chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142901156142901157TG14GENICpossibly homozygous54161995
7142901770142901771CA20GENIChomozygous54161996
7142901917142901918CT12GENIChomozygous54161997
7142902249142902250TC25GENICheterozygous54162000
7142902888142902889TG3GENIChomozygous54162001
7142902892142902893TC3GENIChomozygous54162002
7142902912142902913CG8GENIChomozygous54162003
7142903045142903046GT14GENICpossibly homozygous54162005
7142903172142903173GA26GENICpossibly homozygous54162006
7142904820142904821AT15GENIChomozygous54162007
7142905253142905254AG14GENICheterozygous54162008
7142905922142905923GA7GENICpossibly homozygous54162011
7142906866142906867AG21GENICpossibly homozygous54162012
7142906952142906953GA15GENICpossibly homozygous54162013
7142907515142907516GA15GENIChomozygous54162014
7142911046142911047T-5GENIChomozygous54162022
7142911541142911542GA11GENICheterozygous54162023
7142912010142912011GA21GENIChomozygous54162024
7142913287142913288GT15GENICpossibly homozygous54162039
7142914094142914095TTAG8GENIChomozygous54162040
7142914478142914479AAGGGCTAGCTGTTTT2GENICheterozygous54162041
7142914977142914978GA15GENIChomozygous54162043
7142915480142915481GA33GENICpossibly homozygous54162044
7142919378142919379GA23GENICpossibly homozygous55961157