chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95390677853906779GA14GENIChomozygous117341812
95390765553907656TC21GENIChomozygous117341813
95390916453909165AG39GENIChomozygous117341814
95390920553909206GT32GENIChomozygous117341815
95391064053910641CT34GENIChomozygous117341816
95391065853910659TA25GENICpossibly homozygous117341817
95391140753911408TA21GENIChomozygous117341818
95391144753911448GA18GENIChomozygous117341819
95391315853913159TG24GENIChomozygous117341820
95391366953913670GA27GENIChomozygous117341821
95391376553913766CT28GENIChomozygous117341822
95391381053913811AG25GENIChomozygous117341823
95391430053914301CT28GENIChomozygous117341824
95391740953917410GA34GENIChomozygous117341825
95392080653920807CT30GENIChomozygous117341826
95392117753921178CA21GENIChomozygous117341827
95392513953925140GA27GENICpossibly homozygous117341828
95393465553934656AG28GENIChomozygous117341829
95393468053934681GA29GENIChomozygous117341830
95393689153936892GA28GENIChomozygous117341831
95393925453939255TC19GENIChomozygous117341832
95394043653940437AT40GENIChomozygous117341833
95394242553942426CA17GENIChomozygous117341838
95394279353942794TC36GENIChomozygous117341839
95394461253944613GT24GENIChomozygous117341840
95394545853945459TC17GENIChomozygous117341842