chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25846295758462958TC4GENIChomozygous109772444
25846412758464128CT14GENIChomozygous120359886
25846540058465401CT37GENIChomozygous120359887
25846666058466661AG9GENICpossibly homozygous120359888
25846783858467839TC22GENIChomozygous120143507
25846839058468391GA24GENIChomozygous120359889
25846981258469813CT30GENIChomozygous120359890
25847068458470685CT21GENIChomozygous120359891
25847539258475393CT27GENIChomozygous120359892
25847790858477909GA6GENIChomozygous120359893
25847867458478675AG11GENIChomozygous109772458
25847994558479946TC18GENIChomozygous120143524
25848065458480655TC13GENIChomozygous109772460
25848178258481783AG26GENIChomozygous120143527
25848234458482345GA29GENIChomozygous120359894
25848355058483551AT31GENIChomozygous120143529
25848355158483552AC30GENIChomozygous120143530
25848423858484239GC20GENIChomozygous109772464
25848769658487697GA23GENIChomozygous120359895
25848901058489011GA13GENIChomozygous109772468
25848927358489274CG24GENIChomozygous109772470
25849183358491834TC11GENIChomozygous109772476
25849244458492445AG24GENIChomozygous109772480
25849385258493853CT19GENIChomozygous109772482
25849439158494392TC24GENIChomozygous120359896
25849486358494864CT22GENIChomozygous120359897
25849696158496962TG19GENIChomozygous120359898
25849725758497258AG24GENIChomozygous120143548
25849781258497813GA14GENIChomozygous120359899
25849878858498789GA30GENIChomozygous109772492
25849967458499675GT20GENIChomozygous120359900
25850059058500591CT17GENIChomozygous120359901
25850147858501479CT18GENIChomozygous120359902
25850156158501562AG37GENIChomozygous109772497
25850188158501882CT28GENIChomozygous120359903
25850203858502039TC27GENIChomozygous120359904
25850208358502084GC31GENIChomozygous120143552
25850259558502596GA30GENIChomozygous120359905
25850296558502966AG22GENIChomozygous120359906
25850367758503678AG39GENIChomozygous120143555
25850383758503838AT34GENIChomozygous120143557
25850418658504187CT34GENIChomozygous120143558