chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224443454224443455GA29GENIChomozygous57110567
4224443693224443695GC--14GENIChomozygous57110569
4224443694224443695C-15GENIChomozygous57110570
4224445266224445267TTA17GENICpossibly homozygous57110572
4224445574224445575GA28GENIChomozygous57110574
4224445935224445936TTCA19GENICpossibly homozygous57110576
4224446259224446260GA18GENICpossibly homozygous57110578
4224447219224447220TA19GENIChomozygous57110580
4224447661224447662GA38GENIChomozygous57110581
4224448697224448698GA26GENICheterozygous57110585
4224448701224448702AG25GENICheterozygous57110586
4224449620224449621GGGCGC14GENIChomozygous57110588
4224450890224450891A-1GENIChomozygous58023308
4224449656224449657GA22GENICpossibly homozygous57110590
4224450299224450300TTG22GENIChomozygous57110592
4224450382224450383A-29GENIChomozygous57110594