chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5161859805161859806AG16GENICpossibly homozygous55819590
5161861355161861356C-37GENIChomozygous55819592
5161862204161862205TC41GENIChomozygous55819594
5161862338161862339AG37GENIChomozygous55819596
5161864670161864671AG42GENIChomozygous55819597
5161865141161865142TC15GENICheterozygous55819599
5161865153161865154CT20GENICheterozygous55939832
5161865943161865944C-18GENICheterozygous56072710
5161865945161865946C-17GENICheterozygous56192846
5161865947161865950CTG---10GENICpossibly homozygous55819601
5161865977161865978GC22GENICheterozygous55819605
5161865984161865985CT22GENICheterozygous55819607
5161866000161866001TC23GENICheterozygous55819609
5161866032161866033CT21GENICheterozygous55819611
5161866172161866173AG25GENIChomozygous55819613
5161867014161867015CT33GENIChomozygous55819615
5161867954161867955TC18GENIChomozygous55819617
5161868085161868086GT30GENIChomozygous55819619
5161868339161868340CT26GENIChomozygous55819621
5161869067161869068GA22GENIChomozygous55819623
5161869536161869537CG32GENIChomozygous55819625
5161869884161869885AG54GENIChomozygous55819626
5161869962161869963CT33GENICpossibly homozygous55819628
5161871019161871020GT5GENICheterozygous55819632
5161871030161871031GGGTGTGT1GENIChomozygous55819635
5161871236161871237GA33GENIChomozygous55819637
5161871408161871409TC35GENIChomozygous55819639
5161872217161872218CT40GENIChomozygous55819641
5161873009161873013AAGG----30GENIChomozygous55819643