chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1143632446143632447CCT18GENIChomozygous61675242
1143632835143632836GGGT8GENICheterozygous62162898
1143632835143632836GGGTGT8GENICheterozygous62162900
1143633428143633432GTGT----7GENIChomozygous62162902
1143636500143636501GC28GENIChomozygous60878162
1143636635143636636AG22GENIChomozygous60878163
1143637327143637328AG35GENIChomozygous60878164
1143638171143638172GT24GENIChomozygous60878165
1143638739143638740TC31GENIChomozygous60878166
1143639607143639608GT33GENIChomozygous60878167
1143639723143639724CA14GENIChomozygous60878168
1143639768143639769CT17GENIChomozygous60878169
1143639924143639925GGTGTTT10GENIChomozygous60878170
1143640457143640458TA29GENIChomozygous60878171
1143640743143640744GA25GENIChomozygous60878172
1143641097143641098GC21GENIChomozygous60878173
1143641293143641294GA7GENIChomozygous60878174
1143641811143641812GA18GENIChomozygous60878175
1143643209143643210TC30GENIChomozygous60878177
1143643351143643352TC22GENIChomozygous60878178
1143643560143643561TC30GENIChomozygous60878179
1143643612143643613TC26GENIChomozygous60878180
1143643771143643772TC32GENIChomozygous60878181
1143643805143643806GA29GENIChomozygous60878182
1143643937143643938CT18GENIChomozygous60878183
1143643989143643990TTTTAA6GENIChomozygous61675252
1143644346143644347TTA16GENIChomozygous60878184
1143646194143646195GA19GENIChomozygous61675254
1143644785143644786GA19GENIChomozygous61903013
1143646236143646237CCA19GENIChomozygous61903014
1143646237143646238CCCCCCA19GENIChomozygous61903015