chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141727902141727904GT--15GENICpossibly homozygous54159579
7141727934141727935GC37GENICpossibly homozygous54159580
7141727946141727947GC37GENICpossibly homozygous54159581
7141728910141728911GA64GENICheterozygous54159582
7141728911141728912TTC59GENICheterozygous54159583
7141728940141728941AG62GENICheterozygous54159584
7141728998141728999A-57GENICheterozygous54159585
7141729008141729009CG59GENICheterozygous54159586
7141729197141729198AG53GENICheterozygous54159587
7141729324141729325AG33GENIChomozygous54159588
7141730583141730584GGT30GENICpossibly homozygous54159589
7141731958141731959TC27GENIChomozygous54159590