chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3147716511147716512AT2GENIChomozygous112186144
3147719639147719640CT17GENIChomozygous112186145
3147721896147721897TC16GENIChomozygous112186146
3147723395147723396TC25GENIChomozygous112186147
3147723401147723402AG24GENIChomozygous112186148
3147724357147724358AG19GENIChomozygous112186149
3147724895147724896GA10GENICpossibly homozygous112186150
3147724938147724939TC10GENICpossibly homozygous112186151
3147725102147725103GC27GENIChomozygous111768338
3147725130147725131GA23GENIChomozygous111768340
3147725175147725176GC21GENIChomozygous111768342
3147725599147725600TC13GENIChomozygous112186152
3147728354147728355GA19GENIChomozygous112186153
3147728774147728775GA17GENIChomozygous112186154
3147730217147730218TG14GENIChomozygous112186155
3147731607147731608CT14GENICpossibly homozygous112186156
3147734195147734196AG31GENIChomozygous112186159
3147735559147735560AC29GENIChomozygous112186160
3147738995147738996GA24GENIChomozygous112186161
3147740230147740231GA10GENIChomozygous112186162
3147743366147743367AC18GENIChomozygous112257199
3147743784147743785AC39GENIChomozygous112186163
3147744184147744185CA20GENIChomozygous112186164
3147746132147746133TC26GENIChomozygous112186165
3147748992147748993TC41GENIChomozygous112186166
3147749166147749167AG23GENIChomozygous112186167
3147750215147750216TC25GENIChomozygous112186168
3147750734147750735GT14GENIChomozygous112186169
3147755257147755258AG21GENIChomozygous112186170
3147757270147757271TG17GENIChomozygous112186171