chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266453151266453152AC10GENIChomozygous934165188
1266455573266455574AC24GENIChomozygous934165189
1266455909266455910GT24GENIChomozygous934165190
1266456093266456094AG20GENIChomozygous934165191
1266456616266456617AG21GENIChomozygous934165192
1266456642266456643AG22GENIChomozygous934165193
1266456904266456905GA21GENIChomozygous934165194
1266456977266456978AG18GENIChomozygous934165195
1266457931266457932GA19GENIChomozygous934165196
1266458125266458126TC24GENIChomozygous934165197
1266458150266458151GA26GENIChomozygous934165198
1266458174266458175GA24GENIChomozygous934165199
1266458361266458362CG15GENIChomozygous934165200
1266458398266458399GA22GENIChomozygous934165201
1266458590266458591AG25GENIChomozygous934165202
1266458673266458674CT27GENIChomozygous934165203
1266458945266458946GA22GENIChomozygous934165204
1266459225266459226CT23GENIChomozygous934165205
1266459357266459358AG17GENIChomozygous934165206
1266459377266459378TC15GENIChomozygous934165207
1266459505266459506CT24GENIChomozygous934165208
1266460080266460081TC23GENIChomozygous934165209
1266460290266460291CT27GENIChomozygous934165210
1266460383266460384TC23GENIChomozygous934165211
1266460510266460511GA17GENIChomozygous934165212
1266460616266460617TG23GENIChomozygous934165213
1266460641266460642AG27GENIChomozygous934165214
1266460759266460760TC32GENIChomozygous934165215
1266460885266460886AG14GENIChomozygous934165216
1266460921266460922CT25GENIChomozygous934165217
1266461272266461273CT36GENIChomozygous934165218
1266461367266461368CT17GENIChomozygous934165219
1266461924266461925GA15GENIChomozygous934165220
1266462026266462027CA7GENIChomozygous934165221
1266462028266462029TG8GENIChomozygous934165222
1266462128266462129CT18GENIChomozygous934165223
1266462590266462591TC13GENIChomozygous934165224
1266462736266462737CT21GENIChomozygous934165225
1266462740266462741CT21GENIChomozygous934165226
1266462990266462991AG26GENIChomozygous934165227
1266463178266463179GA22GENIChomozygous934165228