chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4208492880208492881AG18GENIChomozygous57066601
4208495077208495078AG24GENIChomozygous57066602
4208495489208495490GT23GENICheterozygous57066603
4208498471208498472TC28GENIChomozygous57066605
4208498546208498551AAAAA-----1GENIChomozygous57607797
4208498924208498925TC26GENIChomozygous57066606
4208499667208499668T-1GENIChomozygous57066607
4208502120208502121GA23GENIChomozygous57066608
4208504256208504257A-30GENIChomozygous57066609
4208505297208505298TC27GENIChomozygous57066610
4208508035208508036CT24GENICpossibly homozygous57066611
4208510297208510311GAGAGAGAGAGAGA--------------3GENIChomozygous57066612
4208510543208510544TC24GENIChomozygous57066613
4208512238208512239A-2GENIChomozygous57066614
4208512907208512908TC27GENIChomozygous57066615
4208515943208515944AG33GENIChomozygous57066616
4208521280208521281CT32GENIChomozygous57066617
4208521727208521728CT33GENIChomozygous57066618
4208522139208522142TGG---1GENIChomozygous57066619
4208522353208522354TC25GENIChomozygous57066620
4208523079208523080AG29GENIChomozygous57066621
4208529635208529642TTCGTGG-------14GENIChomozygous57066622
4208529860208529861GC30GENIChomozygous57066623
4208530350208530353AAA---1GENIChomozygous57607799
4208531069208531070CT33GENIChomozygous57066624
4208531771208531772AT34GENIChomozygous57066625
4208532744208532745CT25GENIChomozygous57066626
4208533095208533096GA27GENIChomozygous57066627
4208533558208533559AG17GENIChomozygous57066628