chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71504526615045267AACTCTCTCT12GENIChomozygous54956133
71504652815046529TG27GENIChomozygous53799405
71504700815047009AC30GENIChomozygous53799407
71504718815047189GA22GENIChomozygous53799409
71504749315047494CCCCT22GENIChomozygous53799410
71505003415050049TCCTCCTCCTTCTCT---------------12GENICpossibly homozygous55072025
71505255015052551TC21GENIChomozygous53799422
71505760115057602GGAACA25GENIChomozygous53799429
71505800515058006TC17GENIChomozygous53799431
71505825215058253T-12GENICpossibly homozygous53799434
71505842515058426GGTATAGA5GENIChomozygous53799438
71505882415058825G-21GENIChomozygous53799439
71505756615057567GT30GENIChomozygous54303462
71504958515049586GA25GENIChomozygous54303456
71505686015056861AC14GENIChomozygous54303459