chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48528770385287704CT28GENIChomozygous113357152
48528864485288645GA26GENIChomozygous113357154
48529296185292962CG31GENIChomozygous113357156
48530028185300282AG36GENIChomozygous113357158
48530113885301139CT17GENICpossibly homozygous113357160
48530153285301533GC16GENIChomozygous113357162
48530474285304743AT28GENIChomozygous113357164
48530722785307228CA27GENIChomozygous112760763
48531070185310702AG39GENIChomozygous112760771
48531143985311440CT22GENIChomozygous112760775
48531883485318835CT20GENIChomozygous113357166
48532555785325558AT22GENIChomozygous112760821
48532642185326422GA23GENIChomozygous112760823
48532649585326496CT31GENIChomozygous113279132
48532681985326820GA20GENIChomozygous112760825
48532685985326860GA19GENIChomozygous113279134
48532746485327465TC23GENIChomozygous112760827
48532756485327565AC25GENIChomozygous112760829
48532759685327597AG27GENIChomozygous112760831
48532784585327846CT21GENIChomozygous112760833
48532819385328194CT27GENIChomozygous112760837
48532828385328284AG20GENIChomozygous112760839
48532876385328764AG26GENIChomozygous112760841