chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X12881191288120AG22GENIChomozygous108215850
X12887931288794CT28GENIChomozygous108215853
X12890851289086AG32GENIChomozygous108215855
X12895151289516GA36GENIChomozygous108215858
X12912071291208GA34GENIChomozygous108215860
X12928051292806AG30GENIChomozygous108215862
X12933021293303GA16GENIChomozygous108215865
X12957481295756GGATGGAT7GENIChomozygous132247004
X12985951298596AG34GENIChomozygous108215867
X13009641300965AG30GENIChomozygous108215870
X13043961304397GA31GENIChomozygous108215873
X12946761294683AGACTCT37GENIChomozygous129715143
X12992161299217A36GENICpossibly homozygous129715145
X13045071304507C26GENIChomozygous129715146
X12988321298833T28GENICheterozygous132926911