chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105551720455517205CG6GENIChomozygous51459718
105551730755517308AG6GENIChomozygous51459719
105551746455517465AG8GENIChomozygous51459720
105551815755518158AG11GENIChomozygous51459721
105551821955518220CCG9GENIChomozygous51459722
105551823655518237GA8GENIChomozygous51459723
105551877655518777TC6GENIChomozygous51459724
105551888755518888CT7GENIChomozygous51459725
105551924755519248CG13GENIChomozygous51459727
105551966755519668GA12GENIChomozygous51459728
105552040055520401AG5GENIChomozygous51459729
105552119155521192GA14GENIChomozygous51459730
105552135155521366GAGCACCACCCCCTG---------------1GENIChomozygous52319041
105552157755521578AG15GENIChomozygous51459731
105552183455521835CT13GENIChomozygous51459732
105552195855521959GA12GENIChomozygous51459733
105552284355522844AG3GENIChomozygous51459737
105552287655522877GC3GENIChomozygous51459738
105552303655523037GT6GENIChomozygous51459739
105552312855523129TC10GENIChomozygous51459740
105552376255523763TG6GENIChomozygous51459742
105552465655524657TC9GENIChomozygous51459744
105552302055523021GA4GENIChomozygous51653095
105552374755523748CCA6GENIChomozygous51653097
105552467855524803TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCCTACACCCTGTTTTTTTTTTT-----------------------------------------------------------------------------------------------------------------------------6GENIChomozygous52377377
105552492855524929TC7GENIChomozygous51459746