chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1252537663252537664A20GENIChomozygous127504123
1252537783252537783G7GENIChomozygous127504124
1252539372252539373CT23GENIChomozygous109210146
1252540931252540932CT12GENIChomozygous120603873
1252538706252538707TC20GENIChomozygous108612194
1252540204252540205TC23GENIChomozygous108612196
1252539070252539071AG16GENIChomozygous120603869
1252540676252540677TC16GENIChomozygous120603871
1252541014252541015AG14GENIChomozygous108612199
1252541319252541320CT17GENIChomozygous120603875
1252541510252541511CT16GENIChomozygous108612200
1252541966252541967AG20GENIChomozygous108612202
1252542650252542654TTTT24GENIChomozygous127504125
1252542659252542660GA25GENIChomozygous108612207
1252542660252542661TC25GENIChomozygous108612208
1252542661252542662GA25GENIChomozygous108612209
1252543069252543070TC11GENIChomozygous108612210
1252543222252543223TC17GENIChomozygous108612211
1252543419252543420CT24GENIChomozygous120603877
1252543678252543679TA20GENIChomozygous120603879
1252543777252543778AG25GENIChomozygous108612212
1252543912252543913CT16GENIChomozygous120603881
1252546715252546716CT19GENIChomozygous108612215
1252547157252547158TC17GENIChomozygous120603883
1252547256252547257AG14GENIChomozygous108612217
1252548540252548540A17GENIChomozygous127504131
1252548822252548823TA22GENIChomozygous108612220
1252549733252549739CATTTC13GENIChomozygous127504132
1252546505252546507TT12GENIChomozygous131266398
1252546508252546530TTATTATTATTATTATTATTAT12GENIChomozygous131266399