chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17583921375839214CA11GENIChomozygous120867103
17583961475839615CT20GENICpossibly homozygous120867104
17583966875839669CG35GENIChomozygous120867105
17583990275839903CA12GENIChomozygous120867106
17584044875840449GA15GENIChomozygous120867107
17584112675841127AG24GENIChomozygous120867108
17584154175841542AC41GENIChomozygous120867109
17584159375841594CT49GENIChomozygous120867110
17584200775842008TA28GENIChomozygous109502058
17584530275845303CT13GENIChomozygous120867111
17584645275846453CG16GENIChomozygous120867112
17584659475846595AG33GENIChomozygous109502060
17584664975846650CA35GENIChomozygous109502061
17584924775849248AC29GENIChomozygous120867113