chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146994646569946466CA16GENIChomozygous639478311
146995168369951684GGA10GENIChomozygous750686934
146995175469951755AAGG16GENIChomozygous750686935
146995241569952416TG14GENIChomozygous639478312
146995252069952521GGAAA11GENICpossibly homozygous750686936
146995357669953577GGAAA8GENIChomozygous750686937
146995375669953757AG9GENIChomozygous639478313
146995428369954284CT11GENIChomozygous639478314
146995526369955264AATT9GENIChomozygous750686938
146995631869956319AAGGT20GENIChomozygous750686939
146995653569956536AACG7GENIChomozygous750686940
146995657769956584ACACACA-------3GENIChomozygous750686941
146995658769956589CG--3GENIChomozygous750686942
146995896369958964CT13GENIChomozygous639478315
146996195569961956GA14GENIChomozygous639478316
146996222669962227TC13GENIChomozygous639478317
146996285869962859CT15GENIChomozygous639478318
146996692469966925A-4GENIChomozygous750686943
146996711869967119A-7GENIChomozygous750686944
146996916469969165TTAAACAGTTAA14GENIChomozygous750686945
146997052269970523GA16GENIChomozygous639478319