chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
724905922490593C42GENIChomozygous128432151
724906032490604GT39GENIChomozygous115545283
724906092490609T35GENIChomozygous128432152
724906292490630CT62GENIChomozygous115545285
724906602490661C49GENIChomozygous128432153
724906622490663C49GENIChomozygous128432154
724906672490667G47GENIChomozygous128432155
724906752490676G44GENIChomozygous128432156
724906802490681G44GENIChomozygous128432157
724906872490687C48GENIChomozygous128432158
724906912490691G46GENIChomozygous128432159
724906962490697G46GENIChomozygous128432160
724906992490700TA47GENIChomozygous116311229
724907112490712GC49GENIChomozygous118338012
724907122490713CA49GENIChomozygous118338015
724907182490719GT50GENIChomozygous118338018
724907192490720TG51GENIChomozygous118530931
724907372490738G56GENIChomozygous128432161
724907422490743C58GENIChomozygous128432162
724907832490784C55GENIChomozygous128432163
724907872490788G53GENIChomozygous128432164
724907932490794G9GENIChomozygous128432165
724908672490868T9GENIChomozygous128432169
724908222490822T9GENIChomozygous128432166
724908372490838G9GENIChomozygous128432167
724908502490851T9GENIChomozygous128432168