chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108287094482870945GC28GENIChomozygous813202203
108287094582870946TC30GENIChomozygous813202204
108287095082870951AC32GENICpossibly homozygous813202205
108287096182870962GC31GENIChomozygous813202206
108287096382870964GC31GENIChomozygous813202207
108287096982870970TC31GENIChomozygous813202208
108287097182870972TC31GENIChomozygous813202209
108287118782871188CT2GENIChomozygous813202210
108287119082871191CG2GENIChomozygous813202211
108287119982871200CT6GENIChomozygous813202212
108287120482871205CT6GENIChomozygous813202213