chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2051062595106260CT17GENIChomozygous125177158
2051062725106273AG19GENIChomozygous125177159
2051065415106542AG22GENIChomozygous125177160
2051070615107062CT19GENIChomozygous125177163
2051070735107074TC20GENIChomozygous125177164
2051071415107142AG11GENIChomozygous125177165
2051071565107157CA20GENIChomozygous125177166
2051073625107363TC7GENIChomozygous125177167
2051073665107367AG8GENIChomozygous125177168
2051067765106777AT18GENIChomozygous125226368
2051073765107377AT10GENIChomozygous125226369
2051076745107675CT13GENIChomozygous125177171
2051081245108125TG24GENIChomozygous125177172
2051084335108434GA16GENIChomozygous125177175