chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142901156142901157TG13GENICpossibly homozygous54161995
7142901770142901771CA12GENIChomozygous54161996
7142901917142901918CT9GENICpossibly homozygous54161997
7142902249142902250TC11GENICpossibly homozygous54162000
7142902888142902889TG4GENICheterozygous54162001
7142902892142902893TC2GENIChomozygous54162002
7142902912142902913CG8GENIChomozygous54162003
7142903045142903046GT18GENIChomozygous54162005
7142903172142903173GA21GENICpossibly homozygous54162006
7142904820142904821AT6GENIChomozygous54162007
7142905253142905254AG9GENIChomozygous54162008
7142905922142905923GA8GENIChomozygous54162011
7142906866142906867AG19GENIChomozygous54162012
7142906952142906953GA13GENICheterozygous54162013
7142907515142907516GA13GENIChomozygous54162014
7142911046142911047T-7GENIChomozygous54162022
7142911541142911542GA15GENICpossibly homozygous54162023
7142912010142912011GA16GENICpossibly homozygous54162024
7142913287142913288GT4GENICheterozygous54162039
7142914094142914095TTAG5GENIChomozygous54162040
7142914478142914479AAGGGCTAGCTGTTTT1GENIChomozygous54162041
7142914977142914978GA12GENICheterozygous54162043
7142915480142915481GA6GENIChomozygous54162044