chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108691316186913162CT38GENICheterozygous51921850
108691359886913599CT36GENICheterozygous51921852
108691389286913893CA68GENICheterozygous51529079
108691391586913916CG68GENICheterozygous51529080
108691391886913919CA67GENICheterozygous51529081
108691392686913927TC67GENICheterozygous51529082
108691393986913940GT67GENICheterozygous51529083
108691394786913948CCA69GENICheterozygous51529084
108691414586914146TG30GENICheterozygous51921854
108691803486918035CG20GENICheterozygous51921883
108692429086924291AG16GENICheterozygous51724587
108692482786924828GA11GENICheterozygous51724589
108692737286927373CT25GENICheterozygous51529122
108692804586928046GT25GENICheterozygous51529123
108692888686928887CT34GENICheterozygous51529125
108692891286928913TC35GENICheterozygous51529126
108692915486929155CT21GENICheterozygous51921913
108692943586929436GA40GENICheterozygous51921915
108693003186930032GA28GENICheterozygous51921921
108693010786930108GA35GENICheterozygous51921923
108693013286930133AG28GENICheterozygous51529129