chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1115505522115505523CT7GENICheterozygous62445986
1115507488115507489T-5GENIChomozygous60809120
1115507547115507548AT2GENIChomozygous61300781
1115507549115507550GGT2GENIChomozygous62152488
1115513608115513609T-7GENICheterozygous62445987
1115514864115514865A-2GENICheterozygous62152492
1115515879115515881AC--5GENICheterozygous60809134
1115531481115531482T-2GENICheterozygous60809174
1115531500115531501GGT3GENICheterozygous61747038
1115532360115532361AAT1GENIChomozygous60809178
1115543475115543591TTGTTGTTTCGGTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC--------------------------------------------------------------------------------------------------------------------20GENICheterozygous62086184
1115546813115546814T-6GENIChomozygous60809185
1115547414115547415T-2GENICheterozygous62445988
1115548175115548177TG--9GENICheterozygous62295003
1115564984115564985AG15GENICheterozygous60809197
1115567027115567028T-3GENICheterozygous62295006
1115573500115573501CCTTTT1GENIChomozygous62152504
1115580462115580463C-3GENICheterozygous60809223
1115582529115582530GGTTTTTTT4GENICheterozygous62152510
1115591883115591884T-2GENICheterozygous62086185
1115593455115593460TCGGG-----8GENIChomozygous60809243
1115611199115611200T-2GENIChomozygous62350621
1115616927115616928CCA7GENICpossibly homozygous60809297
1115630889115630890GGCA18GENIChomozygous60809320
1115637726115637727A-1GENIChomozygous61747223