chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X3779366237793663TG6GENIChomozygous951337431
X3779369537793696TG5GENIChomozygous951337432
X3780565437805655GA2GENIChomozygous951337433
X3782497837824979TG9GENIChomozygous951337434
X3793179637931797GT9GENIChomozygous951337435
X3793746737937468CT9GENIChomozygous951337436
X3793772537937726CT10GENIChomozygous951337437
X3793772637937727TC10GENIChomozygous951337438
X3795708837957089CA15GENICheterozygous951337439
X3796746337967464TG8GENIChomozygous951337440
X3799591837995919GT10GENIChomozygous951337441
X3799833337998334GA8GENIChomozygous951337442
X3799833737998338GA8GENIChomozygous951337443
X3799833937998340GA7GENIChomozygous951337444
X3799834437998345GA8GENIChomozygous951337445
X3801395538013956AT4GENIChomozygous951337446
X3806253938062540AT6GENIChomozygous951337447
X3806274638062747GT3GENIChomozygous951337448
X3817042238170423TG8GENICpossibly homozygous951337449
X3819409338194094CA13GENICheterozygous951337450
X3819409638194097TA11GENICheterozygous951337451