chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101657006716570068TTAC6GENICheterozygous729696076
101657514416575145TC35GENIChomozygous603471119
101657532216575331GTCCTTCCA---------36GENIChomozygous729696077
101657540116575402AATT22GENIChomozygous729696078
101657561316575614AC32GENIChomozygous601544649
101657571616575717TTA25GENIChomozygous729696080
101657585516575856AG21GENICpossibly homozygous603471120
101657587316575874AG29GENIChomozygous601544650
101657588516575889ACAC----28GENIChomozygous729696081
101657590916575910GA28GENIChomozygous603471121
101657591016575911CT27GENIChomozygous601544651
101657602716576028A-41GENIChomozygous729696082
101657747516577476GGA4GENIChomozygous729696083