chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1499638014996381TC23GENIChomozygous108232974
X1499648514996486TC26GENIChomozygous108232976
X1499654814996549AT16GENIChomozygous108232978
X1499655914996560AG20GENIChomozygous108232980
X1500406815004069GA27GENIChomozygous108232992
X1499786014997861G19GENIChomozygous129722312
X1499787914997879TAACAGATCC19GENIChomozygous129722313
X1500113415001134AG8GENIChomozygous129722314
X1500372815003729A22GENIChomozygous129722315
X1500138115001382AT7GENIChomozygous119905693
X1500327215003273TC20GENICpossibly homozygous108439104
X1499694314996944CT25GENIChomozygous108232982
X1499756114997562AG29GENIChomozygous108232984
X1499903914999040AC21GENIChomozygous108232986
X1499924514999246AG43GENIChomozygous108232988
X1500026915000270CT22GENIChomozygous108232990
X1500422415004225AG24GENIChomozygous108232994
X1500425615004257TC28GENIChomozygous108232996
X1500428115004282G27GENIChomozygous129722316
X1500478515004785T26GENIChomozygous129722317
X1500436515004366TC32GENIChomozygous108369806
X1500466715004668CT29GENIChomozygous108369808