chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1116152810116152811AT27GENIChomozygous108191066
1116153822116153823AG30GENIChomozygous108191067
1116153924116153925CT26GENIChomozygous108191068
1116154294116154295TG30GENIChomozygous108191070
1116156185116156186TC42GENIChomozygous109514885
1116156399116156400GT19GENIChomozygous108191071
1116156475116156476GA20GENIChomozygous108191072
1116156538116156539TC22GENIChomozygous108191073
1116158457116158458CT17GENIChomozygous109514891
1116160641116160642CA24GENIChomozygous108191090
1116160946116160947GA35GENIChomozygous109514895
1116161266116161267TC18GENIChomozygous108191091