chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X12881191288120AG10GENIChomozygous108215850
X12887931288794CT6GENICheterozygous108215853
X12890851289086AG9GENIChomozygous108215855
X12895151289516GA8GENIChomozygous108215858
X12912071291208GA6GENIChomozygous108215860
X12928051292806AG11GENIChomozygous108215862
X12933021293303GA10GENIChomozygous108215865
X12946761294683AGACTCT13GENIChomozygous129715143
X12985951298596AG12GENIChomozygous108215867
X12992161299217A15GENIChomozygous129715145
X13009641300965AG11GENIChomozygous108215870
X13043961304397GA9GENIChomozygous108215873
X13045071304507C7GENIChomozygous129715146