chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10103657968103657969AG10GENIChomozygous664825395
10103658439103658440AG25GENIChomozygous664825396
10103658665103658666CT27GENIChomozygous664825397
10103659475103659476AC20GENIChomozygous664825398
10103662334103662335C-10GENIChomozygous766051559
10103662601103662602CCT12GENIChomozygous766051560
10103662718103662719T-3GENICheterozygous766051562
10103665767103665768AG13GENIChomozygous664825399
10103667623103667624CT24GENIChomozygous664825400
10103667793103667794AG21GENIChomozygous664825401
10103667854103667855AG18GENIChomozygous664825402
10103668206103668210GTGT----16GENIChomozygous766051563
10103668541103668543AA--13GENIChomozygous766051564
10103669968103669969CT20GENIChomozygous664825403
10103670372103670373CT16GENIChomozygous664825404