chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1204622793204622794CT19GENICpossibly homozygous134182151
1204651136204651137G22GENIChomozygous127476178
1204650674204650674T23GENIChomozygous127476175
1204650676204650676C23GENIChomozygous127476176
1204650707204650708C20GENIChomozygous127476177
1204651161204651162C29GENIChomozygous127476179
1204651166204651167G29GENIChomozygous127476180
1204651195204651196C32GENIChomozygous127476181
1204651199204651200C32GENIChomozygous127476182
1204651217204651218T32GENIChomozygous127476183
1204651226204651227G32GENIChomozygous127476184
1204651231204651232C31GENIChomozygous127476185
1204651257204651258C35GENIChomozygous127476186
1204651291204651292T32GENIChomozygous127476187
1204651316204651316T28GENIChomozygous127476188
1204651406204651406T17GENIChomozygous127476189
1204651429204651429A17GENIChomozygous127476190
1204694638204694640CC20GENIChomozygous127476191