chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123055025123055026CT12GENIChomozygous54088981
7123055683123055684AT11GENICheterozygous54235783
7123056263123056264GT9GENICpossibly homozygous54088982
7123057160123057161CT17GENICheterozygous54088983
7123057325123057326C-14GENIChomozygous54088984
7123058614123058616GT--5GENIChomozygous54088985
7123059887123060006CAGAGACTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGGGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC-----------------------------------------------------------------------------------------------------------------------8GENICpossibly homozygous54921391
7123061640123061641GA8GENICheterozygous54088990
7123061668123061669TA3GENIChomozygous54088991
7123061678123061679G-2GENIChomozygous54088992
7123063533123063534CT3GENICheterozygous54088993