chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103003643630036439TTT---10GENIChomozygous51387633
103003806730038075TTTTTTTT--------13GENICpossibly homozygous51834532
103003806830038075TTTTTTT-------13GENICheterozygous51387635
103003860430038605TG28GENIChomozygous51387636
103004010830040111CTT---29GENIChomozygous51387637
103004028230040283CT22GENIChomozygous51387638
103004146630041467TC19INTERGENIChomozygous51387639
103004175830041759TG14INTERGENIChomozygous51387640
103004190930041910CCA17INTERGENIChomozygous51387641
103004211330042114GC21INTERGENIChomozygous51387642
103004235730042358CT23INTERGENIChomozygous51387643
103004300730043015GTGTGTGC--------12INTERGENICpossibly homozygous51387645
103004409530044096GA22INTERGENIChomozygous51387647
103004466430044665GC31INTERGENIChomozygous51387648
103004495930044960TC19INTERGENIChomozygous51387649
103004525830045259GA27INTERGENIChomozygous51387650
103004557830045579CCCCCAA6INTERGENIChomozygous51633661
103004592930045930GA22INTERGENIChomozygous51387652
103004690630046916TGTGTGTGTG----------3INTERGENIChomozygous51387653
103004775830047759CT18INTERGENIChomozygous51387654
103004804030048041AC14INTERGENIChomozygous51387655
103004810630048109CTC---18INTERGENIChomozygous51387656
103004820230048203TC19INTERGENIChomozygous51387657
103004852230048523CA17INTERGENIChomozygous51387658
103004866130048662AG16INTERGENIChomozygous51387659