chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045798724579873TC16GENIChomozygous125175895
2045799974579998GA11GENIChomozygous125209997
2045803694580370GA5GENICheterozygous125209998
2045810414581042AG13GENIChomozygous125175897
2045814334581434GA13GENIChomozygous125209999
2045814944581495GT15GENIChomozygous125210000
2045817874581788GA14GENIChomozygous125210001
2045822864582287GA21GENIChomozygous125210002
2045823984582399CT19GENIChomozygous125210003
2045826224582623GA9GENIChomozygous125175901
2045828284582829CT21GENIChomozygous125175903
2045829074582908AT29GENIChomozygous125210004
2045829544582955CA16GENIChomozygous125175904
2045829934582994CT4GENIChomozygous125175905
2045830464583047GA20GENIChomozygous125210005
2045832554583256GA11GENIChomozygous125175906
2045832584583259AG9GENIChomozygous125210006
2045835604583561CA11GENIChomozygous125175908
2045835974583598CT10GENIChomozygous125210007
2045848784584879GA16GENIChomozygous125210008
2045863364586337CT10GENIChomozygous125175910
2045865334586534AT14GENIChomozygous125175911
2045867224586723TC14GENIChomozygous125175914
2045868204586821CT6GENIChomozygous125210009
2045868754586876GA17GENIChomozygous125210010
2045877344587735AC12GENIChomozygous125210011
2045884714588472AT5GENIChomozygous125210012
2045887454588746GA17GENIChomozygous125210013
2045890234589024CT18GENIChomozygous125175917
2045893644589365GA18GENIChomozygous125210014
2045894204589421AG13GENIChomozygous125175919
2045902424590243CT16GENIChomozygous125210015
2045924594592460CA20GENIChomozygous125210016