chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142334785142334786TC6GENIChomozygous115941758
7142335335142335336GA8GENICheterozygous126541444
7142335416142335417TC13GENIChomozygous126541445
7142335729142335730GT12GENIChomozygous115941759
7142335881142335882AG4GENIChomozygous115941760
7142338618142338619CA7GENIChomozygous115941762
7142356266142356267CT26GENICpossibly homozygous115941764
7142357940142357941TC22GENIChomozygous115941765
7142359050142359051GA29GENIChomozygous115941766