chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265031259265031260TC16GENIChomozygous125327278
1265031412265031413CT15GENIChomozygous108636817
1265031882265031883CT4GENIChomozygous125327279
1265031883265031884TC4GENICheterozygous125327280
1265032828265032829CA31GENIChomozygous108636819
1265032973265032974TC13GENICheterozygous108636820
1265033225265033226GA24GENIChomozygous108636821
1265036061265036062TG6GENIChomozygous108636822
1265036448265036449CG10GENIChomozygous108636825
1265038265265038266TG21GENIChomozygous108636826
1265039224265039225TC20GENIChomozygous108636827
1265039739265039740GC18GENIChomozygous108636828
1265039887265039888AG5GENIChomozygous121218834
1265040637265040638CT26GENIChomozygous108636830
1265041346265041347TC16GENIChomozygous108636831