chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109410430594104306AG67GENIChomozygous51746290
109410549594105497AA--14GENICpossibly homozygous51548071
109410549694105497A-14GENICheterozygous51548072
109410657694106577GA51GENIChomozygous51746292
109410666694106667CT48GENIChomozygous51746294
109410914894109149CT35GENIChomozygous51548075
109410926894109269CA14GENIChomozygous51746296
109410997794109978CA44GENIChomozygous51746298
109411075794110758CT32GENIChomozygous51746300
109411086794110868AT77GENIChomozygous51548077
109411128894111289TG51GENIChomozygous51548079
109411135794111358TC52GENICpossibly homozygous51746302
109411202594112026CA49GENIChomozygous51746304
109411215294112153AG41GENIChomozygous51548082
109411423294114233AC45GENIChomozygous51746306
109411438694114387TC52GENIChomozygous51746308
109411461594114616GA34GENIChomozygous51746310
109411516994115170CCAAAA4GENIChomozygous51746312
109411573494115744TGTGTGTGTG----------16GENICheterozygous52399017
109411573694115744TGTGTGTG--------16GENICheterozygous51746314
109411573894115744TGTGTG------16GENICheterozygous52510803
109411591594115916CA35GENIChomozygous51746316
109411679694116797GA50GENIChomozygous51548091
109411705594117056GC24GENIChomozygous51548092
109412033494120336AA--16GENICpossibly homozygous51746318
109412273294122733AAAAAT1GENIChomozygous51746320
109412353494123542TGTGTGTG--------9GENICheterozygous52399019
109412561394125614T-1GENIChomozygous51548098