chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124722001047220011AG26GENIChomozygous115397506
124722144447221445CG19GENIChomozygous115343458
124722534947225350GT19GENIChomozygous115343460
124722545647225457AG19GENIChomozygous115480603
124722551347225514TC18GENIChomozygous115343462
124722559947225600TC25GENIChomozygous115343464
124722624247226243TC24GENIChomozygous115343466
124722712547227126AG27GENIChomozygous115343468
124722893947228940GA16GENICpossibly homozygous118272643
124723048747230488CG27GENIChomozygous115343472
124723057647230577AG31GENIChomozygous115343474
124723095747230958AG39GENIChomozygous115343476
124723116947231170CG20GENIChomozygous115343478