chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84466502144665022CT71GENIChomozygous149047575
84466645944666460AG90GENIChomozygous145660751
84466753644667537GT80GENIChomozygous145660752
84466766344667664AC61GENIChomozygous145660753
84466781544667816AG50GENIChomozygous145660754
84466801844668019CT59GENIChomozygous145660755
84466961044669610T94GENICpossibly homozygous145644680
84466789544667896G22GENIChomozygous145644678
84466951444669517TGG93GENIChomozygous145644679
84466790644667911TTGGG15GENICpossibly homozygous149046253
84466790944667910G18GENICpossibly homozygous403236264
84466790844667909G18GENICpossibly homozygous403236261
84466790844667909GT18GENICheterozygous403236262
84466790944667910GT18GENICheterozygous403236263
84466791044667911G18GENICpossibly homozygous403236265
84466791044667911GT18GENICheterozygous403236266
84466999044669991GA77GENIChomozygous144819100
84467040944670410AG75GENIChomozygous145660756