chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130111029130111030AG28GENICpossibly homozygous116345856
7130112323130112324CT22GENIChomozygous116345858
7130113369130113370GA24GENIChomozygous116345860
7130114830130114831AG5GENIChomozygous116345864
7130116636130116637CT10GENIChomozygous116345868
7130116743130116744TC23GENIChomozygous115889283
7130117818130117819GA19GENIChomozygous116345870
7130117965130117966AC24GENIChomozygous115889287
7130119970130119971CT15GENIChomozygous116345872
7130120130130120131GA16GENIChomozygous116345874