chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3146696873146696874AG36GENIChomozygous112185612
3146697406146697407AG25GENIChomozygous112185613
3146700594146700595CT24GENIChomozygous112185615
3146704476146704477AT22GENIChomozygous112185617
3146704557146704558CT22GENIChomozygous112185618
3146705651146705652CT33GENIChomozygous112185619
3146705818146705819CT32GENIChomozygous112185620
3146705889146705890GA32GENIChomozygous112185621
3146705930146705931TA30GENIChomozygous112185622
3146706716146706717TA21GENIChomozygous112185623
3146707418146707419GT23GENICpossibly homozygous112185625
3146707605146707606CT27GENIChomozygous112185626
3146707635146707636GA21GENIChomozygous112185627
3146707825146707826CT21GENIChomozygous112185628
3146707878146707879TA26GENIChomozygous119880457
3146707884146707885GA29GENIChomozygous119880458
3146708009146708010GA30GENIChomozygous112185629
3146708083146708084GT37GENIChomozygous112185630
3146708949146708950AG25GENIChomozygous119880459
3146709165146709166CA16GENIChomozygous112185632
3146709385146709386TG17GENIChomozygous112185633
3146709713146709714AC19GENIChomozygous112185634
3146710189146710190TC15GENIChomozygous112185636
3146710196146710197TC16GENIChomozygous112185637
3146710253146710254AC24GENIChomozygous112185638
3146710651146710652TC8GENIChomozygous112185641
3146710768146710769AG13GENIChomozygous112185642
3146710796146710797CA13GENIChomozygous111767754
3146710800146710801GT13GENIChomozygous111767756
3146710804146710805GC13GENIChomozygous111767758
3146710848146710849CT13GENIChomozygous111767760
3146711332146711333AG19GENIChomozygous112185645
3146711593146711594GA18GENIChomozygous112185647
3146712395146712396AG25GENIChomozygous112185648
3146712690146712691AC23GENIChomozygous112185650
3146712824146712825CT35GENIChomozygous112185651
3146714788146714789GA23GENIChomozygous119880460
3146714829146714830AG23GENIChomozygous112185652
3146716099146716100TC11GENIChomozygous119880461
3146716294146716295GA25GENIChomozygous119880462