chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95390630353906304CG7GENIChomozygous117341810
95390677853906779GA21GENIChomozygous117341812
95390765553907656TC17GENIChomozygous117341813
95390916453909165AG25GENIChomozygous117341814
95390920553909206GT24GENIChomozygous117341815
95391064053910641CT31GENIChomozygous117341816
95391065853910659TA34GENIChomozygous117341817
95391140753911408TA27GENIChomozygous117341818
95391144753911448GA28GENIChomozygous117341819
95391315853913159TG24GENIChomozygous117341820
95391366953913670GA20GENIChomozygous117341821
95391376553913766CT27GENIChomozygous117341822
95391381053913811AG27GENIChomozygous117341823
95391430053914301CT31GENIChomozygous117341824
95392080653920807CT27GENIChomozygous117341826
95392117753921178CA26GENIChomozygous117341827
95392513953925140GA19GENIChomozygous117341828
95393465553934656AG31GENIChomozygous117341829
95393468053934681GA32GENIChomozygous117341830
95393689153936892GA25GENIChomozygous117341831
95393925453939255TC22GENIChomozygous117341832
95394043653940437AT34GENIChomozygous117341833
95394242553942426CA19GENIChomozygous117341838
95394279353942794TC35GENIChomozygous117341839
95394461253944613GT27GENIChomozygous117341840
95394489453944895TC30GENICpossibly homozygous117341841
95394545853945459TC15GENIChomozygous117341842