chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101900066919000670AG31GENIChomozygous116919724
101900244719002448AC36GENIChomozygous116919726
101900581919005820AG29GENIChomozygous116504641
101902359219023593TC16GENIChomozygous116504737
101902392419023925AG16GENIChomozygous116504739
101902406319024064TA9GENIChomozygous116504741
101902429819024299GA27GENIChomozygous116919728
101902448119024482CA25GENIChomozygous116504745
101902460719024608AG22GENIChomozygous116504747
101902582019025821CA14GENIChomozygous116504749
101902662519026626CT40GENIChomozygous116741106
101902674319026744AG32GENIChomozygous116741107
101902771319027714CT23GENIChomozygous116504753
101902786319027864AG22GENIChomozygous116504755
101902786919027870GA24GENIChomozygous116741108
101902805919028060TC34GENIChomozygous116504757
101902833619028337TC24GENIChomozygous116504759
101902897719028978AG18GENIChomozygous116504761
101902922919029230GT37GENIChomozygous116504765
101902982119029822GA31GENIChomozygous116504769
101903127719031278TC11GENIChomozygous116504779
101903146319031464GA20GENIChomozygous116741109
101903166519031666TC25GENIChomozygous116504781
101903569419035695TA33GENIChomozygous116741110
101903601819036019GA27GENIChomozygous116741111
101903622719036228AG27GENIChomozygous116504806
101903734219037343TC22GENIChomozygous116504818
101903769219037693CT24GENIChomozygous116741112
101903838819038389GA32GENIChomozygous116741113
101904027519040276AG22GENIChomozygous116504830
101904037519040376GT27GENIChomozygous116741114
101904038619040387AG29GENIChomozygous116741115
101904159719041598GA26GENIChomozygous116741116
101904193019041931CT20GENIChomozygous116741117
101904241519042416CT29GENIChomozygous116504850
101904291519042916TC25GENIChomozygous116504858