chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10103657968103657969AG16GENIChomozygous650046414
10103658439103658440AG21GENIChomozygous650046415
10103658665103658666CT14GENIChomozygous650046416
10103659475103659476AC22GENIChomozygous650046417
10103662334103662335C-4GENICheterozygous757147169
10103662601103662602CCT16GENICheterozygous757147170
10103662715103662719TTTT----9GENICheterozygous757147171
10103665767103665768AG21GENIChomozygous650046418
10103667623103667624CT21GENIChomozygous650046419
10103667793103667794AG28GENIChomozygous650046420
10103667854103667855AG21GENIChomozygous650046421
10103668206103668210GTGT----15GENIChomozygous757147173
10103668541103668543AA--13GENICpossibly homozygous757147174
10103669968103669969CT28GENIChomozygous650046422
10103670372103670373CT20GENIChomozygous650046423