chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104703176547031765GGGTTTGCAACCCCATAGA34GENIChomozygous128814498
104703344047033443CAT21GENIChomozygous128814500
104703345047033451G20GENIChomozygous128814501
104703346847033469G16GENIChomozygous128814502
104703347347033474A15GENIChomozygous128814503
104703348947033490A14GENIChomozygous128814504
104703349647033497A12GENIChomozygous128814505
104703351447033514T11GENIChomozygous128814506
104703351947033520A11GENIChomozygous128814507
104703373547033735T14GENIChomozygous128814513
104703348047033481AT15GENIChomozygous123353954
104703348347033484GA14GENIChomozygous123353955
104703352847033529A7GENIChomozygous128814508
104703354447033545C2GENIChomozygous128814509
104703372347033725AA13GENIChomozygous128814511
104703373247033732G14GENIChomozygous128814512
104703375447033755C18GENIChomozygous128814514
104703375947033776TATTTTTTTTTTTTTTT19GENIChomozygous128814515
104703378647033787T21GENIChomozygous128814516
104703379547033796A22GENIChomozygous128814517
104703380947033811AA27GENIChomozygous128814518
104703383347033834C34GENIChomozygous128814519
104703384547033847GG33GENIChomozygous128814520
104703385247033855CAA31GENIChomozygous128814521
104703385847033858T32GENIChomozygous129968906
104703388147033881T33GENIChomozygous129968907
104703388947033889T34GENIChomozygous128814522
104703390047033901A33GENIChomozygous128814523
104703390447033905A34GENIChomozygous128814524
104703391447033914G36GENIChomozygous128814525
104703391647033919AAT36GENIChomozygous128814526
104703392347033923C35GENIChomozygous128814527
104703392647033927G36GENIChomozygous128814528
104703393147033932C37GENIChomozygous128814529
104703394047033941TA34GENIChomozygous116587123
104703394247033943AG34GENIChomozygous116587125
104703395647033957T35GENIChomozygous128814530
104703396247033964GC34GENIChomozygous128814531