chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139022421390224214T12GENIChomozygous67046728
139022528690225287GA6GENIChomozygous66374529
139022542290225423GA9GENIChomozygous66374531
139022576890225769CT6GENIChomozygous66374537
139022640290226403TC19GENIChomozygous66374541
139022695290226953TG18GENIChomozygous66374543
139022750090227501GA25GENIChomozygous66374545
139022772190227722GA21GENIChomozygous66374547
139022849990228500CT19GENIChomozygous66374549
139022961390229614CA14GENIChomozygous66374551
139023067990230680CT23GENIChomozygous66374553
139023042290230423C14GENIChomozygous66878902
139023473690234737T11GENICheterozygous66878905
139023544290235443GT11GENIChomozygous66374559
139023652890236529AT18GENIChomozygous66374561
139023667190236672GA5GENIChomozygous66374563
139023770490237705AG27GENIChomozygous66374565
139023832990238330CA20GENIChomozygous66374567
139023918490239185CT21GENIChomozygous66374569
139023750790237507CAGAG8GENICheterozygous67476091