chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53421799934218000AG18GENIChomozygous55290850
53421802834218029AT16GENIChomozygous55990653
53421820834218209TA30GENIChomozygous55290851
53421823034218231GC30GENIChomozygous55990654
53421872334218724TC53GENIChomozygous55290852
53421882434218828TGTG----9GENICheterozygous56407051
53421882634218828TG--9GENICheterozygous56407053
53421887634218877G-24GENIChomozygous55990655
53421888634218887AG24GENIChomozygous55290854
53421892234218924AT--27GENIChomozygous55290855
53421925234219253AAT14GENIChomozygous55290856
53421926234219263CCT15GENIChomozygous55290857
53422005234220053CT23GENIChomozygous55290860
53422068234220683GA37GENIChomozygous55990656
53422096734220968GT33GENIChomozygous55290861
53422299634222997GGT17GENIChomozygous55869572
53422413734224138CT28GENIChomozygous55990657
53422415734224158CA28GENIChomozygous56407055
53422646134226462GGT35GENIChomozygous55990658
53422988734229888AAAT15GENICpossibly homozygous55290875
53423083834230839GA29GENIChomozygous55290877
53423193434231935CT26GENIChomozygous55290883
53423416334234164GA27GENIChomozygous55990659
53423672434236725TC39GENIChomozygous55290888
53423794334237944T-15GENICheterozygous55990660
53423809434238110ATATATATATATATAT----------------7GENICpossibly homozygous56526248
53423972334239724CT35GENIChomozygous55990661
53423809634238110ATATATATATATAT--------------7GENICheterozygous56486327