chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1217020245217020246AC22GENIChomozygous108536539
1217020825217020826AG24GENIChomozygous108992493
1217020852217020853GA27GENIChomozygous108536540
1217021048217021049AG35GENIChomozygous108536541
1217021612217021613GA29GENIChomozygous108536542
1217021688217021689GA38GENIChomozygous109193672
1217021861217021862GT31GENIChomozygous108536543
1217023556217023557AG9GENIChomozygous108536544
1217023571217023572AG9GENIChomozygous108536545
1217024452217024453TC23GENIChomozygous108536548
1217024826217024827GA32GENIChomozygous109193678
1217025032217025033AG20GENIChomozygous108536550
1217025176217025177CT20GENIChomozygous109193680
1217026725217026726AG23GENIChomozygous108536553
1217027134217027135GA20GENIChomozygous108992497
1217027487217027488GT33GENIChomozygous109193684
1217027828217027829AG33GENIChomozygous109193686
1217027844217027845GA35GENIChomozygous108536554
1217028768217028769AG27GENIChomozygous108536556
1217029411217029412TC35GENIChomozygous108536557
1217029771217029772GA44GENIChomozygous108536558
1217030904217030905AG19GENIChomozygous108536560
1217031148217031149GC16GENICpossibly homozygous108536561
1217031195217031196GA9GENIChomozygous120512118
1217032514217032515AC25GENIChomozygous108536563
1217032519217032520CT25GENIChomozygous108536564
1217032554217032555CT22GENIChomozygous108536565
1217032605217032606CT24GENIChomozygous108536566
1217032606217032607AG22GENIChomozygous108536567
1217032974217032975TC18GENIChomozygous108536568
1217033224217033225CG19GENIChomozygous108536570
1217033305217033306TG26GENIChomozygous108536571
1217033324217033325TC22GENIChomozygous108536572
1217033449217033450GT19GENIChomozygous108536573
1217033507217033508GA23GENIChomozygous108536574
1217033815217033816CG19GENIChomozygous108536575
1217034082217034083GA22GENIChomozygous108536576
1217034168217034169GA26GENIChomozygous108536577
1217034194217034195CT28GENIChomozygous108536578
1217034428217034429TC30GENIChomozygous109193688
1217034518217034519GA29GENIChomozygous108536579