chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103587314435873145CA47GENIChomozygous808619496
103587341735873418GA49GENIChomozygous808619497
103587413535874136AG27GENIChomozygous808619498
103587418835874189GA25GENIChomozygous808619499
103587461535874616GA63GENICheterozygous808619500
103587462235874623GA65GENICheterozygous808619501
103587464635874647AC56GENICheterozygous808619502
103587635135876352CT60GENICpossibly homozygous808619503
103587660035876601AC38GENIChomozygous808619504
103587669035876691AG38GENIChomozygous808619505
103587690635876907AG36GENIChomozygous808619506
103587690735876908AT35GENIChomozygous808619507
103587690835876909AT34GENIChomozygous808619508
103587690935876910CT35GENIChomozygous808619509
103587693235876933TC45GENIChomozygous808619510
103587696335876964AG45GENIChomozygous808619511
103587760235877603CT41GENIChomozygous808619512
103587761235877613CT43GENIChomozygous808619513
103587764935877650TC31GENIChomozygous808619514
103587774335877744CA43GENIChomozygous808619515
103587905335879054AG35GENIChomozygous808619516