chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71182846611828467GA39GENIChomozygous53789460
71182902711829028CCG50GENIChomozygous53789462
71183045511830456TTC23GENICheterozygous53789463
71183045511830456TTCC23GENICheterozygous54954578
71183148111831527GTGTGTGTGTGTGCGTGCGTGCGTGTGCGTGTGCGTGTGTGTGTGC----------------------------------------------43GENICpossibly homozygous54954580
71183272211832723AT56GENIChomozygous53789468
71183321511833216AAGAGGAC85GENIChomozygous53789469
71183342411833425GGTGT49GENICheterozygous54954582
71183391611833917CT38GENIChomozygous53789470
71183456511834566TG68GENIChomozygous53789471
71183505111835052TC42GENIChomozygous53789472
71183666911836670GA83GENIChomozygous53789473
71183773511837736CT70GENIChomozygous53789474
71183949611839497AG39GENIChomozygous53789475
71184247411842475CT57GENIChomozygous53789476
71184295011842951AG68GENIChomozygous53789477
71184309111843092GA55GENIChomozygous53789481
71184363311843634CA78GENIChomozygous53789482
71184368111843682CT56GENIChomozygous53789483
71184304711843073ATGCTGTCATGTCGTGATGTCATGTG--------------------------61GENIChomozygous54884904