chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109410430594104306AG28GENIChomozygous51746290
109410549594105497AA--9GENICpossibly homozygous51548071
109410549694105497A-9GENICheterozygous51548072
109410657694106577GA21GENIChomozygous51746292
109410666694106667CT27GENIChomozygous51746294
109410914894109149CT25GENIChomozygous51548075
109410926894109269CA24GENIChomozygous51746296
109410997794109978CA30GENIChomozygous51746298
109411075794110758CT38GENIChomozygous51746300
109411086794110868AT26GENIChomozygous51548077
109411128894111289TG20GENIChomozygous51548079
109411135794111358TC24GENIChomozygous51746302
109411202594112026CA25GENIChomozygous51746304
109411215294112153AG31GENIChomozygous51548082
109411423294114233AC31GENIChomozygous51746306
109411438694114387TC25GENIChomozygous51746308
109411461594114616GA31GENIChomozygous51746310
109411516994115170CCAAAA15GENIChomozygous51746312
109411573694115744TGTGTGTG--------12GENICheterozygous51746314
109411591594115916CA35GENIChomozygous51746316
109411679694116797GA36GENIChomozygous51548091
109411705594117056GC30GENIChomozygous51548092
109412033494120336AA--25GENICpossibly homozygous51746318
109412033594120336A-25GENICheterozygous51548094
109412273294122733AAAAAT2GENIChomozygous51746320
109412561394125614T-13GENIChomozygous51548098
109411248094112482CA--12GENICheterozygous52732878
109411573494115744TGTGTGTGTG----------12GENICheterozygous52399017
109412353494123542TGTGTGTG--------2GENIChomozygous52399019