chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
44493630644936307CT9GENICheterozygous112620823
44493955344939554CG4GENIChomozygous112620833
44493955844939559GA4GENIChomozygous112620835
44494616744946168TG27GENIChomozygous112620841
44494821244948213AG36GENIChomozygous112620843
44495462544954626AG16GENIChomozygous112620845
44495538544955386GT27GENIChomozygous112620847
44496445444964455AG28GENIChomozygous112620849
44496476844964769GA25GENIChomozygous112620851
44496721944967220GC20GENIChomozygous112620853
44496762444967625TA32GENIChomozygous112620855
44496957144969572TC17GENIChomozygous112620857