chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25846295758462958TC10GENIChomozygous109772444
25846412758464128CT26GENIChomozygous120359886
25846540058465401CT27GENICpossibly homozygous120359887
25846783858467839TC16GENIChomozygous120143507
25846839058468391GA23GENICpossibly homozygous120359889
25846981258469813CT29GENIChomozygous120359890
25847068458470685CT30GENIChomozygous120359891
25847539258475393CT15GENIChomozygous120359892
25847790858477909GA30GENICpossibly homozygous120359893
25847867458478675AG31GENIChomozygous109772458
25847994558479946TC15GENIChomozygous120143524
25848065458480655TC14GENIChomozygous109772460
25848178258481783AG33GENIChomozygous120143527
25848234458482345GA28GENIChomozygous120359894
25848355058483551AT21GENIChomozygous120143529
25848355158483552AC22GENIChomozygous120143530
25848423858484239GC31GENIChomozygous109772464
25848769658487697GA27GENICpossibly homozygous120359895
25848901058489011GA18GENIChomozygous109772468
25848927358489274CG19GENIChomozygous109772470
25849183358491834TC17GENIChomozygous109772476
25849244458492445AG33GENIChomozygous109772480
25849385258493853CT33GENIChomozygous109772482
25849439158494392TC33GENICpossibly homozygous120359896
25849486358494864CT22GENICpossibly homozygous120359897
25849696158496962TG36GENIChomozygous120359898
25849725758497258AG30GENIChomozygous120143548
25849781258497813GA23GENIChomozygous120359899
25849878858498789GA35GENIChomozygous109772492
25850059058500591CT28GENIChomozygous120359901
25850147858501479CT24GENIChomozygous120359902
25850156158501562AG34GENIChomozygous109772497
25850188158501882CT23GENICpossibly homozygous120359903
25850203858502039TC22GENICpossibly homozygous120359904
25850208358502084GC25GENIChomozygous120143552
25850259558502596GA24GENIChomozygous120359905
25850296558502966AG27GENIChomozygous120359906
25850367758503678AG27GENIChomozygous120143555
25850379758503798GA16GENIChomozygous120143556
25850383758503838AT17GENIChomozygous120143557
25850418658504187CT32GENIChomozygous120143558