chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2066910606691061G-43GENIChomozygous45400169
2066910826691083CA50GENIChomozygous45400171
2066910876691088TC48GENIChomozygous45400173
2066911606691161GA40GENIChomozygous45400175
2066925096692510AAT38GENIChomozygous45400177
2066926256692626CT60GENIChomozygous45400179
2066928076692808GA41GENIChomozygous45400182
2066928686692878TGTGTGTGGT----------22GENIChomozygous45400184
2066928716692876GTGTG-----18GENICheterozygous45400186
2066928756692876G-18GENICpossibly homozygous45400188
2066929796692980AT71GENIChomozygous45400190
2066931676693168AG54GENIChomozygous45400192
2066933546693355AAT27GENIChomozygous45400194
2066934116693412GGTT9GENICpossibly homozygous45400198
2066934746693475TA26GENICpossibly homozygous45400200
2066935066693507A-34GENIChomozygous45400202
2066937736693774GA63GENIChomozygous45400204
2066938606693861GT54GENIChomozygous45400206
2066941026694103CG63GENIChomozygous45400208
2066941256694126CT64GENICpossibly homozygous45400210
2066948436694844AT47GENIChomozygous45400212
2066950476695048TC35GENIChomozygous45400214
2066951006695101GA31GENICpossibly homozygous45400216
2066951206695121TC30GENIChomozygous45400219
2066951316695143ACACACACACAC------------12GENIChomozygous45400221
2066952246695225CCA38GENICpossibly homozygous45400223