chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126165100126165101CT16GENIChomozygous113996564
5126165746126165747CT22GENIChomozygous113996566
5126165851126165852AC17GENIChomozygous113996568
5126166239126166240CT26GENIChomozygous113996570
5126166284126166285AC28GENIChomozygous113996572
5126166446126166447CT32GENIChomozygous113996574
5126166507126166508AC22GENIChomozygous113996576
5126166659126166660GC22GENIChomozygous113996578
5126166941126166942TC22GENIChomozygous113996579
5126167819126167820GA15GENIChomozygous113996583
5126168599126168600GT16GENIChomozygous113996585
5126169791126169792CG13GENIChomozygous113996589
5126170417126170418TC18GENIChomozygous113996591
5126171274126171275CT18GENIChomozygous113996595
5126171453126171454TC25GENIChomozygous113996597
5126173208126173209AG5GENIChomozygous113996609
5126173292126173293TC16GENIChomozygous113996611
5126173476126173477TC22GENIChomozygous113996613
5126174024126174025AG14GENIChomozygous113996615
5126175600126175601CT16GENIChomozygous113996617
5126175784126175785AG18GENIChomozygous113996618
5126175867126175868CT25GENIChomozygous113996620
5126175903126175904AG20GENIChomozygous113996622
5126178445126178446AG35GENIChomozygous113996624
5126179112126179113AG15GENIChomozygous113996626
5126179863126179864CG25GENIChomozygous113996628
5126182103126182104AG16GENIChomozygous113996630
5126182136126182137GA6GENIChomozygous126202891
5126182138126182139AG5GENIChomozygous126202892
5126186983126186984AC27GENIChomozygous113996632
5126187664126187665AG18GENIChomozygous113996634
5126188582126188583GA19GENIChomozygous113996636