chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1128692439128692440GA22GENIChomozygous108927523
1128693611128693612AG15GENIChomozygous108927527
1128694723128694724AC16GENIChomozygous108927533
1128695179128695180CT18GENIChomozygous109137450
1128697260128697261TC21GENIChomozygous108927538
1128697941128697942GA13GENIChomozygous109137452
1128698510128698511AG20GENIChomozygous108927541
1128698977128698978TC10GENIChomozygous108927542
1128699218128699219CT21GENIChomozygous109137454
1128699932128699933CT21GENIChomozygous109137456
1128700144128700145AG27GENIChomozygous109137458
1128701181128701182AG14GENIChomozygous108927544
1128701750128701751CT7GENIChomozygous120485702
1128702452128702453AC4GENIChomozygous108927549
1128703649128703650TA16GENIChomozygous109137462
1128703935128703936AG9GENIChomozygous108927551
1128703967128703968TC8GENIChomozygous108927552
1128703996128703997CT17GENIChomozygous109137464
1128704172128704173AG7GENIChomozygous108927554
1128704245128704246TC17GENIChomozygous108927555
1128704686128704687GA12GENIChomozygous109137466
1128705158128705159TA29GENIChomozygous108927560
1128705633128705634CA12GENIChomozygous109137468
1128705697128705698AG4GENIChomozygous109137470
1128706421128706422AT26GENIChomozygous109137474
1128706685128706686TC24GENIChomozygous108927568
1128706984128706985AT10GENIChomozygous109517011
1128706985128706986TC9GENIChomozygous109517012
1128707198128707199GA9GENIChomozygous109137476
1128707379128707380AT21GENICpossibly homozygous109137478
1128707526128707527CA8GENIChomozygous108927573
1128711638128711639TC10GENIChomozygous108927580
1128715549128715550CT16GENIChomozygous109137480
1128718375128718376CA3GENICheterozygous109137482
1128719098128719099AG13GENIChomozygous108927596
1128704389128704390CT4GENIChomozygous125429806