chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17239813572398136CT17GENIChomozygous108865785
17239852272398523TC31GENICpossibly homozygous108865786
17239853772398538GT28GENIChomozygous108865787
17239895672398957TC9GENIChomozygous108865788
17239937372399374GC14GENIChomozygous108865790
17239970172399702CT7GENIChomozygous108865791
17239977172399772TC10GENIChomozygous108865792
17240173072401731TC7GENIChomozygous108865793