chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117989279117989280TC17GENIChomozygous145491151
4117989788117989789G20GENIChomozygous145444948
4117990227117990228TG16GENIChomozygous145491152
4117993009117993022TTTTTCTTTTTTT14GENIChomozygous145444949
4117993754117993755CT9GENIChomozygous145491153
4117993869117993870TC19GENIChomozygous145491154
4117994170117994171GT18GENIChomozygous145491155
4117995528117995529GA17GENIChomozygous145491156
4117993186117993186TTAG26GENIChomozygous136911178
4117993754117993755C9GENICheterozygous404396482
4117996725117996731TGTTTG16GENIChomozygous145444950
4117996732117996732CC16GENIChomozygous145444951
4117998594117998595CA28GENIChomozygous145491157
4117999017117999018CA18GENIChomozygous145491158
4117999212117999213GA24GENIChomozygous145491159
4118000854118000855CT16GENIChomozygous145491160
4118002040118002040GATGA18GENIChomozygous145444952
4118002183118002184CT31GENIChomozygous145491161
4118002636118002637TC40GENIChomozygous137191664
4118002924118002925G22GENIChomozygous145444953
4118003609118003610TA15GENIChomozygous145491162
4118004252118004253GC28GENIChomozygous145491163
4118005950118005951AG32GENIChomozygous145491164