chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155294274155294275CT13GENIChomozygous943964871
5155294360155294361TC8GENIChomozygous943964872
5155295748155295749TC19GENIChomozygous943964873
5155297253155297254TA21GENIChomozygous943964874
5155300981155300982TG22GENIChomozygous943964875
5155302190155302191GA27GENIChomozygous943964876
5155307760155307761AG19GENIChomozygous943964877
5155308085155308086CT26GENIChomozygous943964878
5155308199155308200AC27GENIChomozygous943964879
5155308271155308272CT17GENIChomozygous943964880
5155308396155308397TC28GENIChomozygous943964881
5155308975155308976TC25GENIChomozygous943964882
5155309320155309321TG21GENIChomozygous943964883
5155309638155309639TG17GENIChomozygous943964884
5155309712155309713CT33GENIChomozygous943964885
5155311536155311537GC24GENIChomozygous943964886
5155311877155311878AG20GENIChomozygous943964887
5155311999155312000AG27GENIChomozygous943964888
5155312352155312353AT34GENIChomozygous943964889
5155316409155316410AG31GENIChomozygous943964890
5155316472155316473TA34GENIChomozygous943964891
5155316661155316662CT29GENIChomozygous943964892
5155317165155317166TC15GENIChomozygous943964893
5155318171155318172CT26GENIChomozygous943964894
5155318392155318393CT18GENIChomozygous943964895
5155318688155318689AG20GENIChomozygous943964896
5155319466155319467GA31GENIChomozygous943964897