chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X124635881124635882GC31GENIChomozygous108326124
X124636223124636224GA12GENIChomozygous108326126
X124637404124637405AC12GENICheterozygous119951603
X124637429124637430GA9GENIChomozygous119951604
X124642068124642069AG44GENICheterozygous119951605
X124642122124642123AG18GENICheterozygous108621613
X124642452124642453AG19GENIChomozygous108326128
X124643201124643202CT33GENIChomozygous108326130
X124644532124644533CT17GENIChomozygous108326132
X124644755124644756CT29GENIChomozygous108326134
X124648028124648029GT12GENIChomozygous108326136
X124648043124648044CT13GENIChomozygous108326138
X124648547124648548AG34GENIChomozygous108326140
X124648836124648837TC30GENIChomozygous108326142
X124651865124651866GC21GENIChomozygous108326144
X124651980124651981CT18GENIChomozygous108326146