chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
730625723062573TC5GENIChomozygous115546561
730626723062673CT22GENIChomozygous115546563
730668803066881CG8GENICheterozygous126594424
730670903067091CA21GENIChomozygous115546567
730671583067159CT21GENIChomozygous115546569
730672773067278GA12GENIChomozygous115546571
730673013067302GA11GENIChomozygous115546573
730689453068946GC13GENIChomozygous115546575
730707343070735TC28GENIChomozygous115546579
730715753071576AT10GENIChomozygous115546581
730727493072750TG12GENIChomozygous115546585
730779933077994AG12GENIChomozygous115546589
730791163079117CT31GENIChomozygous115546591
730722583072259AC21GENIChomozygous126503308
730788573078858CG16GENIChomozygous126503310
730796783079679CT12GENICheterozygous126594425
730797043079705AT25GENICheterozygous126503316
730812143081215CT19GENIChomozygous115546593
730820853082086GT4GENICheterozygous126594426
730830403083041CT7GENIChomozygous126503318
730838843083885AG21GENICheterozygous115546601
730847203084721TG29GENIChomozygous115546603
730872163087217AG21GENIChomozygous115546607
730874003087401AG11GENICheterozygous115546609
730885803088581GA20GENIChomozygous115546611
730887693088770GA8GENICheterozygous122882630
730887933088794GA9GENICheterozygous116360490
730893583089359TG9GENICheterozygous126556975
730902353090236TC18GENIChomozygous115546613
730913203091321TC14GENIChomozygous115546615
730921453092146CT7GENICheterozygous115546617
730941693094170CT5GENIChomozygous126594427