chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130430881130430882CT16GENIChomozygous947311769
7130431011130431012GC14GENIChomozygous947311770
7130431993130431994GA28GENIChomozygous947311771
7130432239130432240CT21GENIChomozygous947311772
7130432938130432939CT24GENIChomozygous947311773
7130435663130435664GC20GENIChomozygous947311774
7130435830130435831CT17GENIChomozygous947311775
7130436509130436510AG17GENIChomozygous947311776
7130439443130439444TC20GENIChomozygous947311777
7130439854130439855GA25GENICpossibly homozygous947311778
7130440127130440128TC22GENIChomozygous947311779
7130440225130440226AG22GENIChomozygous947311780
7130440411130440412TC28GENIChomozygous947311781
7130440629130440630CT32GENIChomozygous947311782
7130440747130440748CA26GENIChomozygous947311783