chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
22798435927984360TC8GENIChomozygous109662152
22798451727984518AT14GENIChomozygous109662154
22798474127984742GC12GENIChomozygous109662156
22798482927984830GC11GENIChomozygous109662158
22798572327985724TC18GENIChomozygous109662160
22798599627985997AG11GENIChomozygous109662164
22798600127986002AC8GENIChomozygous109662166
22798647227986473TC10GENIChomozygous109662168
22798695527986956AG8GENIChomozygous109662170
22798715127987152TC17GENIChomozygous109662172
22798721327987214GA23GENIChomozygous109662174
22798741527987416AG14GENIChomozygous109662176
22798783827987839AG8GENIChomozygous109662178
22798808927988090GA24GENIChomozygous109662180
22798811627988117GA11GENIChomozygous109662182
22798819327988194TA10GENIChomozygous109662184
22798825227988253CT22GENIChomozygous109662186
22798836627988367TC24GENIChomozygous109662188
22798840827988409CG19GENIChomozygous109662190
22798908627989087CT21GENIChomozygous109662192
22799029627990297CT12GENIChomozygous109662194
22799070427990705GA9GENIChomozygous109662196
22799099727990998TC11GENIChomozygous109662198
22799170127991702GA28GENIChomozygous109662200
22799244327992444AG21GENIChomozygous109662208
22799251427992515AC13GENIChomozygous109662210
22799270327992704TC19GENIChomozygous109662212
22799281027992811GA23GENIChomozygous109662214
22799300027993001AG15GENIChomozygous109662216
22799487827994879CG13GENIChomozygous109662218
22799321527993216AT4GENICheterozygous125638184
22799810127998102AG14GENICheterozygous109662222
22800026328000264CT4GENIChomozygous109662224