chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109294823092948231TC27GENIChomozygous958815808
109294823292948233GA27GENIChomozygous958815809
109294896792948968TC16GENIChomozygous958815810
109294897692948977TC15GENIChomozygous958815811
109294929592949296CT17GENIChomozygous958815812
109294937292949373AT21GENIChomozygous958815813
109294939092949391TC18GENIChomozygous958815814
109294957992949580AG31GENIChomozygous958815815
109294992192949922CT23GENIChomozygous958815816
109294996492949965CA20GENIChomozygous958815817
109295023892950239CT16GENIChomozygous958815818
109295046692950467CT21GENIChomozygous958815819
109295047892950479TC18GENIChomozygous958815820
109295048292950483GT17GENIChomozygous958815821
109295049392950494CT21GENIChomozygous958815822
109295080492950805GA26GENIChomozygous958815823
109295087392950874CT25GENIChomozygous958815824
109295100592951006AC20GENIChomozygous958815825
109295107892951079GA14GENIChomozygous958815826
109295117092951171CA12GENIChomozygous958815827
109295119692951197GT14GENIChomozygous958815828
109295124592951246GT13GENIChomozygous958815829
109295126592951266TA11GENIChomozygous958815830
109295127892951279CT11GENIChomozygous958815831
109295141992951420GA18GENIChomozygous958815832
109295160992951610CT19GENIChomozygous958815833
109295179092951791GT13GENIChomozygous958815834
109295182692951827GT14GENIChomozygous958815835
109295252492952525CT33GENIChomozygous958815836
109295259992952600CT33GENIChomozygous958815837
109295260292952603GA31GENIChomozygous958815838
109295260992952610GA32GENIChomozygous958815839
109295335992953360GA22GENIChomozygous958815840
109295366292953663GA19GENIChomozygous958815841
109295469192954692AG16GENIChomozygous958815842
109295805792958058AG22GENIChomozygous958815843