chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199155650199155651AG22GENIChomozygous61043327
1199156086199156087TC14GENIChomozygous61043328
1199158385199158386GA16GENIChomozygous61043332
1199158394199158395AC14GENIChomozygous61043333
1199160153199160154GA15GENIChomozygous61043335
1199160184199160185CT18GENIChomozygous61043336
1199160375199160376CCAT12GENIChomozygous61043337
1199160541199160542TTA8GENIChomozygous61043341
1199160543199160544TA8GENIChomozygous61043342
1199161452199161453AG22GENIChomozygous61043343
1199163392199163393GA15GENIChomozygous61043344
1199163626199163627C-11GENIChomozygous61043346
1199164480199164481TC20GENIChomozygous61043347
1199164607199164608AACCTGCTTTTCATT10GENIChomozygous61043348
1199164978199164979GA24GENIChomozygous61043349
1199165051199165052GA16GENIChomozygous61043350
1199167792199167793GA14GENIChomozygous61043351
1199167828199167829T-14GENIChomozygous61043352