chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87569301875693019TTA1GENIChomozygous52677065
87569302875693029TC2GENIChomozygous52677066
87569303075693031CA2GENIChomozygous52998347
87569304175693042CG1GENIChomozygous52677067
87569304275693043TC1GENIChomozygous52677068
87569305475693055TC1GENIChomozygous52677069
87570612675706128TG--6GENICheterozygous53469940
87570624375706244G-8GENICpossibly homozygous52677074
87572943075729432CC--1GENIChomozygous53396436
87573344575733446C-7GENIChomozygous52677081
87573347175733472AG1GENIChomozygous52998348
87573347275733473GC1GENIChomozygous52677082
87573348475733485GC1GENIChomozygous53364445
87573348675733487CT1GENIChomozygous53364446
87573349275733493TC2GENIChomozygous52677084
87574885075748851T-4GENICheterozygous52998350
87578052275780523CA1GENIChomozygous52677093
87578052575780526CG1GENIChomozygous52677094
87578582075785821GC6GENICheterozygous53126627
87578745675787556TATGACAGGCAGCTCTGGGTTTGTATGACAGGCAGCCCTGGGTTTGTATGACTGACAGGCAGCCCTGGGTTTGTATGACTGACAGGCAGCCCTGGGTTTC----------------------------------------------------------------------------------------------------29GENICheterozygous53537366