chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43122855331228554TG39GENICheterozygous774925161
43122857131228572GA56GENICpossibly homozygous774925162
43122858231228583AG67GENICheterozygous774925163
43122859931228600GC78GENICheterozygous774925164
43122861431228615AC87GENICheterozygous774925165
43122863931228640TC101GENICheterozygous774925166
43122866031228661GA114GENICheterozygous774925167
43122867831228679CT106GENICheterozygous774925168
43122873031228731AT84GENICheterozygous774925169
43122874731228748CT87GENICheterozygous774925170
43122875731228758GC71GENICheterozygous774925171
43122875931228760CT73GENICheterozygous774925172
43122877631228777AG74GENICheterozygous774925173
43122879131228792CA70GENICheterozygous774925174
43122881131228812GA69GENICheterozygous774925175
43122896931228970GA44GENICheterozygous774925176
43122917531229176CA49GENICheterozygous774925177
43122929031229291TA49GENICheterozygous774925178
43122935331229354AG89GENICheterozygous774925179
43122936531229366AC95GENICheterozygous774925180
43122938131229382GT100GENICheterozygous774925181
43122939031229391TA102GENICheterozygous774925182
43122942231229423GA123GENICheterozygous774925183
43122944031229441CT117GENICheterozygous774925184
43122945131229452GA121GENICheterozygous774925185
43122949931229500GT144GENICheterozygous774925186
43122951831229519AG143GENICheterozygous774925187
43122956031229561CT115GENICheterozygous774925188
43122957231229573TG110GENICheterozygous774925189
43122960031229601CG81GENICheterozygous774925190
43122960331229604AG78GENICheterozygous774925191
43122960531229606AC77GENICheterozygous774925192
43122960831229609CT77GENICheterozygous774925193
43122961731229618AG80GENICheterozygous774925194
43122961831229619CT80GENICheterozygous774925195
43122962231229623AG79GENICheterozygous774925196
43122964531229646GC65GENICheterozygous774925197
43122964731229648AC66GENICheterozygous774925198