chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X123900994123900995AG18GENIChomozygous931005629
X123901333123901334TC18GENIChomozygous931005630
X123901666123901667CA17GENIChomozygous931005631
X123902771123902772CT26GENIChomozygous931005632
X123903040123903041CT8GENIChomozygous931005633
X123903719123903720TA18GENIChomozygous931005634
X123904966123904967GA19GENIChomozygous931005635
X123905627123905628AG19GENIChomozygous931005636
X123906352123906353GT15GENIChomozygous931005637
X123906808123906809AG9GENIChomozygous931005638
X123906932123906933TA15GENIChomozygous931005639
X123907599123907600CT15GENIChomozygous931005640
X123911321123911322TC7INTERGENIChomozygous931005641
X123911461123911462GT18INTERGENIChomozygous931005642
X123911482123911483GA18INTERGENIChomozygous931005643
X123911483123911484TG18INTERGENIChomozygous931005644
X123912197123912198TC22INTERGENIChomozygous931005645
X123912664123912665GA25INTERGENIChomozygous931005646
X123914613123914614AG13INTERGENIChomozygous931005647
X123916196123916197AG24INTERGENIChomozygous931005648
X123916552123916553GA11INTERGENIChomozygous931005649
X123916936123916937AG21INTERGENIChomozygous931005650