chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2177457433177457434CG52GENIChomozygous59255382
2177457600177457601TTGG5GENIChomozygous59766458
2177457601177457602TG24GENIChomozygous59255384
2177457678177457679AG22GENIChomozygous59255386
2177459070177459071CT26GENICpossibly homozygous59255388
2177459775177459776GA21GENIChomozygous59255390
2177460562177460563CT30GENIChomozygous59255392
2177461594177461595AC19GENIChomozygous59255394
2177461976177461977AG37GENIChomozygous59255396
2177462783177462787TTTG----13GENICpossibly homozygous59255398
2177462786177462787G-3GENIChomozygous59766459
2177462797177462798AT15GENICheterozygous59255400