chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135536516135536517CT35GENIChomozygous114018118
5135536529135536530GC35GENIChomozygous114018119
5135536707135536708TC52GENIChomozygous114018120
5135537929135537930GA31GENIChomozygous114018123
5135538098135538099AG37GENIChomozygous114018124
5135538264135538265TC46GENIChomozygous114018125
5135539644135539645TA26GENIChomozygous114018126
5135540816135540817TC30GENIChomozygous114018128
5135540951135540952CT42GENIChomozygous114018129
5135541461135541462CT31GENIChomozygous114018130
5135541784135541785AG23GENIChomozygous114018131
5135541882135541883CT25GENIChomozygous114018132
5135542180135542181AC35GENIChomozygous114018134
5135542961135542962GA17GENIChomozygous114018135
5135543680135543681GT26GENIChomozygous114018136
5135544064135544065CT40GENIChomozygous114018138
5135544187135544188GT42GENIChomozygous114018139
5135544316135544317AG29GENIChomozygous114018140
5135544343135544344AG26GENIChomozygous114018141
5135544889135544890AG28GENIChomozygous114018142
5135545269135545270CT31GENIChomozygous114018144
5135547274135547275TC37GENICpossibly homozygous114018146
5135547493135547494TA33GENIChomozygous114018147
5135548228135548229AT42GENIChomozygous114018149
5135548368135548369GC26GENIChomozygous114018150
5135548412135548413CA28GENIChomozygous114018151
5135548550135548551GA28GENIChomozygous114018152
5135548774135548775AC18GENIChomozygous114018153
5135550212135550213GT35GENIChomozygous114018160
5135550214135550215GA35GENIChomozygous114018161
5135550992135550993TC29GENIChomozygous114018163
5135551026135551027GA29GENIChomozygous114018164
5135551032135551033AC27GENIChomozygous114018165
5135551456135551457TG51GENIChomozygous114018166
5135551593135551594CG44GENIChomozygous114018167
5135551950135551951CT15GENIChomozygous118845739