chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103921430539214306GC82GENICheterozygous118065799
103921431839214319TC82GENICheterozygous118065800
103921441539214416TC79GENICheterozygous117989751
103921443039214431TC90GENIChomozygous117989752
103921449839214499TC117GENICheterozygous117989753
103921459839214599TC99GENICheterozygous117989754
103921460439214605CT100GENICheterozygous117989755
103921471939214720G75GENICheterozygous128808754
103921472139214722AT75GENICheterozygous123344053
103921481739214818T79GENICheterozygous128808755
103921482739214828AC83GENICheterozygous117277730
103921488539214886TC99GENICheterozygous116566513
103921490039214901GC104GENICheterozygous117277732
103921512139215122AT61GENICheterozygous123344056
103921512239215123GA61GENICheterozygous123344057
103921515639215159CTT73GENICheterozygous128808756
103921530339215304AG67GENICheterozygous117217674
103921531339215315TC62GENICheterozygous128808757
103921532239215324TG68GENICheterozygous128808758
103921532739215327AC65GENICheterozygous128808759
103921729939217299ACACTCTGGTTT63GENICheterozygous128808760
103921763439217635TC50GENICheterozygous117989756
103922559139225592TC50GENIChomozygous116566535
103922804939228050AG59GENIChomozygous116566549
103921526139215262TC70GENICheterozygous116763000
103921526739215268AG68GENICheterozygous116763002