chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106269221262692213CT28GENIChomozygous116891034
106269402062694021GA28GENIChomozygous116891038
106269413562694136TC27GENIChomozygous116614123
106269472762694728GA19GENIChomozygous116891040
106269567062695671G25GENICpossibly homozygous128823495
106269653962696540GA30GENIChomozygous116939779
106269667762696678GA29GENIChomozygous116891042
106269671962696720AG35GENIChomozygous116891044
106269785362697854TC22GENIChomozygous116614135
106269796162697962CG24GENIChomozygous118084062
106269868062698680AGG20GENIChomozygous128823497
106269986062699861GC38GENIChomozygous116891046