chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3141409656141409657GA22GENIChomozygous120090030
3141412144141412145AG9GENIChomozygous112168398
3141412244141412245GA13GENIChomozygous120090032
3141412507141412508TC17GENIChomozygous120090034
3141414931141414935GAGT3GENICheterozygous135164126
3141414977141414978GC15GENIChomozygous111755862
3141412970141412971GT14GENIChomozygous111755858
3141414527141414528AT13GENICpossibly homozygous111755860
3141415010141415011TC10GENIChomozygous111755864
3141415817141415818AC16GENIChomozygous111755870
3141416938141416939GA13GENIChomozygous120090036
3141417176141417176CTTCCTTT17GENIChomozygous135164127
3141417767141417768AG11GENIChomozygous112168406
3141418458141418459CA10GENIChomozygous120090038
3141415885141415886C15GENIChomozygous130912257
3141415958141415959AT12GENIChomozygous119805961