chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107136959071369591AG43GENICpossibly homozygous116630184
107137032771370328CT60GENICheterozygous118043194
107137077371370774GT42GENIChomozygous117131253
107137253271372533GA74GENICpossibly homozygous117131254
107137302371373024CT74GENICpossibly homozygous117131255
107137392071373921CT57GENICpossibly homozygous117131256
107137457671374577TA58GENIChomozygous117131258
107137516371375164CT55GENIChomozygous117131259
107137614571376146CT51GENICpossibly homozygous116630192
107137627171376272GA64GENICpossibly homozygous117131260
107137928971379290CT56GENIChomozygous117131261
107138193471381935TC64GENIChomozygous116630194