chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109410430594104306AG36GENIChomozygous51746290
109410549694105497A-11GENIChomozygous51548072
109410657694106577GA36GENIChomozygous51746292
109410666694106667CT22GENIChomozygous51746294
109410914894109149CT37GENIChomozygous51548075
109410926894109269CA12GENIChomozygous51746296
109410997794109978CA23GENIChomozygous51746298
109411075794110758CT35GENIChomozygous51746300
109411086794110868AT40GENIChomozygous51548077
109411128894111289TG24GENIChomozygous51548079
109411135794111358TC27GENIChomozygous51746302
109411202594112026CA45GENIChomozygous51746304
109411215294112153AG29GENIChomozygous51548082
109411423294114233AC18GENIChomozygous51746306
109411438694114387TC31GENIChomozygous51746308
109411461594114616GA24GENIChomozygous51746310
109411516994115170CCAAAA6GENIChomozygous51746312
109411573694115744TGTGTGTG--------4GENICheterozygous51746314
109411591594115916CA34GENIChomozygous51746316
109411679694116797GA37GENIChomozygous51548091
109411705594117056GC24GENIChomozygous51548092
109412033494120336AA--18GENICpossibly homozygous51746318
109412033594120336A-18GENICheterozygous51548094
109412113994121140T-3GENICheterozygous51548095
109412561394125614T-2GENIChomozygous51548098
109413226994132270CCTT9GENICheterozygous51548102