chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
61022942310229424TC11GENIChomozygous70128671
61023047810230479TC14GENIChomozygous70128673
61023155910231560CT11GENIChomozygous70128675
61023331810233319GA7GENIChomozygous70128677
61023362510233626TC8GENIChomozygous70128678
61023405910234060TC8GENIChomozygous70128679
61023514510235146AG5GENIChomozygous70128681
61023571010235711AC18GENIChomozygous70128683
61023760110237602AG16GENIChomozygous70128685
61023894110238942TA6GENIChomozygous70128687
61023953710239538GA10GENIChomozygous70128689
61023973210239733CT7GENIChomozygous70128693
61024008410240085TC6GENIChomozygous70128695
61024009810240099TC6GENIChomozygous70128696
61024034210240343AT9GENIChomozygous70128698
61024085910240860TA2GENIChomozygous70128700
61024089810240899AG6GENIChomozygous70128702
61024151110241512CT13GENICheterozygous70128716
61024177910241780AG12GENIChomozygous70128718
61024185910241860GC9GENIChomozygous70128720
61024211010242111TC11GENIChomozygous70128722
61024211510242116GA13GENIChomozygous70128724
61024225510242256GA8GENIChomozygous70128726
61024246110242462CA13GENIChomozygous70128728
61024252710242528AG13GENIChomozygous70128730
61024252910242530TA12GENIChomozygous70128731
61024267410242675GA11GENIChomozygous70128733
61024288710242888GA11GENIChomozygous70128735
61024299410242995AG8GENIChomozygous70128737