chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122395622923956230AC21GENIChomozygous118336940
122395666323956664TC21GENIChomozygous115286247
122395843823958439CT13GENIChomozygous118336941
122395850823958509GA27GENIChomozygous115286249
122396198423961985AG16GENIChomozygous118336942
122396444223964443CT10GENIChomozygous118336943
122396548923965490CT15GENIChomozygous115286259
122396869523968696CA14GENIChomozygous118336946
122396943723969438CT17GENIChomozygous115446259
122397294223972943AT9GENIChomozygous118336949
122397297323972974TA11GENIChomozygous118336950
122397439323974394AG18GENIChomozygous115286267
122397491023974911CT25GENIChomozygous118336952
122397653823976539CT21GENIChomozygous115422070
122397669423976695AG22GENIChomozygous115286271
122397726623977267TC11GENIChomozygous115286273
122397880823978809AG20GENIChomozygous118336959
122398124023981241CT7GENIChomozygous126244576
122396491523964916CG14GENIChomozygous126244572
122397652723976528CA16GENIChomozygous126244573
122397747223977473CT18GENIChomozygous126244574
122398088023980881AT18GENIChomozygous126244575
122398126523981266GT21GENIChomozygous115446261
122398129323981294TC25GENIChomozygous115286279
122398204123982042CG13GENIChomozygous115286281
122398296323982964TC8GENICheterozygous118336966
122398306323983064AC9GENICheterozygous126244577
122398325823983259AG9GENIChomozygous115422072
122398584023985841TC10GENIChomozygous115286283
122398684223986843TA12GENIChomozygous126244578
122398695723986958TG26GENICpossibly homozygous126244579