chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146994646569946466CA7GENIChomozygous611673712
146995168369951684GGA11GENICpossibly homozygous734381064
146995175469951755AAGG8GENIChomozygous734381065
146995241569952416TG15GENIChomozygous611673713
146995252069952521GGAAA14GENIChomozygous734381066
146995357669953577GGAAA4GENIChomozygous734381067
146995375669953757AG22GENIChomozygous611673714
146995428369954284CT12GENIChomozygous611673715
146995526369955264AATT10GENIChomozygous734381068
146995631869956319AAGGT29GENIChomozygous734381069
146995653569956536AACG14GENICpossibly homozygous734381070
146995657769956584ACACACA-------5GENIChomozygous734381071
146995658769956589CG--4GENIChomozygous734381072
146995896369958964CT15GENIChomozygous611673716
146996195569961956GA17GENIChomozygous611673717
146996222669962227TC5GENIChomozygous611673718
146996285869962859CT9GENIChomozygous611673719
146996692469966925A-6GENICheterozygous734381073
146996711869967119A-8GENICpossibly homozygous734381074
146996916469969165TTAAACAGTTAA12GENIChomozygous734381075
146997052269970523GA33GENIChomozygous611673720