chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10103657968103657969AG54GENIChomozygous657649126
10103658439103658440AG25GENIChomozygous657649127
10103658665103658666CT63GENIChomozygous657649128
10103659475103659476AC18GENIChomozygous657649129
10103662334103662335C-9GENIChomozygous761660800
10103662601103662602CCT16GENICpossibly homozygous761660801
10103662718103662719T-5GENICheterozygous761660803
10103665767103665768AG90GENIChomozygous657649130
10103667623103667624CT25GENIChomozygous657649131
10103667793103667794AG67GENIChomozygous657649132
10103667854103667855AG41GENIChomozygous657649133
10103668206103668210GTGT----52GENIChomozygous761660804
10103668541103668543AA--22GENIChomozygous761660805
10103669968103669969CT60GENIChomozygous657649134
10103670372103670373CT47GENIChomozygous657649135