chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130192219130192220GT56GENICpossibly homozygous138223920
7130192740130192741CG11GENICheterozygous403618426
7130192740130192741C11GENICheterozygous403618427
7130192821130192822GA19GENIChomozygous138223921
7130193297130193298CT63GENIChomozygous138223922
7130193469130193470TC53GENIChomozygous138223923
7130195666130195667GC61GENIChomozygous138223924
7130194706130194706T69GENIChomozygous137983769
7130198000130198001TC53GENIChomozygous138223925
7130198528130198529TC54GENIChomozygous138223926