chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1222478664222478665CT21GENIChomozygous108546750
1222478742222478743CA7GENIChomozygous108770295
1222479073222479074GA19GENIChomozygous108546752
1222481309222481310TA4GENIChomozygous108546754
1222482552222482553AG16GENIChomozygous108546756
1222488385222488386GA22GENIChomozygous108546765
1222488573222488574GA29GENIChomozygous108546767
1222488662222488663CG25GENIChomozygous108546769
1222489157222489158CG29GENIChomozygous108546772
1222490125222490126AG27GENIChomozygous108546774
1222494485222494486TG27GENIChomozygous108546778