chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117115342117115343GA29GENIChomozygous119406993
4117115925117115926AG20GENIChomozygous113152738
4117116220117116221GA26GENIChomozygous119406994
4117116337117116338TC33GENIChomozygous113152739
4117120859117120860TC33GENIChomozygous113152744
4117126928117126929CT20GENIChomozygous119406995
4117134988117134989AC11GENIChomozygous119406996
4117139110117139111CT25GENIChomozygous119406997
4117141851117141852TC25GENIChomozygous119406998
4117141880117141881GA24GENIChomozygous119406999
4117142287117142288CT29GENIChomozygous119407000
4117142636117142637TC36GENIChomozygous119407001
4117143617117143618AG22GENIChomozygous119407002
4117143656117143657TA29GENIChomozygous119407003
4117144303117144304GA28GENIChomozygous113152750
4117144856117144857CG41GENIChomozygous119407004
4117145515117145516AC28GENIChomozygous119407005
4117146589117146590CT28GENIChomozygous119407006
4117147225117147226CT29GENIChomozygous119407007
4117147445117147446CT24GENIChomozygous119407008
4117147554117147555CT31GENIChomozygous119407009
4117147555117147556AG31GENIChomozygous119407010
4117148084117148085CT31GENIChomozygous119407011
4117148657117148658TC27GENIChomozygous113152755
4117149209117149210CG25GENIChomozygous119407012
4117149477117149478AG25GENIChomozygous113152756
4117152024117152025AG19GENIChomozygous113152757
4117153222117153223CG38GENIChomozygous119407013
4117153223117153224TC40GENIChomozygous119407014
4117153313117153314GC29GENIChomozygous113152758