chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264060117264060118AG68GENIChomozygous978059129
1264061026264061027AG36GENIChomozygous978059130
1264061283264061284GA78GENIChomozygous978059131
1264061466264061467TC39GENIChomozygous978059132
1264062297264062298TC42GENIChomozygous978059133
1264062501264062502AG56GENIChomozygous978059134
1264062532264062533CT60GENIChomozygous978059135
1264062601264062602CT44GENIChomozygous978059136
1264062947264062948GA38GENIChomozygous978059137
1264064003264064004AG27GENIChomozygous978059138
1264064234264064235TG32GENIChomozygous978059139
1264064641264064642CT38GENIChomozygous978059140
1264064988264064989AG40GENIChomozygous978059141
1264065424264065425CA32GENIChomozygous978059142
1264065813264065814AT47GENIChomozygous978059143
1264066832264066833GA64GENICpossibly homozygous978059144
1264066841264066842CT67GENICpossibly homozygous978059145
1264067060264067061TC27GENIChomozygous978059146
1264067293264067294AG19GENIChomozygous978059147
1264069621264069622CT22GENIChomozygous978059148
1264069737264069738CT41GENIChomozygous978059149
1264069747264069748GA40GENIChomozygous978059150
1264070790264070791CT45GENICpossibly homozygous978059151
1264071386264071387GA25GENIChomozygous978059152
1264071462264071463CA36GENIChomozygous978059153