chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1217019195217019196AC10GENIChomozygous108536538
1217020245217020246AC16GENIChomozygous108536539
1217020852217020853GA25GENIChomozygous108536540
1217021048217021049AG13GENIChomozygous108536541
1217021612217021613GA26GENIChomozygous108536542
1217021861217021862GT26GENIChomozygous108536543
1217023556217023557AG10GENIChomozygous108536544
1217023760217023761CG10GENIChomozygous108536546
1217024452217024453TC26GENIChomozygous108536548
1217024877217024878GC12GENIChomozygous108536549
1217025032217025033AG26GENIChomozygous108536550
1217025356217025357AG27GENIChomozygous108536551
1217026216217026217GA13GENIChomozygous108536552
1217026725217026726AG32GENIChomozygous108536553
1217027844217027845GA23GENIChomozygous108536554
1217028768217028769AG32GENIChomozygous108536556
1217029411217029412TC27GENIChomozygous108536557
1217029771217029772GA16GENIChomozygous108536558
1217029848217029849CT12GENIChomozygous108536559
1217030904217030905AG22GENIChomozygous108536560
1217031148217031149GC18GENIChomozygous108536561
1217032514217032515AC24GENIChomozygous108536563
1217032519217032520CT25GENIChomozygous108536564
1217032554217032555CT19GENIChomozygous108536565
1217032605217032606CT17GENIChomozygous108536566
1217032606217032607AG17GENIChomozygous108536567
1217032974217032975TC12GENIChomozygous108536568
1217033010217033011GA18GENIChomozygous108536569
1217033224217033225CG22GENIChomozygous108536570
1217033305217033306TG17GENIChomozygous108536571
1217033324217033325TC16GENIChomozygous108536572
1217033449217033450GT11GENIChomozygous108536573
1217033507217033508GA11GENIChomozygous108536574
1217034082217034083GA17GENIChomozygous108536576
1217034168217034169GA12GENIChomozygous108536577
1217034194217034195CT12GENIChomozygous108536578
1217034518217034519GA24GENIChomozygous108536579
1217031195217031196GA13GENIChomozygous120512118