chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261301676261301677GA26GENIChomozygous109025965
1261302618261302619GT23GENIChomozygous109025966
1261304622261304623GA38GENIChomozygous108629282
1261309265261309266CT19GENIChomozygous109025967
1261309656261309657TC15GENIChomozygous109025968
1261309686261309687TC18GENIChomozygous109025969
1261311281261311282AC29GENIChomozygous108629298
1261312557261312558TC25GENIChomozygous108629300
1261313651261313652CT31GENIChomozygous109025970
1261315423261315424GA28GENICpossibly homozygous109025971
1261316342261316343CG32GENICpossibly homozygous109025973
1261316487261316488CT22GENIChomozygous109025974
1261316958261316959GT20GENIChomozygous108629305
1261317226261317227AG20GENIChomozygous108629306
1261317442261317443GC19GENIChomozygous109025975
1261317678261317679CT23GENIChomozygous109025976
1261319682261319683GA19GENIChomozygous109025977