chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174764157347641574CT31GENIChomozygous111057584
174764304947643050GA26GENICpossibly homozygous111057585
174764408847644089TC27GENIChomozygous111057586
174764435147644352CT21GENIChomozygous111057587
174764466447644665TG21GENIChomozygous111245371
174764523147645232GC39GENIChomozygous111057588
174764612747646128GA28GENIChomozygous111057589
174764810647648107GA35GENIChomozygous111057590
174764854647648547AG39GENIChomozygous111057591
174764875647648757AC27GENIChomozygous111057592
174764996847649969TC10GENIChomozygous111057593