chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191034292510342926GA19GENIChomozygous46058614
191034326110343262CCA14GENIChomozygous46058615
191034362110343622TTATCCATCC14GENIChomozygous46058616
191034372510343726GT17GENIChomozygous46058624
191034387710343883CACACC------3GENICheterozygous46397183
191034388610343887CG4GENICheterozygous46397185
191034388810343889AG8GENICpossibly homozygous46208006
191034630410346305TC31GENIChomozygous46058626
191034669510346696GA16GENIChomozygous46058627
191034673110346732TTTG6GENIChomozygous46058628
191034809210348093CT22GENIChomozygous46058630
191034927410349275TC28GENICpossibly homozygous46058631
191035053410350535AG28GENIChomozygous46058632
191035314010353141GT22GENIChomozygous46058633
191035522410355225TTTGTG6GENICheterozygous46058634
191035522410355225TTTG6GENICheterozygous46507199
191035562510355626CCCCAGTTATTT3GENIChomozygous46058635
191035567110355672AACTCTCTCTCT3GENIChomozygous46397189
191035759810357599TC26GENIChomozygous46058636