chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103877951738779518CT31GENIChomozygous116762466
103877965838779659AG40GENICpossibly homozygous116762468
103878005338780054AC37GENICpossibly homozygous116762470
103878009538780096CG15GENICpossibly homozygous116762472
103878019938780200CA34GENICpossibly homozygous116762474
103878054638780547TC13GENICheterozygous116762476
103878090238780903AG33GENICpossibly homozygous116762480
103878095738780958AC21GENICpossibly homozygous116762482
103878104738781048GA29GENIChomozygous116762484
103878116338781164AG25GENIChomozygous116762486
103878155038781551CT17GENICpossibly homozygous116762488
103878210638782107AG22GENICpossibly homozygous116762492
103878238538782386GA15GENIChomozygous116762494