chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137116396871163969AG23GENIChomozygous114383681
137116657671166577TC13GENIChomozygous114637508
137116657771166578GA13GENIChomozygous114637510
137116667171166672GA18GENICpossibly homozygous114637512
137116691371166914CT21GENIChomozygous114383685
137116695271166953GA17GENIChomozygous114637514
137116702271167023GA20GENIChomozygous114637516
137116736571167366AG15GENIChomozygous114383686
137116784571167846CA13GENIChomozygous114637518
137116963671169637GA29GENIChomozygous114637520
137116968371169684AG24GENIChomozygous114383687
137116997171169972AG24GENIChomozygous114383688
137117027071170271CT14GENIChomozygous114383689
137117688371176884GA19GENIChomozygous114383690
137117808671178087GA25GENIChomozygous114637522
137117836371178364GT38GENIChomozygous114637524