chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159486904159486905TC21GENIChomozygous118847300
5159486909159486910GA20GENIChomozygous114072707
5159488990159488991GT7GENIChomozygous114072709
5159490025159490026TG18GENIChomozygous114072710
5159490121159490122AG20GENIChomozygous114072711
5159490509159490510GA14GENIChomozygous114072712
5159493066159493067GA21GENIChomozygous114159757
5159494903159494904TG13GENIChomozygous114072716
5159495830159495831CT15GENIChomozygous114072717
5159496926159496927CT25GENIChomozygous114072718
5159497352159497353AC17GENIChomozygous114072719
5159498395159498396GA19GENIChomozygous114072721
5159498468159498469TC15GENIChomozygous114072722
5159498864159498865AG15GENIChomozygous114072723
5159499927159499928CT16GENIChomozygous114072724
5159500467159500468TA18GENIChomozygous114072725
5159500622159500623AG8GENIChomozygous114072726
5159501392159501393GA15GENIChomozygous114072728
5159501538159501539CT17GENIChomozygous114072729
5159501649159501650TC21GENIChomozygous114072730
5159503339159503340GA15GENIChomozygous114072735
5159502657159502658GA13GENIChomozygous114072731
5159503138159503139GC16GENIChomozygous114072733
5159503160159503161GC16GENIChomozygous114072734
5159503347159503348CT16GENIChomozygous114072736
5159503504159503505AG9GENIChomozygous114072737
5159503690159503691GA14GENIChomozygous114072738
5159504476159504477CT9GENIChomozygous114072740
5159504689159504690CT24GENIChomozygous114072741
5159504805159504806AG13GENIChomozygous114072742
5159504816159504817GA11GENIChomozygous114072743