chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2041679544167955CG43GENIChomozygous109389768
2041679814167982TC42GENIChomozygous109233193
2041682964168297CT63GENIChomozygous109389769
2041690294169030CT31GENIChomozygous109233196
2041690304169031AG30GENIChomozygous109233197
2041690624169063AC25GENIChomozygous109233198
2041690804169081CT27GENIChomozygous109233199
2041691244169125AC28GENIChomozygous109233200
2041692954169296CT22GENIChomozygous109389770
2041693484169349CT19GENIChomozygous109233206
2041693824169383GA22GENIChomozygous109389771
2041695224169523CA25GENIChomozygous109233207
2041699804169981TC72GENIChomozygous109389772
2041700064170007CT60GENIChomozygous109389773
2041702794170280TC48GENIChomozygous109233212
2041702814170282CA47GENIChomozygous109233213
2041703344170335AG68GENIChomozygous109233215
2041704134170414AG83GENIChomozygous109233216
2041704694170470TG56GENIChomozygous109389774
2041690794169080CA27GENIChomozygous109547412
2041695474169548CT24GENIChomozygous109547413
2041697074169708GA34GENIChomozygous109547414
2041697244169725AT36GENIChomozygous109547415
2041691904169191TC30GENIChomozygous109296021