chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107248684772486848TC13GENIChomozygous116632677
107248698772486988GA18GENIChomozygous116632679
107248737472487375GT18GENIChomozygous116632683
107248829672488297CT17GENIChomozygous116632685
107248845472488455CT14GENIChomozygous116632687
107248851472488515GA10GENIChomozygous117084573
107248859272488593AC8GENIChomozygous116632689
107248874172488742AG13GENIChomozygous117084575
107248884372488844AG15GENIChomozygous116632691
107248947972489480GA21GENIChomozygous117084577
107248953472489535AG25GENIChomozygous117084579
107249010272490103TG24GENIChomozygous117084581
107249014072490141AG20GENIChomozygous117084583
107249025572490256TC22GENIChomozygous116632693
107249071972490720CT15GENIChomozygous117084585
107249082472490825CT18GENIChomozygous117084587
107249111672491117AG15GENIChomozygous117084589
107249179172491792GA17GENIChomozygous117084591
107249186372491864AG11GENIChomozygous116632699
107249306272493063GA13GENIChomozygous117084593
107249313072493131GT8GENIChomozygous117084595
107249335772493358CT17GENIChomozygous117084597
107249370072493701TC13GENIChomozygous117084599
107249378772493788TC22GENIChomozygous116632705
107249383672493837AG20GENIChomozygous116632707
107249409872494099AG27GENIChomozygous117084600
107249411272494113TC23GENIChomozygous117084602
107249435172494352GA10GENIChomozygous117084604
107249439172494392TC14GENIChomozygous117084606
107249447972494480TC19GENIChomozygous117084608
107249456772494568AG8GENIChomozygous117084610
107249556472495565AG18GENIChomozygous117084612
107249603972496040AC12GENIChomozygous117084614
107249629972496300CT12GENIChomozygous117084616
107249647372496474GA15GENIChomozygous116632713
107249658372496584TA17GENIChomozygous116632715
107249690172496902CT12GENIChomozygous116632717