chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182470913824709139AG15GENIChomozygous110309042
182471123124711232GA19GENIChomozygous110309044
182471470124714702TC5GENIChomozygous110309048
182471471024714711AC4GENIChomozygous110309050
182471520424715205GA19GENIChomozygous110309057
182471569824715699TC43GENIChomozygous110309059
182471603824716039CA39GENIChomozygous110309061
182471891424718915GT34GENIChomozygous110309063
182472100024721001AG23GENIChomozygous110309065
182472246624722467AG24GENIChomozygous110309067
182472293324722934TG37GENICheterozygous110831896
182472293724722938TG38GENICheterozygous110831898
182472294124722942TG39GENICheterozygous119485376
182472158024721581GA54GENICheterozygous119485372
182472181124721812CG52GENICheterozygous119485374
182472292924722930TG38GENICpossibly homozygous119485375
182472164124721642CG78GENICheterozygous119566568
182472294524722946TG41GENICheterozygous119485377
182472905424729055AG44GENIChomozygous110309069
182473044524730446CT37GENIChomozygous110309071
182473241424732415TC36GENIChomozygous110309073
182473264624732647AG26GENIChomozygous110309075
182473281924732820AG36GENIChomozygous110309077
182473299524732996GA54GENIChomozygous110309079
182473328624733287GA34GENIChomozygous110309081
182473361724733618GA26GENIChomozygous110309083
182473520324735204GA37GENICpossibly homozygous110309085
182473587024735871AG34GENIChomozygous110309087
182473616724736168CT36GENIChomozygous110309089
182473668724736688TC35GENIChomozygous110309091
182474030224740303AT27GENIChomozygous110309093
182474129524741296CT31GENIChomozygous110309095
182474296424742965TA27GENIChomozygous110309097
182474358124743582GA25GENICheterozygous119519974
182474358524743586GA27GENICheterozygous119566569
182474361524743616GA20GENICpossibly homozygous119485378
182474361924743620GA23GENICpossibly homozygous119485379
182474485124744852CT34GENIChomozygous110309099
182474493524744936CT42GENIChomozygous110309101
182474553424745535CT37GENIChomozygous110309103