chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103003643630036439TTT---7GENIChomozygous51387633
103003806730038075TTTTTTTT--------16GENICpossibly homozygous51834532
103003806830038075TTTTTTT-------16GENICheterozygous51387635
103003860430038605TG26GENIChomozygous51387636
103004010830040111CTT---25GENIChomozygous51387637
103004028230040283CT23GENIChomozygous51387638
103004146630041467TC17INTERGENIChomozygous51387639
103004175830041759TG30INTERGENIChomozygous51387640
103004190930041910CCA30INTERGENIChomozygous51387641
103004211330042114GC37INTERGENIChomozygous51387642
103004235730042358CT21INTERGENIChomozygous51387643
103004300730043015GTGTGTGC--------8INTERGENICheterozygous51387645
103004409530044096GA23INTERGENIChomozygous51387647
103004466430044665GC26INTERGENIChomozygous51387648
103004495930044960TC26INTERGENIChomozygous51387649
103004525830045259GA22INTERGENIChomozygous51387650
103004557830045579CCCAA1INTERGENIChomozygous52135486
103004592930045930GA21INTERGENIChomozygous51387652
103004690630046916TGTGTGTGTG----------7INTERGENIChomozygous51387653
103004775830047759CT20INTERGENIChomozygous51387654
103004804030048041AC15INTERGENIChomozygous51387655
103004810630048109CTC---26INTERGENIChomozygous51387656
103004820230048203TC35INTERGENIChomozygous51387657
103004852230048523CA23INTERGENIChomozygous51387658
103004866130048662AG27INTERGENIChomozygous51387659