chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7110485690110485691AG22GENIChomozygous138181280
7110486624110486625GA27GENIChomozygous138181282
7110486649110486650AG30GENIChomozygous138181283
7110486669110486670CT26GENIChomozygous148021998
7110486972110486973AC5GENIChomozygous138181284
7110487097110487098CT19GENIChomozygous138181285
7110487116110487117TC19GENIChomozygous138181286
7110487287110487288GA29GENIChomozygous138181287
7110487605110487606GA33GENIChomozygous138181288
7110487835110487836TC41GENIChomozygous138181289
7110487871110487872TC42GENIChomozygous138181290
7110487978110487979CG44GENIChomozygous138181292
7110488001110488002CT43GENIChomozygous138181293
7110488043110488044TA43GENIChomozygous138181294