chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71506713415067135CT17GENIChomozygous115576124
71506741515067416TC31GENIChomozygous115576125
71506756815067569TC27GENIChomozygous115576126
71506773515067736AC26GENIChomozygous115576127
71506788815067889CA17GENIChomozygous115576128
71506837615068377TG10GENIChomozygous115576129
71506873615068737CT10GENIChomozygous115576130
71506892615068927TG25GENIChomozygous115576131
71507021415070215GA26GENIChomozygous115576132
71507026315070264TC28GENIChomozygous115576133
71507060415070605TC21GENIChomozygous115576134
71507084715070848AC24GENIChomozygous115576135
71507087515070876AG28GENIChomozygous115576136
71507102415071025AG21GENIChomozygous115576137
71507105015071051AG17GENIChomozygous115576138
71507334015073341CA21GENIChomozygous115576144
71507361715073618GA9GENIChomozygous115576145
71507428915074290AT30GENIChomozygous115576146
71507452115074522AG23GENIChomozygous115576147
71507484515074846GC20GENIChomozygous115576148
71507541715075418CG21GENIChomozygous115576150
71507560015075601TC31GENIChomozygous115576151
71507578815075789TC25GENIChomozygous115576152
71507598615075987CA29GENIChomozygous115576153
71507617315076174AC20GENIChomozygous115576155
71507650515076506CG16GENIChomozygous115576159
71507681515076816TC8GENIChomozygous115576160
71507699715076998AG17GENIChomozygous115576161
71507713115077132TC20GENIChomozygous115576162
71507741715077418AG24GENIChomozygous115576164
71507785715077858AG22GENIChomozygous115576165
71507864715078648GA16GENIChomozygous115576166
71507938115079382GA19GENIChomozygous115576167