chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6104961749104961750CG13GENICheterozygous55046995
6104961761104961762GC16GENICheterozygous54610890
6104963606104963607TTG16GENICpossibly homozygous54610891
6104963608104963609TG16GENIChomozygous54610892
6104963707104963708GGT1GENIChomozygous54610894
6104964282104964283GA5GENIChomozygous54610895
6104964287104964288GC7GENIChomozygous54610896
6104964300104964301A-11GENICpossibly homozygous54610897
6104967102104967103A-1GENIChomozygous54610898
6104969097104969111AGAGAGAGAGAGAG--------------9GENIChomozygous54610899
6104969121104969122A-18GENICheterozygous54610900
6104969179104969183AAGG----4GENICheterozygous54610901
6104969187104969188AG9GENICheterozygous54610902
6104969218104969222AAAG----7GENIChomozygous54610903
6104970046104970047AG31GENIChomozygous54610904
6104970516104970517TTAA9GENICheterozygous54610905
6104974669104974670A-22GENIChomozygous54610906
6104975113104975114AG27GENIChomozygous54610907
6104976265104976266AG40GENIChomozygous54610908
6104977504104977505AG38GENIChomozygous54610909