chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1175632073175632074GT39GENICpossibly homozygous108961934
1175632425175632426CA35GENIChomozygous108961935
1175633750175633751CT42GENIChomozygous108394628
1175638358175638359AG48GENIChomozygous108961936
1175643635175643636GT52GENIChomozygous108961937
1175643791175643792TC41GENIChomozygous108394638
1175644318175644319GA63GENIChomozygous108961938
1175645119175645120GA37GENIChomozygous108394640
1175647180175647181TA39GENIChomozygous108394648
1175650459175650460AG34GENIChomozygous108394652
1175651347175651348AG32GENICheterozygous108394658
1175653236175653237AC42GENIChomozygous108394664
1175654448175654449GA45GENIChomozygous108961939
1175656148175656149GC59GENIChomozygous108961940
1175656648175656649TC53GENICpossibly homozygous108961941
1175656924175656925TC50GENIChomozygous108961942
1175657102175657103GC21GENIChomozygous108961943
1175657158175657159GA29GENIChomozygous108961944