chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8111694971111694972GA26GENIChomozygous958558580
8111695985111695986CT22GENIChomozygous958558581
8111696079111696080CT21GENIChomozygous958558582
8111696890111696891CT18GENIChomozygous958558583
8111698989111698990GA23GENIChomozygous958558584
8111699238111699239GA24GENIChomozygous958558585
8111700389111700390CT21GENIChomozygous958558586
8111700490111700491TC32GENIChomozygous958558587
8111700575111700576TC34GENIChomozygous958558588
8111701225111701226TC34GENIChomozygous958558589
8111701419111701420AG35GENIChomozygous958558590
8111701475111701476AG30GENIChomozygous958558591
8111701800111701801CT22GENIChomozygous958558592
8111702381111702382AG16GENIChomozygous958558593
8111702844111702845AT12GENIChomozygous958558594
8111702865111702866CT12GENIChomozygous958558595
8111702954111702955CA13GENIChomozygous958558596
8111703036111703037GA19GENIChomozygous958558597
8111703159111703160GA20GENIChomozygous958558598
8111703220111703221GA18GENIChomozygous958558599
8111703564111703565GA18GENIChomozygous958558600
8111703637111703638GC23GENIChomozygous958558601
8111703761111703762AT18GENIChomozygous958558602
8111703862111703863CT13GENIChomozygous958558603
8111704388111704389TG16GENIChomozygous958558604
8111704515111704516GA30GENIChomozygous958558605
8111704774111704775CT17GENIChomozygous958558606
8111706076111706077GC33GENICpossibly homozygous958558607
8111706234111706235GA34GENIChomozygous958558608
8111708481111708482TC32GENIChomozygous958558609
8111709172111709173GC15GENIChomozygous958558610
8111712865111712866CA41GENIChomozygous958558611
8111712963111712964AG35GENIChomozygous958558612
8111713977111713978AG18GENIChomozygous958558613
8111713989111713990CG21GENIChomozygous958558614
8111719885111719886AG16GENIChomozygous958558615