chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71182846611828467GA24GENIChomozygous53789460
71182901211829013GT26GENIChomozygous53789461
71182902711829028CCG25GENIChomozygous53789462
71183045511830456TTC8GENIChomozygous53789463
71183148111831527GTGTGTGTGTGTGCGTGCGTGCGTGTGCGTGTGCGTGTGTGTGTGC----------------------------------------------10GENIChomozygous54954580
71183272211832723AT48GENIChomozygous53789468
71183321511833216AAGAGGAC29GENIChomozygous53789469
71183342411833425GGTGT26GENICheterozygous54954582
71183391611833917CT51GENIChomozygous53789470
71183456511834566TG37GENIChomozygous53789471
71183505111835052TC50GENIChomozygous53789472
71183666911836670GA29GENIChomozygous53789473
71183773511837736CT28GENIChomozygous53789474
71183949611839497AG43GENIChomozygous53789475
71184247411842475CT36GENIChomozygous53789476
71184295011842951AG61GENIChomozygous53789477
71184304711843073ATGCTGTCATGTCGTGATGTCATGTG--------------------------45GENICpossibly homozygous54884904
71184309111843092GA48GENIChomozygous53789481
71184363311843634CA27GENIChomozygous53789482
71184368111843682CT25GENIChomozygous53789483