chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
82888279828882799TC3GENICheterozygous126678506
82893991628939917CT10GENIChomozygous126662624
82901621029016211TG21GENIChomozygous126662625
82906264229062643AT3GENICheterozygous126678507
82918375929183760GC10GENIChomozygous126662626
82919618829196189CG9GENIChomozygous126662627
82922177229221773TG4GENIChomozygous126678508
82937255829372559GC5GENIChomozygous126678509
82937950229379503GA33GENICpossibly homozygous126662628
82942776729427768GA13GENIChomozygous126662629
82943563829435639GC5GENIChomozygous126678510
82943567029435671GT9GENIChomozygous116443242
82951865129518652CA4GENIChomozygous126662633
82951866629518667AT5GENIChomozygous126678511
82951869629518697CA8GENIChomozygous126678512
82967951129679512CA9GENIChomozygous126662635
82969455029694551CT18GENIChomozygous117909724
82969455129694552TC18GENIChomozygous117154063
82973773229737733GA3GENICheterozygous126678513
82977174929771750TC16GENIChomozygous126678514
82980432029804321GT5GENIChomozygous126678515
82980461729804618GA6GENICheterozygous116443375
82980471229804713TC12GENICheterozygous126678516
82983970629839707AG12GENICheterozygous126678517
82986773229867733CA16GENIChomozygous126662639
82986785829867859TG14GENIChomozygous126662641
82986793329867934CA13GENIChomozygous126662642
82986802029868021CA4GENIChomozygous116443548
82988431629884317CT12GENIChomozygous116443563
82988435229884353GT19GENIChomozygous116443564
82988440529884406CA11GENIChomozygous116443565
82989213629892137GA15GENIChomozygous126662644
82991839029918391TG7GENICheterozygous126662645
82994254529942546AT4GENICheterozygous126678518