chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6135493566135493567AT6GENICheterozygous54739818
6135494472135494473AG9GENIChomozygous54739820
6135495664135495665TC14GENICheterozygous54739822
6135495953135495955AT--4GENIChomozygous54739824
6135496440135496441TA8GENICpossibly homozygous54739826
6135497050135497051AG18GENIChomozygous54739832
6135500669135500673TTGT----2GENIChomozygous54739836
6135501276135501277AATGG17GENICpossibly homozygous54739838
6135502604135502605AG13GENIChomozygous54739840
6135508418135508419A-6GENIChomozygous55435689
6135508700135508701AG20GENICpossibly homozygous54739844
6135511028135511029AT28GENIChomozygous54739854
6135511082135511083GA21GENICpossibly homozygous54739856
6135512011135512021ACGGCAGGTT----------1GENIChomozygous54739858
6135514667135514668AT4GENIChomozygous54739867
6135516495135516496GA11GENIChomozygous54739871
6135517904135517905CG15GENIChomozygous54739873
6135518000135518001GA15GENICpossibly homozygous54739875
6135518059135518060TC16GENICpossibly homozygous54739877
6135518547135518548GC18GENICpossibly homozygous54739879
6135518740135518741TC24GENIChomozygous54739881