chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3147714175147714176AC5GENIChomozygous119652192
3147716511147716512AT14GENIChomozygous112186144
3147719639147719640CT32GENIChomozygous112186145
3147721896147721897TC26GENIChomozygous112186146
3147723395147723396TC14GENIChomozygous112186147
3147723401147723402AG14GENIChomozygous112186148
3147724357147724358AG22GENIChomozygous112186149
3147725102147725103GC22GENIChomozygous111768338
3147725130147725131GA28GENICpossibly homozygous111768340
3147725175147725176GC24GENIChomozygous111768342
3147725599147725600TC15GENIChomozygous112186152
3147728354147728355GA31GENIChomozygous112186153
3147728774147728775GA25GENIChomozygous112186154
3147730217147730218TG17GENIChomozygous112186155
3147730921147730922AC19GENICheterozygous119704678
3147730946147730947AT30GENIChomozygous119685933
3147730947147730948TC30GENIChomozygous119685934
3147734195147734196AG35GENIChomozygous112186159
3147735559147735560AC23GENIChomozygous112186160
3147738995147738996GA7GENIChomozygous112186161
3147743784147743785AC24GENIChomozygous112186163
3147744184147744185CA32GENIChomozygous112186164
3147746132147746133TC16GENIChomozygous112186165
3147748992147748993TC29GENIChomozygous112186166
3147749166147749167AG29GENIChomozygous112186167
3147750215147750216TC28GENIChomozygous112186168
3147750734147750735GT12GENIChomozygous112186169
3147755257147755258AG30GENIChomozygous112186170
3147757270147757271TG19GENIChomozygous112186171