chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116151057061510571CG2GENIChomozygous128943727
116151065161510652AC4GENICheterozygous132336962
116151073261510733GA6GENICheterozygous132336963
116151075661510757TC8GENICheterozygous132336964
116151124961511252GAA13GENICheterozygous128916052
116151126161511262AC13GENICheterozygous128943728
116151127761511278AC12GENICheterozygous128943729
116151129461511295AG12GENIChomozygous128943730
116151129561511296GA12GENIChomozygous128943731
116151130161511302AC12GENIChomozygous118207802
116151135761511358CT25GENICheterozygous128943732
116151135961511360GT25GENICheterozygous128943733
116151137361511373A30GENICheterozygous128916053
116151156161511561G86GENICheterozygous128916054
116151169661511697AG20GENICheterozygous118161863
116151180561511806GC30GENICheterozygous128943734
116151187561511875T47GENICheterozygous128916055
116151198061511981TG43GENICheterozygous128943735
116152278761522787G6GENICheterozygous132334869