chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121921163121921164TC10GENIChomozygous116689726
8121921185121921186AC19GENIChomozygous116689728
8121921212121921213AT22GENIChomozygous116689730
8121921228121921229GT22GENIChomozygous116689732
8121921255121921256CA30GENIChomozygous116689734
8121921289121921290GT34GENIChomozygous116689736
8121928737121928738CA17GENIChomozygous116689738
8121929539121929540CG23GENIChomozygous116689740
8121930189121930190CT12GENIChomozygous116895064
8121930793121930794AC29GENIChomozygous116689742
8121930814121930815CG24GENIChomozygous116689744
8121930846121930847GA21GENIChomozygous116689746
8121930866121930867TG18GENIChomozygous116689748
8121930953121930954GT15GENIChomozygous116689750
8121930965121930966CT5GENIChomozygous116689752
8121931845121931846AC19GENIChomozygous116689754
8121941983121941984AC29GENICpossibly homozygous116689758