chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159486904159486905TC27GENIChomozygous118847300
5159486909159486910GA27GENIChomozygous114072707
5159488990159488991GT18GENIChomozygous114072709
5159490025159490026TG18GENIChomozygous114072710
5159490121159490122AG22GENIChomozygous114072711
5159490509159490510GA25GENIChomozygous114072712
5159494903159494904TG13GENIChomozygous114072716
5159495830159495831CT19GENIChomozygous114072717
5159496926159496927CT29GENIChomozygous114072718
5159497352159497353AC18GENIChomozygous114072719
5159497736159497737GC17GENIChomozygous114072720
5159498395159498396GA25GENIChomozygous114072721
5159498468159498469TC26GENIChomozygous114072722
5159498864159498865AG18GENIChomozygous114072723
5159499927159499928CT34GENIChomozygous114072724
5159500467159500468TA24GENIChomozygous114072725
5159500622159500623AG31GENIChomozygous114072726
5159501392159501393GA31GENIChomozygous114072728
5159501538159501539CT31GENIChomozygous114072729
5159501649159501650TC28GENIChomozygous114072730
5159502657159502658GA29GENIChomozygous114072731
5159503138159503139GC23GENIChomozygous114072733
5159503160159503161GC21GENIChomozygous114072734
5159503339159503340GA9GENIChomozygous114072735
5159503347159503348CT10GENIChomozygous114072736
5159503504159503505AG13GENIChomozygous114072737
5159503690159503691GA20GENIChomozygous114072738
5159504476159504477CT21GENIChomozygous114072740
5159504689159504690CT17GENIChomozygous114072741
5159504805159504806AG23GENIChomozygous114072742
5159504816159504817GA24GENIChomozygous114072743