chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96165636461656365TA11GENIChomozygous117358630
96165719261657193AC23GENIChomozygous117358631
96165763461657635GT16GENIChomozygous117358634
96165770661657707AG29GENIChomozygous117358635
96165808461658085TC14GENIChomozygous117358636
96165825361658254TA11GENIChomozygous117358637
96165866361658664CT27GENIChomozygous117358638
96165934361659344CT22GENIChomozygous117358639
96165937861659379GA18GENIChomozygous117358640
96165976861659769GA6GENIChomozygous117358642
96166026961660270GC20GENIChomozygous117358643
96166030661660307CT20GENIChomozygous117358644
96166030961660310AC20GENIChomozygous117358645
96166205761662058TC21GENIChomozygous117358646
96166245961662460GT26GENIChomozygous117358647
96166317561663176TA16GENIChomozygous117358648
96166372461663725CT31GENIChomozygous117358649
96166403061664031CG31GENIChomozygous117358650
96166420861664209AG41GENIChomozygous117358651
96166450461664505AG15GENIChomozygous117358652
96166549661665497CA18GENIChomozygous117358656
96166623861666239CT29GENIChomozygous117358657
96166770061667701AG34GENIChomozygous117358658
96166793661667937GA8GENIChomozygous117358659
96167204061672041CT6GENIChomozygous120385708
96167204261672043CT6GENIChomozygous120385709
96167243961672440CT24GENIChomozygous117358675
96167248561672486AG28GENIChomozygous117358676
96167254061672541CT26GENIChomozygous117358677
96167279361672794GA13GENIChomozygous117358678
96167308661673087GC14GENIChomozygous117358679
96167371461673715GA25GENIChomozygous117358681
96167396661673967TC22GENIChomozygous117358682
96167438861674389GT27GENIChomozygous117358683
96167473161674732CT30GENIChomozygous117358684
96167481661674817AT22GENIChomozygous117358685
96167532561675326CT37GENIChomozygous117358687
96167582361675824AC12GENIChomozygous117570275
96167582461675825GA11GENIChomozygous117570277