chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122150594122150595GC51GENIChomozygous583352089
7122150826122150827CCCA7GENICheterozygous719848159
7122153558122153559GA22GENIChomozygous583352090
7122155180122155181AAG4GENIChomozygous719848162
7122155864122155865TC67GENIChomozygous583352091
7122156385122156386TTTGTTTCTTGGGGTTGGGGATTTAGCTCA25GENICheterozygous719848163
7122156620122156621T-16GENICpossibly homozygous719848164
7122156951122156952AT13GENIChomozygous583352092
7122157951122157952CT33GENIChomozygous583352093
7122158468122158469CT16GENIChomozygous583352094
7122158658122158659TC37GENIChomozygous583352095
7122158661122158662AG37GENIChomozygous583352096
7122170066122170067T-22GENICheterozygous719848165
7122173531122173543GTTTGTTTGTTT------------22GENIChomozygous719848167