chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91795246817952469AG16GENIChomozygous117769617
91795454517954546CT15GENIChomozygous117769619
91795666517956666CT22GENIChomozygous117271140
91795718417957185GT13GENIChomozygous126497956
91795724617957247GA8GENIChomozygous126497957
91795951817959519TA10GENIChomozygous117271149
91796282717962828GA21GENIChomozygous117769621
91796428217964283GA13GENIChomozygous117271160
91796802017968021AG11GENIChomozygous117769623
91797012217970123AT3GENICheterozygous126590067
91797067317970674AG18GENIChomozygous117271178
91797105117971052CT15GENIChomozygous117271180
91797359217973593GA6GENIChomozygous117769625
91797400717974008AG16GENIChomozygous117271183
91797424317974244CT21GENIChomozygous117769627
91798081217980813TC15GENIChomozygous117271202
91798181517981816GA30GENICpossibly homozygous117769629
91798265817982659TG22GENIChomozygous117769631
91798645717986458TA21GENIChomozygous117271219
91798760317987604AG20GENIChomozygous117271224