chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4208492880208492881AG44GENIChomozygous57066601
4208495077208495078AG35GENIChomozygous57066602
4208495489208495490GT32GENICheterozygous57066603
4208497974208497975T-2GENIChomozygous57066604
4208498471208498472TC23GENICpossibly homozygous57066605
4208498924208498925TC46GENIChomozygous57066606
4208499667208499668T-1GENIChomozygous57066607
4208502120208502121GA36GENIChomozygous57066608
4208504256208504257A-34GENIChomozygous57066609
4208505297208505298TC44GENIChomozygous57066610
4208508035208508036CT49GENIChomozygous57066611
4208510297208510311GAGAGAGAGAGAGA--------------10GENICheterozygous57066612
4208510543208510544TC65GENIChomozygous57066613
4208512238208512239A-20GENIChomozygous57066614
4208512907208512908TC47GENIChomozygous57066615
4208515943208515944AG51GENIChomozygous57066616
4208521280208521281CT65GENIChomozygous57066617
4208521727208521728CT62GENICpossibly homozygous57066618
4208522139208522142TGG---5GENIChomozygous57066619
4208522353208522354TC37GENIChomozygous57066620
4208523079208523080AG44GENIChomozygous57066621
4208529635208529642TTCGTGG-------27GENIChomozygous57066622
4208529860208529861GC41GENIChomozygous57066623
4208531069208531070CT49GENIChomozygous57066624
4208531771208531772AT53GENIChomozygous57066625
4208532744208532745CT48GENIChomozygous57066626
4208533095208533096GA59GENIChomozygous57066627
4208533558208533559AG53GENIChomozygous57066628