chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105634097656340977TA17GENIChomozygous52059151
105634191856341919AAT5GENICheterozygous52059153
105634300556343006G-13GENIChomozygous52059155
105634778456347785GC10GENICpossibly homozygous51654988
105635330756353308AG7GENIChomozygous52059159
105635713856357151AGTGATGCGATCT-------------6GENICheterozygous52059161
105635914756359149TC--5GENICheterozygous52059163
105636318856363189GA16GENICpossibly homozygous52059165
105636339156363392TC6GENIChomozygous51654994
105636453156364532GA9GENIChomozygous51654996