chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
22798435927984360TC7GENIChomozygous109662152
22798451727984518AT16GENIChomozygous109662154
22798474127984742GC8GENIChomozygous109662156
22798482927984830GC18GENIChomozygous109662158
22798572327985724TC20GENIChomozygous109662160
22798599627985997AG16GENICheterozygous109662164
22798600127986002AC13GENICheterozygous109662166
22798647227986473TC20GENIChomozygous109662168
22798695527986956AG25GENIChomozygous109662170
22798715127987152TC15GENIChomozygous109662172
22798721327987214GA21GENIChomozygous109662174
22798741527987416AG19GENIChomozygous109662176
22798783827987839AG14GENIChomozygous109662178
22798808927988090GA16GENIChomozygous109662180
22798811627988117GA9GENIChomozygous109662182
22798819327988194TA11GENIChomozygous109662184
22798825227988253CT18GENIChomozygous109662186
22798836627988367TC22GENIChomozygous109662188
22798840827988409CG16GENIChomozygous109662190
22798908627989087CT18GENIChomozygous109662192
22799029627990297CT16GENIChomozygous109662194
22799070427990705GA14GENIChomozygous109662196
22799072727990728AG9GENIChomozygous125565618
22799099727990998TC18GENIChomozygous109662198
22799170127991702GA8GENIChomozygous109662200
22799244327992444AG25GENIChomozygous109662208
22799251427992515AC15GENIChomozygous109662210
22799270327992704TC16GENIChomozygous109662212
22799281027992811GA21GENIChomozygous109662214
22799300027993001AG23GENIChomozygous109662216
22799487827994879CG13GENIChomozygous109662218
22799810127998102AG11GENIChomozygous109662222
22800026328000264CT4GENIChomozygous109662224