chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2177457433177457434CG29GENICpossibly homozygous59255382
2177457678177457679AG4GENIChomozygous59255386
2177459070177459071CT15GENIChomozygous59255388
2177459775177459776GA16GENICpossibly homozygous59255390
2177460562177460563CT24GENIChomozygous59255392
2177461122177461123CA14GENICheterozygous61050945
2177461594177461595AC16GENICpossibly homozygous59255394
2177461976177461977AG31GENICpossibly homozygous59255396
2177462786177462787G-4GENICheterozygous59766459