chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
498818419881842AC22GENIChomozygous112492720
498821159882116GT24GENIChomozygous112492722
498823949882395GA27GENIChomozygous112492724
498826919882692AG18GENIChomozygous112492726
498827329882733AC21GENIChomozygous112492728
498828159882816CT11GENIChomozygous112492730
498829369882937TC6GENIChomozygous112492731
498831699883170AC6GENIChomozygous112492733
498839749883975TC24GENIChomozygous112492735
498840489884049TA33GENIChomozygous112492737
498855309885531GA23GENIChomozygous112492739
498856899885690GA28GENIChomozygous112492741
498857889885789GA28GENIChomozygous112492743
498890459889046GA20GENIChomozygous112492753
498899719889972CT17GENIChomozygous112492755
498907689890769AG23GENIChomozygous112492757
498908559890856CT23GENIChomozygous112492759
498915089891509GT13GENIChomozygous119273134
498928609892861AG28GENIChomozygous112492763
498940089894009CT18GENIChomozygous112492765
498970109897011CT19GENIChomozygous112492767
498977069897707TC25GENIChomozygous112492769
498982009898201TC6GENIChomozygous112492771
498996379899638TA26GENIChomozygous112492773
498997189899719AG37GENIChomozygous112492775
499017529901753AG29GENIChomozygous112492779
499022829902283TC21GENIChomozygous112492781
499027559902756CT17GENIChomozygous112492785
499028959902896AG27GENIChomozygous112492787
499046039904604AG19GENIChomozygous112492789
499048079904808TC15GENIChomozygous112492791
499050639905064CT12GENIChomozygous112492793
499060069906007GA23GENIChomozygous112492795
499062269906227AG10GENIChomozygous112492797
499079809907981CT24GENIChomozygous112492799