chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119393736119393737GA24GENIChomozygous115851796
7119394959119394960GA6GENIChomozygous118399035
7119395344119395345CT18GENIChomozygous115851798
7119396232119396233TC17GENIChomozygous115851800
7119396676119396677TG11GENICheterozygous115851802
7119396723119396724GA25GENIChomozygous115851804
7119396763119396764TC20GENIChomozygous115851806
7119397783119397784CT17GENIChomozygous115851810
7119398460119398461CA6GENIChomozygous115851822
7119398614119398615TC18GENIChomozygous115851826
7119399000119399001TC25GENIChomozygous115851830
7119399379119399380GA22GENIChomozygous115851832
7119399858119399859TC6GENIChomozygous115851834
7119399863119399864GT4GENIChomozygous126602189
7119399896119399897TG17GENIChomozygous115851836
7119401662119401663TC17GENIChomozygous115851840
7119401856119401857GA22GENIChomozygous115851842
7119403063119403064AG16GENIChomozygous115851844
7119403232119403233TC15GENIChomozygous115851846
7119403587119403588AT9GENIChomozygous115851848
7119404929119404930AG17GENIChomozygous115851854
7119405725119405726TG32GENIChomozygous115851856
7119406914119406915GA16GENIChomozygous115851862
7119406930119406931AG14GENIChomozygous115851864
7119407117119407118TA19GENIChomozygous115851866
7119408265119408266TA10GENIChomozygous115851868
7119409121119409122CT19GENIChomozygous115851870
7119409136119409137AC19GENIChomozygous115851872
7119409494119409495GT6GENIChomozygous115851874
7119409664119409665GA14GENIChomozygous115851876