chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8132000323132000324CG29GENIChomozygous116904096
8132000468132000469TG32GENICpossibly homozygous116904098
8132000495132000496CT31GENICpossibly homozygous116728745
8132000611132000612GA23GENIChomozygous116904100
8132001122132001123AG20GENIChomozygous116904102
8132002697132002698TC27GENICheterozygous116904104
8132004606132004607TC17GENIChomozygous116728760
8132006092132006093GA16GENIChomozygous116904106
8132006177132006178CT36GENIChomozygous116904108
8132009111132009112TC21GENIChomozygous116728764
8132009983132009984AG45GENIChomozygous116728765