chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103917165939171660TC18GENIChomozygous51422590
103917176539171766GA19GENIChomozygous51422591
103917215339172154GA17GENIChomozygous51422592
103917299139172992GT1GENIChomozygous51422594
103917314439173145TC17GENIChomozygous51422595
103917331239173313CT19GENIChomozygous51422596
103917367139173681CACACACACA----------5GENICheterozygous52436953
103917367339173681CACACACA--------5GENICheterozygous52369541
103917988439179885GA26GENIChomozygous51422597
103918020039180201CCATGCTCACTTACTCTCT17GENIChomozygous52369547
103918046539180466CT22GENIChomozygous51422599
103918234439182345CA18GENICpossibly homozygous51422600
103918403139184039AGCCTGTC--------14GENIChomozygous51422601
103918471639184717G-15GENIChomozygous51422602
103917998839179989GT21GENIChomozygous52043630