chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226233332226233333TC26GENIChomozygous61601812
1226233655226233656AACCAGTG34GENIChomozygous61601813
1226233826226233827GA43GENIChomozygous61601814
1226234349226234350GA31GENIChomozygous61601816
1226235419226235420GT43GENIChomozygous61601818
1226236252226236253TC26GENIChomozygous61601819
1226237335226237336CCTTTTT12GENIChomozygous61103797
1226237488226237489CT27GENIChomozygous61601821
1226237914226237915GA18GENIChomozygous61601823
1226238567226238568CT17GENIChomozygous61601824
1226238594226238595TC25GENICpossibly homozygous61601826
1226239519226239521AC--19GENIChomozygous61601828
1226239595226239596AC26GENICpossibly homozygous61601829
1226241522226241523AG15GENIChomozygous61103802
1226242167226242168TC31GENIChomozygous61103804
1226242483226242484AAAC17GENIChomozygous61103805
1226242977226242978GA10GENIChomozygous61601831
1226243051226243052A-2GENIChomozygous61321642
1226243066226243067G-16GENICheterozygous61103806
1226243652226243653AG42GENIChomozygous61103807
1226244331226244332GC26GENIChomozygous61601832