chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45068780350687804AG43GENIChomozygous112647808
45068799550687996TC42GENIChomozygous112647810
45068800750688008AG43GENIChomozygous112647812
45068828050688281TC53GENIChomozygous112647814
45068856550688566GA32GENIChomozygous112647816
45068895150688952GA21GENIChomozygous112647818
45068957950689580TC35GENIChomozygous112647820
45068965750689658AG29GENIChomozygous112647822
45069005550690056AT28GENIChomozygous119276358
45069006050690061AT29GENIChomozygous119276360
45069016550690166AT36GENIChomozygous112647824
45069020650690207AG38GENIChomozygous112647826
45069051350690514CT36GENIChomozygous112647828
45069079450690795CT25GENIChomozygous112647830
45069128950691290AG29GENIChomozygous112647832
45069243750692438GT17GENIChomozygous112647834
45069266750692668GA4GENICheterozygous119276362
45069266850692669GA4GENICheterozygous119276364
45069266950692670CA4GENICheterozygous119276366