibly homozygous116627298
107023120070231201AC62GENIChomozygous117222455
107023138370231384AC67GENIChomozygous117222457
107023144870231449GA50GENIChomozygous117222459
107023161670231617GT58GENIChomozygous117222461
107023189770231898CT53GENICpossibly homozygous118042673
107023196670231967TC50GENIChomozygous118042674
107023242070232421GA76GENIChomozygous117222463
107023254270232543GA79GENIChomozygous117222465
107023322270233223AG59GENIChomozygous117222467
107023324670233247CA56GENIChomozygous116627304
107023447870234479CT34GENICpossibly homozygous117222469
107023198970231990AG62GENICpossibly homozygous117999903