chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159486909159486910GA25GENIChomozygous114072707
5159488990159488991GT25GENIChomozygous114072709
5159490025159490026TG33GENIChomozygous114072710
5159490121159490122AG22GENIChomozygous114072711
5159490509159490510GA28GENIChomozygous114072712
5159493066159493067GA24GENICpossibly homozygous114159757
5159493534159493535CA8GENIChomozygous114072714
5159494903159494904TG26GENICpossibly homozygous114072716
5159495830159495831CT24GENIChomozygous114072717
5159496926159496927CT36GENIChomozygous114072718
5159497352159497353AC26GENIChomozygous114072719
5159497736159497737GC33GENIChomozygous114072720
5159498395159498396GA30GENIChomozygous114072721
5159498468159498469TC32GENIChomozygous114072722
5159498864159498865AG31GENIChomozygous114072723
5159499927159499928CT31GENIChomozygous114072724
5159500467159500468TA45GENIChomozygous114072725
5159500622159500623AG40GENIChomozygous114072726
5159501141159501142GC26GENIChomozygous114072727
5159501392159501393GA38GENIChomozygous114072728
5159501538159501539CT34GENIChomozygous114072729
5159501649159501650TC28GENIChomozygous114072730
5159502657159502658GA33GENIChomozygous114072731
5159502872159502873CG20GENIChomozygous114072732
5159503138159503139GC33GENIChomozygous114072733
5159503160159503161GC31GENIChomozygous114072734
5159503339159503340GA29GENIChomozygous114072735
5159503347159503348CT28GENIChomozygous114072736
5159503504159503505AG29GENIChomozygous114072737
5159503690159503691GA29GENIChomozygous114072738
5159503850159503851TA32GENIChomozygous114072739
5159504476159504477CT31GENIChomozygous114072740
5159504689159504690CT35GENIChomozygous114072741
5159504805159504806AG37GENIChomozygous114072742
5159504816159504817GA40GENIChomozygous114072743