chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73645800936458010TC7GENIChomozygous53875435
73645822536458228ATG---1GENIChomozygous55076280
73645824636458247TA2GENIChomozygous54192920
73645841236458413GA6GENIChomozygous55076284
73646110036461101AC6GENIChomozygous53875438
73646119136461192GC6GENICheterozygous53875439
73646219836462199GA12GENICpossibly homozygous55076294
73646283636462837AG7GENIChomozygous53875444
73646334236463343TC10GENIChomozygous53875446
73646338636463387TA12GENICpossibly homozygous53875447
73646386436463865AG16GENIChomozygous53875448
73646559936465600TC11GENIChomozygous53875450
73646578436465786TG--5GENIChomozygous54192930
73646642536466426AAAGCGCTCTACCACTGAGCTAAATCCCCAGCC3GENICheterozygous54893344
73646765836467659GA5GENIChomozygous53875461
73646766136467662CT4GENIChomozygous53875462
73646766836467669AC2GENIChomozygous53875463
73646767736467678CT2GENIChomozygous53875464
73646986836469869AG4GENIChomozygous53875472
73647070336470707AAAT----2GENIChomozygous54192932
73646446536464466AG8GENICheterozygous55557566
73646618636466187TG3GENIChomozygous55557569
73646630036466301CG14GENIChomozygous55557572