chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7114819561114819562TC30GENIChomozygous115835542
7114819710114819711AG23GENIChomozygous115835544
7114821075114821076AT16GENIChomozygous116080132
7114822415114822416TC37GENIChomozygous115835548
7114823896114823897CA28GENIChomozygous115835558
7114826043114826044AG25GENIChomozygous115835562
7114831751114831752AG20GENIChomozygous115835566
7114833401114833402AG29GENIChomozygous115835572
7114838456114838457AT35GENIChomozygous116080136
7114839050114839051TC34GENIChomozygous115835590
7114840116114840117AC18GENIChomozygous115835602
7114844746114844747AG20GENIChomozygous115835608
7114845647114845648CA36GENIChomozygous116080139
7114845671114845672TC29GENIChomozygous116080140
7114851118114851119TC15GENIChomozygous116080141
7114855437114855438GA29GENIChomozygous115835610
7114859571114859572CT36GENIChomozygous116080142
7114861045114861046TC34GENIChomozygous115835616
7114862036114862037AG35GENIChomozygous115835620
7114866925114866926CT20GENIChomozygous116080143
7114869999114870000CT28GENIChomozygous116080144
7114870899114870900TA27GENIChomozygous116080145
7114872384114872385AC27GENIChomozygous116080146
7114872877114872878GA25GENIChomozygous116080147
7114876892114876893TC23GENIChomozygous115835632
7114879257114879258TG24GENIChomozygous116080148
7114880256114880257TA33GENIChomozygous115835634
7114881634114881635TC38GENIChomozygous115835640
7114886823114886824GA19GENIChomozygous116080149