chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31249163212491633AG20GENIChomozygous111449988
31249548012495480A7GENIChomozygous127850541
31249548212495482AGGA7GENIChomozygous127850542
31249548312495484CA7GENIChomozygous119667067
31249579512495796GT8GENIChomozygous111449991
31249582712495828TC8GENIChomozygous119712219
31249582912495829T8GENIChomozygous129887641
31249583112495831A8GENIChomozygous129887642
31249583512495837GA8GENIChomozygous129887643
31249584212495843T8GENIChomozygous129887644
31249585112495851A8GENIChomozygous129887645
31249585512495855G8GENIChomozygous129887646
31249586212495862G7GENIChomozygous129887647
31249586912495869AA7GENIChomozygous129887648
31249587112495872CA7GENIChomozygous129894010
31249587312495874CA7GENIChomozygous129894011
31249587512495875TAGAT6GENIChomozygous129887649
31249587512495876CA6GENIChomozygous129894012
31249588412495885G6GENIChomozygous129887650
31249588712495887GC6GENIChomozygous129887651
31249588912495889C6GENIChomozygous129887652
31249589512495895AG6GENIChomozygous129887653
31249589812495898A6GENIChomozygous129887654
31249671512496719CCAT12GENIChomozygous132038581
31249760112497602AG18GENIChomozygous111449995
31250143012501431AG13GENIChomozygous111876985
31250214212502143C2GENICheterozygous134480051
31250383312503834TC10GENIChomozygous111450000
31250768212507682AAAC9GENIChomozygous132038582
31250788412507890ACAAGA16GENIChomozygous132038583