chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101657514416575145TC17GENIChomozygous616468453
101657532216575331GTCCTTCCA---------18GENIChomozygous741101022
101657540116575402AATT12GENIChomozygous741101023
101657561316575614AC17GENIChomozygous616468454
101657571616575717TTA15GENIChomozygous741101025
101657585516575856AG20GENICpossibly homozygous616468455
101657587316575874AG28GENIChomozygous616468456
101657588516575889ACAC----28GENIChomozygous741101026
101657590916575910GA29GENIChomozygous616468457
101657591016575911CT28GENIChomozygous616468458
101657602716576028A-15GENICpossibly homozygous741101027
101657747516577476GGA2GENIChomozygous741101028