chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6103762600103762601GC52GENICheterozygous114924768
6103762602103762603TG53GENICheterozygous114924770
6103762623103762624AG50GENICheterozygous114924772
6103762630103762631CA50GENICheterozygous114924774
6103762633103762634CT49GENICheterozygous114924776
6103762696103762697CG59GENICheterozygous114924778
6103762699103762700GA62GENICheterozygous114924780
6103762706103762707CT63GENICheterozygous114924782
6103762707103762708CG62GENICheterozygous114924784
6103762710103762711CT61GENICheterozygous114924786
6103762756103762757TC70GENICheterozygous114924788
6103762849103762850TC34GENICheterozygous114924790
6103762978103762979GA42GENICheterozygous114924792
6103763017103763018AC41GENICheterozygous114924794
6103763105103763106AC28GENIChomozygous114924796
6103763279103763280GA70GENICheterozygous114924798
6103763438103763439CT39GENICheterozygous114924800
6103763920103763921AC44GENICheterozygous115074984
6103763926103763927TA46GENICheterozygous115074986
6103763931103763932GA43GENICheterozygous115074988