chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122539944122539945CT18GENIChomozygous115860892
7122540053122540054TC13GENIChomozygous115860894
7122542658122542659GA24GENIChomozygous115860896
7122543559122543560CA19GENIChomozygous115860898
7122545534122545535AG15GENIChomozygous115860900
7122548356122548357AT21GENIChomozygous115860902
7122548718122548719CA8GENIChomozygous115860904
7122551704122551705CT16GENIChomozygous115860908
7122559179122559180AG7GENICheterozygous126587205
7122559354122559355GT4GENICheterozygous126539226
7122559376122559377GT7GENICheterozygous116082088
7122559383122559384CG6GENICheterozygous126620133
7122560055122560056TC21GENIChomozygous115860920
7122563717122563718GA22GENIChomozygous115860922
7122565436122565437CG20GENIChomozygous115860924
7122567026122567027GA30GENIChomozygous115860928
7122568574122568575TA29GENIChomozygous115860930
7122573650122573651AG4GENIChomozygous115860933
7122574735122574736AG18GENIChomozygous115860935
7122574753122574754TA14GENIChomozygous115860937
7122577597122577598AG15GENIChomozygous115860941
7122579456122579457AG25GENIChomozygous115860943
7122580221122580222AG16GENIChomozygous115860945
7122581613122581614GA7GENIChomozygous115860947
7122581619122581620AG9GENIChomozygous115860949