chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1204660119204660120GGT1GENIChomozygous62314512
1204660633204660634C-3GENIChomozygous62314513
1204660688204660689TTG2GENIChomozygous62314514
1204660690204660691CCTGT2GENIChomozygous62314515
1204661115204661116GA2GENIChomozygous62029988
1204661141204661142GGT1GENIChomozygous61062926
1204662335204662336GA17GENIChomozygous61062929
1204662419204662420GGT9GENIChomozygous61062930
1204662995204662996GGACCCCAAACAGA3GENIChomozygous62314516
1204663014204663018TCTG----3GENIChomozygous62236013
1204663276204663277AG15GENIChomozygous61062936
1204663417204663418GA6GENICheterozygous62029992