chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
724880712488072CT8GENIChomozygous115545271
724880762488077GC8GENIChomozygous115545273
724905922490593C22GENIChomozygous128432151
724906032490604GT23GENIChomozygous115545283
724906092490609T23GENIChomozygous128432152
724906292490630CT24GENIChomozygous115545285
724906602490661C19GENIChomozygous128432153
724906622490663C19GENIChomozygous128432154
724906672490667G19GENIChomozygous128432155
724906752490676G22GENIChomozygous128432156
724906802490681G22GENIChomozygous128432157
724906872490687C23GENIChomozygous128432158
724906912490691G25GENIChomozygous128432159
724906962490697G25GENIChomozygous128432160
724906992490700TA25GENIChomozygous116311229
724907112490712GC25GENIChomozygous118338012
724907122490713CA24GENIChomozygous118338015
724907182490719GT24GENIChomozygous118338018
724907192490720TG24GENIChomozygous118530931
724907372490738G23GENIChomozygous128432161
724907422490743C22GENIChomozygous128432162
724907832490784C2GENIChomozygous128432163
724907872490788G2GENIChomozygous128432164
724907932490794G2GENIChomozygous128432165
724908222490822T2GENIChomozygous128432166
724908372490838G2GENIChomozygous128432167
724908502490851T2GENIChomozygous128432168
724908672490868T2GENIChomozygous128432169