chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11662260416622605CT12GENICheterozygous62610224
11662365316623654TG14GENICpossibly homozygous62668311
11662397716623978TC15GENIChomozygous62288751
11662401716624018TA11GENIChomozygous62668312
11662418416624185CT22GENIChomozygous62668313
11662443816624439CCCTTGACTCTAA2GENIChomozygous62668314
11662559716625598AG17GENIChomozygous62288754
11662588816625889TC10GENIChomozygous62668315
11662592016625921TC10GENIChomozygous62668316
11662593416625935CT6GENIChomozygous62668317
11662594016625941TC5GENIChomozygous62668318
11662611416626115TA8GENIChomozygous62288756
11662616216626163GA11GENIChomozygous62668319
11662619216626193AG12GENIChomozygous62288757