chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1535983815359839GA4GENIChomozygous45096490
X1536021515360216AG4GENIChomozygous45096491
X1536175915361760GA12GENIChomozygous45273613
X1536187915361880TC11GENIChomozygous45273614
X1536210815362109TA6GENIChomozygous45096495
X1536228315362284AG9GENIChomozygous45273615
X1536237415362375AG9GENIChomozygous45273616
X1536298715362989AC--5GENIChomozygous45273617
X1536303715363039CA--7GENIChomozygous45273618
X1536305915363060CT8GENIChomozygous45273619
X1536307615363080CACA----8GENIChomozygous45273620
X1536374515363746CA10GENIChomozygous45096499
X1536397115363972GC5GENIChomozygous45273621
X1536402915364030GA14GENIChomozygous45273622
X1536407615364077AG14GENIChomozygous45096500
X1536413815364145GGATAAA-------6GENICheterozygous45795315
X1536421115364212T-15GENIChomozygous45273623
X1536597715365978CT12GENIChomozygous45273624
X1536660315366604TC4GENIChomozygous45096502
X1536665215366653TTA10GENIChomozygous45273625
X1536694315366944CT13GENIChomozygous45273626
X1536707915367080C-10GENIChomozygous45096503
X1536740715367408AG13GENIChomozygous45096506
X1536747515367476AG12GENIChomozygous45096507
X1536812415368125AT19GENICpossibly homozygous45273627
X1536896915368970CT13GENIChomozygous45096509
X1536897415368975CT13GENIChomozygous45096510
X1536897615368977TTTGTTG12GENIChomozygous45273628
X1536929315369294CT12GENIChomozygous45273629
X1536933615369342AAAAAA------10GENICheterozygous45795316
X1536933715369342AAAAA-----10GENICheterozygous45768169
X1536980715369808CCATATA6GENICheterozygous45096511
X1537001415370015TA16GENIChomozygous45273631
X1537087915370880AG17GENIChomozygous45273632
X1537091415370915AG16GENIChomozygous45273633
X1537107615371079TTA---11GENIChomozygous45795317
X1537500215375003CCA11GENICheterozygous45273634
X1537925915379260GGAC5GENICheterozygous45665344
X1538504715385048AC6GENIChomozygous45273635
X1538973415389735GA7GENIChomozygous45096531