chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84858378848583789GA29GENICpossibly homozygous116957116
84858380648583807CT23GENIChomozygous116957118
84858381148583812CT25GENIChomozygous116957120
84858381348583814AG24GENIChomozygous116957122
84858390548583906GA31GENIChomozygous116957124
84858459448584595GA19GENIChomozygous116957126
84858494248584943AG18GENIChomozygous116957128
84858540048585401TC13GENIChomozygous116957130
84858542048585421TC10GENICheterozygous116957132
84858542548585426CT10GENICheterozygous116957134
84858544648585447TC7GENICheterozygous116957136
84858592848585929TC8GENIChomozygous116957138
84858747248587473GA21GENICpossibly homozygous116957140
84858810148588102CT23GENIChomozygous116957142
84858823148588232GA24GENIChomozygous116957144
84858827948588280TC27GENICpossibly homozygous116957146
84858952448589525AC23GENIChomozygous116957148
84859030148590302CT18GENICpossibly homozygous116957150
84859036248590363CT26GENIChomozygous116957152
84859093248590933AC28GENIChomozygous116957154
84859156548591566CT17GENIChomozygous116957156
84859229248592293GT36GENIChomozygous116957158
84859535848595359TG28GENIChomozygous116957160
84859544648595447AG21GENIChomozygous116957162
84859577648595777TC25GENIChomozygous116957164
84859700648597007CT18GENIChomozygous116957166
84859814448598145TA21GENIChomozygous116957168
84859834048598341TG63GENICheterozygous116957170
84859835048598351TG77GENICheterozygous116957172
84859839848598399CT62GENICheterozygous116957174
84859840448598405CT56GENICheterozygous116957176
84859845648598457CT26GENIChomozygous116957178