chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266257617266257618GA39GENIChomozygous806126198
1266259480266259481TG54GENIChomozygous806126199
1266259955266259956TC49GENIChomozygous806126200
1266260071266260072AC73GENIChomozygous806126201
1266260704266260705GA40GENICpossibly homozygous806126202
1266260846266260847TA35GENIChomozygous806126203
1266261396266261397GC50GENIChomozygous806126204
1266262051266262052TC25GENICpossibly homozygous806126205
1266262303266262304AG44GENIChomozygous806126206
1266262580266262581CT49GENIChomozygous806126207
1266263068266263069CA52GENICpossibly homozygous806126208
1266264337266264338TA57GENIChomozygous806126209
1266264589266264590AG48GENIChomozygous806126210
1266265228266265229AG37GENIChomozygous806126211
1266266414266266415GT24GENIChomozygous806126212
1266266712266266713CT50GENIChomozygous806126213
1266267954266267955TC37GENIChomozygous806126214
1266268309266268310GA48GENICpossibly homozygous806126215
1266270325266270326AG28GENIChomozygous806126216