chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135537929135537930GA18GENIChomozygous114018123
5135538098135538099AG18GENIChomozygous114018124
5135538264135538265TC33GENIChomozygous114018125
5135539644135539645TA30GENIChomozygous114018126
5135540816135540817TC27GENIChomozygous114018128
5135540951135540952CT30GENIChomozygous114018129
5135541461135541462CT21GENIChomozygous114018130
5135541784135541785AG10GENIChomozygous114018131
5135541882135541883CT12GENIChomozygous114018132
5135542961135542962GA25GENIChomozygous114018135
5135544187135544188GT14GENIChomozygous114018139
5135544316135544317AG12GENIChomozygous114018140
5135544343135544344AG13GENIChomozygous114018141
5135544889135544890AG24GENIChomozygous114018142
5135545269135545270CT9GENIChomozygous114018144
5135546920135546921TC20GENIChomozygous114144582
5135547274135547275TC32GENIChomozygous114018146
5135548228135548229AT20GENIChomozygous114018149
5135548368135548369GC19GENIChomozygous114018150
5135548412135548413CA12GENIChomozygous114018151
5135548550135548551GA20GENIChomozygous114018152
5135548774135548775AC24GENIChomozygous114018153
5135549686135549687AG20GENIChomozygous114018159
5135550212135550213GT16GENIChomozygous114018160
5135550214135550215GA15GENIChomozygous114018161
5135550992135550993TC10GENIChomozygous114018163
5135551026135551027GA14GENIChomozygous114018164
5135551032135551033AC12GENIChomozygous114018165
5135551456135551457TG26GENIChomozygous114018166
5135551593135551594CG31GENIChomozygous114018167