chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84012799240127993AG19GENIChomozygous116802086
84012799540127996CT18GENIChomozygous116802088
84012805940128060AG21GENIChomozygous116802090
84012845740128458GA33GENIChomozygous116802092
84013019540130196AG35GENIChomozygous116802094
84013061940130620CT27GENIChomozygous116802096
84013062940130630AG24GENIChomozygous116802098
84013093240130933GA33GENIChomozygous116802100
84013103140131032CT23GENIChomozygous116802102
84013111040131111TC26GENIChomozygous116802104
84013170140131702CT22GENIChomozygous116802108
84013180040131801GA35GENIChomozygous116802110
84013206140132062TC26GENIChomozygous116802112
84013240240132403AC21GENIChomozygous116802114
84013478140134782CT29GENIChomozygous116802132
84013487740134878CT29GENIChomozygous116802134
84013494040134941CG27GENIChomozygous116802136
84013505140135052CT26GENIChomozygous116802138
84013505340135054TA25GENIChomozygous116802140
84013569540135696GA23GENIChomozygous116802142
84013603840136039CT19GENIChomozygous116802144
84013648840136489TC25GENIChomozygous116802146
84013669240136693AG30GENIChomozygous116802148
84013688940136890TC24GENIChomozygous116802150
84013730640137307TC40GENIChomozygous116802152
84013469640134697TC28GENIChomozygous116463744