chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10103657968103657969AG12GENIChomozygous646242078
10103658439103658440AG14GENIChomozygous646242079
10103658665103658666CT15GENIChomozygous646242080
10103659475103659476AC22GENIChomozygous646242081
10103662334103662335C-5GENIChomozygous754867920
10103662601103662602CCT16GENICheterozygous754867921
10103665767103665768AG9GENIChomozygous646242082
10103667623103667624CT16GENIChomozygous646242083
10103667793103667794AG15GENIChomozygous646242084
10103667854103667855AG20GENIChomozygous646242085
10103668206103668210GTGT----14GENIChomozygous754867922
10103668541103668543AA--13GENIChomozygous754867923
10103669968103669969CT14GENIChomozygous646242086
10103670372103670373CT25GENIChomozygous646242087