chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1535983815359839GA2GENIChomozygous45096490
X1536021515360216AG7GENIChomozygous45096491
X1536175915361760GA6GENIChomozygous45273613
X1536187915361880TC1GENIChomozygous45273614
X1536210815362109TA9GENIChomozygous45096495
X1536228315362284AG12GENIChomozygous45273615
X1536237415362375AG8GENIChomozygous45273616
X1536298715362989AC--8GENIChomozygous45273617
X1536303715363039CA--17GENIChomozygous45273618
X1536305915363060CT15GENIChomozygous45273619
X1536307515363076CCCA6GENICheterozygous45096497
X1536307615363080CACA----6GENICheterozygous45273620
X1536374515363746CA7GENIChomozygous45096499
X1536397115363972GC5GENIChomozygous45273621
X1536402915364030GA4GENIChomozygous45273622
X1536407615364077AG8GENIChomozygous45096500
X1536421115364212T-8GENIChomozygous45273623
X1536597715365978CT18GENIChomozygous45273624
X1536660315366604TC7GENIChomozygous45096502
X1536694315366944CT12GENIChomozygous45273626
X1536707915367080C-6GENIChomozygous45096503
X1536707915367080CCAAA6GENICheterozygous45096504
X1536740715367408AG16GENIChomozygous45096506
X1536747515367476AG11GENIChomozygous45096507
X1536812415368125AT9GENIChomozygous45273627
X1536896915368970CT7GENIChomozygous45096509
X1536897415368975CT9GENIChomozygous45096510
X1536897615368977TTTGTTG8GENIChomozygous45273628
X1536929315369294CT11GENICheterozygous45273629
X1536933615369341AAAAA-----4GENIChomozygous45273630
X1536980715369808CCATATA1GENIChomozygous45096511
X1537001415370015TA13GENIChomozygous45273631
X1537087915370880AG9GENIChomozygous45273632
X1537091415370915AG10GENIChomozygous45273633
X1537107015371073TTA---1GENIChomozygous45096514
X1537500215375003CCA4GENIChomozygous45273634
X1538504715385048AC7GENIChomozygous45273635
X1538682615386827GA17GENIChomozygous45273636
X1538973415389735GA10GENIChomozygous45096531
X1536898115368982TG10GENICheterozygous45323268
X1538107315381077AGAT----5GENIChomozygous45252022