chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104703176547031765GGGTTTGCAACCCCATAGA12GENIChomozygous128814498
104703344047033443CAT12GENIChomozygous128814500
104703345047033451G12GENIChomozygous128814501
104703346847033469G11GENIChomozygous128814502
104703347347033474A10GENIChomozygous128814503
104703348047033481AT10GENIChomozygous123353954
104703348347033484GA10GENIChomozygous123353955
104703348947033490A9GENIChomozygous128814504
104703349647033497A9GENIChomozygous128814505
104703351447033514T7GENIChomozygous128814506
104703351947033520A7GENIChomozygous128814507
104703352847033529A4GENIChomozygous128814508
104703373247033732G5GENIChomozygous128814512
104703354447033545C3GENIChomozygous128814509
104703370747033708C5GENIChomozygous128814510
104703372347033725AA5GENIChomozygous128814511
104703368147033682A4GENIChomozygous130776720
104703368947033692TCG4GENIChomozygous130776721
104703369647033696T4GENIChomozygous130776722
104703373547033735T5GENIChomozygous128814513
104703375447033755C5GENIChomozygous128814514
104703375947033776TATTTTTTTTTTTTTTT5GENIChomozygous128814515
104703378647033787T5GENIChomozygous128814516
104703379547033796A5GENIChomozygous128814517
104703380947033811AA5GENIChomozygous128814518
104703388947033889T5GENIChomozygous128814522
104703390047033901A5GENIChomozygous128814523
104703390447033905A5GENIChomozygous128814524
104703391447033914G6GENIChomozygous128814525
104703391647033919AAT6GENIChomozygous128814526
104703392347033923C6GENIChomozygous128814527
104703392647033927G6GENIChomozygous128814528
104703393147033932C6GENIChomozygous128814529
104703394047033941TA7GENIChomozygous116587123
104703394247033943AG7GENIChomozygous116587125
104703395647033957T8GENIChomozygous128814530
104703396247033964GC8GENIChomozygous128814531
104703388147033881T5GENIChomozygous129968907