chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X124635881124635882GC28GENIChomozygous931006025
X124636223124636224GA12GENIChomozygous931006026
X124642452124642453AG18GENIChomozygous931006027
X124643201124643202CT27GENIChomozygous931006028
X124644532124644533CT15GENIChomozygous931006029
X124644755124644756CT27GENIChomozygous931006030
X124648028124648029GT10GENIChomozygous931006031
X124648043124648044CT10GENIChomozygous931006032
X124648547124648548AG33GENIChomozygous931006033
X124648836124648837TC28GENIChomozygous931006034
X124651865124651866GC21GENIChomozygous931006035
X124651980124651981CT16GENIChomozygous931006036