chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96376999963770000AG34GENIChomozygous68455281
96377184463771845GA21GENIChomozygous68455284
96377270063772701AG32GENIChomozygous68455287
96377313663773137CT32GENIChomozygous68455290
96377385563773856AG26GENIChomozygous68455292
96377394563773946TG26GENIChomozygous68455295
96377447863774479TC26GENIChomozygous68455298
96377496563774966TG27GENIChomozygous68455301
96377666563776666CT22GENIChomozygous68455304
96377714363777144TA29GENICpossibly homozygous68455307
96377777763777778GA23GENIChomozygous68455313
96377778163777782AG23GENIChomozygous68455316
96377848763778488GA38GENIChomozygous68455319
96377924863779249GT23GENIChomozygous68455322
96377955063779551AG24GENIChomozygous68455324
96378021463780215AG13GENIChomozygous68455327
96378304963783050AC24GENIChomozygous68455330
96378554563785546AG27GENIChomozygous68455332
96378809463788095GA20GENIChomozygous68455335
96378824963788250TA22GENIChomozygous68455338
96378975363789754AG19GENIChomozygous68455341
96378979863789799GA19GENIChomozygous68455344