chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3149628938149628939TC20INTERGENIChomozygous72226664
3149628977149628978TC19INTERGENIChomozygous72226666
3149629032149629033CT18INTERGENIChomozygous72226668
3149629308149629309TA40INTERGENIChomozygous72226670
3149629374149629375TC28INTERGENIChomozygous72226672
3149629477149629478CT35INTERGENIChomozygous72226673
3149629514149629515CA43INTERGENIChomozygous72226675
3149629741149629742AG35INTERGENIChomozygous72226677
3149629802149629803GA22INTERGENIChomozygous72226679
3149630285149630286TG18INTERGENIChomozygous72226681
3149630376149630377TC11INTERGENIChomozygous72226685
3149630384149630385AG15INTERGENIChomozygous72226687
3149630487149630488AG34INTERGENIChomozygous72226689
3149630660149630661AG32INTERGENIChomozygous72226691
3149631225149631226AG45INTERGENIChomozygous72226695
3149631700149631701TC12INTERGENIChomozygous72226697
3149632150149632151GA28INTERGENIChomozygous72226699
3149632300149632301TC26INTERGENICpossibly homozygous72226701