chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185595296555952966AC16GENIChomozygous110360866
185595326055953261TG34GENIChomozygous110542610
185595337855953379CT36GENIChomozygous110542612
185595926555959266AG23GENIChomozygous110360876
185596194555961946AG28GENIChomozygous110542614
185596501755965018GA31GENIChomozygous110542616
185596590555965906AG24GENIChomozygous110360884
185596601555966016TC21GENIChomozygous110542618
185596681955966820TC28GENIChomozygous110360886
185596840855968409AG20GENIChomozygous110360890
185596969655969697GA37GENIChomozygous110542620
185597116855971169CT30GENIChomozygous110360892
185597179055971791CG27GENIChomozygous110542622
185597429555974296CT24GENIChomozygous110542624
185597916155979162TC29GENIChomozygous110360894
185598000255980003GT7GENIChomozygous110360896
185598081255980813GA27GENIChomozygous110542626
185598115755981158CT23GENIChomozygous110542628
185598118755981188GA23GENIChomozygous110542630
185598200055982001GA23GENIChomozygous110360902
185598332155983322AG27GENIChomozygous110360904
185598361755983618CT36GENIChomozygous110360906
185598842955988430CT24GENIChomozygous110360914
185598917855989179AG34GENIChomozygous110360916
185599399855993999GA28GENIChomozygous110542636
185599412955994130AG31GENIChomozygous110360923
185599762855997629TC32GENIChomozygous110542638
185600035156000352CT30GENIChomozygous110542640
185600082156000822CT24GENIChomozygous110542642
185600143756001438GA21GENIChomozygous110542644
185600188056001881GA35GENIChomozygous110542647
185600560056005601GA29GENIChomozygous110360927
185600616856006169TG21GENIChomozygous110592620
185600745656007457GA27GENIChomozygous110542649
185600890656008907TC32GENIChomozygous110360933
185600930256009303TC26GENIChomozygous110360937
185600690056006901AT14GENIChomozygous110631221
185600941656009417CT17GENIChomozygous110631223
185600938656009387GC23GENIChomozygous110360939