chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101334879313348794GT33GENIChomozygous116495796
101334973913349740TG37GENIChomozygous116994648
101335211913352120CA30GENIChomozygous116735731
101335292013352921TC24GENIChomozygous116735733
101335316913353170AG33GENIChomozygous116735734
101335419713354198AG23GENIChomozygous116735737
101335469413354695TC39GENICpossibly homozygous116495832
101335484613354847CT25GENICpossibly homozygous116915174
101335135813351359CT30GENIChomozygous116915168
101335182213351823GA29GENIChomozygous116915170
101335321613353217TC25GENIChomozygous116915172