chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121057492110574922TA34GENICpossibly homozygous776770897
121057494010574941GT34GENICpossibly homozygous776770898
121057514210575143TG24GENIChomozygous776770899
121057647310576474TA21GENIChomozygous776770900
121057726310577264GT22GENIChomozygous776770901
121057776610577767GT29GENIChomozygous776770902
121057816510578166AG55GENIChomozygous776770903
121058054410580545TC27GENIChomozygous776770904
121058068210580683TC34GENIChomozygous776770905
121058252610582527TC51GENIChomozygous776770906
121058277210582773CT56GENIChomozygous776770907
121058298310582984AG19GENICheterozygous776770908