chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108722578387225784CT14GENIChomozygous116898785
108722638287226383TC26GENIChomozygous116898787
108722877787228778TA9GENIChomozygous116898789
108722989687229897GC29GENIChomozygous116898793
108723041087230411TC7GENIChomozygous116669476
108723218987232190GC8GENIChomozygous116669490
108723324387233244GA32GENIChomozygous116898795
108723388587233886CT17GENIChomozygous116669496
108723390087233901GT14GENIChomozygous116669498
108723409087234091AG8GENIChomozygous116669500
108723426087234261TC13GENIChomozygous116669502
108723452187234522CT10GENIChomozygous116669504
108723453987234540GA8GENIChomozygous116669506
108723481587234816GA25GENIChomozygous116669508
108723482487234825AT23GENIChomozygous116817487
108723486487234865AG17GENIChomozygous116669510
108723532487235325CT14GENIChomozygous116817489
108723544087235441CT21GENIChomozygous116817491
108723545187235452TA18GENIChomozygous116669512
108723559687235597AG17GENIChomozygous116669514
108723612887236129AC18GENIChomozygous116669518
108723647687236477GA12GENIChomozygous116669522
108723650987236510CA8GENIChomozygous116669524
108723655387236554AG9GENIChomozygous116669526
108723675487236755CT26GENIChomozygous116669528
108723744787237448CT23GENIChomozygous116817493
108723764987237650CT29GENIChomozygous116817495
108723766387237664TC31GENIChomozygous116669530
108723781187237812CT16GENIChomozygous116898799
108723798687237987CT20GENIChomozygous116669532
108723800887238009GT20GENIChomozygous116817497
108723825787238258TC27GENIChomozygous116669534