chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53421799934218000AG14GENIChomozygous55290850
53421802834218029AT9GENIChomozygous55990653
53421820834218209TA23GENIChomozygous55290851
53421823034218231GC17GENIChomozygous55990654
53421872334218724TC20GENIChomozygous55290852
53421882634218828TG--3GENIChomozygous56407053
53421887634218877G-11GENIChomozygous55990655
53421888634218887AG12GENIChomozygous55290854
53421892234218924AT--21GENIChomozygous55290855
53421925234219253AAT12GENIChomozygous55290856
53421926234219263CCT13GENIChomozygous55290857
53422005234220053CT25GENIChomozygous55290860
53422068234220683GA20GENIChomozygous55990656
53422096734220968GT21GENIChomozygous55290861
53422299634222997GGTTT16GENICheterozygous55290863
53422299634222997GGT16GENICpossibly homozygous55869572
53422413734224138CT24GENIChomozygous55990657
53422415734224158CA20GENIChomozygous56407055
53422646134226462GGT18GENIChomozygous55990658
53422988734229888AAAT11GENIChomozygous55290875
53423083834230839GA22GENIChomozygous55290877
53423193434231935CT16GENIChomozygous55290883
53423416334234164GA30GENIChomozygous55990659
53423672434236725TC26GENIChomozygous55290888
53423794334237944T-9GENIChomozygous55990660