chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64051100840511009GGGT9GENIChomozygous56213698
64051279640512797TC2GENIChomozygous54869581
64051377440513775TC8GENIChomozygous54869583
64051524540515246GGTT7GENICpossibly homozygous54869589
64051541140515412TC5GENIChomozygous54869590
64051542340515424AG6GENIChomozygous54869591
64051451140514517GGCTCC------5GENIChomozygous56577496
64051264640512647CT8GENIChomozygous56577493
64051450740514509CC--5GENIChomozygous56577494
64051764740517648GA8GENIChomozygous56577498
64051451940514520AG5GENIChomozygous56581126
64051452440514525T-5GENIChomozygous56581127
64051712140517122T-5GENIChomozygous56052460
64051932140519322GA4GENIChomozygous56577499
64052120340521204TC6GENIChomozygous54869594
64052232440522325CA6GENIChomozygous56577501
64052402140524022CT5GENIChomozygous54869596
64052407140524072GT8GENIChomozygous56577503
64052426540524266TTCACCACCACCAC3GENIChomozygous56581128
64052467540524676CT6GENIChomozygous56577505
64052470940524710GT7GENIChomozygous54869600
64052522340525224AG6GENIChomozygous54869601
64052535140525352CT7GENIChomozygous54869603
64052574240525743GT10GENIChomozygous56577506
64052587940525880CT5GENIChomozygous54869605