chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1200037846200037847CG19GENICpossibly homozygous806050138
1200082399200082400CT16GENIChomozygous806050139
1200082407200082408TC16GENIChomozygous806050140
1200091092200091093CT22GENIChomozygous806050141
1200091436200091437CT56GENIChomozygous806050142
1200092336200092337TC63GENIChomozygous806050143
1200094808200094809GT39GENICheterozygous806050144
1200094844200094845GT46GENICheterozygous806050145
1200098783200098784CA27GENIChomozygous806050146
1200101883200101884TA38GENIChomozygous806050147
1200102337200102338GC23GENIChomozygous806050148
1200102768200102769AG43GENIChomozygous806050149
1200103259200103260AG52GENIChomozygous806050150
1200103287200103288AG47GENIChomozygous806050151
1200103734200103735CA51GENIChomozygous806050152
1200105292200105293GA30GENIChomozygous806050153
1200105691200105692TC29GENICpossibly homozygous806050154
1200107695200107696TC62GENIChomozygous806050155
1200108550200108551GA45GENIChomozygous806050156
1200111121200111122CT50GENIChomozygous806050157
1200111280200111281GA44GENIChomozygous806050158
1200111928200111929TC57GENIChomozygous806050159
1200112449200112450AG46GENIChomozygous806050160
1200112829200112830AG29GENIChomozygous806050161
1200114822200114823GA53GENIChomozygous806050162
1200115095200115096GC42GENIChomozygous806050163
1200115478200115479TC46GENIChomozygous806050164
1200116078200116079GA47GENIChomozygous806050165
1200116373200116374GA56GENIChomozygous806050166