chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18002988480029885GA28GENIChomozygous120481133
18003028280030283AG45GENIChomozygous109298046
18003061880030619CG41GENIChomozygous109298050
18003066280030663TG40GENIChomozygous120481134
18003113680031137AT22GENIChomozygous120481135
18003248880032489AG34GENIChomozygous109298054
18003270580032706CT13GENIChomozygous120481136
18003573580035736AG54GENICpossibly homozygous109298060
18003603580036036GA33GENIChomozygous120481138
18003656080036561AG28GENIChomozygous120481139
18003708480037085TC23GENIChomozygous120481140
18003897280038973GA13GENIChomozygous109298068
18004168480041685GA30GENIChomozygous120481141
18004191380041914TC30GENIChomozygous109298082