chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137880615178806152CT16GENIChomozygous114402000
137880616878806169CA16GENIChomozygous114402002
137880618578806186GA16GENICpossibly homozygous114402004
137880623778806238GA24GENIChomozygous114402006
137880629878806299GT26GENIChomozygous114402008
137880633578806336TC25GENIChomozygous114402010
137880710578807106AG33GENIChomozygous114402012
137880781378807814TC29GENIChomozygous114402014
137880929578809296TC26GENIChomozygous114402016
137880991678809917AG27GENIChomozygous114402018
137881013278810133GA38GENIChomozygous114402020
137881052078810521TC37GENIChomozygous114402022
137881085378810854CA32GENIChomozygous114402024
137881105378811054CT29GENIChomozygous114402026
137881190278811903GA19GENIChomozygous114402028
137881215878812159CT20GENIChomozygous114402030
137881286978812870GC30GENIChomozygous114402032
137881310978813110GT22GENIChomozygous114402034
137881373278813733CT23GENIChomozygous114402036
137881373678813737GT22GENIChomozygous114402038
137881375278813753AT27GENICpossibly homozygous114402040
137881394578813946TC29GENIChomozygous114402042
137880880678808807TA12GENIChomozygous114689362
137881493478814935GT36GENIChomozygous114402044
137881616178816162AG25GENIChomozygous114402046
137881806578818066GA33GENIChomozygous114402048
137881848378818484AG42GENIChomozygous114402050
137881914578819146CT30GENIChomozygous114402052