chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2238107169238107170AG40GENIChomozygous110326149
2238107530238107531TC49GENICpossibly homozygous110326151
2238107624238107625AG53GENIChomozygous110326153
2238108576238108577AT69GENICpossibly homozygous110326155
2238108718238108719AG49GENIChomozygous110326157
2238108742238108743TC59GENIChomozygous110326159
2238108756238108757CT60GENICpossibly homozygous110326161
2238108774238108775TC63GENIChomozygous110326163
2238109297238109298GA59GENIChomozygous110326165
2238109391238109392CT55GENIChomozygous110326167
2238109503238109504CT32GENICpossibly homozygous110326169
2238109504238109505AG34GENICpossibly homozygous110326171
2238109668238109669GC70GENIChomozygous110326173