chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6111477209111477210GC23GENIChomozygous785508107
6111477596111477597TG25GENIChomozygous785508108
6111477775111477776AG28GENIChomozygous785508109
6111477962111477963GC26GENIChomozygous785508110
6111478157111478158GT21GENIChomozygous785508111
6111478175111478176GA24GENIChomozygous785508112
6111478376111478377TA13GENIChomozygous785508113
6111478447111478448CT30GENIChomozygous785508114
6111478449111478450GA29GENIChomozygous785508115
6111478551111478552CT29GENIChomozygous785508116
6111478766111478767AG26GENIChomozygous785508117
6111478980111478981CT21GENIChomozygous785508118
6111479360111479361CT15GENIChomozygous785508119
6111479664111479665AG23GENIChomozygous785508120
6111479806111479807GA10GENIChomozygous785508121
6111480069111480070CT29GENIChomozygous785508122
6111480093111480094AG32GENIChomozygous785508123
6111480357111480358CT36GENIChomozygous785508124
6111480406111480407GA38GENIChomozygous785508125
6111480449111480450GA29GENIChomozygous785508126
6111480611111480612TC23GENIChomozygous785508127
6111480630111480631TC19GENIChomozygous785508128
6111480894111480895CT31GENIChomozygous785508129
6111481514111481515GA22GENIChomozygous785508130
6111481601111481602AG21GENIChomozygous785508131
6111482451111482452GA17GENIChomozygous785508132
6111482981111482982TC21GENIChomozygous785508133
6111483352111483353AG23GENIChomozygous785508134
6111483811111483812CT21GENIChomozygous785508135
6111484855111484856GA34GENIChomozygous785508136
6111485417111485418TC30GENIChomozygous785508137
6111485509111485510AT25GENICheterozygous785508138
6111485516111485517CT23GENIChomozygous785508139
6111485625111485626AC28GENIChomozygous785508140
6111485846111485847TC32GENIChomozygous785508141
6111486035111486036GA31GENIChomozygous785508142