chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7114819561114819562TC23GENIChomozygous115835542
7114819710114819711AG10GENIChomozygous115835544
7114821075114821076AT19GENIChomozygous116080132
7114822415114822416TC22GENIChomozygous115835548
7114823896114823897CA7GENIChomozygous115835558
7114826043114826044AG4GENIChomozygous115835562
7114831751114831752AG14GENIChomozygous115835566
7114833401114833402AG22GENIChomozygous115835572
7114838456114838457AT11GENIChomozygous116080136
7114839050114839051TC24GENIChomozygous115835590
7114839318114839319AG13GENIChomozygous116080138
7114840116114840117AC12GENIChomozygous115835602
7114844746114844747AG8GENIChomozygous115835608
7114845647114845648CA21GENIChomozygous116080139
7114845671114845672TC14GENIChomozygous116080140
7114851118114851119TC17GENIChomozygous116080141
7114855437114855438GA8GENIChomozygous115835610
7114859571114859572CT20GENIChomozygous116080142
7114861045114861046TC15GENIChomozygous115835616
7114862036114862037AG21GENIChomozygous115835620
7114866925114866926CT20GENIChomozygous116080143
7114869999114870000CT11GENIChomozygous116080144
7114870899114870900TA18GENIChomozygous116080145
7114872384114872385AC18GENIChomozygous116080146
7114872877114872878GA14GENIChomozygous116080147
7114876892114876893TC32GENIChomozygous115835632
7114879257114879258TG25GENIChomozygous116080148
7114886823114886824GA15GENIChomozygous116080149