chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109410430594104306AG25GENIChomozygous51746290
109410549594105497AA--13GENICheterozygous51548071
109410549694105497A-13GENICheterozygous51548072
109410657694106577GA33GENIChomozygous51746292
109410666694106667CT31GENIChomozygous51746294
109410914894109149CT29GENIChomozygous51548075
109410926894109269CA23GENIChomozygous51746296
109410997794109978CA40GENIChomozygous51746298
109411075794110758CT27GENIChomozygous51746300
109411086794110868AT25GENIChomozygous51548077
109411128894111289TG27GENIChomozygous51548079
109411135794111358TC28GENIChomozygous51746302
109411202594112026CA26GENIChomozygous51746304
109411215294112153AG19GENIChomozygous51548082
109411423294114233AC25GENIChomozygous51746306
109411438694114387TC34GENIChomozygous51746308
109411461594114616GA28GENIChomozygous51746310
109411516994115170CCAAAA3GENIChomozygous51746312
109411573694115744TGTGTGTG--------12GENIChomozygous51746314
109411591594115916CA30GENIChomozygous51746316
109411679694116797GA29GENICpossibly homozygous51548091
109411705594117056GC21GENIChomozygous51548092
109412033494120336AA--16GENIChomozygous51746318
109412561394125614T-3GENIChomozygous51548098
109412918494129187TAG---13GENICheterozygous51746322
109413226994132270CCT15GENICheterozygous51548101
109411518794115188TA12GENIChomozygous51998077