chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207391510207391511TC24GENICheterozygous925975177
2207392115207392116TC19GENICheterozygous925975178
2207399526207399529TGT---8GENICheterozygous926082929
2207401532207401533TC5GENICheterozygous925975179
2207404637207404638TA17GENICheterozygous925975180
2207405115207405116CT35GENICheterozygous925975181
2207405228207405229AG54GENICheterozygous925975182
2207406084207406085AG32GENICheterozygous925975183
2207406284207406285AG37GENICheterozygous925975184
2207408740207408741GA23GENICheterozygous925975185
2207410892207410893TC7GENICheterozygous925975186
2207411151207411152TG49GENICheterozygous925975187
2207412016207412017TC34GENICheterozygous925975188
2207412023207412024CA37GENICheterozygous925975189
2207412049207412050GA30GENICheterozygous925975190
2207413599207413600CT39GENICheterozygous925975191
2207415980207415981GA37GENICheterozygous925975192
2207417935207417936A-18GENICheterozygous926082930
2207419362207419363GA11GENICheterozygous925975193
2207419413207419414GA8GENICheterozygous925975194
2207419483207419484CT7GENICheterozygous925975195
2207422891207422892TTG27GENICheterozygous926082931
2207423030207423031TC28GENICheterozygous925975196
2207423580207423581AC31GENICheterozygous925975197