chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57766844677668447A-9GENIChomozygous55475862
57767055877670559AG10GENIChomozygous55475863
57767152177671522TC8GENICpossibly homozygous55475864
57767184677671847AT16GENIChomozygous55475865
57767381477673815A-7GENIChomozygous55475869
57767722777677228AG7GENICpossibly homozygous55475871
57767893577678936AG10GENICheterozygous56028488
57768006777680068CA5GENICheterozygous55475874
57768119377681194TC9GENICpossibly homozygous55475875
57768142277681423AC14GENICheterozygous55475877
57768440177684402T-5GENIChomozygous55475878
57768440777684409AG--5GENIChomozygous55475879
57768617777686178GA5GENIChomozygous55475880
57768643477686435CG13GENIChomozygous55475881
57768673777686738AC13GENIChomozygous55475882
57768713077687131TG6GENICheterozygous55475883
57768716477687165TG4GENIChomozygous55475884
57768738777687388CT14GENIChomozygous55475885
57768763077687631GA8GENIChomozygous55475886
57768771977687720AAAGGAAGG1GENIChomozygous55475887
57768777977687780AG2GENIChomozygous55475893
57768781877687819TTA6GENICheterozygous55475894
57768784577687846AG10GENIChomozygous55475895
57768824777688248AC6GENIChomozygous55475896
57768856777688568TC16GENIChomozygous55475897
57768922777689228AG18GENICpossibly homozygous55475898
57768975477689757AGC---2GENIChomozygous55475899
57769274377692744AG8GENICpossibly homozygous55475901
57769319677693197CT11GENIChomozygous55475902
57769806177698062GT14GENICheterozygous55475905
57770191677701917TTA7GENICheterozygous55475906
57770671277706713TTA2GENIChomozygous55475915
57770900877709009AG7GENICpossibly homozygous55475917
57770641177706412TA7GENIChomozygous56681860