chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108286463082864631CT64GENIChomozygous116898557
108286490782864908TC39GENICpossibly homozygous116812792
108287094482870945GC30GENIChomozygous116812826
108287094582870946TC29GENIChomozygous116812828
108287095082870951AC32GENIChomozygous116812830
108287096182870962GC25GENIChomozygous117257834
108287096382870964GC26GENIChomozygous117104905
108287096982870970TC25GENIChomozygous117257836
108287097182870972TC25GENIChomozygous117257838
108287119082871191CG3GENIChomozygous117152289
108287119982871200CT16GENIChomozygous116980621
108287120482871205CT15GENIChomozygous117152290
108287257582872576GC44GENICheterozygous116812832
108287261182872612GA37GENICheterozygous118125626