chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8106451570106451571TA52GENIChomozygous808306097
8106453272106453273TC57GENIChomozygous808306098
8106453565106453566CT54GENIChomozygous808306099
8106454816106454817TG56GENICheterozygous808306100
8106454969106454970CA41GENIChomozygous808306101
8106456895106456896AG50GENICpossibly homozygous808306102
8106458365106458366AC43GENICheterozygous808306103
8106458388106458389CG43GENIChomozygous808306104
8106460360106460361TG45GENIChomozygous808306105
8106461462106461463GA59GENIChomozygous808306106
8106462917106462918TC54GENIChomozygous808306107
8106463968106463969GA62GENIChomozygous808306108
8106464866106464867AG55GENIChomozygous808306109
8106465096106465097CT41GENIChomozygous808306110
8106466972106466973AG42GENIChomozygous808306111
8106468644106468645TC62GENIChomozygous808306112