chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154513783154513784TC13GENICheterozygous821605891
3154513902154513903CT13GENICheterozygous821605892
3154514044154514045CT7GENICheterozygous821605893
3154514276154514277TG10GENICheterozygous821605894
3154515131154515132TC7GENICheterozygous821605895
3154515744154515745GA8GENICheterozygous821605896
3154516160154516161GA11GENICheterozygous821605897
3154516260154516261TC15GENICheterozygous821605898
3154516301154516302CT17GENICheterozygous821605899
3154516344154516345CT8GENICheterozygous821605900
3154516642154516643CT18GENICheterozygous821605901
3154516671154516672CT19GENICheterozygous821605902
3154516726154516727CT17GENICheterozygous821605903
3154516727154516728AG19GENICheterozygous821605904
3154516884154516885AG8GENICheterozygous821605905
3154517017154517018TA19GENICheterozygous821605906
3154517287154517288AG13GENICheterozygous821605907
3154517593154517594TC9GENICheterozygous821605908
3154517632154517633G-9GENICheterozygous821605909
3154517846154517847TC17GENICheterozygous821605910
3154517898154517899TC12GENICheterozygous821605911
3154518068154518069GA7GENICheterozygous821605912
3154518158154518159TTA16GENICheterozygous821605913
3154518166154518167TC19GENICheterozygous821605914
3154519645154519646CG10GENICheterozygous821605915
3154519852154519853CT10GENICheterozygous821605916
3154519985154519986AG11GENICheterozygous821605917
3154520656154520657TG12GENICheterozygous821605918
3154520987154520988CT9GENICheterozygous821605919
3154521686154521687CT10GENICheterozygous821605920