chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
22798451727984518AT22GENIChomozygous109662154
22798474127984742GC28GENIChomozygous109662156
22798482927984830GC17GENIChomozygous109662158
22798572327985724TC8GENIChomozygous109662160
22798599627985997AG15GENIChomozygous109662164
22798600127986002AC14GENIChomozygous109662166
22798647227986473TC39GENIChomozygous109662168
22798695527986956AG35GENIChomozygous109662170
22798715127987152TC28GENIChomozygous109662172
22798721327987214GA31GENIChomozygous109662174
22798811627988117GA12GENIChomozygous109662182
22798741527987416AG26GENIChomozygous109662176
22798783827987839AG30GENIChomozygous109662178
22798808927988090GA16GENIChomozygous109662180
22798819327988194TA12GENIChomozygous109662184
22798825227988253CT14GENIChomozygous109662186
22798836627988367TC31GENIChomozygous109662188
22798840827988409CG23GENIChomozygous109662190
22798908627989087CT29GENIChomozygous109662192
22799029627990297CT31GENIChomozygous109662194
22799070427990705GA8GENIChomozygous109662196
22799099727990998TC27GENIChomozygous109662198
22799170127991702GA29GENIChomozygous109662200
22799244327992444AG17GENIChomozygous109662208
22799251427992515AC30GENIChomozygous109662210
22799270327992704TC35GENIChomozygous109662212
22799281027992811GA26GENIChomozygous109662214
22799300027993001AG17GENIChomozygous109662216
22799487827994879CG13GENIChomozygous109662218