chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X12881191288120AG18GENIChomozygous108215850
X12887931288794CT25GENIChomozygous108215853
X12890851289086AG25GENIChomozygous108215855
X12895151289516GA15GENIChomozygous108215858
X12912071291208GA32GENIChomozygous108215860
X12928051292806AG20GENIChomozygous108215862
X12933021293303GA18GENIChomozygous108215865
X12985951298596AG21GENIChomozygous108215867
X13009641300965AG28GENIChomozygous108215870
X13043961304397GA27GENIChomozygous108215873
X12946761294683AGACTCT25GENIChomozygous129715143
X12992161299217A19GENICpossibly homozygous129715145
X13045071304507C24GENIChomozygous129715146