chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3147714175147714176AC32GENIChomozygous119652192
3147716511147716512AT10GENIChomozygous112186144
3147719639147719640CT20GENIChomozygous112186145
3147721896147721897TC20GENIChomozygous112186146
3147723395147723396TC21GENIChomozygous112186147
3147723401147723402AG21GENIChomozygous112186148
3147724357147724358AG47GENIChomozygous112186149
3147725102147725103GC25GENIChomozygous111768338
3147725130147725131GA24GENIChomozygous111768340
3147725175147725176GC40GENIChomozygous111768342
3147725599147725600TC33GENIChomozygous112186152
3147728354147728355GA21GENIChomozygous112186153
3147728774147728775GA35GENIChomozygous112186154
3147730217147730218TG13GENIChomozygous112186155
3147734195147734196AG38GENIChomozygous112186159
3147738995147738996GA34GENIChomozygous112186161
3147743784147743785AC56GENIChomozygous112186163
3147744184147744185CA22GENIChomozygous112186164
3147746132147746133TC54GENIChomozygous112186165
3147748992147748993TC37GENIChomozygous112186166
3147749166147749167AG29GENICpossibly homozygous112186167
3147750215147750216TC33GENIChomozygous112186168
3147755257147755258AG35GENIChomozygous112186170
3147757270147757271TG36GENIChomozygous112186171