chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46159076461590765GA11GENIChomozygous56916623
46159078661590787TC16GENIChomozygous56916624
46159113261591133AC19GENIChomozygous56916625
46159214261592143GA33GENIChomozygous56916626
46159237961592380AG19GENIChomozygous56916627
46159323561593236A-22GENICpossibly homozygous58587638
46159343261593433T-22GENICpossibly homozygous57733192
46159500061595001CT20GENIChomozygous56916631
46159508761595088T-20GENIChomozygous56916632
46159568961595690CG29GENIChomozygous56916633
46159646361596464CT24GENIChomozygous56916634
46159739361597394GA26GENIChomozygous56916635
46159772761597728T-9GENICpossibly homozygous56916636
46159773161597738TGTTGTG-------9GENICpossibly homozygous56916637
46159858361598584CA25GENIChomozygous56916639
46159883561598836CA34GENIChomozygous56916640
46159987261599873TC27GENIChomozygous56916641