chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X124635881124635882GC18GENIChomozygous810305513
X124636223124636224GA29GENIChomozygous810305514
X124637400124637401CA29GENICheterozygous810305515
X124637404124637405AC31GENICheterozygous810305516
X124637429124637430GA28GENICpossibly homozygous810305517
X124642068124642069AG72GENICheterozygous810305518
X124642093124642094GA38GENICheterozygous810305519
X124642452124642453AG31GENIChomozygous810305520
X124643201124643202CT41GENIChomozygous810305521
X124644532124644533CT24GENIChomozygous810305522
X124644755124644756CT12GENIChomozygous810305523
X124648028124648029GT29GENIChomozygous810305524
X124648043124648044CT30GENIChomozygous810305525
X124648547124648548AG26GENIChomozygous810305526
X124648836124648837TC11GENIChomozygous810305527
X124651865124651866GC20GENIChomozygous810305528
X124651980124651981CT17GENIChomozygous810305529