chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124183114741831148GT30INTERGENIChomozygous66751571
124183134841831349TC14INTERGENIChomozygous66751573
124183212941832130TC9INTERGENIChomozygous66751575
124183213041832131GA9INTERGENIChomozygous66751577
124183221241832213CG17INTERGENIChomozygous66751579
124183241441832415TA24INTERGENIChomozygous66751581
124183251241832513CG30INTERGENIChomozygous66751583
124183319541833196GA13INTERGENICpossibly homozygous66751585
124183322141833222AG7INTERGENIChomozygous66751587
124183329541833296GC17INTERGENIChomozygous66751589
124183355141833552AG20INTERGENICheterozygous66751595
124183367641833677GA28INTERGENICpossibly homozygous66751599
124183370041833701TA24INTERGENIChomozygous66751601
124183395941833960GA18INTERGENIChomozygous66751603
124183418841834189CT13INTERGENIChomozygous66751605
124183419941834200CT12INTERGENIChomozygous66751607
124183422141834222AG14INTERGENIChomozygous66751609
124183428041834281GT13INTERGENIChomozygous66751611
124183430241834303AG19INTERGENIChomozygous66751613
124183444841834449AG12INTERGENIChomozygous66751615
124183445941834460TC13INTERGENIChomozygous66751617
124183452441834525AG14INTERGENIChomozygous66751619
124183460841834609CT19INTERGENIChomozygous66751623
124183488341834884TC28INTERGENIChomozygous66751625
124183488541834886TC29INTERGENIChomozygous66751627
124183494841834949TC28INTERGENIChomozygous66751629
124183505141835052GA16INTERGENIChomozygous66751635
124183524941835250TG18INTERGENIChomozygous66751643
124183526941835270TC18INTERGENIChomozygous66751645
124183532641835327GC25INTERGENIChomozygous66751647
124183549941835500AG26INTERGENICpossibly homozygous66751649
124183550441835505TC23INTERGENICpossibly homozygous66751651
124183553441835535GA24INTERGENIChomozygous66751653
124183559141835592AC18INTERGENIChomozygous66751655
124183563841835639CT22INTERGENICpossibly homozygous66751657
124183570041835701TG23INTERGENIChomozygous66751659
124183578341835784CT29INTERGENIChomozygous66751661