chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138828851288288513GA4GENIChomozygous49852408
138828869388288694AG6GENIChomozygous49852409
138828896088288961GA8GENIChomozygous49852410
138828900588289006CT7GENIChomozygous50953624
138828945888289461CGG---7GENIChomozygous50953626
138828946288289463TA7GENIChomozygous50953628
138828949288289493GC7GENIChomozygous49852411
138829098488291001AAAAGAAAGAAAGAAAG-----------------2GENIChomozygous50953632
138829157588291584CAGCCAGAG---------1GENIChomozygous49852420
138829228788292288T-4GENIChomozygous49960540
138829235288292353GGT1GENIChomozygous49852422
138829298288292983T-8GENIChomozygous49852433
138829329988293300TC6GENIChomozygous49852434
138829331788293318GA6GENIChomozygous51221108
138829338488293385TC1GENIChomozygous49852435
138829472388294724AG5GENIChomozygous49852437
138829480288294803GA9GENIChomozygous49852438
138829575888295762ACAC----3GENICheterozygous50584704
138829580888295809GGCA1GENIChomozygous49852444
138829622488296225CT5GENIChomozygous49852447
138829871788298718TA8GENIChomozygous49852450
138829880888298809GA9GENIChomozygous49852451
138829894688298947GGCACA2GENIChomozygous49960545
138829936688299367GA14GENIChomozygous49852458
138829940388299404CCATAGGCTTGTCCATATAGGCTTGTCCAT8GENIChomozygous50497059
138829945788299458GA13GENIChomozygous49852459
138829972588299726GT10GENIChomozygous49852460
138830022688300227GA8GENIChomozygous49852461
138830147988301480CCTG4GENIChomozygous49852467
138830330288303306CACA----1GENIChomozygous50528892
138830341288303413TTA11GENICpossibly homozygous49852475
138830364988303650GA9GENIChomozygous49852476
138830539588305396A-5GENIChomozygous49852477
138830594588305947CA--8GENICheterozygous50566299
138830597888305979GA11GENIChomozygous51221110
138830659988306600A-4GENIChomozygous49852480
138830674488306745AG6GENIChomozygous49852481
138830749388307494CT4GENIChomozygous49852483
138830753288307540ACACACAC--------3GENIChomozygous50953638
138830801188308012A-8GENIChomozygous50128219