chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119393736119393737GA18GENIChomozygous115851796
7119394959119394960GA11GENIChomozygous118399035
7119395344119395345CT22GENIChomozygous115851798
7119396232119396233TC14GENIChomozygous115851800
7119396676119396677TG13GENIChomozygous115851802
7119396723119396724GA23GENIChomozygous115851804
7119396763119396764TC10GENIChomozygous115851806
7119397274119397275GA6GENIChomozygous115851808
7119397783119397784CT18GENIChomozygous115851810
7119398386119398387CT8GENIChomozygous126538934
7119398614119398615TC12GENIChomozygous115851826
7119398829119398830CT8GENIChomozygous115851828
7119399000119399001TC22GENIChomozygous115851830
7119399379119399380GA26GENIChomozygous115851832
7119399858119399859TC4GENIChomozygous115851834
7119399896119399897TG10GENIChomozygous115851836
7119400019119400020AG9GENIChomozygous115851838
7119401662119401663TC24GENIChomozygous115851840
7119401856119401857GA21GENIChomozygous115851842
7119403063119403064AG17GENIChomozygous115851844
7119403232119403233TC15GENIChomozygous115851846
7119403587119403588AT9GENIChomozygous115851848
7119404929119404930AG24GENIChomozygous115851854
7119405725119405726TG22GENIChomozygous115851856
7119406914119406915GA14GENIChomozygous115851862
7119406930119406931AG13GENIChomozygous115851864
7119407117119407118TA21GENIChomozygous115851866
7119408265119408266TA17GENIChomozygous115851868
7119409121119409122CT18GENIChomozygous115851870
7119409136119409137AC19GENIChomozygous115851872
7119409494119409495GT12GENIChomozygous115851874
7119409664119409665GA17GENIChomozygous115851876