chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130228472130228473AG75GENIChomozygous54110633
7130229049130229050C-19GENICheterozygous54110634
7130229426130229427CT37GENIChomozygous54110635
7130229650130229651TG46GENICheterozygous54521241
7130230110130230111AG33GENIChomozygous54110636
7130230113130230114A-27GENIChomozygous54110637
7130230217130230218CT57GENIChomozygous54110638
7130230385130230386GA43GENIChomozygous54110639
7130231477130231478GA36GENIChomozygous54110640
7130232650130232651TTC36GENIChomozygous54110641
7130233261130233262AG35GENICpossibly homozygous54110642
7130233699130233700TTAC13GENICheterozygous54110643
7130233699130233700TTACAC13GENICheterozygous54110644