chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109580530109580531GA28GENIChomozygous51599521
10109584504109584505GC20GENIChomozygous51599522
10109586642109586643CT26GENIChomozygous51599523
10109589444109589445CG33GENICpossibly homozygous51599524
10109594253109594254CT26GENIChomozygous51599525
10109596161109596162G-26GENIChomozygous51599526