chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106759356867593686TTGAAAAATATTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGATCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC----------------------------------------------------------------------------------------------------------------------4GENICheterozygous722155162
106762714267627143TTAA1GENIChomozygous722155165
106770459067704591T-6GENICheterozygous722155169
106771254867712549AAT5GENICheterozygous722155170
106772979367729794AG17GENICheterozygous588407395
106772979467729795AG17GENICheterozygous588407396
106773145467731455TTG7GENIChomozygous722155171
106773146067731461GGT8GENIChomozygous722155172
106774212567742126A-12GENICheterozygous722155179
106777478867774789A-1GENIChomozygous722155180
106780745067807451AAG12GENICpossibly homozygous722155182