chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124183114741831148GT32INTERGENIChomozygous66751571
124183134841831349TC13INTERGENIChomozygous66751573
124183212941832130TC21INTERGENIChomozygous66751575
124183213041832131GA21INTERGENIChomozygous66751577
124183221241832213CG25INTERGENIChomozygous66751579
124183241441832415TA23INTERGENIChomozygous66751581
124183251241832513CG36INTERGENIChomozygous66751583
124183319541833196GA55INTERGENICpossibly homozygous66751585
124183322141833222AG47INTERGENIChomozygous66751587
124183329541833296GC50INTERGENIChomozygous66751589
124183355141833552AG46INTERGENICpossibly homozygous66751595
124183367641833677GA54INTERGENICpossibly homozygous66751599
124183370041833701TA34INTERGENIChomozygous66751601
124183395941833960GA29INTERGENIChomozygous66751603
124183418841834189CT27INTERGENIChomozygous66751605
124183419941834200CT26INTERGENIChomozygous66751607
124183422141834222AG27INTERGENIChomozygous66751609
124183428041834281GT26INTERGENIChomozygous66751611
124183430241834303AG22INTERGENIChomozygous66751613
124183444841834449AG28INTERGENIChomozygous66751615
124183445941834460TC29INTERGENIChomozygous66751617
124183452441834525AG23INTERGENIChomozygous66751619
124183460841834609CT22INTERGENIChomozygous66751623
124183488341834884TC32INTERGENIChomozygous66751625
124183488541834886TC33INTERGENIChomozygous66751627
124183494841834949TC25INTERGENIChomozygous66751629
124183505141835052GA12INTERGENIChomozygous66751635
124183524941835250TG12INTERGENIChomozygous66751643
124183526941835270TC34INTERGENIChomozygous66751645
124183532641835327GC24INTERGENIChomozygous66751647
124183549941835500AG28INTERGENIChomozygous66751649
124183550441835505TC28INTERGENIChomozygous66751651
124183553441835535GA31INTERGENIChomozygous66751653
124183559141835592AC35INTERGENIChomozygous66751655
124183563841835639CT32INTERGENIChomozygous66751657
124183570041835701TG48INTERGENIChomozygous66751659
124183578341835784CT33INTERGENIChomozygous66751661